串联
催化作用
一氧化碳
二氧化碳电化学还原
乙烯
二氧化碳
电解
法拉第效率
碳纤维
材料科学
化学
镍
化学工程
无机化学
甲烷化器
合成气
金属
碳化合物
法拉第电流
碱金属
纳米技术
检出限
作者
Xianhui Ma,Juan Zhang,Dayin He,Wei Jiang,Y W Sun,Jiayi Cui,Cai Chen,Yue Lin,Tao Yao,Huang Zhou,Yafei Li,Y N Wu
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-05-13
卷期号:12 (20): eaea2538-eaea2538
标识
DOI:10.1126/sciadv.aea2538
摘要
Tandem carbon dioxide reduction reaction (CO 2 RR) to multicarbon products (CO 2 -CO-C 2+ ) such as ethylene represents a pivotal strategy for carbon valorization. However, conventional alkaline or neutral tandem systems limit the carbon dioxide utilization and stability due to severe (bi)carbonate formation. Here, we design a durable acidic-alkaline tandem system to efficiently synthesize C 2+ products, especially ethylene. In the acidic CO 2 RR step, a catalyst with precisely controlled metal site distance was used to regulate *COOH adsorption. Typically, a 99.7 ± 0.4% carbon monoxide Faradaic efficiency (FE) at 1.4 amperes per square centimeter can be achieved using a catalyst with 0.5-nanometer nickel sites, surpassing the previously reported metal catalysts. When this catalyst was integrated into the acidic-alkaline tandem system and coupled with the alkaline carbon monoxide electroreduction, the ethylene and C 2+ FE reached 75.3 ± 1.2 and 92.5 ± 1.3% at 10 amperes, respectively, and remained stable for 400 hours. Our work provides solutions for the durable conversion of carbon dioxide to C 2+ products from catalyst and electrolyzer design.
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