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Stabilities of multiply charged dimers and clusters of fullerenes
Stockholms universitet.
Stockholms universitet.
Stockholms universitet.
Stockholms universitet.
Vise andre og tillknytning
2007 (engelsk)Inngår i: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 126, nr 22, s. 224303-Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The authors find even-odd variations as functions of r (...+[C60]2(r+)([C60C70](r+)) electron-transfer collisions. This even-odd behavior is in sharp contrast to the smooth one for fullerene monomers and may be related to even-odd effects in dimer ionization energies in agreement with results from an electrostatic model. The kinetic energy releases for dimer dissociations [predominantly yielding intact fullerenes [C60]2(r+)-->C60(r1+)+C60(r2+) in the same (r1=r2) or nearby (r1=r2+/-1) charge states] are found to be low in comparison with the corresponding model results indicating that internal excitations of the separating (intact) fullerenes are important. Experimental appearance sizes for the heavier clusters of fullerenes [C60]n(r+) (n>3 and r=2-5) compare well with predictions from a new nearest-neighbor model assuming that r unit charges in [C60]n(r+) are localized to r C60 molecules such that the Coulomb energy of the system is minimized. The system is then taken to be stable if (i) two (singly) charged C60 are not nearest neighbors and (ii) the r C60(+) molecules have binding energies to their neutral nearest neighbors which are larger than the repulsive energies for the (r-1) C60(+)-C60(+) pairs. Essential ingredients in the nearest-neighbor model are cluster geometries and the present results on dimer stabilities.

sted, utgiver, år, opplag, sider
2007. Vol. 126, nr 22, s. 224303-
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Identifikatorer
URN: urn:nbn:se:uu:diva-12710DOI: 10.1063/1.2743433ISI: 000247247400015OAI: oai:DiVA.org:uu-12710DiVA, id: diva2:40479
Tilgjengelig fra: 2008-01-10 Laget: 2008-01-10 Sist oppdatert: 2017-12-11bibliografisk kontrollert

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