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  • 1.
    Bäckström, Erik
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Hanstorp, D.
    Hole, Odd Magnar
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Stockholm University, Faculty of Science, Department of Physics. Jan Kochanowski University, Poland.
    Nascimento, Rodrigo F.
    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.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    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.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    Storing keV negative ions for an hour: The lifetime of the metastable 2P1/2 level in 32S−2015In: Physical Review Letters, ISSN 0031-9007, E-ISSN 1079-7114, Vol. 114, no 14, article id 143003Article in journal (Refereed)
    Abstract [en]

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

  • 2.
    Chartkunchand, Kiattichart C.
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Kaminska, Magdalena
    Stockholm University, Faculty of Science, Department of Physics. Jan Kochanowski University, Poland.
    Anderson, Emma K.
    Stockholm University, Faculty of Science, Department of Physics.
    Kristiansson, M. K.
    Eklund, Gustav
    Stockholm University, Faculty of Science, Department of Physics.
    Hole, Odd Magnar
    Stockholm University, Faculty of Science, Department of Physics.
    Nascimento, Rodrigo F.
    Stockholm University, Faculty of Science, Department of Physics. Centro Federal de Educação Tecnológica Celso Suckow da Fonseca, Brazil.
    Blom, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Björkhage, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    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.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Davis, V. T.
    Neill, P. A.
    Thompson, J. S.
    Hanstorp, D.
    Zettergren, Henning
    Stockholm University, Faculty of Science, Department of Physics.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Radiative lifetimes of the bound excited states of Pt-2016In: Physical Review A, ISSN 2469-9926, Vol. 94, no 3, article id 032501Article in journal (Refereed)
    Abstract [en]

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

  • 3.
    Gatchell, Michael
    et al.
    Stockholm University, Faculty of Science, Department of Physics.
    Stockett, Mark H.
    Stockholm University, Faculty of Science, Department of Physics. Aarhus University, Denmark.
    de Ruette, Nathalie
    Stockholm University, Faculty of Science, Department of Physics.
    Chen, Tao
    Stockholm University, Faculty of Science, Department of Physics.
    Giacomozzi, Linda
    Stockholm University, Faculty of Science, Department of Physics.
    Nascimento, Rodrigo F.
    Stockholm University, Faculty of Science, Department of Physics.
    Wolf, Michael
    Stockholm University, Faculty of Science, Department of Physics.
    Anderson, Emma K.
    Stockholm University, Faculty of Science, Department of Physics.
    Delaunay, R.
    Vizcaino, V.
    Rousseau, P.
    Adoui, L.
    Huber, B. A.
    Schmidt, Henning T.
    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.
    Failure of hydrogenation in protecting polycyclic aromatic hydrocarbons from fragmentation2015In: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 92, no 5, article id 050702Article in journal (Refereed)
    Abstract [en]

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

  • 4.
    Kamińska, Magdalena
    et al.
    Stockholm University, Faculty of Science, Department of Physics. Jan Kochanowski University, Poland.
    Davis, V. T.
    Hole, Odd Magnar
    Stockholm University, Faculty of Science, Department of Physics.
    Nascimento, Rodrigo F.
    Stockholm University, Faculty of Science, Department of Physics. Centro Federal de Educação Tecnológica Celso Suckow da Fonseca, Brazil.
    Chartkunchand, Kiattichart C.
    Stockholm University, Faculty of Science, Department of Physics. University of Nevada, USA.
    Blom, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Björkhage, Mikael
    Stockholm University, Faculty of Science, Department of Physics.
    Källberg, Anders
    Stockholm University, Faculty of Science, Department of Physics.
    Löfgren, Patrik
    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.
    Simonsson, Ansgar
    Stockholm University, Faculty of Science, Department of Physics.
    Thomas, Richard D.
    Stockholm University, Faculty of Science, Department of Physics.
    Mannervik, Sven
    Stockholm University, Faculty of Science, Department of Physics.
    Neill, P. A.
    Thompson, J. S.
    Schmidt, Henning T.
    Stockholm University, Faculty of Science, Department of Physics.
    Cederquist, Henrik
    Stockholm University, Faculty of Science, Department of Physics.
    Hanstorp, D.
    Lifetime of the bound excited level in Ni-2016In: Physical Review A. Atomic, Molecular, and Optical Physics, ISSN 1050-2947, E-ISSN 1094-1622, Vol. 93, no 1, article id 012512Article in journal (Refereed)
    Abstract [en]

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

  • 5. Santos, L. O.
    et al.
    Rocha, A. B.
    Nascimento, Rodrigo F.
    Stockholm University, Faculty of Science, Department of Physics. UnED Petrópolis, Brazil.
    de Castro Faria, N. V.
    Jalbert, Ginette
    Potential energy curves and generalized oscillator strength for doubly excited states of hydrogen molecule2015In: Journal of Physics B: Atomic, Molecular and Optical Physics, ISSN 0953-4075, E-ISSN 1361-6455, Vol. 48, no 18, article id 185104Article in journal (Refereed)
    Abstract [en]

    We report calculations of potential energy curves for doubly excited states of the H-2 molecule in the 1.2a. u. <= R <= 12a. u. range at the multireference configuration interaction (MRCI) level based on multiconfigurational self-consistent field (MCSCF) orbitals. We focus on the Q(2) states which lie between the second and third ionization thresholds of the H-2(+) molecular ion, i.e. the (2)Sigma(+)(u) and (2)Pi(u) states, respectively, and dissociate in the H(2l) + H(2l) channels. The MCSCF/ MRCI approach allows us to successfully identify the molecular optically forbidden Q(2) (1)Sigma(+)(g) state which dissociates into two H(2s) atoms. Generalized oscillator strength as a function of transferred momentum for three doubly excited states is also presented.

  • 6.
    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).

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