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• W2533575565 abstract "A theoretical study on the geometric and electronic structure of C60 and Sc3N@C80 absorbed on pristine graphene nanoflakes (GNFs) is presented. C60 is found to adsorb in two nearly degenerate configurations: with a pentagon facing the GNF, which is the most stable one, and with a hexagon facing the GNF in a face-to-face perfect alignment, rarely common in π–π interactions, 0.06 eV higher in energy. The calculated binding energy of 0.76 eV, which includes dispersion effects, is in good agreement with previous theoretical and experimental reports. On the contrary, Sc3N@C80 adsorption on the GNF resulted in a higher binding energy of 1.00 eV for nearly degenerate isomers that have a pentagon and a hexagon facing the SLG. This larger binding energy is explained in terms of a higher dispersion interaction between the larger metallofullerene and the GNF, and due to the fact that charge separation in Sc3N@C80, which results in a positively charged Sc3N inside a negatively charged C80, favors binding with the GNF. Furthermore, the Sc3N moiety is found to rotate inside the supported C80 fullerene, which in combination with the orientation of the fullerene on the SLG leads to a series of isomers with binding energies ranging from 0.76 to 1.00 eV. Our results show that it could be possible to adsorb metallofulleres on graphene nanoflakes with an energy large enough to prevent diffusion, therefore opening the possibility to potential applications." @default.
• W2533575565 created "2016-10-28" @default.
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• W2533575565 date "2016-11-02" @default.
• W2533575565 modified "2023-09-25" @default.
• W2533575565 title "Electronic and Structural Properties of C60 and Sc3N@C80 Supported on Graphene Nanoflakes" @default.
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• W2533575565 doi "https://doi.org/10.1021/acs.jpcc.6b07405" @default.
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