双金属片
电化学
法拉第效率
电极
扩散
二氧化碳电化学还原
材料科学
可逆氢电极
吸附
氢
化学工程
氢气储存
无机化学
化学
催化作用
纳米技术
一氧化碳
物理化学
工作电极
有机化学
热力学
物理
工程类
作者
Chang Zhu,Aohui Chen,Jianing Mao,Gangfeng Wu,Shoujie Li,Xiao Dong,Guihua Li,Zheng Jiang,Yanfang Song,Wei Wei,Wei Wei
标识
DOI:10.1002/sstr.202200328
摘要
Carbon dioxide electroreduction driven by renewable electricity into high‐value chemicals enables energy storage while contributing to climate change mitigation. Herein, a CuPd bimetallic catalyst is developed by electrodeposition for efficient CO 2 electroreduction, achieving a C 2+ Faradaic efficiency as high as 75.6% with a current density of −200 mA cm −2 at −1.15 V versus reversible hydrogen electrode. Upon incorporation of Pd, the average d ‐band center of the CuPd bimetallic catalyst downward shifts relative to the Fermi level, making the adsorbed CO intermediates active for further C–C coupling. Theoretical calculations confirm that CO generated on the Pd domain can spill over to the CuPd interface for C–C coupling with a lower energy barrier, further promoting the formation of C 2+ compounds. This study provides insights into the rational design of Cu‐based bimetallic catalysts for highly efficient CO 2 electroreduction to multicarbon products.
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