Porous Bilayer Electrode-Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction

被引:13
作者
Wang, Yucheng [1 ]
Lei, Hanhui [1 ]
Xiang, Hang [2 ]
Fu, Yongqing [1 ]
Xu, Chenxi [2 ,3 ]
Jiang, Yinzhu [4 ]
Xu, Ben Bin [1 ]
Yu, Eileen Hao [2 ,5 ]
Gao, Chao [6 ]
Liu, Terence Xiaoteng [1 ]
机构
[1] Northumbria Univ, Fac Engn & Environm, Newcastle Upon Tyne NE1 8ST, Tyne & Wear, England
[2] Newcastle Univ, Sch Engn, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Hefei Univ Technol, Dept Mat Sci & Engn, Hefei 230009, Peoples R China
[4] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Peoples R China
[5] Loughborough Univ, Dept Chem Engn, Loughborough LE11 3TU, Leics, England
[6] Zhejiang Univ, MOE Key Lab Macromol Synth & Functionalizat, Dept Polymer Sci & Engn, Key Lab Adsorpt & Separat Mat & Technol Zhejiang, 38 Zheda Rd, Hangzhou 310027, Peoples R China
来源
ADVANCED ENERGY AND SUSTAINABILITY RESEARCH | 2021年 / 2卷 / 11期
基金
英国工程与自然科学研究理事会;
关键词
CO2 reduction reaction; gas diffusion electrodes; graphene aerogels; mass transfer; ELECTROCATALYTIC REDUCTION; CARBON-DIOXIDE; ETHYLENE; ELECTROREDUCTION; EFFICIENCY; STABILITY; INSIGHTS; CATALYST; CAPTURE; FORMATE;
D O I
10.1002/aesr.202100083
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Comparing with the massive efforts in developing innovative catalyst materials system and technologies, structural design of cells has attracted less attention on the road toward high-performance electrochemical CO2 reduction reaction (eCO(2)RR). Herein, a hybrid gas diffusion electrode-based reaction cell is proposed using highly porous carbon paper (CP) and graphene aerogels (GAs), which is expected to offer directional diffusion of gas molecules onto the catalyst bed, to sustain a high performance in CO2 conversion. The above-mentioned hypothesis is supported by the experimental and simulation results, which show that the CP+GA combined configuration increases the Faraday efficiency (FE) from approximate to 60% to over 94% toward carbon monoxide (CO) and formate production compared with a CP only cell with Cu2O as the catalyst. It also suppresses the undesirable side reaction-hydrogen evolution over 65 times than the conventional H-type cell (H-cell). By combining with advanced catalysts with high selectivity, a 100% FE of the cell with a high current density can be realized. The described strategy sheds an extra light on future development of eCO(2)RR with a structural design of cell-enabled high CO2 conversion.
引用
收藏
页数:8
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