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  • 1. Andersson, Patrik U.
    et al.
    Ojekull, Jenny
    Pettersson, Jan B. C.
    Markovic, Nikola
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Ehlerding, Anneli
    Stockholm University, Faculty of Science, Department of Physics.
    Österdahl, Fabian
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Uggerud, Einar
    Danared, Hakan
    Kallberg, Anders
    Formation of Highly Rovibrationally Excited Ammonia from Dissociative Recombination of NH4+2010In: The journal of physical chemistry letters, ISSN 1948-7185, Vol. 1, no 17, p. 2519-2523Article in journal (Refereed)
    Abstract [en]

    The internal energy distribution of ammonia formed in the dissociative recombination (DR) of NH4+ with electrons has been studied by an imaging technique at the ion storage ring CRYRING. The DR process resulted in the formation of NH3 + H (0,90 +/- 0.01), with minor contributions from channels producing NH2 + H-2 (0.05 +/- 0.01) and NH2 + 2H (0.04 +/- 0.02). The formed NH3 molecules were highly internally excited, with a mean rovibrational energy of 3.3 +/- 0.4 eV, which corresponds to 70% of the energy released in the neutralization process. The internal energy distribution was semiquantitatively reproduced by ab initio direct dynamics simulations, and the calculations suggested that the NH3 molecules are highly vibrationally excited while rotational excitation is limited. The high internal,excitation and the translational energy of NH3 and H will influence their subsequent reactivity, an aspect that should be taken into account when developing detailed models of the interstellar medium and ammonia-containing plasmas.

  • 2. Angelova, G.
    et al.
    Ziemann, V.
    Meseck, A.
    Salén, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    van der Meulen, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Boedewadt, J.
    Khan, S.
    Winter, A.
    Schlarb, H.
    Loehl, F.
    Saldin, E.
    Schneidmiller, E.
    Yurkov, M.
    Observation of two-dimensional longitudinal-transverse correlations in an electron beam by laser-electron interactions2008In: Physical Review Special Topics. Accelerators and Beams, ISSN 1098-4402, E-ISSN 1098-4402, Vol. 11, no 7, article id 70702Article in journal (Refereed)
    Abstract [en]

    During the preparatory work for the optical-replica synthesizer experiment in the free-electron laser FLASH at DESY, we were able to superimpose a short, approximately 200 fs long pulse from a frequencydoubled mode-locked erbium laser with titanium-sapphire amplifier and an approximately 20 ps long electron bunch in an undulator. This induces an energy modulation in a longitudinal slice of the electron bunch. A magnetic chicane downstream of the undulator converts the energy modulation into a density modulation within the slice that causes the emission of coherent optical transition radiation from a silver-coated silicon screen. Varying the relative timing between electron and laser, we use a camera to record two-dimensional images of the slices as a function of the longitudinal position within the electron bunch.

  • 3.
    Bergstrand, Märta
    et al.
    Stockholm University, Faculty of Humanities, Department of Slavic Languages and Literatures.
    Larsson, Mats
    Stockholm University, Faculty of Humanities, Department of Slavic Languages and Literatures.
    Från Königinhofer-handskriften till Novemberorkanen: en bibliografi över tjeckisk och slovakisk skönlitteratur i svensk översättning 1862-19911992Book (Other academic)
  • 4. Berrah, Nora
    et al.
    Fang, Li
    Murphy, Brendan
    Osipov, Timur
    Ueda, Kiyoshi
    Kukk, Edwin
    Feifel, Raimund
    van der Meulen, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Salén, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    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 laser2011In: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 108, no 41, p. 16912-16915Article in journal (Refereed)
    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.

  • 5.
    Brinne Roos, Johanna
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Larson, Åsa
    Stockholm University, Faculty of Science, Department of Physics.
    Orel, Ann
    Deptartment of Applied Science, University of California, Davis.
    Dissociative recombination of BeH+Manuscript (Other academic)
    Abstract [en]

    The cross section for dissociative recombination of BeH+ is calculated by solution of the timedependent Schrödinger equation in the local complex potential approximation. The effects of couplings between resonant states and the Rydberg states converging to the ground state of the ionare studied. The relevant potentials, couplings and autoionization widths are extracted using abinitio electron scattering and structure calculations, followed by a diabatization procedure. Thecalculated cross sections shows a sizable magnitude at low energy, followed by a high-energy peakcentered around 1 eV. The electronic couplings between the neutral states induce oscillations in thecross section. Analytical forms for the cross sections at low collision energies are given.

  • 6.
    Danielsson, Mathias
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Paál, Andreas
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitaly
    Stockholm University, Faculty of Science, Department of Physics.
    Ehlerding, Anneli
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Stockholm University, Faculty of Science, Department of Physics.
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard
    Stockholm University, Faculty of Science, Department of Physics.
    Österdal, Fabian
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Källberg, Anders
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    The cross-section and branching fractions for dissociative recombination of the diacetylene cation C4D2+2008In: International Journal of Mass Spectrometry, ISSN 1387-3806, E-ISSN 1873-2798, Vol. 273, no 3, p. 111-116Article in journal (Refereed)
    Abstract [en]

    In this paper we report the results of a study on the dissociative recombination (DR) of the diacetylene cation, C4D2+, which has been carried out at the ion storage ring CRYRING in Stockholm, Sweden. The energy-dependent absolute DR cross-section as well as the branching fractions at 0 eV collision energy were measured. The DR cross-section was best fitted using the expression σ(E) = (7.5 ± 1.5) × 10−16 × E−(1.29±0.03) cm2 over the collision energy range 1–100 meV. The thermal rate coefficient was deduced from the cross-section to be α(T) = (1.10 ± 0.15) × 10−6 × (T/300)−(0.79±0.03) cm3/s. The reported branching fractions for C4D2+ agree with previous experiments on the DR of C4H2+ performed at the ASTRID storage ring in Aarhus, Denmark, and furthermore, indicate that the DR of C4D2+ possesses only two channels leading to the following products: C4D + D (75%) and C2D + C2D (25%).

  • 7. Frasinski, L. J.
    et al.
    Zhaunerchyk, V.
    Mucke, M.
    Squibb, R. J.
    Siano, M.
    Eland, J. H. D.
    Linusson, Per
    Stockholm University, Faculty of Science, Department of Physics.
    van der Meulen, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Sahlén, Martin
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Foucar, L.
    Ullrich, J.
    Motomura, K.
    Mondal, S.
    Ueda, K.
    Osipov, T.
    Fang, L.
    Murphy, B. F.
    Berrah, N.
    Bostedt, C.
    Bozek, J. D.
    Schorb, S.
    Messerschmidt, M.
    Glownia, J. M.
    Cryan, J. P.
    Coffee, R. N.
    Takahashi, O.
    Wada, S.
    Piancastelli, M. N.
    Richter, R.
    Prince, K. C.
    Feifel, R.
    Dynamics of Hollow Atom Formation in Intense X-Ray Pulses Probed by Partial Covariance Mapping2013In: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 111, no 7, p. 073002-Article in journal (Refereed)
    Abstract [en]

    When exposed to ultraintense x-radiation sources such as free electron lasers (FELs) the innermost electronic shell can efficiently be emptied, creating a transient hollow atom or molecule. Understanding the femtosecond dynamics of such systems is fundamental to achieving atomic resolution in flash diffraction imaging of noncrystallized complex biological samples. We demonstrate the capacity of a correlation method called partial covariance mapping'' to probe the electron dynamics of neon atoms exposed to intense 8 fs pulses of 1062 eV photons. A complete picture of ionization processes competing in hollow atom formation and decay is visualized with unprecedented ease and the map reveals hitherto unobserved nonlinear sequences of photoionization and Auger events. The technique is particularly well suited to the high counting rate inherent in FEL experiments.

