法拉第效率
甲酸
阳极
甲醇
阴极
制氢
二氧化碳电化学还原
联轴节(管道)
氢
电催化剂
化学工程
化学
工作(物理)
材料科学
二氧化碳
选择性
无机化学
催化作用
合金
产量(工程)
电流密度
过电位
航程(航空)
氧化还原
偶联反应
电压
电化学
电极
作者
Zhikeng Zheng,Xiaobo Zheng,François Maréchal,Huiming Wen,Ke Li,Zhenhao Xu,Yameng Fan,Peng Li,Suyu Zhang,Bin Liu,Dingsheng Wang,Kai Yan,Guoxiu Wang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-06
卷期号:64 (43): e202512078-e202512078
被引量:22
标识
DOI:10.1002/anie.202512078
摘要
Abstract The coupling of electrocatalytic CO 2 reduction (ECR) and methanol oxidation reaction (MOR) presents a promising strategy for simultaneous cogeneration of formic acid (FA) at both cathode and anode. However, sluggish kinetics, low selectivity and efficiency hinder practical application. Herein, we demonstrate an integrated ECR||MOR system employing CuBi cathode and NiCo anode for energy‐efficient FA cogeneration. The CuBi alloy achieves high Faradaic efficiencies (FE > 90%) for FA generation over an extensive potential range (>400 mV), attributed to the accelerated formation of HCOO * intermediates in facilitating FA production. Meanwhile, the NiCo alloy reached a remarkable FE of 97.5% for FA generation at 1.4 V versus reversible hydrogen electrode, benefiting from rapid HCOO * intermediate formation that effectively mitigates CO toxicity. This unique system delivered a current density of 10 mA cm −2 at a voltage of 2.07 V, representing a substantial reduction of 320 mV compared to water electrolysis. Across a wide operational voltage window (2.0–2.8 V), the system consistently delivered total Faradaic efficiencies ranging between 189% and 192%, alongside exceptional FA production capacities surpassing 400 g kWh −1 , which significantly outperformed traditional methods (∼220 g kWh −1 ). This work provides an efficient pathway for low‐energy CO 2 utilization and sustainable FA production.
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