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Research Article

Interfacial oxidized Pd species dominate catalytic hydrogenation of polar unsaturated bonds

Pengyao You1Shaoqi Zhan2,3Pengpeng Ruan1Ruixuan Qin1Shiguang Mo1Yazhou Zhang1Kunlong Liu1Lansun Zheng1Nanfeng Zheng1( )
State Key Laboratory for Physical Chemistry of Solid Surfaces, Collaborative Innovation Center of Chemistry for Energy Materials, and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China
Department of Chemistry─BMC, Uppsala University, BMC Box 576, Uppsala S-751 23, Sweden
Department of Chemistry, University of Oxford, Oxford OX1 3QZ, UK
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Graphical Abstract

The metal–support interface plays a crucial role in stabilizing oxidized Pd species for the selective hydrogenation polar unsaturated bonds.

Abstract

The determination of catalytically active sites is crucial for the design of efficient and stable catalysts toward desired reactions. However, the complexity of supported noble metal catalysts has led to controversy over the locations of catalytically active sites (e.g., metal, support, and metal/support interface). Here we develop a structurally controllable catalyst system (Pd/SBA-15) to reveal the catalytic active sites for the selective hydrogenation of ketones to alcohol using acetophenone hydrogenation as model reaction. Systematic investigations demonstrated that unsupported Pd nanocrystals have no catalytic activity for acetophenone hydrogenation. However, oxidized Pd species were catalytically highly active for acetophenone hydrogenation. The catalytic activity decreased with the decreased oxidation state of Pd. This work provides insights into the hydrogenation mechanism of ketones but also other unsaturated compounds containing polar bonds, e.g., nitrobenzene, N-benzylidene-benzylamine, and carbon dioxide.

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Nano Research
Pages 228-234
Cite this article:
You P, Zhan S, Ruan P, et al. Interfacial oxidized Pd species dominate catalytic hydrogenation of polar unsaturated bonds. Nano Research, 2024, 17(1): 228-234. https://doi.org/10.1007/s12274-023-5538-9
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Received: 23 November 2022
Revised: 26 January 2023
Accepted: 30 January 2023
Published: 15 March 2023
© Tsinghua University Press 2023
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