  • 8.
    Gatchell, Michael
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Alexander, John D.
    Stockholm University, Faculty of Science, Department of Physics.
    Andler, Guillermo
    Stockholm University, Faculty of Science, Department of Physics.
    Björkhage, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Blom, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Brännholm, Lars
    Stockholm University, Faculty of Science, Department of Physics.
    Bäckström, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Chen, Tao
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf
    Stockholm University, Faculty of Science, Department of Physics.
    Halldén, Per
    Stockholm University, Faculty of Science, Department of Physics.
    Hanstorp, Dag
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Leontein, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Liljeby, Leif
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Paal, Andras
    Stockholm University, Faculty of Science, Department of Physics.
    Reinhed, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Rensfelt, Karl-Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Rosén, Stefan
    Stockholm University, Faculty of Science, Department of Physics.
    Seitz, Fabian
    Stockholm University, Faculty of Science, Department of Physics.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Stockett, Mark H.
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    First results from the Double ElectroStatic Ion-Ring ExpEriment, DESIREE2014In: Journal of Physics, Conference Series, ISSN 1742-6588, E-ISSN 1742-6596, Vol. 488, p. 092003-Article in journal (Refereed)
    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.

  • 9.
    Gatchell, Michael
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Rosén, Stefan
    Stockholm University, Faculty of Science, Department of Physics.
    Reinhed, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    Stockholm University, Faculty of Science, Department of Physics.
    Brännholm, Lars
    Stockholm University, Faculty of Science, Department of Physics.
    Blom, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Björkhage, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Bäckström, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Alexander, John D.
    Stockholm University, Faculty of Science, Department of Physics.
    Leontein, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Hanstorp, D.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Liljeby, Leif
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Rensfelt, Karl-Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Danared, Håkan
    Stockholm University, Faculty of Science, Department of Physics. European Spallation Source, Sweden.
    Paál, Andras
    Stockholm University, Faculty of Science, Department of Physics.
    Masuda, Masaharu
    Stockholm University, Faculty of Science, Department of Physics.
    Halldén, Per
    Stockholm University, Faculty of Science, Department of Physics.
    Andler, Guillermo
    Stockholm University, Faculty of Science, Department of Physics.
    Stockett, Mark H.
    Stockholm University, Faculty of Science, Department of Physics.
    Chen, Tao
    Stockholm University, Faculty of Science, Department of Physics.
    Källersjö, Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Weimer, Jan
    Stockholm University, Faculty of Science, Department of Physics.
    Hansen, K.
    Hartman, H.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    Commissioning of the DESIREE storage rings - a new facility for cold ion-ion collisions2014In: Journal of Physics, Conference Series, ISSN 1742-6588, E-ISSN 1742-6596, Vol. 488, p. 012040-Article in journal (Refereed)
    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.

  • 10.
    Geppert, W.D.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, M.
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, R.D.
    Stockholm University, Faculty of Science, Department of Physics.
    Österdahl, F.
    Hellberg, F.
    Stockholm University, Faculty of Science, Department of Physics.
    Zhauernerchyk, V.
    Stockholm University, Faculty of Science, Department of Physics.
    Ehlerding, A.
    Stockholm University, Faculty of Science, Department of Physics.
    Millar, T.J.
    Roberts, H.
    Semaniak, J.
    af Ugglas, M.
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Källberg, Anders
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Kaminska, M.
    Larsson, M.
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative recombination of protonated methanol2006In: Journal of the Chemical Society, Faraday Transactions, ISSN 0956-5000, E-ISSN 1364-5455, Vol. 133, p. 177-190Article in journal (Refereed)
  • 11.
    Geppert, Wolf D.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Experimental Investigations into Astrophysically Relevant Ionic Reactions2013In: Chemical Reviews, ISSN 0009-2665, E-ISSN 1520-6890, Vol. 113, no 12, p. 8872-8905Article, review/survey (Refereed)
  • 12.
    Hamberg, Mathias
    et al.
    Stockholm University, Faculty of Science, Department of Physics. Uppsala University, Sweden.
    Kashperka, Iryna
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Roueff, Evelyne
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics. Uppsala University, Sweden.
    Danielsson, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Österdahl, Fabian
    Stockholm University, Faculty of Science, Department of Physics.
    Vigren, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Paál, Andras
    Stockholm University, Faculty of Science, Department of Physics.
    Gerin, Maryvonne
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Experimental Studies of (HCO+)-C-13 Recombining with Electrons at Energies between 2-50 000 meV2014In: Journal of Physical Chemistry A, ISSN 1089-5639, E-ISSN 1520-5215, Vol. 118, no 31, p. 6034-6049Article in journal (Refereed)
    Abstract [en]

    An investigation into the dissociative recombination process for (HCO+)-C-13 using merged ion-electron beam methods has been performed at the heavy ion storage ring CRYRING, Stockholm, Sweden. We have measured the branching fractions of the different product channels at similar to 0 eV collision energy to be the following: CO + H 87 +/- 2%, OH + C 9 +/- 2%, and O + CH 4 +/- 2%. The formation of electronically excited CO in the dominant reaction channel has also been studied, and we report the following tentative branching fractions for the different CO product electronic states: CO(X (1)Sigma(+)) + H, 54 +/- 10%; CO(a (3)Pi) + H, 23 +/- 4%; and CO(a' (3)Sigma(+)) + H, 23 +/- 4%. The absolute cross section between similar to 2-50 000 meV was measured and showed resonance structures between 3 and 15 eV. The cross section was fitted in the energy range relevant to astrophysics, i.e., between 1 and 300 meV, and was found to follow the expression sigma = 1.3 +/- 0.3 X 10(-16) E-1.29 +/- 0.05 cm(2) and the corresponding thermal rate constant was determined to be k(T) = 2.0 +/- 0.4 X 10(-7)(T/300)(-0.79 +/- 0.05) cm(3) s(-1). Radioastronomical observations with the IRAM 30 m telescope of HCO+ toward the Red Rectangle yielded an upper column density limit of 4 X 10(11) cm(-2) of HCO+ at the 1 sigma level in that object, indicating that previous claims that the dissociative recombination of HCO+ plays an important role in the production of excited CO molecules emitting the observed Cameron bands in that object are not supported.

  • 13.
    Hamberg, Mathias
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Vigren, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Jan Kochanowski University, Kielce, Poland.
    Kashperka, Iryna
    Stockholm University, Faculty of Science, Department of Physics.
    Zhang, Mingwu
    Institute of Modern Physics.
    Trippel, Sebastian
    Albert-Ludwigs-Universität Freiburg, Tyskland.
    Österdahl, Fabian
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Paál, András
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf
    Stockholm University, Faculty of Science, Department of Physics.
    Experimental studies of the dissociative recombination for CD3CDOD+ and CH3CH2OH2+Manuscript (preprint) (Other academic)
    Abstract [en]

    Aims:  Determination of branching fractions, cross sections and thermal rate constants for the dissociative recombination of CD3CDOD+ and CH3CH2OH2+ at the low relative kinetic energies encountered in the interstellar medium.

    Methods: The experiments were carried out by merging an ion and electron beam at the heavy ion storage ring CRYRING, Stockholm, Sweden.

    Results: Break-up of the CCO structure into three heavy fragments is not found for either of the ions. Instead the CCO structure is retained in 23 ± 3% of the DR reactions of CD3CDOD+ and 7 ± 3% in the DR of CH3CH2OH2+, whereas rupture into two heavy fragments occurs in 77 ± 3% and 93 ± 3% of the DR events of the respective ions. The measured cross sections were fitted between 1-200 meV yielding the following thermal rate constants and cross-section dependencies on the relative kinetic energy: σ(Ecm[eV]) = 1.7 ± 0.3 × 1015(Ecm[eV])1.23±0.02 cm2 and k(T) = 1.9 ± 0.4 × 106(T/300)0.73±0.02 cm3s1 for CH3CH2OH2+  as well as k(T) = 1.1 ± 0.4 × 106(T/300)0.74±0.05 cm3s1 and σ(Ecm[eV]) = 9.2 ± 4 × 1016(Ecm[eV])1.24±0.05 cm2 for CD3CDOD+.

