石墨烯
催化作用
电化学
Atom(片上系统)
材料科学
选择性
对偶(语法数字)
密度泛函理论
纳米技术
化学工程
碳纤维
纳米颗粒
无机化学
化学
组合化学
计算化学
物理化学
电极
有机化学
复合数
复合材料
计算机科学
嵌入式系统
艺术
工程类
文学类
作者
Yifan Li,Chang Chen,Rui Cao,Ziwei Pan,Hua He,Kebin Zhou
标识
DOI:10.1016/j.apcatb.2020.118747
摘要
Electrochemical reduction of CO2 into value-added carbon compounds offers a promising strategy to mitigate global warming, but present challenges for chemistry due to the poor selectivity and stability of electrocatalysts. In this work, we report a dual-atom Ag2/graphene catalyst featuring well-defined AgN3-AgN3 active site for CO2 electrochemical reduction. This dual-atom catalyst can drive CO2 reduction reaction at a potential as high as -0.25 V, and exhibit excellent CO Faradic efficiency up to 93.4 % with a current density of 11.87 mA cm−2 at -0.7 V and long-term stability, far surpassing the single-atom Ag1/graphene and the traditional silver nanoparticle catalysts. DFT calculations reveal that the dual-atom Ag site lowers the barrier for the formation of *COOH by stabilizing the *CO2 through the concomitant interactions with the C and an O atom of CO2, resulting in excellent catalytic performance.
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