Abstract

In the present work we show, how a high pressure hydrogenation of commercial anatase or anatase/rutile powder can create a photocatalyst for hydrogen evolution that is highly effective and stable without the need of any additional co-catalyst. This activation effect can not be observed for rutile. For anatase/rutile mixtures, however, a strong synergistic effect is found (similar to findings commonly observed for noble metal decorated TiO2). ESR measurements indicate the intrinsic co-catalytic activation of anatase TiO2 to be due to specific defect centers formed during hydrogenation.

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