  • 14.
    Hamberg, Mathias
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Österdahl, Fabian
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Vigren, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Jan Kochanowski University.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics, The Manne Siegbahn Laboratory.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics, The Manne Siegbahn Laboratory.
    Paál, András
    Stockholm University, Faculty of Science, Department of Physics, The Manne Siegbahn Laboratory.
    Larsson, Mats
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Experimental studies of the dissociative recombination processes for the dimethyl ether ions CD3OCD2+ and (CD3)2OD+2010In: Astronomy and Astrophysics, ISSN 0004-6361, E-ISSN 1432-0746, Vol. 514, p. A83-Article in journal (Refereed)
    Abstract [en]

    Aims: Determination of branching fractions, cross sections and thermal rate coefficients for the dissociative recombination of CD3OCD2+ (0-0.3 eV) and (CD3)2OD+ (0-0.2 eV) at the low relative kinetic energies encountered in the interstellar medium.

    Methods: The measurements were carried out using merged electron and ion beams at the CRYRING storage ring, Stockholm, Sweden.

    Results: For (CD3)2OD+ we have experimentally determined the branching fraction for ejection of a single hydrogen atom in the DR process to be maximally 7% whereas 49% of the reactions involve the break up of the COC chain into two heavy fragments and 44% ruptures both C-O bonds. The DR of CD3OCD2+ is dominated by fragmentation of the COC chain into two heavy fragments. The measured thermal rate constants and cross sections are k(T) =1.7 ± 0.5 × 106(T/300)0.77±0.01 cm3s−1,  σ= 1.2 ± 0.4 × 1015(Ecm[eV])1.27 ± 0.01 cm2 and k(T) = 1.7 ± 0.6 × 106(T/300)0.70±0.02 cm3s1,σ= 1.7 ± 0.6 × 1015(Ecm[eV])1.20±0.02 cm2 for CD3OCD2+ and (CD3)2OD+, respectively.

  • 15.
    Kulyk, Kostiantyn
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Palianytsia, Borys
    Alexander, John D.
    Stockholm University, Faculty of Science, Department of Physics.
    Azizova, Liana
    Borysenko, Mykola
    Kartel, Mykola
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Kulik, Tetiana
    Kinetics of Valeric Acid Ketonization and Ketenization in Catalytic Pyrolysis on Nanosized SiO2, gamma-Al2O3, CeO2/SiO2, Al2O3/SiO2 and TiO2/SiO22017In: ChemPhysChem, ISSN 1439-4235, E-ISSN 1439-7641, Vol. 18, no 14, p. 1943-1955Article in journal (Refereed)
    Abstract [en]

    Valeric acid is an important renewable platform chemical that can be produced efficiently from lignocellulosic biomass. Upgrading of valeric acid by catalytic pyrolysis has the potential to produce value added biofuels and chemicals on an industrial scale. Understanding the different mechanisms involved in the thermal transformations of valeric acid on the surface of nanometer-sized oxides is important for the development of efficient heterogeneously catalyzed pyrolytic conversion techniques. In this work, the thermal decomposition of valeric acid on the surface of nanoscale SiO2, gamma-Al2O3, CeO2/SiO2, Al2O3/SiO2 and TiO2/SiO2 has been investigated by temperature-programmed desorption mass spectrometry (TPD MS). Fourier transform infrared spectroscopy (FTIR) has also been used to investigate the structure of valeric acid complexes on the oxide surfaces. Two main products of pyrolytic conversion were observed to be formed depending on the nano-catalyst used-dibutylketone and propylketene. Mechanisms of ketene and ketone formation from chemisorbed fragments of valeric acid are proposed and the kinetic parameters of the corresponding reactions were calculated. It was found that the activation energy of ketenization decreases in the order SiO2 > gamma-Al2O3 > TiO2/SiO2 > Al2O3/SiO2, and the activation energy of ketonization decreases in the order gamma-Al2O3 > CeO2/SiO2. Nanooxide CeO2/SiO2 was found to selectively catalyze the ketonization reaction.

  • 16.
    Kulyk, Kostiantyn
    et al.
    Stockholm University, Faculty of Science, Department of Physics. SCA R&D Centre, Sweden.
    Rebrov, Oleksii
    Stockholm University, Faculty of Science, Department of Physics.
    Ryding, M.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Uggerud, E.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Low-Energy Collisions of Protonated Enantiopure Amino Acids with Chiral Target Gases2017In: Journal of the American Society for Mass Spectrometry, ISSN 1044-0305, E-ISSN 1879-1123, Vol. 28, no 12, p. 2686-2691Article in journal (Refereed)
    Abstract [en]

    Here we report on the gas-phase interactions between protonated enantiopure amino acids (l- and d-enantiomers of Met, Phe, and Trp) and chiral target gases [(R)- and (S)-2-butanol, and (S)-1-phenylethanol] in 0.1-10.0 eV low-energy collisions. Two major processes are seen to occur over this collision energy regime, collision-induced dissociation and ion-molecule complex formation. Both processes were found to be independent of the stereo-chemical composition of the interacting ions and targets. These data shed light on the currently debated mechanisms of gas-phase chiral selectivity by demonstrating the inapplicability of the three-point model to these interactions, at least under single collision conditions.

  • 17.
    Kulyk, Kostiantyn
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Rebrov, Oleksii
    Stockholm University, Faculty of Science, Department of Physics.
    Stockett, Mark H.
    Stockholm University, Faculty of Science, Department of Physics.
    Alexander, John D.
    Stockholm University, Faculty of Science, Department of Physics.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    High-energy collisions of protonated enantiopure amino acids with a chiral target gas2015In: International Journal of Mass Spectrometry, ISSN 1387-3806, E-ISSN 1873-2798, Vol. 388, p. 59-64Article in journal (Refereed)
    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.

  • 18.
    Kulyk, Kostiantyn
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Gatchell, Michael
    Stockholm University, Faculty of Science, Department of Physics.
    Alexander, John D.
    Stockholm University, Faculty of Science, Department of Physics.
    Borysenko, Mykola
    Palianytsia, Borys
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Kulik, Tetiana
    Dimethylsilanone Generation from Pyrolysis of Polysiloxanes Filled with Nanosized Silica and Ceria/Silica2016In: chempluschem, ISSN 2192-6506, Vol. 81, no 9, p. 1003-1013Article in journal (Refereed)
    Abstract [en]

    Temperature-programmed desorption mass spectrometry (TPDMS) was used to study the pyrolysis of PDMS and its composites with nanosized silica and ceria/silica. The results suggest that the elusive organosilicon compound, dimethylsilanone, is generated from PDMS over a broad temperature range (in some cases starting at 70 degrees C). The presence of nano-oxides catalyzes this process. Ions characteristic of the fragmentation of dimethylsilanone under electron ionization are assigned with the aid of DFT structure calculations. Possible reaction mechanisms for dimethylsilanone generation are discussed in the context of the calculated kinetic parameters. Observed accompanying products of PDMS pyrolysis, such as tetramethylcyclodisiloxane and hexamethylcyclotrisiloxane, indicate that multiple channels are involved in the dimethylsilanone release.

  • 19.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative recombination of H-3(+): 10 years in retrospect2012In: Philosophical Transactions. Series A: Mathematical, physical, and engineering science, ISSN 1364-503X, E-ISSN 1471-2962, Vol. 370, no 1978, p. 5118-5129Article, review/survey (Refereed)
    Abstract [en]

    The dissociative recombination of H-3(+) has been an intriguing problem for more than half a century. The early experiments on H-3(+) during the first 20 years were carried out without mass analysis in decaying plasma afterglows, and thus the measured rates pertained to an uncontrolled mixture of H-3(+) and impurity ions. When mass analysis was used, the rate coefficient was determined to be an uneventful value of about 10(-7) cm(3) s(-1), a very common rate coefficient for many molecular ions. But this was not the end of the story, not even the beginning of the end; it marked only the end of the beginning. The story I will tell in this article started about 10 years ago, when the dissociative recombination of H-3(+) was approaching its deepest crisis. Today, owing to an extensive experimental and theoretical effort, the state of affairs has reached a historically unique level of harmony, although there still remains many things to sort out.

