镍
催化作用
还原(数学)
Atom(片上系统)
材料科学
比例(比率)
化学工程
冶金
无机化学
化学
工程类
物理
有机化学
嵌入式系统
数学
几何学
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 BV]
日期:2018-11-08
卷期号:3 (1): 265-278
被引量:873
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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