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Ions colliding with...
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Seitz, FabianStockholms universitet,Fysikum
(author)
Ions colliding with clusters of fullerenes-Decay pathways and covalent bond formations
- Article/chapterEnglish2013
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AIP Publishing,2013
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LIBRIS-ID:oai:DiVA.org:su-92922
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https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-92922URI
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https://doi.org/10.1063/1.4812790DOI
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Language:English
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Summary in:English
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
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AuthorCount:23;
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We report experimental results for the ionization and fragmentation of weakly bound van der Waals clusters of n C-60 molecules following collisions with Ar2+, He2+, and Xe20+ at laboratory kinetic energies of 13 keV, 22.5 keV, and 300 keV, respectively. Intact singly charged C-60 monomers are the dominant reaction products in all three cases and this is accounted for by means of Monte Carlo calculations of energy transfer processes and a simple Arrhenius-type [C-60](n)(+) -> C-60(+) + (n - 1)C-60 evaporation model. Excitation energies in the range of only similar to 0.7 eV per C-60 molecule in a [C-60](13)(+) cluster are sufficient for complete evaporation and such low energies correspond to ion trajectories far outside the clusters. Still we observe singly and even doubly charged intact cluster ions which stem from even more distant collisions. For penetrating collisions the clusters become multiply charged and some of the individual molecules may be promptly fragmented in direct knock-out processes leading to efficient formations of new covalent systems. For Ar2+ and He2+ collisions, we observe very efficient C-119(+) and C-118(+) formation and molecular dynamics simulations suggest that they are covalent dumb-bell systems due to bonding between C-59(+) or C-58(+) and C-60 during cluster fragmentation. In the Ar2+ case, it is possible to form even smaller C-120-2m(+) molecules (m = 2-7), while no molecular fusion reactions are observed for the present Xe20+ collisions.
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Zettergren, HenningStockholms universitet,Fysikum(Swepub:su)henning
(author)
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Rousseau, P.
(author)
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Wang, Y.
(author)
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Chen, TaoStockholms universitet,Fysikum(Swepub:su)tache
(author)
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Gatchell, MichaelStockholms universitet,Fysikum(Swepub:su)miga8512
(author)
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Alexander, John D.Stockholms universitet,Fysikum(Swepub:su)jalex
(author)
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Stockett, Mark H.Stockholms universitet,Fysikum(Swepub:su)mstoc
(author)
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Rangama, J.
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Chesnel, J. Y.
(author)
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Capron, M.
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Poully, J. C.
(author)
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Domaracka, A.
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Mery, A.
(author)
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Maclot, S.
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Vizcaino, V.
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Schmidt, Henning T.Stockholms universitet,Fysikum(Swepub:su)schmidt
(author)
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Adoui, L.
(author)
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Alcami, M.
(author)
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Tielens, A. G. G. M.
(author)
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Martin, F.
(author)
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Huber, B. A.
(author)
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Cederquist, HenrikStockholms universitet,Fysikum(Swepub:su)cederq
(author)
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Stockholms universitetFysikum
(creator_code:org_t)
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In:Journal of Chemical Physics: AIP Publishing139:30021-96061089-7690
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Seitz, Fabian
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Zettergren, Henn ...
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Rousseau, P.
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Wang, Y.
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Chen, Tao
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Gatchell, Michae ...
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Alexander, John ...
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Stockett, Mark H ...
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Rangama, J.
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Chesnel, J. Y.
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Capron, M.
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Poully, J. C.
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Domaracka, A.
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Mery, A.
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Maclot, S.
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Vizcaino, V.
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Schmidt, Henning ...
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Adoui, L.
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Alcami, M.
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Tielens, A. G. G ...
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Martin, F.
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Huber, B. A.
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Cederquist, Henr ...
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Stockholm University