  • 20.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative recombination of H-3(+) and D-5(+)2019In: Philosophical Transactions. Series A: Mathematical, physical, and engineering science, ISSN 1364-503X, E-ISSN 1471-2962, Vol. 377, no 2154, article id 20180397Article, review/survey (Refereed)
    Abstract [en]

    Compared with earlier years, the dissociative recombination of H-3(+) has not been very actively studied in recent years. New results from afterglow experiments are quoted and compared with results from ion storage rings and theory. New results for D-5(+) are discussed. This article also contains some historical remarks on hydrogen and its importance for the advancement of physics and chemistry. This article is part of a discussion meeting issue 'Advances in hydrogen molecular ions: H-3(+), H-5(+) and beyond'.

  • 21.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    H-3(+): the initiator of interstellar chemistry2008In: International Journal of Astrobiology, ISSN 1473-5504, E-ISSN 1475-3006, Vol. 7, no 04-mar, p. 237-241Article in journal (Refereed)
    Abstract [en]

    Second only to H-2, protonated molecular hydrogen, H-3(+), is the most abundantly produced interstellar molecule. Owing to its high reactivity and acidity, it plays the pivotal role in initiating interstellar chemical reactions, something which also reduces its steady-state concentration. Interstellar H-3(+) is not only destroyed in chemical reactions but also in dissociative recombination with electrons. The rate constant and mechanism of recombination have long been controversial, but great advances have been made during recent years, with the important consequence that the cosmic ray ionization rate in diffuse Clouds is now believed to be higher by an order of magnitude than previously assumed.

  • 22.
    Larsson, Mats
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Balatsky, Alexander V.
    Stockholm University, Nordic Institute for Theoretical Physics (Nordita). Los Alamos National Laboratory, USA.
    Landau's Nobel Prize in Physics2016In: JETP Letters: Journal of Experimental And Theoretical Physics Letters, ISSN 0021-3640, E-ISSN 1090-6487, Vol. 103, no 12, p. 795-798Article in journal (Refereed)
    Abstract [en]

    Work of Lev Landau had a profound impact on the physics in 20th century. Landau had created the paradigms that had framed the conversations on the outstanding problems in physics for decades. He had laid foundations for our understanding of quantum matter like superfluidity, superconductivity and the theory of Fermi liquid. Here we present some Nobel Archive data on the winning nomination that led to the Nobel Prize in Physics in 1962.

  • 23.
    Larsson, Mats
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf. D.
    Stockholm University, Faculty of Science, Department of Physics.
    Nyman, G.
    Ion chemistry in space2012In: Reports on progress in physics (Print), ISSN 0034-4885, E-ISSN 1361-6633, Vol. 75, no 6, p. 066901-Article, review/survey (Refereed)
    Abstract [en]

    We review the gas-phase chemistry in extraterrestrial space that is driven by reactions with atomic and molecular ions. Ions are ubiquitous in space and are potentially responsible for the formation of increasingly complex interstellar molecules. Until recently, positively charged atoms and molecules were the only ions known in space; however, this situation has changed with the discovery of various molecular anions. This review covers not only the observation, distribution and reactions of ions in space, but also laboratory-based experimental and theoretical methods for studying these ions. Recent results from space-based instruments, such as those on the Cassini-Huygens space mission and the Herschel Space Observatory, are highlighted.

  • 24.
    Larsson, Mats
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    McCall, B. J.
    Orel, A. E.
    The dissociative recombination of H-3(+) - a saga coming to an end?2008In: Chemical Physics Letters, ISSN 0009-2614, E-ISSN 1873-4448, Vol. 462, no 06-apr, p. 145-151Article in journal (Refereed)
    Abstract [en]

    Major progress has been made in the understanding of how H-3(+) recombines with thermal and sub-thermal electrons, a process of great importance to the chemistry of diffuse interstellar clouds. Two independent ion storage ring experiments with rovibrationally cold H-3(+) ions are in excellent agreement, and quantum mechanical calculations agree with the storage ring results quantitatively for the thermal rate constant, if not in all details concerning the cross section. The recombination mechanism is understood. A direct consequence of this progress is that the cosmic-ray ionization rate in diffuse clouds must be shifted upwards to a value larger than 10 (16)s (1). 

  • 25.
    Larsson, Mats
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Salén, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    van der Meulen, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    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 laser2013In: Journal of Physics B: Atomic, Molecular and Optical Physics, ISSN 0953-4075, E-ISSN 1361-6455, Vol. 46, no 16, p. 164030-Article in journal (Refereed)
    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.

  • 26. Li, Cui
    et al.
    Salén, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Yatsyna, Vasyl
    Schio, Luca
    Feifel, Raimund
    Squibb, Richard
    Kaminska, Magdalena
    Stockholm University, Faculty of Science, Department of Physics. Jan Kochanowski University, Poland.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Richter, Robert
    Alagia, Michele
    Stranges, Stefano
    Monti, Susanna
    Carravetta, Vincenzo
    Zhaunerchyk, Vitali
    Experimental and theoretical XPS and NEXAFS studies of N-methylacetamide and N-methyltrifluoroacetamide2016In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 18, no 3, p. 2210-2218Article in journal (Refereed)
    Abstract [en]

    Experimental Near-Edge X-ray Absorption Fine-Structure (NEXAFS) spectra of N-methyltrifluoroacetamide (FNMA), which is a peptide model system, measured at the C, N, O and F K-edges are reported. The features in the spectra have been assigned by Static-Exchange (STEX) calculations. Using the same method, we have also assigned previously measured NEXAFS spectra of another peptide model system, N-methylacetamide (NMA). To facilitate the NEXAFS feature assignments, X-ray Photoelectron Spectroscopy (XPS) measurements for NMA and FNMA have been carried out with the aim of obtaining the 1s electron ionization potentials, which are compared with the values predicted by our Hartree-Fock (Delta HF) and Multi Configuration Self Consistent Field (Delta MCSCF) calculations. We also demonstrate an approach to compensate for screening effects that are neglected in the STEX method. Ion yield measurements of FNMA associated with the excitation of several C, N, O, and F K-shell pre-edge resonances have revealed site-specific fragmentation in some cases which we interpret with the aid of our theoretical calculations.

  • 27. Mucke, M.
    et al.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics. Uppsala University, Sweden; University of Gothenburg, Sweden.
    Frasinski, L. J.
    Squibb, R. J.
    Siano, M.
    Eland, J. H. D.
    Linusson, Per
    Stockholm University, Faculty of Science, Department of Physics.
    Salén, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    vab der Meulen, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Foucar, L.
    Ullrich, J.
    Motomura, K.
    Mondal, S.
    Ueda, K.
    Osipov, T.
    Fang, L.
    Murphy, B. F.
    Berrah, N.
    Bostedt, C.
    Bozek, J. D.
    Schorb, S.
    Messerschmidt, M.
    Glownia, J. M.
    Cryan, J. P.
    Coffee, R. N.
    Takahashi, O.
    Wada, S.
    Piancastelli, M. N.
    Richter, R.
    Prince, K. C.
    Feifel, R.
    Covariance mapping of two-photon double core hole states in C2H2 and C2H6 produced by an x-ray free electron laser2015In: New Journal of Physics, ISSN 1367-2630, E-ISSN 1367-2630, Vol. 17, article id 073002Article in journal (Refereed)
    Abstract [en]

    Few-photon ionization and relaxation processes in acetylene (C2H2) and ethane (C2H6) were investigated at the linac coherent light source x-ray free electron laser (FEL) at SLAC, Stanford using a highly efficient multi-particle correlation spectroscopy technique based on a magnetic bottle. The analysis method of covariance mapping has been applied and enhanced, allowing us to identify electron pairs associated with double core hole (DCH) production and competing multiple ionization processes including Auger decay sequences. The experimental technique and the analysis procedure are discussed in the light of earlier investigations of DCH studies carried out at the same FEL and at third generation synchrotron radiation sources. In particular, we demonstrate the capability of the covariance mapping technique to disentangle the formation of molecular DCH states which is barely feasible with conventional electron spectroscopy methods.

