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  • 1.
    Anderson, Emma K.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kamińska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    Chartkunchand, Kiattichart C.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Eklund, Gustav
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. University of Innsbruck, Austria.
    Hansen, K.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Decays of excited silver-cluster anions Ag-n, n=4 to 7, in the Double ElectroStatic Ion Ring ExpEriment2018Inngår i: Physical Review A: covering atomic, molecular, and optical physics and quantum information, ISSN 2469-9926, E-ISSN 2469-9934, Vol. 98, nr 2, artikkel-id 022705Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Spontaneous decays of small, hot silver-cluster anions Ag-n(-), n = 4-7, have been studied using one of the rings of the Double ElectroStatic Ion Ring ExpEriment (DESIREE). Observation of these decays over very long time scales is possible due to the very low residual gas pressure (similar to 10(-14)) and cryogenic (13 K) operation of DESIREE. The yield of neutral particles from stored beams of Ag-6(-) and Ag-2(-) anions were measured for 100 milliseconds and were found to follow single power-law behavior with millisecond time-scale exponential cutoffs. The Ag-4(-) and Ag-5(-) anions were stored for 60 s and the observed decays show two-component power-law behaviors. We present calculations of the rate constants for electron detachment from and fragmentation of Ag-4(-) and Ag-5(-). In these calculations, we assume that the internal energy distribution of the clusters are flat and with this we reproduce the early steep parts of the experimentally measured decay curves for Ag-4(-) and Ag-5(-) which extends to tens and hundreds of milliseconds, respectively. The fact that the calculations reproduce the early slopes of Ag-4(-) and Ag-5(-), which differ for the two cases, suggests that it is the changes in fragmentation rates with internal cluster energies of Ag-4(-) and Ag-5(-) rather than conditions in the ion source that determine this behavior. Comparisons with the measurements strongly suggest that the neutral particles detected in these time domains originate from Ag-4(-) -> Ag-3(-) + Ag and Ag-5(-) -> Ag-3(-) +Ag-2 fragmentation processes.

  • 2.
    Anderson, Emma K.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt-May, Alice F.
    Najeeb, Punnakayathil K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Eklund, Gustav
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chartkunchand, Kiattichart C.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kaminska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Nascimento, Rodrigo
    Hansen, Klavs
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Fragmentaion and detachemnt of hot silver and copper dimer anionsManuskript (preprint) (Annet vitenskapelig)
  • 3. Aumayr, Friedrich
    et al.
    Ueda, Kiyoshi
    Sokell, Emma
    Schippers, Stefan
    Sadeghpour, Hossein
    Merkt, Frederic
    Gallagher, Thomas F.
    Dunning, F. Barry
    Scheier, Paul
    Eche, Olof
    Kirchner, Tom
    Fritzsche, Stephan
    Surzhykov, Andrey
    Ma, Xinwen
    Rivarola, Roberto
    Fojon, Omar
    Tribedi, Lokesh
    Lamour, Emily
    Lopez-Urrutia, Jose R. Crespo
    Litvinov, Yuri A.
    Shabaev, Vladimir
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schleberger, Marika
    Wilhelm, Richard A.
    Azuma, Toshiyuki
    Boduch, Philippe
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stoehlker, Thomas
    Roadmap on photonic, electronic and atomic collision physics: III. Heavy particles2019Inngår i: Journal of Physics B: Atomic, Molecular and Optical Physics, ISSN 0953-4075, E-ISSN 1361-6455, Vol. 52, nr 17, artikkel-id 171003Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We publish three Roadmaps on photonic, electronic and atomic collision physics in order to celebrate the 60th anniversary of the ICPEAC conference. Roadmap III focusses on heavy particles: with zero to relativistic speeds. Modern theoretical and experimental approaches provide detailed insight into the wide range of many-body interactions involving projectiles and targets of varying complexity ranging from simple atoms, through molecules and clusters, complex biomolecules and nanoparticles to surfaces and crystals. These developments have been driven by technological progress and future developments will expand the horizon of the systems that can be studied. This Roadmap aims at looking back along the road, explaining the evolution of the field, and looking forward, collecting nineteen contributions from leading scientists in the field.

  • 4. Bernard, J.
    et al.
    Montagne, G.
    Bredy, R.
    Terpend-Ordaciere, B.
    Bourgey, A.
    Kerleroux, M.
    Chen, L.
    Schmidt, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Martin, S.
    A ""tabletop"" electrostatic ion storage ring: Mini-Ring2008Inngår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 79, nr 7, s. 75109-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report on the design, construction, and commissioning of a novel electrostatic ion storage ring of small dimensions-in the following referred to as ""Mini-Ring."" Mini-Ring consists of four horizontal parallel-plate deflectors and two conical electrostatic mirrors. Ions are injected through the two deflectors on the injection side and off axis with respect to the conical mirrors which face each other. The first injection deflector, originally at zero voltage, is switched to its set value such that the ions after one turn follow stable trajectories of lengths of roughly 30 cm. This design reduces the number of electrodes necessary to guide the ion beam through the ring in stable orbits. The six elements (deflectors and mirrors) are placed on a common grounded plate-the tabletop. Here, we present the design, ion trajectory simulations, and results of the first test experiments demonstrating the successful room-temperature operation of Mini-Ring at background pressures of 10(-6)-10(-7) mbar.

  • 5. Bernigaud, Virgile
    et al.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Haag, Nicole
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Holm, Anne I. S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Huber, Bernd A.
    Hvelplund, Preben
    Kadhane, Umesh
    Larsen, Mikkel Koefod
    Manil, Bruno
    Nielsen, Steen Bröndsted
    Panja, Subhasis
    Ptasinska, Sylwia
    Rangama, Jimmy
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Streletskii, Alexey V.
    Stöchkel, Kristian
    Worm, Esben S.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Electron capture-induced dissociation of AK dipeptide dications: Influence of ion velocity, crown-ether complexation and collision gas2008Inngår i: International Journal of Mass Spectrometry, ISSN 1387-3806, E-ISSN 1873-2798, Vol. 276, nr 2-3, s. 77-81Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The fragmentation of doubly protonated AK dipeptide ions has been investigated after collisional electron transfer. Electron capture leads to three dominant channels, H loss, NH3 loss, and N–Cα bond breakage to give either c+ or z+ fragment ions. The relative importance of these channels has been explored as a function of ion velocity, the degree of complexation with crown ether, and collision gas. Our results indicate that H loss and NH3 loss are competing channels whereas the probability of N–Cα bond breakage is more or less constant.

  • 6. Berrah, Nora
    et al.
    Fang, Li
    Murphy, Brendan
    Osipov, Timur
    Ueda, Kiyoshi
    Kukk, Edwin
    Feifel, Raimund
    van der Meulen, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Salén, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Larsson, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Richter, Robert
    Prince, Kevin C.
    Bozek, John D.
    Bostedt, Christoph
    Wada, Shin-ichi
    Piancastelli, Maria N.
    Tashiro, Motomichi
    Ehara, Masahiro
    Double-core-hole spectroscopy for chemical analysis with an intense X-ray femtosecond laser2011Inngår i: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 108, nr 41, s. 16912-16915Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Theory predicts that double-core-hole (DCH) spectroscopy can provide a new powerful means of differentiating between similar chemical systems with a sensitivity not hitherto possible. Although DCH ionization on a single site in molecules was recently measured with double-and single-photon absorption, double-core holes with single vacancies on two different sites, allowing unambiguous chemical analysis, have remained elusive. Here we report that direct observation of double-core holes with single vacancies on two different sites produced via sequential two-photon absorption, using short, intense X-ray pulses from the Linac Coherent Light Source free-electron laser and compare it with theoretical modeling. The observation of DCH states, which exhibit a unique signature, and agreement with theory proves the feasibility of the method. Our findings exploit the ultrashort pulse duration of the free-electron laser to eject two core electrons on a time scale comparable to that of Auger decay and demonstrate possible future X-ray control of physical inner-shell processes.

