二氧化碳电化学还原
一氧化碳
电解
化学
电化学
无机化学
二氧化碳
氧化还原
法拉第效率
气体扩散电极
铋
锌
电极
催化作用
有机化学
电解质
物理化学
作者
Shaoyun Hao,Ahmad Elgazzar,Shou-Kun Zhang,Tae‐Ung Wi,Feng-Yang Chen,Yuge Feng,Peng Zhu,Haotian Wang
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-06-12
卷期号:388 (6752): eadr3834-eadr3834
被引量:111
标识
DOI:10.1126/science.adr3834
摘要
(Bi)carbonate salt formation has been widely recognized as a primary factor in poor operational stability of the electrochemical carbon dioxide reduction reaction (CO 2 RR). We demonstrate that flowing CO 2 gas into an acid bubbler—which carries trace amounts of acid vapor into a gas diffusion electrode for silver-catalyzed CO 2 RR to carbon monoxide (CO)—can prevent salt accumulation. In a 100-square-centimeter, scaled-up CO 2 RR membrane electrode assembly electrolyzer with single serpentine flow channels, the acid humidification method achieved the 4500 hours of stability milestone at 100 mA cm −2 without compromising the CO faradaic efficiency, whereas a conventional water-humidified CO 2 feed only operated stably for ~80 hours. The acid-humidified CO 2 approach was extended to bismuth, copper, and zinc catalysts.
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