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• W2009117565 abstract "We present the optimization of a genetic algorithm (GA) that is designed to predict the most stable structural isomers of hydrogenated and hydroxylated fullerene cages. Density functional theory (DFT) and density functional tight binding (DFTB) methods are both employed to compute isomer energies. We show that DFTB and DFT levels of theory are in good agreement with each other and that therefore both sets of optimized GA parameters are very similar. As a prototypical fullerene cage, we consider the functionalization of the C20 species, since for this smallest possible fullerene cage it is possible to compute all possible isomer energies for evaluation of the GA performance. An energy decomposition analysis for both C20Hn and C20(OH)n systems reveals that, for only few functional groups, the relative stabilities of different structural isomers may be rationalized simply with recourse to π-Hückel theory. However, upon a greater degree of functionalization, π-electronic effects alone are incapable of describing the interaction between the functional groups and the distorted cage, and both σ- and π-electronic structure must be taken into account in order to understand the relative isomer stabilities." @default.
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• W2009117565 date "2012-04-24" @default.
• W2009117565 modified "2023-10-06" @default.
• W2009117565 title "Optimization of a Genetic Algorithm for the Functionalization of Fullerenes" @default.
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• W2009117565 doi "https://doi.org/10.1021/ct300190u" @default.
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