材料科学
双金属片
化学工程
二氧化碳电化学还原
催化作用
可逆氢电极
碳纤维
电化学
电解质
铜
成核
基质(水族馆)
锡
电极
纳米技术
无机化学
过电位
化学
工作电极
一氧化碳
复合材料
冶金
有机化学
物理化学
工程类
地质学
海洋学
金属
复合数
作者
Luwei Peng,Yongxia Wang,Israr Masood ul Hasan,Bo Zhou,Yaofeng Wang,Jia Lin,Jinli Qiao,Feng‐Yuan Zhang
标识
DOI:10.1016/j.apcatb.2019.118447
摘要
The electrochemical CO2 reduction reaction (CO2RR) into liquid fuels is a promising avenue to both store intermittent renewable energy and reduce global CO2 emission, but daunting bottlenecks owing to poor selectivity, low activity and stability of the electrocatalysts. Herein, we report that bimetallic copper and tin are simultaneously deposited on the nitrogen doped porous carbon cloth (N-CC) via an efficient and facile co-electroplating strategy. The highly conductive N-doped porous carbon cloth as substrate enables a largely uniform distribution of N-doped defects, which can provide more active sites for the nucleation and growth of anchoring nano-sized Cn/Sn (3.39 nm). The as-prepared electrode (Cu(1)Sn(4)-N-CC), with a 3D-hierarchical porous honeycomb structure, could not only favor the diffusion of electrolyte and serve as “transfer posts” to confine the intermediates of reduced CO2, but also provide abundant terrace, ledge and kink atoms to function as active site for highly efficient CO2RR. As such, the obtained Cu(1)Sn(4)-N-CC electrode convert CO2 to formate with allured faradic efficiency (90.24 %), partial current density (15.56 mA cm−2) and production rate (173 μmol h-1 cm−2) at −0.97 VRHE, along with a long-term tolerance in CO2RR. This study may provide a new design for self-growing bimetallic catalyst on N-doped porous substrate to regulate advanced catalysts/electrodes for different applications.
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