  • 7.
    Bäckström, Erik
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hanstorp, D.
    Hole, Odd Magnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kaminska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    Nascimento, Rodrigo F.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mannervik, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Storing keV negative ions for an hour: The lifetime of the metastable 2P1/2 level in 32S−2015Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 114, nr 14, artikkel-id 143003Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We use a novel electrostatic ion storage ring to measure the radiative lifetime of the upper level in the 3p 5  P 2  o 1/2 →3p 5  P 2  o 3/2   spontaneous radiative decay in S −  32   to be 503±54  sec . This is by orders of magnitude the longest lifetime ever measured in a negatively charged ion. Cryogenic cooling of the storage ring gives a residual-gas pressure of a few times 10 −14   mbar at 13 K and storage of 10 keV sulfur anions for more than an hour. Our experimental results differ by 1.3σ  from the only available theoretical prediction.

  • 8.
    Chartkunchand, Kiattichart C.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kaminska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    Anderson, Emma K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kristiansson, M. K.
    Eklund, Gustav
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hole, Odd Magnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Nascimento, Rodrigo F.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Centro Federal de Educação Tecnológica Celso Suckow da Fonseca, Brazil.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mannervik, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Davis, V. T.
    Neill, P. A.
    Thompson, J. S.
    Hanstorp, D.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Radiative lifetimes of the bound excited states of Pt-2016Inngår i: Physical Review A, ISSN 2469-9926, Vol. 94, nr 3, artikkel-id 032501Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The intrinsic radiative lifetimes of the 5d(10)6s(2)S(1/2) and 5d(9)6s(2) D-2(3/2) bound excited states in the platinum anion Pt- have been studied at cryogenic temperatures at the Double ElectroStatic Ion Ring Experiment (DESIREE) facility at Stockholm University. The intrinsic lifetime of the higher-lying 5d(10)6s S-2(1/2) state was measured to be 2.54 +/- 0.10 s, while only a lifetime in the range of 50-200 ms could be estimated for the 5d(9)6s(2) D-2(3/2) fine-structure level. The storage lifetime of the Pt- ion beam was measured to be a little over 15 min at a ring temperature of 13 K. The present study reports the lifetime of an atomic negative ion in an excited bound state with an electron configuration different from that of the ground state.

  • 9.
    Chartkunchand, Kiattichart C.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Anderson, Emma K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Eklund, Gustav
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kristiansson, Moa K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kamińska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    de Ruette, Nathalie
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Dianion diagnostics in DESIREE: High-sensitivity detection of C-n(2-) from a sputter ion source2018Inngår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 89, nr 3, artikkel-id 033112Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A sputter ion source with a solid graphite target has been used to produce dianions with a focus on carbon cluster dianions, C-n(2-), with n = 7-24. Singly and doubly charged anions from the source were accelerated together to kinetic energies of 10 keV per atomic unit of charge and injected into one of the cryogenic (13 K) ion-beam storage rings of the Double ElectroStatic Ion Ring Experiment facility at Stockholm University. Spontaneous decay of internally hot C-n(2-) dianions injected into the ring yielded C-n(2-) anions with kinetic energies of 20 keV, which were counted with a microchannel plate detector. Mass spectra produced by scanning the magnetic field of a 90 degrees analyzing magnet on the ion injection line reflect the production of internally hot C-7(2-) - C-24(2-) dianions with lifetimes in the range of tens of microseconds to milliseconds. In spite of the high sensitivity of this method, no conclusive evidence of C-6(2-) was found while there was a clear C-7(2-) signal with the expected isotopic distribution. This is consistent with earlier experimental studies and with theoretical predictions. An upper limit is deduced for a C-6(2-) signal that is two orders-of-magnitude smaller than that for C-7(2-). In addition, CnO2- and CnCu2- dianions were detected.

  • 10.
    Chen, Tao
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zhang, Y.
    Rousseau, P.
    Domaracka, A.
    Maclot, S.
    Delaunay, R.
    Adoui, L.
    Huber, B. A.
    Schlatholter, T.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Absolute fragmentation cross sections in atom-molecule collisions: Scaling laws for non-statistical fragmentation of polycyclic aromatic hydrocarbon molecules2014Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 140, nr 22, artikkel-id 224306Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We present scaling laws for absolute cross sections for non-statistical fragmentation in collisions between Polycyclic Aromatic Hydrocarbons (PAH/PAH(+)) and hydrogen or helium atoms with kinetic energies ranging from 50 eV to 10 keV. Further, we calculate the total fragmentation cross sections (including statistical fragmentation) for 110 eV PAH/PAH(+) + He collisions, and show that they compare well with experimental results. We demonstrate that non-statistical fragmentation becomes dominant for large PAHs and that it yields highly reactive fragments forming strong covalent bonds with atoms (H and N) and molecules (C6H5). Thus nonstatistical fragmentation may be an effective initial step in the formation of, e. g., Polycyclic Aromatic Nitrogen Heterocycles (PANHs). This relates to recent discussions on the evolution of PAHNs in space and the reactivities of defect graphene structures.

  • 11.
    Chen, Tao
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rudy, Delaunay
    Domaracka, Alicja
    Micelotta, Elisabetta R.
    Tielens, Alexander G. G. M.
    Rousseau, Patrick
    Adoui, Lamri
    Huber, Bernd A.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Formation of H2 from internally heated polycyclic aromatic hydrocarbons: Excitation energy dependence2015Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 142, nr 14, artikkel-id 144305Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have investigated the effectiveness of molecular hydrogen (H-2) formation from Polycyclic Aromatic Hydrocarbons (PAHs) which are internally heated by collisions with keV ions. The present and earlier experimental results are analyzed in view of molecular structure calculations and a simple collision model. We estimate that H-2 formation becomes important for internal PAH temperatures exceeding about 2200 K, regardless of the PAH size and the excitation agent. This suggests that keV ions may effectively induce such reactions, while they are unlikely due to, e.g., absorption of single photons with energies below the Lyman limit. The present analysis also suggests that H-2 emission is correlated with multi-fragmentation processes, which means that the [PAH-2H](+) peak intensities in the mass spectra may not be used for estimating H-2-formation rates.

  • 12.
    de Ruette, Nathalie
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Dochain, A.
    Launoy, T.
    Nascimento, Rodrigo F.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Centro Federal de Educação Tecnológica Celso Suckow da Fonseca, Brazil.
    Kaminska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Vaeck, N.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Urbain, X.
    Mutual Neutralization of O- with O+ and N+ at Subthermal Collision Energies2018Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 121, nr 8, artikkel-id 083401Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have measured total absolute cross sections for the mutual neutralization (MN) of O- with O+ and N+. A fine resolution (of about 50 meV) in the kinetic energy spectra of the product neutral atoms allows unique identification of the atomic states participating in the mutual neutralization process. Cross sections and branching ratios have also been calculated down to 1 meV center-of-mass collision energy for these two systems, with a multichannel Landau-Zener model and an asymptotic method for the ionic-covalent coupling matrix elements. The importance of two-electron processes in one-electron transfer is demonstrated by the dominant contribution of a core-excited configuration of the nitrogen atom in N+ + O- collisions. This effect is partially accounted for by introducing configuration mixing in the evaluation of coupling matrix elements.

  • 13.
    de Ruette, Nathalie
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Wolf, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Giacomozzi, Linda
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Universität Innsbruck, Austria.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Haag, Nicole
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    DESIREE electrospray ion source test bench and setup for collision induced dissociation experiments2018Inngår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 89, nr 7, artikkel-id 075102Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    In this paper, we give a detailed description of an electrospray ion source test bench and a single-pass setup for ion fragmentation studies at the Double ElectroStatic Ion Ring ExpEriment infrastructure at Stockholm University. This arrangement allows for collision-induced dissociation experiments at the center-of-mass energies between 10 eV and 1 keV. Charged fragments are analyzed with respect to their kinetic energies (masses) by means of an electrostatic energy analyzer with a wide angular acceptance and adjustable energy resolution.

