期刊
ACS CATALYSIS
卷 12, 期 15, 页码 9579-9588出版社
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.2c02230
关键词
hydrogen evolution; photocatalysis; cluster size; platinum; nickel; alcohols; titania
资金
- DFG [EXC 2089/1-390776260]
- Luxembourg National Research Fund (FNR) [12531916]
- TUM International Graduate School of Science and Engineering
In the past decade, photocatalytic hydrogen evolution from metal-loaded TiO2 has received significant attention. This study compares size-selected Ni and Pt clusters as co-catalysts on a TiO2(110) single crystal and investigates the size- and coverage-dependent effects on the catalyst performance. Larger clusters and higher coverages of Ni enhance the product formation rate, while Pt co-catalysts exhibit a stable and higher activity, but size-specific effects need to be considered.
In the past decade, hydrogen evolution from photocatalytic alcohol oxidation on metal-loaded TiO2 has emerged as an active research field. While the presence of a metal cluster co-catalyst is crucial as a H-2 recombination center, size and coverage effects on the catalyst performance are not yet comprehensively understood. To some extent, this is due to the fact that common deposition methods do not allow for an independent change in size and coverage, which can be overcome by the use of cluster sources and the deposition of size-selected clusters. This study compares size-selected Ni and Pt clusters as co-catalysts on a TiO2(110) single crystal and the resulting size- and coverage-dependent effects in the photocatalytic hydrogen evolution from alcohols in ultrahigh vacuum (UHV). Larger clusters and higher coverages of Ni enhance the product formation rate, although deactivation over time occurs. In contrast, Pt co-catalysts exhibit a stable and higher activity and size-specific effects have to be taken into account. While H-2 evolution is improved by a higher concentration of Pt clusters, an increase in the metal content by the deposition of larger particles can even be detrimental to the performance of the photocatalyst. The acquired overall mechanistic picture is corroborated by H-2 formation kinetics from mass spectrometric data. Consequently, for some metals, size effects are relevant for improving the catalytic performance, while for other co-catalyst materials, merely the coverage is decisive. The elucidation of different size and coverage dependencies represents an important step toward a rational catalyst design for photocatalytic hydrogen evolution.
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