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Paper | Open Access

Light-driven ethanol dehydrogenation for hydrogen production over CuPt bimetallic catalysts

Shihao Dua,bRun Shia ( )Jiaqi ZhaoaPu Wanga,bJinhu Wanga,bZhenhua LiaPeng Miaoa,bQianqian ShangcChi Duana,bTierui Zhanga,b ( )
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China
Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences, Beijing 100049, China
College of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252000, China
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Abstract

The ethanol dehydrogenation (ED) reaction is considered a sustainable pathway for hydrogen production. However, the ED reaction is energy-intensive as it requires high temperatures. Here, we report a layered double hydroxide-derived catalyst composed of CuPt bimetallic nanoparticles for efficient light-driven ED reaction without additional thermal energy input, achieving a hydrogen production rate of 136.9 μmol g−1 s−1. This rate is 1.4 times higher than that achieved at the same temperature in the dark. Experimental results and theoretical simulations suggest that the localized surface plasmon resonance (LSPR) effect of Cu reduces the apparent activation energy of the light-driven ED reaction. The presence of Pt nanoparticles around Cu enhances the LSPR effect, thereby significantly increasing the hydrogen production efficiency.

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Industrial Chemistry & Materials
Pages 332-341

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Cite this article:
Du S, Shi R, Zhao J, et al. Light-driven ethanol dehydrogenation for hydrogen production over CuPt bimetallic catalysts. Industrial Chemistry & Materials, 2025, 3(3): 332-341. https://doi.org/10.1039/d4im00158c

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Received: 22 December 2024
Accepted: 14 March 2025
Published: 14 March 2025
© 2025 The Author(s).

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.