催化作用
掺杂剂
法拉第效率
材料科学
铜
电化学
欠电位沉积
选择性
无机化学
化学工程
氢
兴奋剂
表面工程
金属有机骨架
金属
多相催化
纳米技术
钯
沉积(地质)
工作(物理)
化学物理
生物量(生态学)
电子效应
作者
M H Zhao,Chenyang Pan,Xinyi Han,Yifan Fu,Y Xu,Jisheng Xie,Beibei Xu,Jihan Zhou,Zipeng Zhao,Tao Cheng,Mufan Li
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-06-05
卷期号:20 (23): 16976-16986
标识
DOI:10.1021/acsnano.6c04674
摘要
Electrochemical hydrogenation of biomass-derived aldehydes is a sustainable alternative to thermochemical routes, yet its efficiency is often limited by competitive hydrogen evolution and poorly defined surface–adsorption relationships on nonprecious metal catalysts. Here, we report a copper core/surface gradient tin-doping strategy that enables adsorption-controlled electrohydrogenation of 5-hydroxymethylfurfural (HMF) to 2,5-bis(hydroxymethyl)furan (BHMF). Unlike conventional bulk alloying, gradient Sn enrichment selectively tailors the Cu surface electronic structure, stabilizing carbon-centered intermediates while suppressing hydrogen adsorption. The optimized CuSn 0.18 catalyst achieves a BHMF Faradaic efficiency of 81.4% with excellent stability and scalability in both H-cell and membrane–electrode assembly configurations. By integrating Pb underpotential deposition with operando spectroscopy, we establish a quantitative structure–activity framework correlating Sn surface coverage, active site density, and electronic modulation with catalytic performance. This work demonstrates surface-specific dopant engineering as a general strategy for rationally controlling selectivity in electrocatalytic biomass valorization.
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