| Literature DB >> 25327934 |
Ning Liu1, Christopher Schneider, Detlef Freitag, Umamaheswari Venkatesan, V R Reddy Marthala, Martin Hartmann, Benjamin Winter, Erdmann Spiecker, Andres Osvet, Eva M Zolnhofer, Karsten Meyer, Tomohiko Nakajima, Xuemei Zhou, Patrik Schmuki.
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.Entities:
Keywords: TiO2; co-catalyst; hydrogenation; titanium(III); water splitting
Year: 2014 PMID: 25327934 DOI: 10.1002/anie.201408493
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336