过电位
电催化剂
催化作用
可逆氢电极
法拉第效率
镍
碳纤维
二氧化碳电化学还原
氧化还原
材料科学
电化学
化学
无机化学
热解
化学工程
电极
工作电极
一氧化碳
物理化学
有机化学
复合数
冶金
工程类
复合材料
作者
Yibo Guo,Sai Yao,Yuanyuan Xue,Xu Hu,Huijuan Cui,Zhen Zhou
标识
DOI:10.1016/j.apcatb.2021.120997
摘要
The electrochemical reduction reaction of carbon dioxide (CO2RR) is an effective way towards carbon neutralization. Single-atom catalysts (SACs) are expected to be efficient for CO2RR due to maximum atom utilization and excellent catalytic performance. Here, nitrogen-doped carbon supported Ni SACs (Ni-SAC@NCs) were prepared through effective fast pyrolysis. CO2 can convert into CO efficiently with Ni-SAC@NCs as electrocatalysts for CO2RR. The faradaic efficiency kept well above 80% in the applied potential window of −0.6 to −0.9 V (vs. reversible hydrogen electrode (RHE)), with a highest FECO of 95% at −0.6 V (vs. RHE). Ni-SAC@NCs can achieve the best CO selectivity under a small overpotential, surpassing most other state-of-the-art catalysts. Computations also indicate that the unique defect-Ni-N3 structure is the active site. This work not only provides a simple and promising new route for the preparation of SACs, but also proves the key role of the coordination environment in electrocatalysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI