http://www.cnr.it/ontology/cnr/individuo/prodotto/ID167021
Direct role of surface oxygen vacancies in visible light emission of tin dioxide nanowires (Articolo in rivista)
- Type
- Label
- Direct role of surface oxygen vacancies in visible light emission of tin dioxide nanowires (Articolo in rivista) (literal)
- Anno
- 2008-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1063/1.3041775? (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- S. Lettieri; M. Causà; A. Setaro; F. Trani; V. Barone; D. Ninno; P. Maddalena (literal)
- Pagina inizio
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- [S. Lettieri]: CNR-INFM Coherentia, I-80126 Naples, Italy
[M. Causa]: Univ Naples Federico 2, Dipartimento Chim, I-80126 Naples, Italy
[A. Setaro, F. Trani, P. Maddalena]: Univ Naples Federico 2, Dipartimento Sci Fis, I-80126 Naples, Italy
[V. Barone]: Univ Naples Federico 2, Dipartimento Chim, I-80126 Naples, Italy
and Area Ric, CNR, Ist Proc Chim Fis, I-56124 Pisa, Italy (literal)
- Titolo
- Direct role of surface oxygen vacancies in visible light emission of tin dioxide nanowires (literal)
- Abstract
- Tin dioxide ?SnO2? nanowires exhibit a strong visible photoluminescence that is not observed in
bulk crystalline SnO2. To explain such effect, oxygen vacancies are often invoked without clarifying
if they represent the direct origin of luminescence or if their presence triggers other radiative
processes. Here we report an investigation of the nature of the visible light emission in SnO2
nanowires, showing that both experimental and theoretical ab initio analyses support the first
hypothesis. On the basis of photoluminescence quenching analysis and of first-principles
calculations we show that surface bridging oxygen vacancies in SnO2 lead to formation of occupied
and empty surface bands whose transition energies are in strong agreement with luminescence
features and whose luminescence activity can be switched off by surface adsorption of oxidizing
molecules. Finally, we discuss how such findings may explain the decoupling between
\"electrical-active\" and \"optical-active\" states in SnO2 gas nanosensors. (literal)
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