催化作用
甲酸
法拉第效率
化学工程
纳米棒
制氢
生物量(生态学)
材料科学
电解
可逆氢电极
电催化剂
氢
吸附
碳纤维
无机化学
化学
电极
纳米技术
电化学
有机化学
工作电极
电解质
复合数
地质学
复合材料
物理化学
海洋学
工程类
作者
Qiang Zhao,Zhenzheng Gui,Zhao Xu,Jiaxue Hu,Xiaojing Liu,Haian Xia,Peng Fei Zhang,Yuhui Chen,Fenfen Wang
出处
期刊:Small
[Wiley]
日期:2025-07-31
卷期号:21 (38): e04985-e04985
被引量:1
标识
DOI:10.1002/smll.202504985
摘要
Abstract Electrocatalytic of biomass‐derived glucose into formic acid integrated with hydrogen generation represents a highly advantageous strategy for sustainable biomass utilization and carbon neutrality, but is frequently hindered by high energy demands and suboptimal conversion efficiency. Herein, a CuO‐CoMOF/NF catalyst is reported, comprising a rough nanorod array CuO grown on nickel foam (NF) and decorated with Co‐Metal‐Organic Framework (Co‐MOF), which demonstrates extraordinary performance and stability at a low potential of 1.45 V (vs RHE), achieving a Faradaic efficiency (FE) of 98.5% and a formic acid production rate of 1.4 mmol cm −2 h −1 , significantly outperforming that of CuO/NF catalyst. The remarkable performance is primarily attributed to the instantaneous formation of CoOOH active species on the surface of the catalyst, which synergistically promotes the swift consumption of glucose through spontaneous chemical reactions, enhancing charge transfer and optimizing the adsorption behavior of the catalyst. Notably, at a current density of 10 mA cm −2 , the voltage requires for a two‐electrode electrolyzer is 494 mV lower than that for conventional overall water splitting. This study offers new perspectives for the rational design of electrocatalysts for the efficient conversion of biomass‐derived alcohols into value‐added chemicals while simultaneously generating hydrogen.
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