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Hydrogenated anatase: strong photocatalytic dihydrogen evolution without the use of a co-catalyst.
Liu, Ning; Schneider, Christopher; Freitag, Detlef; Venkatesan, Umamaheswari; Marthala, V R Reddy; Hartmann, Martin; Winter, Benjamin; Spiecker, Erdmann; Osvet, Andres; Zolnhofer, Eva M; Meyer, Karsten; Nakajima, Tomohiko; Zhou, Xuemei; Schmuki, Patrik.
Afiliação
  • Liu N; Department of Materials Science WW-4, LKO, University of Erlangen-Nuremberg, Martensstrasse 7, 91058 Erlangen (Germany).
Angew Chem Int Ed Engl ; 53(51): 14201-5, 2014 Dec 15.
Article em En | MEDLINE | ID: mdl-25327934
ABSTRACT
The high-pressure hydrogenation of commercially available anatase or anatase/rutile TiO2 powder can create a photocatalyst for H2 evolution that is highly effective and stable without the need for any additional co-catalyst. This activation effect cannot be observed for rutile; however, for anatase/rutile mixtures, a strong synergistic effect can be found (similar to results commonly observed for noble-metal-decorated TiO2). EPR and PL measurements indicated the intrinsic co-catalytic activation of anatase TiO2 to be due to specific defect centers formed during hydrogenation. These active centers can be observed specifically for high-pressure hydrogenation; other common reduction treatments do not result in this effect.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2014 Tipo de documento: Article