  • 28. Nastasiienko, Nataliia
    et al.
    Palianytsia, Borys
    Kartel, Mykola
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Kulik, Tetiana
    Thermal Transformation of Caffeic Acid on the Nanoceria Surface Studied by Temperature Programmed Desorption Mass-Spectrometry, Thermogravimetric Analysis and FT-IR Spectroscopy2019In: Colloids and Interfaces, ISSN 2504-5377, Vol. 3, no 1, article id 34Article in journal (Refereed)
    Abstract [en]

    The studies of pyrolysis of caffeic acid (CA) and its surface complexes is important for the development of technologies of heterogeneous catalytic pyrolysis of plant- and wood- based renewable biomass components. In this work, the structure and thermal transformations of the surface complexes of CA on the surface of nanoceria were investigated using Fourier transform-infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA) and temperature-programmed desorption mass spectrometry (TPD MS). It was found that CA on the surface of cerium dioxide forms several types of complexes: bidentate carboxylates, monodentate carboxylates and complexes formed as a result of interaction with phenolic hydroxyl groups. This is due to the ability of nanosized cerium dioxide to generate basic hydroxyl groups that can deprotonate phenolic groups to form phenolates on the surface. The main pyrolysis products were identified. The possible ways of forming 3,4-dihydroxyphenylethylene, acetylene carboxylic acid, pyrocatechol and phenol from surface complexes of CA were suggested. It was established that on the nanoceria surface effectively occur the decarboxylation, decarbonylation, and dehydration reactions of the CA, which are the desirable processes in biomass conversion technologies.

  • 29. Pettersson, J. B. C.
    et al.
    Andersson, P. U.
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Öjekull, J.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative recombination and excitation of D-5(+) by collisions with low-energy electrons2015In: Molecular Physics, ISSN 0026-8976, E-ISSN 1362-3028, Vol. 113, no 15-16, p. 2099-2104Article in journal (Refereed)
    Abstract [en]

    We report results from high-resolution studies of D-5(+) cluster ion collisions with low-energy electrons performed in a heavy ion storage ring. Absolute dissociative recombination (DR) and dissociative excitation (DE) cross sections were determined for the energy range from 0.0005 to 20eV. The DR cross sections were exceedingly large at low energies, and DR resulted in efficient internal energy redistribution and pronounced fragmentation with two main product channels: D-2+3D (0.62 +/- 0.03) and 2D(2)+D (0.35 +/- 0.01). The DR and DE cross sections were comparable in the energy range from 0.2 to 20eV, which suggest that the two processes follow similar dynamics and are competing outcomes of the ion-electron interaction. A simple picture of the recombination process of D-5(+) which captures the essential physics is suggested.

  • 30.
    Rebrov, Oleksii
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Kulyk, Kostiantyn
    Stockholm University, Faculty of Science, Department of Physics.
    Ryding, Mauritz
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Uggerud, Einar
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Chirally sensitive collision induced dissociation of proton-bound diastereomeric complexes of tryptophan and 2-butanol2017In: Chirality, ISSN 0899-0042, E-ISSN 1520-636X, Vol. 29, no 3-4, p. 115-119Article in journal (Refereed)
    Abstract [en]

    In this work we report the stereo-dependent collision-induced dissociation (CID) of proton-bound complexes of tryptophan and 2-butanol. The dissociation efficiency was measured as a function of collision energy in single collision mode. The homochiral complex was found to be less stable against CID than a heterochiral one. Additional gas dependence measurements were performed with diastereomeric complexes that confirm the findings.

  • 31.
    Rebrov, Oleksii
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Poline, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Ryding, M. J.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Uggerud, E.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Non-covalently bonded diastereomeric adducts of amino acids and (S)-1-phenylethanol in low-energy dissociative collisions2019In: Molecular Physics, ISSN 0026-8976, E-ISSN 1362-3028Article in journal (Refereed)
    Abstract [en]

    We have studied the collision induced dissociation reactions of proton-bound diastereomeric adducts of S-1-phenylethanol and enantiomers of three different amino acids (tryptophan, phenylalanine, methionine). In all cases, the loss of S-1-phenylethanol from the adduct ion is the only observed process, and the relative abundance is found to be independent of the chirality of the amino acid. This is in contrast to earlier experiments on the dissociation of protonated tryptophan-2-butanol adducts, where chirality affected the results. Results obtained from quantum chemical computations support and provide a rationale for the experimental observations and highlight temperature as a possible factor of importance for the chiral effect in these types of systems. [GRAPHICS] .

  • 32.
    Rebrov, Oleksii
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Poline, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Yatsyna, Vasyl
    Maitre, Philippe
    Loire, Estelle
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    IRMPD spectroscopy of protonated tryptophan diastereomersManuscript (preprint) (Other academic)
  • 33.
    Rebrov, Oleksii
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Ryding, Mauritz J.
    Thomas, Richard
    Stockholm University, Faculty of Science, Department of Physics.
    Uggerud, Einar
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Non-covalently Bonded Diastereomeric Adducts of Amino Acids and (S)-1-Phenylethanol in Low-energy Dissociative CollisionsManuscript (preprint) (Other academic)
    Abstract [en]

    We have studied the collision induced dissociation reactions of proton-bound diastereomeric adducts of S-(-)-1-phenylethanol and enantiomers of three different amino acids (tryptophan, phenylalanine, methionine) with argon at a collision energy of 0.5 eV in the center-of-mass frame. At this energy, fragmentation into the alcohol and the protonated amino acid was the only observed product channel. Contrary to anticipation, the fragmentation was found to be insensitive to the chirality of the constituents. The results obtained from quantum chemical calculations show that the hetero-chiral adducts are more stable than the homo-chiral forms. However, given the experimental conditions in the ion source, it is likely that multiple conformers which lie close in energy to the ground-state configuration are populated, limiting the experimental sensitivity to observe the predicted differences.

  • 34.
    Roos, J. B.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Larson, A.
    Stockholm University, Faculty of Science, Department of Physics.
    Orel, A. E.
    Dissociative recombination of BeH+2009In: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 80, no 1, p. 12501-Article in journal (Refereed)
    Abstract [en]

    The cross section for dissociative recombination of BeH+ is calculated by the solution of the time-dependent Schrodinger equation in the local complex potential approximation. The effects of couplings between resonant states and the Rydberg states converging to the ground state of the ion are studied. The relevant potentials, couplings, and autoionization widths are extracted using ab initio electron scattering and structure calculations, followed by a diabatization procedure. The calculated cross sections show a sizable magnitude at low energy, followed by a high-energy peak centered around 1 eV. The electronic couplings between the neutral states induce oscillations in the cross section. Analytical forms for the cross sections at low collision energies are given.

  • 35.
    Sahlén, Martin
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    van der Meulen, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Feifel, Raimund
    Stockholm University, Faculty of Science, Department of Physics.
    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 Laser2012In: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 108, no 15, p. 153003-Article in journal (Refereed)
    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.

