详细信息

The Effect of the Coordination Environment of Atomically Dispersed Fe and N Co-doped Carbon Nanosheets on CO2 Electroreduction  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:The Effect of the Coordination Environment of Atomically Dispersed Fe and N Co-doped Carbon Nanosheets on CO2 Electroreduction

作者:Tuo, Jinqin[1];Zhu, Yihua[1];Jiang, Hongliang[2];Shen, Jianhua[1];Li, Chunzhong[1,2]

机构:[1]East China Univ Sci & Technol, Key Lab Ultra Fine Mat Minist Educ, Frontiers Sci Ctr Materiobiol & Dynam Chem, Shanghai Engn Res Ctr Hierarch Nanomat,Sch Mat Sc, 130 Meilong Rd, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Chem Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China

年份:2020

卷号:7

期号:23

起止页码:4767

外文期刊名:CHEMELECTROCHEM

收录:;EI(收录号:20205009619101);WOS:【SCI-EXPANDED(收录号:WOS:000597323800009)】;

语种:英文

外文关键词:CO2 electroreduction; confinement anchoring effect; single atom; coordination environment

摘要:Single-atom metal and nitrogen co-doped carbon catalysts have caused an extensive research boom for electrochemical CO2 reduction reaction (CO2RR). The diversity of metal-N coordination environment at high temperature limits the accurate study of electrocatalytic active sites. In this work, Fe porphyrin is anchored on a nitrogen-doped graphene substrate through the coordination between Fe and N atoms to form atomically dispersed Fe and N co-doped graphene nanosheets. The confinement anchoring effect of the nitrogen-doped graphene substrate prevents Fe atoms from agglomerating into Fe nanoparticles. Apart from that, the different Fe-N coordination environments and their catalytic effects on CO2RR are investigated by temperature changes. Electrochemical tests and density functional theory (DFT) calculations indicate that the atomically dispersed saturated Fe-N coordination catalyst have excellent performance for CO2RR and the Faradaic efficiency towards CO can up to 97 % at a potential of -0.5 V (vs. reversible hydrogen electrode, RHE).

参考文献:

正在载入数据...

版权所有©华东理工大学 重庆维普资讯有限公司 渝B2-20050021-7 
渝公网安备 50019002500408号 违法和不良信息举报中心