TY - JOUR
T1 - Surface Gradient Sn Doping of Copper Enables Adsorption-Controlled Electrohydrogenation of Biomass-Derived Aldehydes
AU - Zhao, Mengyao
AU - Pan, Chenyang
AU - Han, Xinyi
AU - Fu, Yifan
AU - Xu, Yifei
AU - Xie, Jisheng
AU - Xu, Bingjun
AU - Zhou, Jihan
AU - Zhao, Zipeng
AU - Cheng, Tao
AU - Li, Mufan
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/6/16
Y1 - 2026/6/16
N2 - 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 CuSn0.18 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.
AB - 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 CuSn0.18 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.
KW - 2,5-bis(hydroxymethyl)furan
KW - 5-hydroxymethylfurfural
KW - bimetallic catalyst
KW - biomass valorization
KW - electrochemical hydrogenation
UR - https://www.scopus.com/pages/publications/105041923713
U2 - 10.1021/acsnano.6c04674
DO - 10.1021/acsnano.6c04674
M3 - Article
AN - SCOPUS:105041923713
SN - 1936-0851
VL - 20
SP - 16976
EP - 16986
JO - ACS Nano
JF - ACS Nano
IS - 23
ER -