  • 36.
    Schmidt, Henning T.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Gatchell, Michael
    Stockholm University, Faculty of Science, Department of Physics.
    Rosén, Stefan
    Stockholm University, Faculty of Science, Department of Physics.
    Reinhed, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    Stockholm University, Faculty of Science, Department of Physics.
    Brännholm, Lars
    Stockholm University, Faculty of Science, Department of Physics.
    Blom, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Björkhage, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Bäckström, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Alexander, John D.
    Stockholm University, Faculty of Science, Department of Physics.
    Leontein, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Hanstorp, D.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Liljeby, Leif
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Rensfelt, Karl-Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Danared, Håkan
    Stockholm University, Faculty of Science, Department of Physics.
    Paal, A.
    Stockholm University, Faculty of Science, Department of Physics.
    Masuda, Masaharu
    Stockholm University, Faculty of Science, Department of Physics.
    Hallden, Per
    Stockholm University, Faculty of Science, Department of Physics.
    Andler, Guillermo
    Stockholm University, Faculty of Science, Department of Physics.
    Stockett, Mark H.
    Stockholm University, Faculty of Science, Department of Physics.
    Chen, Tao
    Stockholm University, Faculty of Science, Department of Physics.
    Källersjö, Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Weimer, Jan
    Stockholm University, Faculty of Science, Department of Physics.
    Hansen, K.
    Hartman, H.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    First storage of ion beams in the Double Electrostatic Ion-Ring Experiment: DESIREE2013In: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 84, no 5, p. 055115-Article in journal (Refereed)
    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.

  • 37.
    Schmidt, Henning
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Johansson, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf
    Stockholm University, Faculty of Science, Department of Physics.
    Haag, Nicole
    Stockholm University, Faculty of Science, Department of Physics.
    Reinhed, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Rosén, Stefan
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Danared, Håkan
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Rensfelt, K.-G
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Liljeby, Leif
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Bagge, Lars
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Björkhage, Mikael
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Blom, Mikael
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Löfgren, Patrik
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Källberg, Anders
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Paál, Andras
    Stockholm University, Faculty of Science, The Manne Siegbahn Laboratory .
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    DESIREE as a new tool for interstellar ion chemistry2008In: International Journal of Astrobiology, ISSN 1473-5504, E-ISSN 1475-3006, Vol. 7, no 3-4, p. 205-208Article in journal (Refereed)
    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.

  • 38.
    Thomas, Richard D.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Ehlerding, Anneli
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Bahati, E.
    Bannister, M. E.
    Fogle, M. R.
    Vane, C. R.
    Dissociative recombination of LiH2+2014In: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 89, no 5, p. 050701-Article in journal (Refereed)
    Abstract [en]

    In this paper, we report results regarding how LiH2+ fragments as a result of a low-energy collision with an electron (dissociative recombination), a reaction that contains only elements and particles created during the very first phase of the universe. The collision-energy-dependent reaction rate and cross sections show detailed structures, more so than predicted by theory, suggesting significant rovibrational coupling in the ion and a complex reaction surface. From the structure of the molecule, the reaction predominantly results in the formation of Li + H-2. However, 23% of the reaction flux leads to more interesting products, with 17% producing Li + 2H and 6% producing LiH + H. These last two channels break the strongest molecular bond in the system and, in the case of the latter channel, form a significantly weaker ionic bond. Possible reasons behind this interesting behavior are discussed, together with the interaction between the available reaction channels.

  • 39.
    Thomas, Richard D.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Kashperka, Iryna
    Stockholm University, Faculty of Science, Department of Physics.
    Vigren, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative Recombination of CH4+2013In: Journal of Physical Chemistry A, ISSN 1089-5639, E-ISSN 1520-5215, Vol. 117, no 39, p. 9999-10005Article in journal (Refereed)
    Abstract [en]

    CH4+ is an important molecular ion in the astrochemistry of diffuse clouds, dense clouds, cometary comae, and planetary ionospheres However, the rate of one of the common destruction mechanisms for molecular ions in these regions, dissociative recombination (DR), is somewhat uncertain. Here, we present absolute measurements for the DR of CH4+ made using the heavy ion storage ring CRYRING hi Stockholm, Sweden. From our collision energy dependent cross sections, we infer a thermal rate constant of k(T-e) = 1.71(+/- 0.02) X 10(-6)(T-e/300)(-0.66(+/- 0.02)) cm(3) s(-1) over the region of electron temperatures 10 <= T-e <= 1000 K. At low collision energies, we have measured the branching fractions of the DR products to be CH4 (0.00 +/- 0.00); CH3 + H (0.18 +/- 0.03); CH2 + 2H (0.51 +/- 0.03); CH2 + H-2 (0.06 +/- 0.01); CH + H-2 + H (0.23 +/- 0.01); and CH + 2H(2) (0.02 +/- 0.01), indicating that two or more C-H bonds are broken in similar to 80% of all collisions.

  • 40.
    Thomas, Richard D.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Andler, Guillermo
    Stockholm University, Faculty of Science, Department of Physics.
    Björkhage, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Blom, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Brännholm, Lars
    Stockholm University, Faculty of Science, Department of Physics.
    Bäckstrom, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Danared, Håkan
    Stockholm University, Faculty of Science, Department of Physics.
    Das, Susanta
    Stockholm University, Faculty of Science, Department of Physics.
    Haag, Nicole
    Stockholm University, Faculty of Science, Department of Physics.
    Halldén, Per
    Stockholm University, Faculty of Science, Department of Physics.
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Holm, Anne I. S.
    Stockholm University, Faculty of Science, Department of Physics.
    Johansson, H. A. B.
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Källersjö, Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Leontein, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Liljeby, Leif
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    Stockholm University, Faculty of Science, Department of Physics.
    Malm, Bo
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Masuda, Masaharu
    Stockholm University, Faculty of Science, Department of Physics.
    Misra, Deepankar
    Stockholm University, Faculty of Science, Department of Physics.
    Orban, A.
    Stockholm University, Faculty of Science, Department of Physics.
    Paál, Andras
    Stockholm University, Faculty of Science, Department of Physics.
    Reinhed, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Rensfelt, Karl-Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Rosén, Stefan
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, K.
    Stockholm University, Faculty of Science, Department of Physics.
    Seitz, Fabian
    Stockholm University, Faculty of Science, Department of Physics.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Weimer, Jan
    Stockholm University, Faculty of Science, Department of Physics.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    The double electrostatic ion ring experiment: A unique cryogenic electrostatic storage ring for merged ion-beams studies2011In: Review of Scientific Instruments, ISSN 0034-6748, E-ISSN 1089-7623, Vol. 82, no 6, p. 065112-Article in journal (Refereed)
    Abstract [en]

    We describe the design of a novel type of storage device currently under construction at Stockholm University, Sweden, using purely electrostatic focussing and deflection elements, in which ion beams of opposite charges are confined under extreme high vacuum cryogenic conditions in separate rings and merged over a common straight section. The construction of this double electrostatic ion ring experiment uniquely allows for studies of interactions between cations and anions at low and well-defined internal temperatures and centre-of-mass collision energies down to about 10 K and 10 meV, respectively. Position sensitive multi-hit detector systems have been extensively tested and proven to work in cryogenic environments and these will be used to measure correlations between reaction products in, for example, electron-transfer processes. The technical advantages of using purely electrostatic ion storage devices over magnetic ones are many, but the most relevant are: electrostatic elements which are more compact and easier to construct; remanent fields, hysteresis, and eddy-currents, which are of concern in magnetic devices, are no longer relevant; and electrical fields required to control the orbit of the ions are not only much easier to create and control than the corresponding magnetic fields, they also set no upper mass limit on the ions that can be stored. These technical differences are a boon to new areas of fundamental experimental research, not only in atomic and molecular physics but also in the boundaries of these fields with chemistry and biology. For examples, studies of interactions with internally cold molecular ions will be particular useful for applications in astrophysics, while studies of solvated ionic clusters will be of relevance to aeronomy and biology.

