Excitonic Resonance in Semiconductor–Metal Nanohybrids
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Scholar |
Altres documents de l'autoria: Climente, Juan I.; Movilla, Jose L.; Goldoni, Guido; Planelles, Josep
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Mostra el registre complet de l'elementcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7013
comunitat-uji-handle3:10234/8638
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http://dx.doi.org/10.1021/jp2047757 |
Metadades
Títol
Excitonic Resonance in Semiconductor–Metal NanohybridsData de publicació
2011-07Editor
ACSISSN
1932-7447Tipus de document
info:eu-repo/semantics/articleVersió de l'editorial
http://pubs.acs.org/doi/full/10.1021/jp2047757Versió
info:eu-repo/semantics/publishedVersionResum
We use a configuration interaction approach within the envelope function approximation to study the nature of the excitonic resonance in nanohybrids, composite nanoparticles (NPs) combining a semiconducting and a ... [+]
We use a configuration interaction approach within the envelope function approximation to study the nature of the excitonic resonance in nanohybrids, composite nanoparticles (NPs) combining a semiconducting and a metallic segment in contact. With reference to recent experimental reports, we specifically study CdS-based nanorods with metallic NPs deposited at the tips (matchstick) or metallic coatings (core–shell). The excitonic states are computed taking into account both the renormalization of the electron–hole interaction and self-energy effects induced by the metallic segment on the electron–hole pair, as well as by the dielectric environment, through an induced charge numerical approach. In neutral matchstick structures, the metal NP has only a minor influence (1 meV) on the excitonic states. When the metallic NP is charged, the exciton becomes rapidly red-shifted and spatially indirect. In contrast, in neutral core–shell structures the exciton energy red-shifts by tens of millielectronvolts. [-]
Publicat a
Journal Physical Chemistry C, 2011, 115 (32)Drets d'accés
Copyright © 2011 American Chemical Society
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