  • 14.
    Fischer, D.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gudmundsson, Magnus
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Berenyi, Zoltan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Haag, Nicole
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Misra, Deepankar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kallberg, A.
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Stochkel, K.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, H. T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Importance of Thomas single-electron transfer in fast p-He collisions2010Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 81, nr 1, s. 12714-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report experimental angular differential cross sections for nonradiative single-electron capture in p-He collisions (p + He -> H + He+) with a separate peak at the 0.47 mrad Thomas scattering angle for energies in the 1.3-12.5 MeV range. We find that the intensity of this peak scales with the projectile velocity as v(P)(-11). This constitutes the first experimental test of the prediction from 1927 by L. H. Thomas [Proc. R. Soc. 114, 561 (1927)]. At our highest energy, the peak at the Thomas angle contributes with 13.5% to the total integrated nonradiative single-electron capture cross section.

  • 15.
    Gatchell, Michael
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rousseau, P.
    Domaracka, A.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chesnel, J. Y.
    Mery, A.
    Maclot, S.
    Adoui, L.
    Huber, B. A.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Ions colliding with mixed clusters of C-60 and coronene: Fragmentation and bond formation2014Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 90, nr 2, artikkel-id 022713Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have studied collisions between 22.5 keV He2+ ions and mixed clusters [(C-60)(m)(C24H12)(n)] of m C-60 and n coronene molecules where m and n range up to about ten. Surprisingly, the cluster fragmentation behavior in distant collisions is dramatically different for pure coronene clusters (m = 0) and clusters containing a single C-60 molecule (m = 1). In the latter case, the clusters may be ionized without also being fragmented on the experimental time scale of tens of microseconds. This does not occur for pure coronene clusters, but is a main characteristic of pure fullerene clusters. For ion trajectories penetrating the mixed cluster, we observe covalent bond formations between C-59 or C-58 and C-60, but not between coronene fragments and C-60, or between C-60 fragments and coronene. These results are explained by means of classical molecular dynamics simulations of collisions inside the fragmenting mixed clusters.

  • 16.
    Gatchell, Michael
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Andler, Guillermo
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Brännholm, Lars
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Bäckström, Erik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Geppert, Wolf
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Halldén, Per
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hanstorp, Dag
    Hellberg, Fredrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Larsson, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Leontein, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Liljeby, Leif
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mannervik, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Paal, Andras
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rensfelt, Karl-Gunnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Seitz, Fabian
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    First results from the Double ElectroStatic Ion-Ring ExpEriment, DESIREE2014Inngår i: Journal of Physics, Conference Series, ISSN 1742-6588, E-ISSN 1742-6596, Vol. 488, s. 092003-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have stored the first beams in one of the rings of the double electrostatic ion-storage ring, DESIREE at cryogenic and at room temperature conditions. At cryogenic operations the following parameters are found. Temperature; T= 13K, pressure; p <10(-13) mbar, initial number of stored ions; N > 10(7) and storage lifetime of a C-2(-) beam; tau = 450 S.

  • 17.
    Gatchell, Michael
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Brännholm, Lars
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Bäckström, Erik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Leontein, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hanstorp, D.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Liljeby, Leif
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hellberg, Fredrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mannervik, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Larsson, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Geppert, Wolf D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rensfelt, Karl-Gunnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Danared, Håkan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. European Spallation Source, Sweden.
    Paál, Andras
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Masuda, Masaharu
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Halldén, Per
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Andler, Guillermo
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källersjö, Gunnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Weimer, Jan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hansen, K.
    Hartman, H.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Commissioning of the DESIREE storage rings - a new facility for cold ion-ion collisions2014Inngår i: Journal of Physics, Conference Series, ISSN 1742-6588, E-ISSN 1742-6596, Vol. 488, s. 012040-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report on the ongoing commissioning of the Double ElectroStatic Ion Ring ExpEriment, DESIREE, at Stockholm University. Beams of atomic carbon anions (C-) and smaller carbon anion molecules (C-2(-), C-3(-), C-4(-) etc.) have been produced in a sputter ion source, accelerated to 10 keV or 20 keV, and stored successfully in the two electrostatic rings. The rings are enclosed in a common vacuum chamber cooled to below 13 Kelvin. The DESIREE facility allows for studies of internally relaxed single isolated atomic, molecular and cluster ions and for collision experiments between cat-and anions down to very low center-of-mass collision energies (meV scale). The total thermal load of the vacuum chamber at this temperature is measured to be 32 W. The decay rates of stored ion beams have two components: a non-exponential component caused by the space charge of the beam itself which dominates at early times and an exponential term from the neutralization of the beam in collisions with residual gas at later times. The residual gas limited storage lifetime of carbon anions in the symmetric ring is over seven minutes while the 1/e lifetime in the asymmetric ring is measured to be about 30 seconds. Although we aim to improve the storage in the second ring, the number of stored ions are now sufficient for many merged beams experiments with positive and negative ions requiring milliseconds to seconds ion storage.

  • 18.
    Gatchell, Michael
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Aarhus University, Denmark.
    de Ruette, Nathalie
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Giacomozzi, Linda
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Nascimento, Rodrigo F.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Wolf, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Anderson, Emma K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Delaunay, R.
    Vizcaino, V.
    Rousseau, P.
    Adoui, L.
    Huber, B. A.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Failure of hydrogenation in protecting polycyclic aromatic hydrocarbons from fragmentation2015Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 92, nr 5, artikkel-id 050702Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A recent study of soft x-ray absorption in native and hydrogenated coronene cations, C24H12+m + m = 0-7, led to the conclusion that additional hydrogen atoms protect (interstellar) polycyclic aromatic hydrocarbon (PAH) molecules from fragmentation [Reitsma et al., Phys. Rev. Lett. 113, 053002 (2014)]. The present experiment with collisions between fast (30-200 eV) He atoms and pyrene (C16H10+m +, m = 0, 6, and 16) and simulations without reference to the excitation method suggests the opposite. We find that the absolute carbon-backbone fragmentation cross section does not decrease but increases with the degree of hydrogenation for pyrene molecules.

  • 19.
    Gatchell, Michael
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rousseau, P.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kulyk, Kostiantyn
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chesnel, J. Y.
    Domaracka, A.
    Méry, A.
    Maclot, S.
    Adoui, L.
    Stöchkel, K.
    Hvelplund, P.
    Wang, Y.
    Alcamí, M.
    Huber, B. A.
    Martín, F.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Non-statistical fragmentation of PAHs and fullerenes in collisions with atoms2014Inngår i: International Journal of Mass Spectrometry, ISSN 1387-3806, E-ISSN 1873-2798, Vol. 365, s. 260-265Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Non-statistical fragmentation processes may be important when Polycyclic Aromatic Hydrocarbon molecules (PAHs), fullerenes, or other large complex molecules collide with atoms and atomic ions. For collisions with hydrogen or helium this occurs for center-of-mass energies between a few tens to a few hundreds of electron volts and typically results in losses of single atoms. In such processes one forms much more reactive fragments than in statistical fragmentation, which instead are dominated by losses of C2- or C2H2-molecules (H-atoms) from fullerenes and PAHs, respectively. An enhanced reactivity has recently been demonstrated for van der Waals clusters of C60 molecules where prompt knockouts of single C-atoms from one of the fullerenes yield highly reactive C59+ fragments, which easily form covalent bonds with a C60 molecule inside the clusters

  • 20.
    Gatchell, Michael
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Seitz, Fabian
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stocket, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Lawicki, A.
    Rangama, J.
    Rousseau, P.
    Capron, M.
    Maclot, S.
    Maisonny, R.
    Domaracka, A.
    Adoui, L.
    Mery, A.
    Chesnel, J-Y
    Manil, B.
    Huber, B. A.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Ions colliding with polycyclic aromatic hydrocarbon clusters2013Inngår i: Physica Scripta, ISSN 0031-8949, E-ISSN 1402-4896, Vol. T156, s. 014062-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have measured the ionization and fragmentation of polycyclic aromatic hydrocarbon (PAH) molecules and their clusters. We find that PAH clusters containing up to roughly 100 individual molecules fragment strongly following collisions with keV ions in low or high charge states (q). For both types of collisions, singly charged PAH molecules are found to be the dominant products but for very different reasons. A high-q ion projectile charge leads to strong multiple ionization of the PAH clusters and subsequent Coulomb explosions. A low-q ion projectile charge often leads to single ionization but stronger internal heating and long evaporation sequences with a singly charged PAH monomer as the end product. We have developed a Monte Carlo method for collision-induced heating of PAH clusters and present an evaporation model where the clusters cool slowly as most of the internal energies are stored in intramolecular vibrations and not in molecule-molecule vibrations.

