镍
选择性
催化作用
电流密度
材料科学
氢
电催化剂
化学工程
冶金
无机化学
电极
化学
电化学
工程类
物理化学
物理
有机化学
量子力学
作者
Tingting Zheng,Kun Jiang,Na Ta,Yongfeng Hu,Jie Zeng,Jingyue Liu,Haotian Wang
出处
期刊:Joule
[Elsevier]
日期:2019-01-01
卷期号:3 (1): 265-278
被引量:708
标识
DOI:10.1016/j.joule.2018.10.015
摘要
Summary
The scaling up of electrocatalytic CO2 reduction for practical applications is still hindered by a few challenges: low selectivity, small current density to maintain a reasonable selectivity, and the cost of the catalytic materials. Here we report a facile synthesis of earth-abundant Ni single-atom catalysts on commercial carbon black, which were further employed in a gas-phase electrocatalytic reactor under ambient conditions. As a result, those single-atomic sites exhibit an extraordinary performance in reducing CO2 to CO, yielding a current density above 100 mA cm−2, with nearly 100% selectivity for CO and around 1% toward the hydrogen evolution side reaction. By further scaling up the electrode into a 10 × 10-cm2 modular cell, the overall current in one unit cell can easily ramp up to more than 8 A while maintaining an exclusive CO evolution with a generation rate of 3.34 L hr−1 per unit cell.
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