电化学
化学
催化作用
法拉第效率
氧合物
稳定器(航空)
氧化还原
化学工程
选择性
二氧化碳电化学还原
组合化学
电极
无机化学
纳米技术
有机化学
材料科学
一氧化碳
物理化学
机械工程
工程类
作者
Xinyu Wang,Yawen Jiang,Keke Mao,Wanbing Gong,Delong Duan,Jun Ma,Yuan Zhong,Jiawei Li,Hengjie Liu,Ran Long,Yujie Xiong
摘要
The electrochemical CO2 reduction reaction (CO2RR) to produce high value-added hydrocarbons and oxygenates presents a sustainable and compelling approach toward a carbon-neutral society. However, uncontrollable migration of active sites during the electrochemical CO2RR limits its catalytic ability to simultaneously achieve high C2 selectivity and ultradurability. Here, we demonstrate that the generated interfacial CuAlO2 species can efficiently stabilize the highly active sites over the Cu-CuAlO2-Al2O3 catalyst under harsh electrochemical conditions without active sites regeneration for a long-term test. We show that this unique Cu-CuAlO2-Al2O3 catalyst exhibits ultradurable electrochemical CO2RR performance with an 85% C2 Faradaic efficiency for a 300 h test. Such a simple interfacial engineering design approach unveiled in this work would be adaptable to develop various ultradurable catalysts for industrial-scale electrochemical CO2RR.
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