  • 21.
    Giacomozzi, Linda
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    D'Angelo, Giovanna
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Universidad Autónoma de Madrid, Spain.
    Diaz-Tendero, S.
    de Ruette, Nathalie
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alcami, M.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Decay pathways for protonated and deprotonated adenine molecules2019Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 151, nr 4, artikkel-id 044306Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have measured fragment mass spectra and total destruction cross sections for protonated and deprotonated adenine following collisions with He at center-of-mass energies in the 20-240 eV range. Classical and ab initio molecular dynamics simulations are used to provide detailed information on the fragmentation pathways and suggest a range of alternative routes compared to those reported in earlier studies. These new pathways involve, for instance, losses of HNC molecules from protonated adenine and losses of NH2 or C3H2N2 from deprotonated adenine. The present results may be important to advance the understanding of how biomolecules may be formed and processed in various astrophysical environments.

  • 22.
    Giacomozzi, Linda
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    D'Angelo, Giovanna
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Diaz-Tendero, Sergio
    de Ruette, Nathalie
    Stockett, Mark
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alcamí, Manuel
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Decay pathways for protonated and deprotonated Adenine moleculesManuskript (preprint) (Annet vitenskapelig)
  • 23.
    Giacomozzi, Linda
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    de Ruette, Nathalie
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Wolf, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    D'Angelo, Giovanna
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Universidade do Porto, Portugal; Universidad Autónoma de Madrid, Spain.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Knockout driven fragmentation of porphyrins2017Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 19, nr 30, s. 19750-19755Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have studied collisions between tetraphenylporphyrin cations and He or Ne at center-of-mass energies in the range 50-110 eV. The experimental results were interpreted in view of density functional theory calculations of dissociation energies and classical molecular dynamics simulations of how the molecules respond to the He/Ne impact. We demonstrate that prompt atom knockout strongly contributes to the total destruction cross sections. Such impulse driven processes typically yield highly reactive fragments and are expected to be important for collisions with any molecular system in this collision energy range, but have earlier been very difficult to isolate for biomolecules.

  • 24.
    Gudmundsson, Magnus
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Fischer, D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Haag, N.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, H. A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Misra, Deepankar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt-Boecking, H.
    Schuch, Reinhold
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schoeffler, M.
    Stochkel, K.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Angular scattering in fast ion-atom electron transfer collisions: projectile wave diffraction and Thomas mechanisms2010Inngår i: Journal of Physics B: Atomic, Molecular and Optical Physics, ISSN 0953-4075, E-ISSN 1361-6455, Vol. 43, nr 18, s. 185209-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report experimental angular differential cross sections for double-electron capture in He2+ + He collisions and single-electron capture in H+ + He collisions for the 1.3-12.5 MeV kinetic energy range. In all cases, the total cross sections are dominated by forward scattering peaks in d sigma/d Omega. The shapes and widths (but not the magnitudes) of these peaks are very similar for all energies and for capture of one or two electrons corresponding also to our measured linear increases in the transverse momentum transfers with increasing projectile velocities. These observations may be ascribed to diffraction limitations which are connected to electron transfer probabilities P(b) which are significant in limited regions of b only. For the H+ + He single-electron capture we observe two additional maxima in the angular differential cross sections. We conclude that while the secondary maxima at similar to 0.5 mrad probably have large contributions from the Thomas proton-electron-nucleus scattering mechanism, the third maxima at similar to 0.75 mrad are most likely mainly due to projectile de Broglie wave diffraction.

  • 25.
    Haag, Nicole
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Holm, Anne I. S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Brøndsted Nielsen, Steen
    Hvelplund, Preben
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Electron capture induced dissociation of doubly protonated pentapeptides: Dependence on molecular structure and charge separation2011Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 134, nr 3, s. 035102-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have studied electron capture induced dissociation of a set of doubly protonated pentapeptides, all composed of one lysine (K) and either four glycine (G) or four alanine (A) residues, as a function of the sequence of these building blocks. Thereby the separation of the two charges, sequestered on the N-terminal amino group and the lysine side chain, is varied. The characteristic cleavage of N–Cα bonds is observed for all peptides over the whole backbone length, with the charge carrying fragments always containing K. The resulting fragmentation patterns are very similar if G is replaced by A. In the case of [XKXXX+2H]2+ (X=A or G), a distinct feature is observed in the distribution of backbone cleavage fragments and the probability for ammonia loss is drastically reduced. This may be due to an isomer with an amide oxygen as protonation site giving rise to the observed increase in breakage at a specific site in the molecule. For the other peptides, a correlation with the distance between amide oxygen and the charge at the lysine side chain has been found. This may be an indication that it is only the contribution from this site to the charge stabilization of the amide π* orbitals which determines relative fragment intensities. For comparison, complexes with two crown ether molecules have been studied as well. The crown ether provides a shielding of the charge and prevents the peptide from folding and internal hydrogen bonding, which leads to a more uniform fragmentation behavior.

  • 26.
    Haag, Nicole
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Liu, Bo
    Brøndsted Nielsen, Steen
    Zettergren, Henning
    Hvelplund, Preben
    Manil, Bruno
    Huber, Bernd A.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Collisions with biomolecules embedded in smallwater clusters2009Konferansepaper (Fagfellevurdert)
    Abstract [en]

    We have studied fragmentation of water embedded adenosine 5’-monophosphate(AMP) anions after collisions with neutral sodium atoms. At a collision energy of 50 keV,loss of water molecules from the collisionally excited cluster ions is the dominant process andfragmentation of the AMP itself is almost completely prohibited if the number of attachedwater molecules is larger than 13. However, regardless of the initial number of water moleculesattached to the ion, capture of an electron, i.e. formation of a dianion, always leads to loss ofa single hydrogen atom accompanied by evaporation of water molecules. This damaging effectbecomes more important as the size of the water cluster increases, which is just the oppositeto the protective behavior observed for collision induced dissociation (CID) without electrontransfer. For both cases, the loss of water molecules within the experimental time frame isqualitatively well described by means of a common model of an evaporative ensemble. Thesesimulations, however, indicate that characteristically different distributions of internal energyare involved in CID and electron capture induced dissociation.

  • 27. Hansen, K.
    et al.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Aarhus University, Denmark.
    Kaminska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    Nascimento, Rodrigo F.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Centro Federal de Educacao Tecnologica Celso Suckow da Fonseca, Brazil.
    Anderson, Emma K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chartkunchand, Kiattichart C.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Eklund, Gustav
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Spontaneous decay of small copper-cluster anions Cu-n(-) (n=3-6), on long time scales2017Inngår i: Physical Review A, ISSN 2469-9926, Vol. 95, nr 2, artikkel-id 022511Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have measured the spontaneous neutral particle emission from copper-cluster anions ( Cu-n(-), n = 3-6) stored at cryogenic temperatures in one of the electrostatic ion storage rings of the Double ElectroStatic Ion Ring ExpEriment facility at Stockholm University. The measured rate of emission from the stored Cu-3(-) ions follows a single power-law decay for about 1 ms but then decreases much more rapidly with time. The latter behavior may be due to a decrease in the density of available final states in Cu-3 as the excitation energies of the decaying ions approach the electron detachment threshold. The emissions from Cu-4(-), Cu-5(-), and Cu-6(-) are well described by sums of two power laws that are quenched by radiative cooling of the stored ions with characteristic times between a few and hundreds of milliseconds. We relate these two-component behaviors to populations of stored ions with higher and lower angular momenta. In a separate experiment, we studied the laser-induced decay of Cu-6(-) ions that were excited by 1.13- or 1.45-eV photons after 46 ms of storage.

