Photoinduced charge shift in Li+ doped giant nested fullerenes
Over the last years, carbon nano-onions (CNOs) have been in focus in material science research. Their red-shifted absorption allows utilizing CNOs as promising photosensitizers. We report here a systematic study of excited state properties of six double-layered Li+ doped fullerenes of Ih symmetry: [...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:10256/16739 |
| Acceso en línea: | http://hdl.handle.net/10256/16739 |
| Access Level: | acceso abierto |
| Palabra clave: | Ful·lerens Fotoquímica Fullerenes Photochemistry |
| Sumario: | Over the last years, carbon nano-onions (CNOs) have been in focus in material science research. Their red-shifted absorption allows utilizing CNOs as promising photosensitizers. We report here a systematic study of excited state properties of six double-layered Li+ doped fullerenes of Ih symmetry: [Li@C60@C240]+, [Li@C60@C540]+, [Li@C60@C960]+, [Li@C240@C540]+, [Li@C240@C960]+ and [Li@C540@C960]+. On the basis of TDDFT calculations, we show that the long-wave absorption by the Li+ doped species leads to charge transfer (CT) between the inner and the outer shells unlike their neutral double-layered precursors. The CT energy depends strongly on the size of the concentric fullerenes and it can easily be tuned by varying both the encapsulated metal ion and the size of the shells. Two types of low-lying excited states are identified (1) capacitor-like structures, as Li+@C60-@C240+, with alternating positive and negative charges, and (2) states, where the positive charge is delocalized over the outer shell, as in Li@C240@C540+. We suggest a simple expression to estimate the energy difference of these excited states and to predict the type of the lowest CT state in nested fullerenes. The effect of nature of the encapsulated ion on the charge transfer state energies is considered. The HOMO - LUMO transition energy is found to vary significantly when going from [Li@C60@C240]+ to [Li@C540@C960]+ |
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