Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 16976-16986 |
| Number of pages | 11 |
| Journal | ACS Nano |
| Volume | 20 |
| Issue number | 23 |
| DOIs | |
| Publication status | Published - 16 Jun 2026 |
| Externally published | Yes |
Keywords
- 2,5-bis(hydroxymethyl)furan
- 5-hydroxymethylfurfural
- bimetallic catalyst
- biomass valorization
- electrochemical hydrogenation
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