  • 28.
    Holm, Anne I. S.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Seitz, Fabian
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosen, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Lawicki, A.
    Rangama, J.
    Rousseau, P.
    Capron, M.
    Maisonny, R.
    Adoui, L.
    Mery, A.
    Manil, B.
    Huber, B. A.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Ions Colliding with Cold Polycyclic Aromatic Hydrocarbon Clusters2010Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 105, nr 21, s. 213401-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report the first experimental study of ions interacting with clusters of polycyclic aromatic hydrocarbon (PAH) molecules. Collisions between 11.25 keV He-3(+) or 360 keV Xe-129(20+) and weakly bound clusters of one of the smallest PAH molecules, anthracene, show that C14H10 clusters have much higher tendencies to fragment in ion collisions than other weakly bound clusters. The ionization is dominated by peripheral collisions in which the clusters, very surprisingly, are more strongly heated by Xe20+ collisions than by He+ collisions. The appearance size is k = 15 for [C14H10](k)(2+).

  • 29.
    Johansson, Henrik A. B.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Holm, Anne I. S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Haag, Nicole
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Brøndsted Nielsen, S.
    Wyer, J. A.
    Kirketerp, M.-B. S.
    Støchkel, K.
    Hvelplund, P.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Unimolecular dissociation of anthracene and acridine cations: The importance of isomerization barriers for the C2H2 loss and HCN loss channels2011Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 135, s. 084304-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The loss of C2H2 is a low activation energy dissociation channel for anthracene (C14H10) and acridine (C13H9N) cations. For the latter ion another prominent fragmentation pathway is the loss of HCN. We have studied these two dissociation channels by collision induced dissociation experiments of 50 keV anthracene cations and protonated acridine, both produced by electrospray ionization, in collisions with a neutral xenon target. In addition, we have carried out density functional theory calculations on possible reaction pathways for the loss of C2H2 and HCN. The mass spectra display features of multi-step processes, and for protonated acridine the dominant first step process is the loss of a hydrogen from the N site, which then leads to C2H2/HCN loss from the acridine cation. With our calculations we have identified three pathways for the loss of C2H2 from the anthracene cation, with three different cationic products: 2-ethynylnaphthalene, biphenylene, and acenaphthylene. The third product is the one with the overall lowest dissociation energy barrier. For the acridine cation our calculated pathway for the loss of C2H2 leads to the 3-ethynylquinoline cation, and the loss of HCN leads to the biphenylene cation. Isomerization plays an important role in the formation of the non-ethynyl containing products. All calculated fragmentation pathways should be accessible in the present experiment due to substantial energy deposition in the collisions.

  • 30.
    Johansson, Henrik A. B.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Stockholms universitet, Naturvetenskapliga fakulteten, Oskar Klein-centrum för kosmopartikelfysik (OKC).
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Holm, Anne I. S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Seitz, Fabian
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rousseau, P.
    Lawicki, A.
    Capron, M.
    Domaracka, A.
    Lattouf, E.
    Maclot, S.
    Maisonny, R.
    Manil, B.
    Chesnel, J.-Y.
    Adoui, L.
    Huber, B. A.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Ionization and fragmentation of polycyclic aromatic hydrocarbon clusters in collisions with keV ions2011Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 84, nr 4, s. 043201-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report on an experimental study of the ionization and fragmentation of clusters of k polycyclic aromatic hydrocarbon (PAH) molecules using anthracene, C14H10, or coronene, C24H12. These PAH clusters are moderately charged and strongly heated in small impact parameter collisions with 22.5-keV He2+ ions, after which they mostly decay in long monomer evaporation sequences with singly charged and comparatively cold monomers as dominating end products. We describe a simple cluster evaporation model and estimate the number of PAH molecules in the clusters that have to be hit by He2+ projectiles for such complete cluster evaporations to occur. Highly charged and initially cold clusters are efficiently formed in collisions with 360-keV Xe20+ ions, leading to cluster Coulomb explosions and several hot charged fragments, which again predominantly yield singly charged, but much hotter, monomer ions than the He2+ collisions. We present a simple formula, based on density-functional-theory calculations, for the ionization energy sequences as functions of coronene cluster size, rationalized in terms of the classic electrostatic expression for the ionization of a charged conducting object. Our analysis indicates that multiple electron removal by highly charged ions from a cluster of PAH molecules rapidly may become more important than single ionization as the cluster size k increases and that this is the main reason for the unexpectedly strong heating in these types of collisions.

  • 31.
    Kamińska, Magdalena
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    Davis, V. T.
    Hole, Odd Magnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Nascimento, Rodrigo F.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Centro Federal de Educação Tecnológica Celso Suckow da Fonseca, Brazil.
    Chartkunchand, Kiattichart C.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. University of Nevada, USA.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mannervik, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Neill, P. A.
    Thompson, J. S.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hanstorp, D.
    Lifetime of the bound excited level in Ni-2016Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 93, nr 1, artikkel-id 012512Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The intrinsic lifetime of the upper level in the bound-bound 3d(9) 4s(2) D-2(3/2) -> 3d(9) 4s(2) D-2(5/2) radiative transition in Ni- was measured to be 15.1 +/- 0.4 s. The experiment was performed at cryogenic temperatures in one of the ion-beam storage rings of the Double ElectroStatic Ion Ring ExpEriment facility at Stockholm University. The storage lifetime of the Ni- ion beam was measured to be close to 5 min at a ring temperature of 13 K.

  • 32.
    Kulyk, Kostiantyn
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rebrov, Oleksii
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Larsson, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    High-energy collisions of protonated enantiopure amino acids with a chiral target gas2015Inngår i: International Journal of Mass Spectrometry, ISSN 1387-3806, E-ISSN 1873-2798, Vol. 388, s. 59-64Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have studied the fragmentation of the singly protonated L- and D-forms of enantiomerically pure phenylalanine (Phe), tryptophan (Trp), and methionine (Met) in high-energy collisions with chiral and achiral gas targets. (S)-(+)-2-butanol, racemic (+/-)-2-butanol, and argon were used as target gases. At center-of-mass frame collision energy of I key, it was found that all of the ions exhibit common fragmentation pathways which are independent of target chirality. For all projectile ions, the elimination of NH3 and H2O + CO were found to be the main reaction channels. The observed fragmentation patterns were dominated by statistically driven processes. The energy deposited into the ions was found to be sufficient to yield multiple fragment ions, which arise from decomposition via various competitive reaction pathways.

  • 33.
    Kulyk, Kostiantyn
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Wolf, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Universität Innsbruck, Austria.
    Giacomozzi, Linda
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Vegvari, Akos
    Kovalenko, Oleksandr
    de Ruette, Nathalie
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Wendt, Ola
    Zubarev, Roman
    Schmidt, T. Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Collision Induced Dissociation of the retinal chromophore Schiff base from sub-eV to keV collision energiesInngår i: Journal of Physical Chemistry A, ISSN 1089-5639, E-ISSN 1520-5215Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The gas-phase fragmentation of the protonated n-butylamine Schiff base of all-trans-retinal (NB-RPSB) was measured in low- and high-energy collisional activation modes. The protonated n-butyl β-ionone Schiff base (NB-BISB) peak at m/z = 248, known to be formed as a result of a complex gas-phase rearrangement reaction, has been reported to dominate in mass spectra of NB-RPSB after photo- and collisionally activated fragmentation processes. Earlier reported high-energy collision (50 keV) mass spectra have shown a broad distribution of the fragments with the peak at m/z = 248 present but not dominating. We observed the formation of a peak at m/z = 248 only in collisional activation of NB-RPSB parent ion below a few eV, which shows that the rearrangement process is extremely efficient and happens in a very narrow energy range. On the other hand, our high-energy collision induced dissociation experiments yielded fragmentation patterns, which are fully accounted for simple bond cleavages of the NB-RPSB molecular backbone. We do not observe any peak corresponding to the formation of NB-BISB in the 10 eV – 1 keV collision energy range. This leaves the question open why this fragment reappears in the mass spectra at much higher energies.

