过电位
材料科学
法拉第效率
催化作用
电化学
化学工程
水溶液
介孔材料
成核
阴极
基质(水族馆)
碳纤维
锰
电解质
无机化学
纳米技术
电极
复合数
有机化学
化学
复合材料
物理化学
冶金
工程类
地质学
海洋学
作者
Meiling Wang,Ying Yao,Yuhui Tian,Yifei Yuan,Liguang Wang,Feiyang Yang,Jingjie Ren,Xinrong Hu,Feng Wu,Shanqing Zhang,Junxiu Wu,Jun Lü
标识
DOI:10.1002/adma.202210658
摘要
CO2 utilization and conversion are of great importance in alleviating the rising CO2 concentration in the atmosphere. Here, a single-atom catalyst (SAC) is reported for electrochemical CO2 utilization in both aqueous and aprotic electrolytes. Specifically, atomically dispersed Mn-N4 sites are embedded in bowl-like mesoporous carbon particles with the functionalization of epoxy groups in the second coordination spheres. Theoretical calculations suggest that the epoxy groups near the Mn-N4 site adjust the electronic structure of the catalyst with reduced reaction energy barriers for the electrocatalytic reduction of CO2 to CO. The resultant Mn-single-atom carbon with N and O doped catalyst (MCs-(N,O)) exhibits extraordinary electrocatalytic performance with a high CO faradaic efficiency of 94.5%, a high CO current density of 13.7 mA cm-2 , and a low overpotential of 0.44 V in the aqueous environment. Meanwhile, as a cathode catalyst for aprotic Li-CO2 batteries, the MCs-(N,O) with well-regulated active sites and unique mesoporous bowl-like morphology optimizes the nucleation behavior of discharge products. MCs-(N,O)-based batteries deliver a low overpotential and excellent cyclic stability of 1000 h. The findings in this work provide a new avenue to design and fabricate SACs for various electrochemical CO2 utilization systems.
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