  • 41.
    Thomas, Richard D.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Gatchell, Michael
    Stockholm University, Faculty of Science, Department of Physics.
    Rosén, Sara
    Stockholm University, Faculty of Science, Department of Physics.
    Reinhed, Peter
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    Stockholm University, Faculty of Science, Department of Physics.
    Brännholm, Lars
    Stockholm University, Faculty of Science, Department of Physics.
    Blom, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Björkhage, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Bäckström, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Alexander, John D.
    Stockholm University, Faculty of Science, Department of Physics.
    Leontein, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Hanstorp, D.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Stockholm University, Faculty of Science, Department of Physics.
    Nascimento, Rodrigo
    Stockholm University, Faculty of Science, Department of Physics.
    Liljeby, Leif
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Hellberg, Fredrik
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Rensfelt, Karl-Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Paál, Andras
    Stockholm University, Faculty of Science, Department of Physics.
    Masuda, Masaharu
    Stockholm University, Faculty of Science, Department of Physics.
    Halldén, Per
    Stockholm University, Faculty of Science, Department of Physics.
    Andler, Guillermo
    Stockholm University, Faculty of Science, Department of Physics.
    Stockett, Mark H.
    Stockholm University, Faculty of Science, Department of Physics.
    Chen, Tao
    Stockholm University, Faculty of Science, Department of Physics.
    Källersjö, Gunnar
    Stockholm University, Faculty of Science, Department of Physics.
    Weimer, Jan
    Stockholm University, Faculty of Science, Department of Physics.
    Hansen, K.
    Hartman, H.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    DESIREE: Physics with cold stored ion beams2015In: DR2013: Ninth international conference on dissociative recombination: theory, experiment, and applications, 2015, Vol. 84, article id 01004Conference paper (Refereed)
    Abstract [en]

    Here we will briefly describe the commissioning of the Double ElectroStatic Ion Ring ExpEriment (DESIREE) facility at Stockholm University, Sweden. This device uses purely electrostatic focussing and deflection elements and allows ion beams of opposite charge to be confined under extreme high vacuum and cryogenic conditions in separate rings and then merged over a common straight section. This apparatus allows for studies of interactions between cations and anions at very low and well-defined centre-of-mass energies (down to a few meV) and at very low internal temperatures (down to a few K).

  • 42.
    Thomas, Richard
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Kashperka, I.
    Stockholm University, Faculty of Science, Department of Physics.
    Vigren, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, M.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Indriolo, N.
    Yagi, K.
    Hirata, S.
    McCall, B. J.
    DISSOCIATIVE RECOMBINATION OF VIBRATIONALLY COLD CH+3 AND INTERSTELLAR IMPLICATIONS2012In: Astrophysical Journal, ISSN 0004-637X, E-ISSN 1538-4357, Vol. 758, no 1, p. 55-Article in journal (Refereed)
    Abstract [en]

    CH3+ is an important molecular ion in the astrochemistry of diffuse clouds, dense clouds, cometary comae, and planetary ionospheres. However, the rate of one of the major destruction mechanisms of CH3+, dissociative recombination (DR), has long been uncertain, hindering the use of CH3+ as an astrochemical probe. Here, we present the first absolute measurement of the DR of vibrationally cold CH3+, which has been made using the heavy storage ring CRYRING in Stockholm, Sweden. From our collision-energy-dependent cross sections, we infer a thermal rate constant of k(T) = 6.97(+/- 0.03) x 10(-7)(T/300)(-0.61(+/- 0.01)) cm(3) s(-1) over the region 10 K <= T <= 1000 K. At low collision energies, we have measured the branching fractions of the DR products to be CH3 (0.00(- 0.00)(+ 0.01)), CH2 + H (0.35(-0.01)(+ 0.01)), CH + 2H (0.20(-0.02)(+0.02)), CH + H-2 (0.10(-0.01)(+0.01)), and C + H-2 + H (0.35(-0.02)(+ 0.01)), indicating that two or more C-H bonds are broken in 65% of all collisions. We also present vibrational calculations which indicate that the CH3+ ions in the storage ring were relaxed to the vibrational ground state by spontaneous emission during the storage time. Finally, we discuss the implications of these new measurements for the observation of CH3+ in regions of the diffuse interstellar medium where CH+ is abundant.

  • 43. Tom, Brian A.
    et al.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Wiczer, Michael B.
    Mills, Andrew A.
    Crabtree, Kyle N.
    Kaminska, Magdalena
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Vigren, Erik
    Stockholm University, Faculty of Science, Department of Physics.
    van der Zande, Wim J.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    McCall, Benjamin J.
    Dissociative recombination of highly enriched para-H-3(+)2009In: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 130, no 3, p. 31101-Article in journal (Refereed)
    Abstract [en]

    The determination of the dissociative recombination rate coefficient of H-3(+) has had a turbulent history, but both experiment and theory have recently converged to a common value. Despite this convergence, it has not been clear if there should be a difference between the rate coefficients for ortho-H-3(+) and para-H-3(+). A difference has been predicted theoretically and could conceivably impact the ortho:para ratio of H-3(+) in the diffuse interstellar medium, where H-3(+) has been widely observed. We present the results of an experiment at the CRYRING ion storage ring in which we investigated the dissociative recombination of highly enriched (similar to 83.6%) para-H-3(+) using a supersonic expansion source that produced ions with T-rot similar to 60-100 K. We observed an increase in the low energy recombination rate coefficient of the enriched para-H-3(+) by a factor of similar to 1.25 in comparison to H-3(+) produced from normal H-2 (ortho:para=3:1). The ratio of the rate coefficients of pure para-H-3(+) to that of pure ortho-H-3(+) is inferred to be similar to 2 at low collision energies; the corresponding ratio of the thermal rate coefficients is similar to 1.5 at electron temperatures from 60 to 1000 K. We conclude that this difference is unlikely to have an impact on the interstellar ortho:para ratio of H-3(+).

  • 44.
    Vigren, E.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, V.
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, W. D.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, M.
    Stockholm University, Faculty of Science, Department of Physics.
    Bahati, E.
    Vane, C. R.
    Bannister, M. E.
    Fogle, M. R.
    Hamberg, M.
    Stockholm University, Faculty of Science, Department of Physics.
    Danielsson, M.
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, M.
    Thomas, R. D.
    Stockholm University, Faculty of Science, Department of Physics.
    Collision-induced dissociation of similar to 2-MeV O-3(+) and N-3(+) ions2013In: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 87, no 5, article id 052707Article in journal (Refereed)
    Abstract [en]

    We present a study into the collision-induced dissociation (possibly including electron stripping) of O-3(+) and N-3(+) with rest gas molecules (predominantly H-2) in the heavy-ion storage ring CRYRING. The projectile ions had kinetic energies of 1.96 MeV (O-3(+)) and 2.25 MeV (N-3(+)) and from the experimental data we could derive the relative importance of the channels that produce at least one neutral product fragment. The dominant type of fragmentation for both ions involves the production of a single neutral fragment, namely an individual atom. We also find pronounced dissimilarities when comparing the O-3(+) and N-3(+) results, which we link to the stronger chemical bonds in the nitrogen system.

  • 45.
    Vigren, Erik
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Semaniak, Jacek
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Kashperka, Iryna
    Stockholm University, Faculty of Science, Department of Physics.
    Millar, T. J.
    Walsh, Catherine
    Roberts, Helen
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative Recombination of Protonated Formic Acid: Implications for Molecular Cloud and Cometary Chemistry2010In: Astrophysical Journal, ISSN 0004-637X, E-ISSN 1538-4357, Vol. 709, no 2, p. 1429-1434Article in journal (Refereed)
    Abstract [en]

    At the heavy ion storage ring CRYRING in Stockholm, Sweden, we have investigated the dissociative recombination of DCOOD2+ at low relative kinetic energies, from similar to 1 meV to 1 eV. The thermal rate coefficient has been found to follow the expression k(T) = 8.43 x 10(-7) (T/300)(-0.78) cm(3) s(-1) for electron temperatures, T, ranging from similar to 10 to similar to 1000 K. The branching fractions of the reaction have been studied at similar to 2 meV relative kinetic energy. It has been found that similar to 87% of the reactions involve breaking a bond between heavy atoms. In only 13% of the reactions do the heavy atoms remain in the same product fragment. This puts limits on the gas-phase production of formic acid, observed in both molecular clouds and cometary comae. Using the experimental results in chemical models of the dark cloud, TMC-1, and using the latest release of the UMIST Database for Astrochemistry improves the agreement with observations for the abundance of formic acid. Our results also strengthen the assumption that formic acid is a component of cometary ices.

