http://www.cnr.it/ontology/cnr/individuo/prodotto/ID58303

DFT Study on Anatase TiO2 Nanowires: Structure and Electronic Properties As Functions of Size, Surface Termination, and Morphology (Articolo in rivista)

Type

Prodotto della ricerca (Classe)
Articolo in rivista (Classe)

Label

DFT Study on Anatase TiO2 Nanowires: Structure and Electronic Properties As Functions of Size, Surface Termination, and Morphology (Articolo in rivista) (literal)

Anno

2010-01-01T00:00:00+01:00 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi

10.1021/jp9090987 (literal)

Alternative label

Iacomino, A; Cantele, G; Trani, F; Ninno, D (2010)
DFT Study on Anatase TiO2 Nanowires: Structure and Electronic Properties As Functions of Size, Surface Termination, and Morphology
in Journal of physical chemistry. C; ACS, American chemical society, Washington, DC (Stati Uniti d'America)
(literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

Iacomino, A; Cantele, G; Trani, F; Ninno, D (literal)

Pagina inizio

12389 (literal)

Pagina fine

12400 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url

http://pubs.acs.org/doi/abs/10.1021/jp9090987 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume

114 (literal)

Rivista

Journal of physical chemistry. C (Rivista)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali

12 (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo

29 (literal)

Note

Scopu (literal)
ISI Web of Science (WOS) (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni

Univ Roma Tre, Dipartimento Fis E Amaldi, I-00146 Rome, Italy; Univ Naples Federico 2, CNISM, Dipartimento Sci Fis, I-80126 Naples, Italy; CNR SPIN, I-80126 Naples, Italy; Scuola Normale Super Pisa, I-56126 Pisa, Italy (literal)

Titolo

DFT Study on Anatase TiO2 Nanowires: Structure and Electronic Properties As Functions of Size, Surface Termination, and Morphology (literal)

Abstract

We have performed first-principles calculations on anatase TiO2 nanowires (NWs) to investigate the dependence of their structural and electronic properties on the size, the surface coverage, and the morphology. We have found that the overall crystallinity of the NWs increases on increasing the diameter size or equivalently upon surface coverage with simple water-derived adsorbates. The NWs grown along the [010] direction are found to be more ordered with respect to the NWs in the [001] direction of the same size, thus highlighting the dependence of the crystallinity on the choice of the morphology. The bare and hydrated NWs do show the band gap blue shift due to the size confinement, but deviations from an ideal trend with the size are found and ascribed to the morphology and the crystallinity. Through the analysis of the valence band maximum and conduction band minimum energies we found that the electrochemical potential variations of the TiO2 NWs profit from the confined size, for example, by favoring the water splitting process. Moreover, the availability of internal channels for an efficient charge transport can be tuned by the surface coverage. The terminal hydroxyl groups of the hydrated NWs cannot be considered as deep hole traps since their related electronic states have binding energies in the same range of the NW oxygen states. The hydrogenated NWs grown along the [001] direction show occupied states at the bottom of the conduction bands, thus we expect that TiO2 NWs can be used as efficient hydrogen sensors. Finally, the surface hydration leads to the most stable NWs among the considered surface configurations with formation energies that are even close to the bulk limit. (literal)

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