  • 34.
    Larsson, Mats
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Salén, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    van der Meulen, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Feifel, R.
    Piancastelli, M. N.
    Fang, L.
    Murphy, B. F.
    Osipov, T.
    Berrah, N.
    Kukk, E.
    Ueda, K.
    Bozek, J. D.
    Bostedt, C.
    Wada, S.
    Richter, R.
    Feyer, V.
    Prince, K. C.
    Double core-hole formation in small molecules at the LCLS free electron laser2013Inngår i: Journal of Physics B: Atomic, Molecular and Optical Physics, ISSN 0953-4075, E-ISSN 1361-6455, Vol. 46, nr 16, s. 164030-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have investigated nonlinear processes in small molecules by x-ray photoelectron spectroscopy using the Linac Coherent Light Source free electron laser, and by simulations. The main focus of the experiments was the formation of the two-site double core-hole (tsDCH) states in the molecules CO2, N2O and N-2. These experiments are described in detail and the results are compared with simulations of the photoelectron spectra. The double core-hole states, and in particular the tsDCH states, have been predicted to be highly sensitive to the chemical environment. The theory behind this chemical sensitivity is validated by the experiments. Furthermore, our simulations of the relative integrated intensities of the peaks associated with the nonlinear processes show that this type of simulation, in combination with experimental data, provides a useful tool for estimating the duration of ultra-short x-ray pulses.

  • 35. Lawicki, A.
    et al.
    Holm, Anne I. S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rousseau, P.
    Capron, M.
    Maisonny, R.
    Maclot, S.
    Seitz, Fabian
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Manil, B.
    Adoui, L.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Huber, B. A.
    Multiple ionization and fragmentation of isolated pyrene and coronene molecules in collision with ions2011Inngår i: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 83, nr 2, s. 022704-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The interaction of multiply charged ions (He2+, O3+, and Xe20+) with gas-phase pericondensed polycyclic aromatic hydrocarbon (PAH) molecules of coronene (C24H12) and pyrene (C16H10) is studied for low-velocity collisions (v <= 0.6 a.u.). The mass spectrometric analysis shows that singly and up to quadruply charged intact molecules are important reaction products. The relative experimental yields are compared with the results of a simple classical over-the-barrier model. For higher molecular charge states, the experimental yields decrease much more strongly than the model predictions due to the instabilities of the multiply charged PAH molecules. Even-odd oscillations with the number of carbon atoms, n, in the intensity distributions of the CnHx+ fragments indicate a linear chain structure of the fragments similar to those observed for ion-C60 collisions. The latter oscillations are known to be due to dissociation energy differences between even-and odd-n Cn-chain molecules. For PAH molecules, the average numbers of H atoms attached to the CnHx chains are larger for even-n reflecting acetylenic bond systems.

  • 36. Lestinsky, M.
    et al.
    Andrianov, V.
    Aurand, B.
    Bagnoud, V.
    Bernhardt, D.
    Beyer, H.
    Bishop, S.
    Blaum, K.
    Bleile, A.
    Borovik, At.
    Bosch, F.
    Bostock, C. J.
    Brandau, C.
    Braeuning-Demian, A.
    Bray, I.
    Davinson, T.
    Ebinger, B.
    Echler, A.
    Egelhof, P.
    Ehresmann, A.
    Engström, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Enss, C.
    Ferreira, N.
    Fischer, D.
    Fleischmann, A.
    Foerster, E.
    Fritzsche, S.
    Geithner, R.
    Geyer, S.
    Glorius, J.
    Goebel, K.
    Gorda, O.
    Goullon, J.
    Grabitz, P.
    Grisenti, R.
    Gumberidze, A.
    Hagmann, S.
    Heil, M.
    Heinz, A.
    Herfurth, F.
    Hess, R.
    Hillenbrand, P. -M.
    Hubele, R.
    Indelicato, P.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kester, O.
    Kiselev, O.
    Knie, A.
    Kozhuharov, C.
    Kraft-Bermuth, S.
    Kuehl, T.
    Lane, G.
    Litvinov, Yu. A.
    Liesen, D.
    Ma, X. W.
    Maertin, R.
    Moshammer, R.
    Mueller, A.
    Namba, S.
    Neumeyer, P.
    Nilsson, T.
    Noertershaeuser, W.
    Paulus, G.
    Petridis, N.
    Reed, M.
    Reifarth, R.
    Reiss, P.
    Rothhardt, J.
    Sanchez, R.
    Sanjari, M. S.
    Schippers, S.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schneider, D.
    Scholz, P.
    Schuch, Reinhold
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schulz, M.
    Shabaev, V.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Sjöholm, Johannes
    Skeppstedt, Örjan
    Stockholm Univ, Fysikum, S-10691 Stockholm, Sweden.
    Sonnabend, K.
    Spillmann, U.
    Stiebing, K.
    Steck, M.
    Stohlker, T.
    Surzhykov, A.
    Torilov, S.
    Trabert, E.
    Trassinelli, M.
    Trotsenko, S.
    Tu, X. L.
    Uschmann, I.
    Walker, P. M.
    Weber, G.
    Winters, D. F. A.
    Woods, P. J.
    Zhao, H. Y.
    Zhang, Y. H.
    Physics book: CRYRING@ESR2016Inngår i: The European Physical Journal Special Topics, ISSN 1951-6355, E-ISSN 1951-6401, Vol. 225, nr 5, s. 797-882Artikkel, forskningsoversikt (Fagfellevurdert)
    Abstract [en]

    The exploration of the unique properties of stored and cooled beams of highly-charged ions as provided by heavy-ion storage rings has opened novel and fascinating research opportunities in the realm of atomic and nuclear physics research. Since the late 1980s, pioneering work has been performed at the CRYRING at Stockholm (Abrahamsson et al. 1993) and at the Test Storage Ring (TSR) at Heidelberg (Baumann et al. 1988). For the heaviest ions in the highest charge-states, a real quantum jump was achieved in the early 1990s by the commissioning of the Experimental Storage Ring (ESR) at GSI Helmholtzzentrum für Schwerionenforschung (GSI) in Darmstadt (Franzke 1987) where challenging experiments on the electron dynamics in the strong field regime as well as nuclear physics studies on exotic nuclei and at the borderline to atomic physics were performed. Meanwhile also at Lanzhou a heavy-ion storage ring has been taken in operation, exploiting the unique research opportunities in particular for medium-heavy ions and exotic nuclei (Xia et al. 2002).

  • 37.
    Misra, Deepankar
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning Thordal
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gudmundsson, Magnus
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Fischer, Daniel
    Max-Planck Institut, Heidelberg.
    Haag, Nicole
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A B
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Najjari, B
    Max-Planck Institut, Heidelberg.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schuch, Reinhold
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schöffler, Marcus
    Frankfurt University.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Voitkiv, A B
    Max-Planck Institut, Heidelberg.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Two-Center Double-Capture Interference in Fast He2++H2 Collisions2009Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 102, nr 15, s. 153201-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report the first observation of Young-type interference effects in a two-electron transfer process. These effects change strongly as the projectile velocity changes in fast (1.2 and 2.0 MeV) He^{2+}-H_2 collisions as manifested in strong variations of the double-electron capture rates with the H_2 orientation. This is consistent with fully quantum mechanical calculations, which ignore sequential electron transfer, and a simple projectile de Broglie wave picture assuming that two-electron transfer probabilities are higher in collisions where the projectile passes close to either one of the H_2 nuclei.

