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

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 (eCO2RR). Herein, a hybrid gas diffusion electrode‐based reaction...

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Autores principales: Yucheng Wang, Hanhui Lei, Hang Xiang, Yongqing Fu, Chenxi Xu, Yinzhu Jiang, Ben Bin Xu, Eileen Hao Yu, Chao Gao, Terence Xiaoteng Liu
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Lenguaje:EN
Publicado: Wiley-VCH 2021
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Acceso en línea:https://doaj.org/article/aefa9f7739e64f2c96db4cbc7436bd56
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spelling oai:doaj.org-article:aefa9f7739e64f2c96db4cbc7436bd562021-11-04T09:03:08ZPorous Bilayer Electrode‐Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction2699-941210.1002/aesr.202100083https://doaj.org/article/aefa9f7739e64f2c96db4cbc7436bd562021-11-01T00:00:00Zhttps://doi.org/10.1002/aesr.202100083https://doaj.org/toc/2699-9412Comparing 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 (eCO2RR). 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 ≈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 eCO2RR with a structural design of cell‐enabled high CO2 conversion.Yucheng WangHanhui LeiHang XiangYongqing FuChenxi XuYinzhu JiangBen Bin XuEileen Hao YuChao GaoTerence Xiaoteng LiuWiley-VCHarticleCO2 reduction reactiongas diffusion electrodesgraphene aerogelsmass transferEnvironmental technology. Sanitary engineeringTD1-1066Renewable energy sourcesTJ807-830ENAdvanced Energy & Sustainability Research, Vol 2, Iss 11, Pp n/a-n/a (2021)
institution DOAJ
collection DOAJ
language EN
topic CO2 reduction reaction
gas diffusion electrodes
graphene aerogels
mass transfer
Environmental technology. Sanitary engineering
TD1-1066
Renewable energy sources
TJ807-830
spellingShingle CO2 reduction reaction
gas diffusion electrodes
graphene aerogels
mass transfer
Environmental technology. Sanitary engineering
TD1-1066
Renewable energy sources
TJ807-830
Yucheng Wang
Hanhui Lei
Hang Xiang
Yongqing Fu
Chenxi Xu
Yinzhu Jiang
Ben Bin Xu
Eileen Hao Yu
Chao Gao
Terence Xiaoteng Liu
Porous Bilayer Electrode‐Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction
description 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 (eCO2RR). 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 ≈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 eCO2RR with a structural design of cell‐enabled high CO2 conversion.
format article
author Yucheng Wang
Hanhui Lei
Hang Xiang
Yongqing Fu
Chenxi Xu
Yinzhu Jiang
Ben Bin Xu
Eileen Hao Yu
Chao Gao
Terence Xiaoteng Liu
author_facet Yucheng Wang
Hanhui Lei
Hang Xiang
Yongqing Fu
Chenxi Xu
Yinzhu Jiang
Ben Bin Xu
Eileen Hao Yu
Chao Gao
Terence Xiaoteng Liu
author_sort Yucheng Wang
title Porous Bilayer Electrode‐Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction
title_short Porous Bilayer Electrode‐Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction
title_full Porous Bilayer Electrode‐Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction
title_fullStr Porous Bilayer Electrode‐Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction
title_full_unstemmed Porous Bilayer Electrode‐Guided Gas Diffusion for Enhanced CO2 Electrochemical Reduction
title_sort porous bilayer electrode‐guided gas diffusion for enhanced co2 electrochemical reduction
publisher Wiley-VCH
publishDate 2021
url https://doaj.org/article/aefa9f7739e64f2c96db4cbc7436bd56
work_keys_str_mv AT yuchengwang porousbilayerelectrodeguidedgasdiffusionforenhancedco2electrochemicalreduction
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