  • 46.
    Vigren, Erik
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Millar, T. J.
    Walsh, Catherine
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    The Dissociative Recombination of Protonated Acrylonitrile, CH2CHCNH+, with implications for the Nitrile Chemistry in Dark Molecular Clouds and the Upper Atmosphere of Titan2009In: Astrophysical Journal, ISSN 0004-637X, E-ISSN 1538-4357, Vol. 695, no 1, p. 317-324Article in journal (Refereed)
    Abstract [en]

    Measurements on the dissociative recombination (DR) of protonated acrylonitrile, CH2CHCNH+, have been performed at the heavy ion storage ring CRYRING located in the Manne Siegbahn Laboratory in Stockholm, Sweden. It has been found that at similar to 2meV relative kinetic energy about 50% of the DR events involve only ruptures of X-Hbonds (where X = C or N) while the rest leads to the production of a pair of fragments each containing two heavy atoms (alongside H and/or H-2). The absolute DR cross section has been investigated for relative kinetic energies ranging from similar to 1 meV to 1 eV. The thermal rate coefficient has been determined to follow the expression k(T) = 1.78 x 10(-6) (T/300)(-0.80) cm(3) s(-1) for electron temperatures ranging from similar to 10 to 1000 K. Gas-phase models of the nitrile chemistry in the dark molecular cloud TMC-1 have been run and results are compared with observations. Also, implications of the present results for the nitrile chemistry of Titan's upper atmosphere are discussed.

  • 47.
    Vigren, Erik
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Kaminska, Magdalena
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Trippel, Sebastian
    Wester, Roland
    Zhang, Mingwu
    Kashperka, Iryna
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics, The Manne Siegbahn Laboratory.
    Semaniak, Jacek
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative Recombination of Protonated Propionitrile, CH3CH2CNH+: Implications for Titan's Upper Atmosphere2010In: Astrophysical Journal, ISSN 0004-637X, E-ISSN 1538-4357, Vol. 722, no 1, p. 847-850Article in journal (Refereed)
    Abstract [en]

    The dissociative recombination of protonated propionitrile, CH3CH2CNH+, has been investigated at the heavy ion storage ring, CRYRING, at the Manne Siegbahn Laboratory, Stockholm University, Sweden. The thermal rate coefficient has been deduced to follow k(T) = (1.5 ± 0.2) × 10–6 (T/300)–0.76 ± 0.02 cm3 s–1 for electron temperatures ranging from ~10 to ~1000 K. Measurements of the branching fractions were performed at ~0 eV relative kinetic energy. It has been found that in 43% ± 2% of the reactions the four heavy atoms remain in the same product fragment. An equal portion of the reactions leads to products where one of the heavy atoms is split off from the other three and 14% ± 1% result in a breakup into two heavy fragments containing two heavy atoms each. We discuss the significance of the data to Titan's upper atmosphere.

  • 48.
    Vigren, Erik
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Trippel, Sebastian
    Zhang, Mingwu
    Stockholm University, Faculty of Science, Department of Physics.
    Kashperka, Iryna
    Stockholm University, Faculty of Science, Department of Physics.
    af Ugglas, Magnus
    Stockholm University, Faculty of Science, Department of Physics.
    Walsh, Catherine
    Wester, Roland
    Semaniak, Jacek
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative recombination of the acetaldehyde cation, CH3CHO+2010In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 12, no 37, p. 11670-11673Article in journal (Refereed)
    Abstract [en]

    The dissociative recombination of the acetaldehyde cation, CH3CHO+, has been investigated at the heavy ion storage ring CRYRING at the Manne Siegbahn Laboratory in Stockholm, Sweden. The dependence of the absolute cross section of the reaction on the relative kinetic energy has been determined and a thermal rate coefficient of k(T) = (1.5 +/- 0.2) x 10(-6) (T/300)(-0.70 +/- 0.02) cm(3) s(-1) has been deduced, which is valid for electron temperatures between similar to 10 and 1000 K. The branching fractions of the reaction were studied at similar to 0 eV relative kinetic energy and we found that breaking one of the bonds between two of the heavy atoms occurs in 72 +/- 2% of the reactions. In the remaining events the three heavy atoms stay in the same product fragment. While the branching fractions are fairly similar to the results from an earlier investigation into the dissociative recombination of the fully deuterated acetaldehyde cation, CD3CDO+, the thermal rate coefficient is somewhat larger for CH3CHO+. Astrochemical implications of the results are discussed.

  • 49.
    Vigren, Erik
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Danielsson, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Semaniak, Jacek
    Andersson, Patrik U.
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative recombination of fully deuterated protonated acetonitrile, CD3CND+: Product branching fractions, absolute cross section and thermal rate coefficient2008In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 10, no 27, p. 4014-4019Article in journal (Refereed)
    Abstract [en]

    The dissociative recombination of fully deuterated protonated acetonitrile, CD3CND+, has been investigated at the CRYRING heavy ion storage ring, located at the Manne Siegbahn Laboratory, Stockholm, Sweden. Branching fractions were measured at similar to 0 eV relative collision energy between the ions and the electrons and in 65% of the DR events there was no rupture of bonds between heavy atoms. In the remaining 35%, one of the bonds between the heavy atoms was broken. The DR cross-section was measured between similar to 0 eV and 1 eV relative collision energy. In the energy region between 1 meV and 0.1 eV the cross section data were best fitted by the expression sigma = 7.37 x 10(-16) (E/eV)(-1.23) cm(2), whereas sigma = 4.12 x 10(-16) (E/eV)(-1.46) cm(2) was the best fit for the energy region between 0.1 and 1.0 eV. From the cross section a thermal rate coefficient of alpha(T) = 8.13 x 10(-7) (T/300)(-0.69) cm(3) s(-1) was deduced.

  • 50.
    Vigren, Erik
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Hamberg, Mathias
    Stockholm University, Faculty of Science, Department of Physics.
    Zhaunerchyk, Vitali
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Semaniak, Jacek
    Danielsson, Mathias
    Larsson, Mats
    Stockholm University, Faculty of Science, Department of Physics.
    Geppert, Wolf D.
    Stockholm University, Faculty of Science, Department of Physics.
    Dissociative recombination of the deuterated acetaldehyde ion, CD3CDO+: product branching fractions, absolute cross sections and thermal rate coefficient2007In: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 9, no 22, p. 2856-2861Article in journal (Refereed)
    Abstract [en]

    Dissociative recombination of the deuterated acetaldehyde ion CD3CDO+ has been studied at the heavy-ion storage ring CRYRING, located at the Manne Siegbahn Laboratory, Stockholm, Sweden. Product branching fractions together with absolute DR cross-sections were measured. The branching fractions were determined at a relative collision energy between the ions and the electrons of 0 eV. With a probability of 34% the DR events resulted in no ruptures of bonds between heavy atoms (i.e. no breakage of the C–C bond or the CO bond). In the remaining 66% of the events one of the bonds between the heavy atoms was broken. The energy-dependent cross-section for the DR reaction was measured between 0 and 1 eV relative kinetic energy. In the energy region between 1 meV and 0.2 eV the absolute cross section could be fitted by the expression σ(E) = 6.8 × 10−16E−1.28 cm2, whereas in the energy interval between 0.2 and 1 eV the data were best fitted by σ(E) = 4.1 × 10−16E−1.60 cm2. From these cross section data the thermal rate coefficient (as a function of the electron temperature), α(T) = 9.2 × 10−7 (T/300)−0.72 cm3 s−1 was obtained.

12 1 - 50 of 57
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