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Research Article

Ultrasmall Au10 clusters anchored on pyramid-capped rectangular TiO2 for olefin oxidation

Lixiong Li1,2, Shuangshuang Huang1,2, Jianjun Song1,2, Nating Yang1,2, Jingwei Liu1, Yuyun Chen1, Yuhan Sun1,3( ), Rongchao Jin4, Yan Zhu1,3( )
CAS Key Laboratory of Low-Carbon Conversion Science and EngineeringShanghai Advanced Research InstituteChinese Academy of SciencesShanghai201210China
University of Chinese Academy of SciencesBeijing100049China
School of Physical Science and TechnologyShanghaiTech UniversityShanghai201210China
Department of ChemistryCarnegie Mellon UniversityPittsburghPA15213USA
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Abstract

Ultrasmall Au10 clusters have a unique electronic structure and can act as a charge reservoir to donate electrons or accept charges. This is particularly important for catalysis, since it leads to facile charge transfer across the interface between the gold species and the oxide substrate. To determine the electronic and structural effects of Au10 on the catalytic oxidation, a TiO2 charge carrier was chosen as the substrate to anchor Au10 for olefin oxidation. Au10 supported on TiO2-RP (RP = pyramid-capped columnar structure) exhibited superior catalytic activity to Au10/TiO2 nanotubes and Au10/P25. In addition, the supported Au10 clusters gave rise to higher activity than supported Au20, Au144 clusters, and 5 nm Au nanocrystals. The superior catalytic ability of Au10/TiO2-RP arises from the charge/discharge effect of the Au10/TiO2-RP interface, which effectively improves the formation of active oxygen species on electron-rich gold atoms at the terminal position of Au10, and promotes the activation of olefin C=C bonds on the electron-deficient gold atoms of Au10.

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Nano Research
Pages 1182-1192

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Cite this article:
Li L, Huang S, Song J, et al. Ultrasmall Au10 clusters anchored on pyramid-capped rectangular TiO2 for olefin oxidation. Nano Research, 2016, 9(4): 1182-1192. https://doi.org/10.1007/s12274-016-1012-2

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Received: 14 October 2015
Revised: 19 December 2015
Accepted: 08 January 2016
Published: 11 March 2016
© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2016