Durable CO 2 conversion in the proton-exchange membrane system

Electrolysis that reduces carbon dioxide (CO ) to useful chemicals can, in principle, contribute to a more sustainable and carbon-neutral future . However, it remains challenging to develop this into a robust process because efficient conversion typically requires alkaline conditions in which CO pre...

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Veröffentlicht in:Nature (London) 2024-02, Vol.626 (7997), p.86
Hauptverfasser: Fang, Wensheng, Guo, Wei, Lu, Ruihu, Yan, Ya, Liu, Xiaokang, Wu, Dan, Li, Fu Min, Zhou, Yansong, He, Chaohui, Xia, Chenfeng, Niu, Huiting, Wang, Sicong, Liu, Youwen, Mao, Yu, Zhang, Chengyi, You, Bo, Pang, Yuanjie, Duan, Lele, Yang, Xuan, Song, Fei, Zhai, Tianyou, Wang, Guoxiong, Guo, Xingpeng, Tan, Bien, Yao, Tao, Wang, Ziyun, Xia, Bao Yu
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container_issue 7997
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container_title Nature (London)
container_volume 626
creator Fang, Wensheng
Guo, Wei
Lu, Ruihu
Yan, Ya
Liu, Xiaokang
Wu, Dan
Li, Fu Min
Zhou, Yansong
He, Chaohui
Xia, Chenfeng
Niu, Huiting
Wang, Sicong
Liu, Youwen
Mao, Yu
Zhang, Chengyi
You, Bo
Pang, Yuanjie
Duan, Lele
Yang, Xuan
Song, Fei
Zhai, Tianyou
Wang, Guoxiong
Guo, Xingpeng
Tan, Bien
Yao, Tao
Wang, Ziyun
Xia, Bao Yu
description Electrolysis that reduces carbon dioxide (CO ) to useful chemicals can, in principle, contribute to a more sustainable and carbon-neutral future . However, it remains challenging to develop this into a robust process because efficient conversion typically requires alkaline conditions in which CO precipitates as carbonate, and this limits carbon utilization and the stability of the system . Strategies such as physical washing, pulsed operation and the use of dipolar membranes can partially alleviate these problems but do not fully resolve them . CO electrolysis in acid electrolyte, where carbonate does not form, has therefore been explored as an ultimately more workable solution . Herein we develop a proton-exchange membrane system that reduces CO to formic acid at a catalyst that is derived from waste lead-acid batteries and in which a lattice carbon activation mechanism contributes. When coupling CO reduction with hydrogen oxidation, formic acid is produced with over 93% Faradaic efficiency. The system is compatible with start-up/shut-down processes, achieves nearly 91% single-pass conversion efficiency for CO at a current density of 600 mA cm and cell voltage of 2.2 V and is shown to operate continuously for more than 5,200 h. We expect that this exceptional performance, enabled by the use of a robust and efficient catalyst, stable three-phase interface and durable membrane, will help advance the development of carbon-neutral technologies.
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However, it remains challenging to develop this into a robust process because efficient conversion typically requires alkaline conditions in which CO precipitates as carbonate, and this limits carbon utilization and the stability of the system . Strategies such as physical washing, pulsed operation and the use of dipolar membranes can partially alleviate these problems but do not fully resolve them . CO electrolysis in acid electrolyte, where carbonate does not form, has therefore been explored as an ultimately more workable solution . Herein we develop a proton-exchange membrane system that reduces CO to formic acid at a catalyst that is derived from waste lead-acid batteries and in which a lattice carbon activation mechanism contributes. When coupling CO reduction with hydrogen oxidation, formic acid is produced with over 93% Faradaic efficiency. The system is compatible with start-up/shut-down processes, achieves nearly 91% single-pass conversion efficiency for CO at a current density of 600 mA cm and cell voltage of 2.2 V and is shown to operate continuously for more than 5,200 h. We expect that this exceptional performance, enabled by the use of a robust and efficient catalyst, stable three-phase interface and durable membrane, will help advance the development of carbon-neutral technologies.</description><identifier>EISSN: 1476-4687</identifier><identifier>PMID: 38297172</identifier><language>eng</language><publisher>England</publisher><ispartof>Nature (London), 2024-02, Vol.626 (7997), p.86</ispartof><rights>2024. 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title Durable CO 2 conversion in the proton-exchange membrane system
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