  • 38.
    Reinhed, Peter
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Orbán, Andrea
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kashperka, Iryna
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Misra, Deepankar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Fardi, Afshin
    Brännholm, Lars
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cryogenic keV ion-beam storage in ConeTrap - a tool for ion-temperature control2010Inngår i: Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment, ISSN 0168-9002, E-ISSN 1872-9576, Vol. 621, nr 1-3, s. 83-90Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have tested the ion-storage capabilities of the compact triple-electrode electrostatic ion-beam trap, ConeTrap, down to cryogenic temperatures. The low-temperature operation of this electrostatic storage device is an important test for the double electrostatic ion-ring experiment, DESIREE, which is presently under construction at Stockholm University. In the present work we measured the pressure dependent storage lifetimes of 2.5 keV He+ and 2.8 keV Ar+ ion beams in ConeTrap at temperatures down to 28 K and pressures down to 1.3·10-10 mbar. The so far longest measured ion storage lifetime using this system is 21.5±3.8 s for Ar+ ions. The present combination of ConeTrap and the cryogenic experimental chamber was recently applied in the first black-body correction-free measurement of the lifetime of the metastable He- ion at 10 K [Phys. Rev. Lett. 103, 213002(2009)].

  • 39.
    Reinhed, Peter
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Orbán, Andrea
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Werner, Josefina
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kashperka, Iryna
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Misra, Deepankar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Brännholm, Lars
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum, Manne Siegbahn-laboratoriet.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum, Manne Siegbahn-laboratoriet.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Precision lifetime measurements of He- in a cryogenic electrostatic ion-beam trap2009Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 103, nr 21, s. 213002-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have developed a small purely electrostatic ion-beam trap which may be operated in thermal equilibrium at precisely controlled temperatures down to 10 K. Thus, we avoid magnetic field induced mixing of quantum states and may effectively eliminate any influence from absorption of photons from black-body radiation. We report the first correction free measurements of the lifetimes of the 1s2s2p 4PoJ state of 4He- and the high precision result 359.0±0.7 μs for the J=5/2 level. The lifetimes for the J=3/2 and J=1/2 levels are determined to be 12.3±0.5 and 7.8±1.0 μs, respectively.

  • 40.
    Rosén, Stefan
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Fischer, Daniel
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Liljeby, Leif
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Bagge, Lars
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Leontein, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Operating a triple stack microchannel plate-phosphor assembly for single particle counting in the 12-300 K temperature range2007Inngår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 78, nr 11, s. 113301-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    An assembly consisting of a stack of three microchannel plates (MCPs) and a phosphor screen anode has been operated over the temperature range from 300 to 12 K. We report on measurements at 6.4 kHz (using an alpha source) and with dark counts only (15 Hz). Without any particle source,  the MCP bias current decreased by a factor of 2.1×103 when the temperature was lowered from 300 to 12 K. Using the alpha source, and a photomultiplier tube (PMT) to monitor the phosphor screen anode, we first observed an increase in the decay time of the phosphor from 12 to 45 μs when the temperature was decreased from 300 to 100 K while the decay time then decreased and reached a value of 5 μs at 12 K. The pulse height distribution from the PMT was measured between300 and 12 K and shows a spectrum typical for a MCP phosphor setup at 300 K and 12 K but is strongly degraded for intermediate temperatures. We conclude that the present MCP-phosphor detector assembly is well suited for position-sensitive particle counting operation at temperatures down to at least 12 K even for count rates beyond 6 kHz. This result is crucial and an important part of ongoing developments of new instrumentation for investigations of, e.g., interactions involving complex molecular ions with internal quantum state control.

  • 41. Rousseau, P.
    et al.
    Lawicki, A.
    Holm, Anne I. S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Capron, M.
    Maisonny, R.
    Maclot, S.
    Lattouf, E.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Seitz, Fabian
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mery, A.
    Rangama, J.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosen, S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chesnel, J. -Y
    Domaracka, A.
    Manil, B.
    Adoui, L.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Huber, B. A.
    Low energy ions interacting with anthracene molecules and clusters2012Inngår i: Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms, ISSN 0168-583X, E-ISSN 1872-9584, Vol. 279, s. 140-143Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The interaction of slow ions (nu similar to 0.4 au.) with a small polycyclic aromatic hydrocarbon, namely anthracene (C14H10), is studied in the gas-phase either with the isolated molecule or with a pure cluster target. We discuss the ionization and fragmentation of the molecule with respect to the projectile charge state, i.e. for singly charged He+ ions and for multiply charged Xe20+. ions. For the isolated C14H10, single or multiple ionization of the molecule occurs under ion impact. The (multi) cation relative yields are compared with those obtained by other ionization methods (electron and fs-laser). The molecular dissociation occurs by loss of hydrogen and small hydrocarbon molecules, leading to the formation of CnHx cations. The interaction of Xe20+ with C14H10 clusters gives surprising results, i.e. the emission of hotter monomer compared to the interaction with He+.

  • 42.
    Sahlén, Martin
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    van der Meulen, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Larsson, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Feifel, Raimund
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Piancastelli, M. N.
    Fang, L.
    Murphy, B.
    Osipov, T.
    Berrah, N.
    Kukk, E.
    Ueda, K.
    Bozek, J. D.
    Bostedt, C.
    Wada, S.
    Richter, R.
    Feyer, V.
    Prince, K. C.
    Experimental Verification of the Chemical Sensitivity of Two-Site Double Core-Hole States Formed by an X-Ray Free-Electron Laser2012Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 108, nr 15, s. 153003-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have performed x-ray two-photon photoelectron spectroscopy using the Linac Coherent Light Source x-ray free-electron laser in order to study double core-hole (DCH) states of CO2, N2O, and N-2. The experiment verifies the theory behind the chemical sensitivity of two-site DCH states by comparing a set of small molecules with respect to the energy shift of the two-site DCH state and by extracting the relevant parameters from this shift.

  • 43.
    Schmidt, Henning T.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Brännholm, Lars
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Bäckström, Erik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Leontein, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hanstorp, D.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Liljeby, Leif
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hellberg, Fredrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mannervik, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Larsson, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Geppert, Wolf D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rensfelt, Karl-Gunnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Danared, Håkan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Paal, A.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Masuda, Masaharu
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hallden, Per
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Andler, Guillermo
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källersjö, Gunnar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Weimer, Jan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Hansen, K.
    Hartman, H.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    First storage of ion beams in the Double Electrostatic Ion-Ring Experiment: DESIREE2013Inngår i: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 84, nr 5, s. 055115-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report on the first storage of ion beams in the Double ElectroStatic Ion Ring ExpEriment, DESIREE, at Stockholm University. We have produced beams of atomic carbon anions and small carbon anion molecules (C-n(-), n = 1, 2, 3, 4) in a sputter ion source. The ion beams were accelerated to 10 keV kinetic energy and stored in an electrostatic ion storage ring enclosed in a vacuum chamber at 13 K. For 10 keV C-2(-) molecular anions we measure the residual-gas limited beam storage lifetime to be 448 s +/- 18 s with two independent detector systems. Using the measured storage lifetimes we estimate that the residual gas pressure is in the 10(-14) mbar range. When high current ion beams are injected, the number of stored particles does not follow a single exponential decay law as would be expected for stored particles lost solely due to electron detachment in collision with the residual-gas. Instead, we observe a faster initial decay rate, which we ascribe to the effect of the space charge of the ion beam on the storage capacity.

