电催化剂
析氧
钝化
法拉第效率
催化作用
分解水
可逆氢电极
双金属片
化学
产量(工程)
化学工程
无机化学
生物量(生态学)
电解质
电极
材料科学
电化学
纳米技术
冶金
物理化学
工作电极
有机化学
图层(电子)
光催化
工程类
海洋学
地质学
作者
Dexin Chen,Yunxuan Ding,Xing Cao,Linqin Wang,Husileng Lee,Gaoxin Lin,Wenlong Li,Guoheng Ding,Licheng Sun
标识
DOI:10.1002/anie.202309478
摘要
Electricity-driven organo-oxidations have shown an increasing potential recently. However, oxygen evolution reaction (OER) is the primary competitive reaction, especially under high current densities, which leads to low Faradaic efficiency (FE) of the product and catalyst detachment from the electrode. Here, we report a bimetallic Ni-Cu electrocatalyst supported on Ni foam (Ni-Cu/NF) to passivate the OER process while the oxidation of 5-hydroxymethylfurfural (HMF) is significantly enhanced. A current density of 1000 mA cm-2 can be achieved at 1.50 V vs. reversible hydrogen electrode, and both FE and yield keep close to 100 % over a wide range of potentials. Both experimental results and theoretical calculations reveal that Cu doping impedes the OH* deprotonation to O* and hereby OER process is greatly passivated. Those instructive results provide a new approach to realizing highly efficient biomass upgrading by regulating the OER activity.
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