Abstract
Integrating value-added chemical upgrading with energy-efficient hydrogen production represents a promising strategy for sustainable electrochemical systems. Herein, we report MOF-derived Pt-incorporated Cu catalysts directly grown on Cu foam (Pt–Cu/CF) as self-supported catalyst-electrode composites for coupled furfural electrochemical hydrogenation (FEH) and formaldehyde oxidation reaction (FOR). The MOF-derived hierarchical porous structure ensures highly dispersed metallic active sites, while Pt incorporation lowers the carbonyl hydrogenation barrier for FEH and establishes a kinetically balanced C–H cleavage/hydrogen recombination profile for FOR, resulting in superior bifunctional activity and selectivity. When integrated into an anion exchange membrane paired electrolyzer (Pt–Cu/CF‖Pt–Cu/CF), the system achieves 10 mA cm−2 at an ultralow operating cell voltage of 0.197 V, which is 1.60 V lower than that required for the conventional HER‖OER process under identical device configurations, directly translating to a substantial reduction in electrical energy consumption. These results demonstrate that MOF-derived hierarchical architecture and Pt-induced electronic modulation of Cu collectively enable high bifunctional activity, establishing a design principle for energy-efficient paired electrolysis systems.
| Original language | English |
|---|---|
| Pages (from-to) | 24589-24599 |
| Number of pages | 11 |
| Journal | Journal of Materials Chemistry A |
| Volume | 14 |
| Issue number | 37 |
| DOIs | |
| Publication status | Published - 23 Jun 2026 |
Bibliographical note
Publisher Copyright:This journal is © The Royal Society of Chemistry, 2026.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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