  • 44.
    Schmidt, Henning
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Fischer, Daniel
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Berenyi, Zoltan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cocke, Charles Lewis
    Gudmundsson, Magnus
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Haag, Nicole
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Levin, Sergey B.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Sassenberg, Ulf
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schuch, Reinhold
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Stöchkel, Kristian
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Evidence of Wave-Particle Duality for Single Fast Hydrogen Atoms2008Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 101, nr 8, s. 083201-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report the direct observation of interference effects in a Young's double-slit experiment where the interfering waves are two spatially separated components of the de Broglie wave of single 1.3 MeV hydrogen atoms formed close to either target nucleus in H+ + H2 electron-transfer collisions. Quantum interference strongly influences the results even though the hydrogen atoms have a de Broglie wavelength, \lambda_dB, as small as 25 fm.

  • 45.
    Schmidt, Henning
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Geppert, Wolf
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Haag, Nicole
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Larsson, Mats
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Danared, Håkan
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Rensfelt, K.-G
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Liljeby, Leif
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Bagge, Lars
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Björkhage, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Blom, Mikael
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Paál, Andras
    Stockholms universitet, Naturvetenskapliga fakulteten, Manne Siegbahn-laboratoriet.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    DESIREE as a new tool for interstellar ion chemistry2008Inngår i: International Journal of Astrobiology, ISSN 1473-5504, E-ISSN 1475-3006, Vol. 7, nr 3-4, s. 205-208Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A novel cryogenic electrostatic storage device consisting of two ion-beam storage rings with a common straight section for studies of interactions between oppositely charged ions at low and well-defined relative velocities is under construction at Stockholm University. Here we consider the prospect of using this new tool to measure cross-sections and rate coefficients for mutual neutralization reactions of importance in interstellar ion chemistry in general and specifically in cosmic pre-biotic ion chemistry.

  • 46.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Electrostatic storage rings for atomic and molecular physics2015Inngår i: Physica Scripta, ISSN 0031-8949, E-ISSN 1402-4896, Vol. T166, artikkel-id 014063Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A significant number of electrostatic ion-storage rings have been built since the late 1990s or are currently in their construction or commisioning phases. In this short contribution, we attempt to supply an overview of these different facilities, while we also mention a selection of the electrostatic ion-beam traps that has been developed through the same time period and by some of the same research groups.

  • 47.
    Schmidt, Henning T.
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Eklund, Gustav
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Chartkunchand, Kiattichart C.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Anderson, Emma K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kamińska, Magdalena
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Jan Kochanowski University, Poland.
    de Ruette, Nathalie
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Thomas, Richard D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Kristiansson, Moa K.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Reinhed, Peter
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosen, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Simonsson, Ansgar
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Källberg, Anders
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Löfgren, Patrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Mannervik, Sven
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rotationally Cold OH- Ions in the Cryogenic Electrostatic Ion-Beam Storage Ring DESIREE2017Inngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 119, nr 7, artikkel-id 073001Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We apply near-threshold laser photodetachment to characterize the rotational quantum level distribution of OH- ions stored in the cryogenic ion-beam storage ring DESIREE at Stockholm University. We find that the stored ions relax to a rotational temperature of 13.4 +/- 0.2 K with 94.9 +/- 0.3% of the ions in the rotational ground state. This is consistent with the storage ring temperature of 13.5 +/- 0.5 K as measured with eight silicon diodes but in contrast to all earlier studies in cryogenic traps and rings where the rotational temperatures were always much higher than those of the storage devices at their lowest temperatures. Furthermore, we actively modify the rotational distribution through selective photodetachment to produce an OH- beam where 99.1 +/- 0.1% of approximately one million stored ions are in the J = 0 rotational ground state. We measure the intrinsic lifetime of the J = 1 rotational level to be 145 +/- 28 s.

  • 48.
    Seitz, Fabian
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Holm, Anne I. S.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Johansson, Henrik A. B.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rosén, Stefan
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Lawicki, A.
    Rangama, J.
    Rousseau, P.
    Capron, M.
    Maisonny, R.
    Domaracka, A.
    Adoui, L.
    Mery, A.
    Manil, B.
    Huber, B. A.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Polycyclic aromatic hydrocarbon-isomer fragmentation pathways: Case study for pyrene and fluoranthene molecules and clusters2011Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 135, nr 6, s. 064302-Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report on measurements of the ionization and fragmentation of polycyclic aromatic hydrocarbon (PAH) targets in Xe(20+) + C(16)H(10) and Xe(20+) + [C(16)H(10)](k) collisions and compare results for the two C(16)H(10) isomers: pyrene and fluoranthene. For both types of targets, i.e., for single PAH molecules isolated in vacuum or for isomerically pure clusters of one of the molecules, the resulting fragment spectra are surprisingly similar. However, we do observe weak but significant isomer effects. Although these are manifested in very different ways for the monomer and cluster targets, they both have at their roots small differences (<2.5 eV) between the total binding energies of neutral, and singly and multiply charged pyrene and fluoranthene monomers. The results will be discussed in view of the density functional theory calculations of ionization and dissociation energies for fluoranthene and pyrene. A simple classical over-the-barrier model is used to estimate cross sections for single-and multiple-electron transfer between PAHs and ions. Calculated single and multiple ionization energies, and the corresponding model PAH ionization cross sections, are given.

  • 49.
    Seitz, Fabian
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rousseau, P.
    Wang, Y.
    Chen, Tao
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Alexander, John D.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Stockett, Mark H.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Rangama, J.
    Chesnel, J. Y.
    Capron, M.
    Poully, J. C.
    Domaracka, A.
    Mery, A.
    Maclot, S.
    Vizcaino, V.
    Schmidt, Henning T.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Adoui, L.
    Alcami, M.
    Tielens, A. G. G. M.
    Martin, F.
    Huber, B. A.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Ions colliding with clusters of fullerenes-Decay pathways and covalent bond formations2013Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 139, nr 3, artikkel-id 034309Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We report experimental results for the ionization and fragmentation of weakly bound van der Waals clusters of n C-60 molecules following collisions with Ar2+, He2+, and Xe20+ at laboratory kinetic energies of 13 keV, 22.5 keV, and 300 keV, respectively. Intact singly charged C-60 monomers are the dominant reaction products in all three cases and this is accounted for by means of Monte Carlo calculations of energy transfer processes and a simple Arrhenius-type [C-60](n)(+) -> C-60(+) + (n - 1)C-60 evaporation model. Excitation energies in the range of only similar to 0.7 eV per C-60 molecule in a [C-60](13)(+) cluster are sufficient for complete evaporation and such low energies correspond to ion trajectories far outside the clusters. Still we observe singly and even doubly charged intact cluster ions which stem from even more distant collisions. For penetrating collisions the clusters become multiply charged and some of the individual molecules may be promptly fragmented in direct knock-out processes leading to efficient formations of new covalent systems. For Ar2+ and He2+ collisions, we observe very efficient C-119(+) and C-118(+) formation and molecular dynamics simulations suggest that they are covalent dumb-bell systems due to bonding between C-59(+) or C-58(+) and C-60 during cluster fragmentation. In the Ar2+ case, it is possible to form even smaller C-120-2m(+) molecules (m = 2-7), while no molecular fusion reactions are observed for the present Xe20+ collisions.

  • 50.
    Stockett, H. Mark
    et al.
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Wolf, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Gatchell, Michael
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum. Universität Innsbruck, Austria.
    Schmidt, T. Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Zettergren, Henning
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    Cederquist, Henrik
    Stockholms universitet, Naturvetenskapliga fakulteten, Fysikum.
    The threshold displacement energy of buckminsterfullerene and formation of endohedral defect fullerenesInngår i: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    We have measured the threshold center-of-mass energy for knocking out a single carbon atom from C60 in C60-+He collisions.  Combining this experimental result with classical molecular dynamics simulations of such collisions we deduce a semi-empirical value of 24.1±0.5 eV for the C60 → C59+C threshold displacement energy, the minimum energy needed to remove a single carbon atom from the C60 cage. In addition, we oberserve the formation of the endohedral defect fullerene complex He@C59- and its decay product He@C58-.

12 1 - 50 of 67
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