化学
电化学
还原(数学)
甲烷
电极
无机化学
物理化学
有机化学
几何学
数学
作者
Jin Cai,Qing Zhao,Wei-You Hsu,Chungseok Choi,Yang Liu,John Mark P. Martirez,Chih Chen,Jin Huang,Emily A. Carter,Yu Huang
摘要
High Resolution Image Download MS PowerPoint Slide The electrochemical carbon dioxide reduction reaction (CO 2 RR) is a promising route to close the carbon cycle by reducing CO 2 into valuable fuels and chemicals. Electrocatalysts with high selectivity toward a single product are economically desirable yet challenging to achieve. Herein, we demonstrated a highly (111)-oriented Cu foil electrocatalyst with dense twin boundaries (TB) (tw-Cu) that showed a high Faradaic efficiency of 86.1 ± 5.3% toward CH 4 at −1.2 ± 0.02 V vs the reversible hydrogen electrode. Theoretical studies suggested that tw-Cu can significantly lower the reduction barrier for the rate-determining hydrogenation of CO compared to planar Cu(111) under working conditions, which suppressed the competing C–C coupling, leading to the experimentally observed high CH 4 selectivity.
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