Size and Coverage Effects of Ni and Pt Co-Catalysts in the Photocatalytic Hydrogen Evolution from Methanol on TiO2(110)

催化作用 光催化 星团(航天器) 金属 材料科学 多相催化 沉积(地质) 甲醇 化学工程 化学 纳米技术 有机化学 古生物学 工程类 生物 程序设计语言 计算机科学 沉积物
作者
Moritz Eder,Carla Courtois,Philip Petzoldt,Sonia Mackewicz,Martin Tschurl,Ueli Heiz
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:12 (15): 9579-9588 被引量:28
标识
DOI:10.1021/acscatal.2c02230
摘要

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 H2 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 H2 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 H2 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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