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Durable CO2 conversion in the proton-exchange membrane system.

Authors :
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
Source :
Nature; Feb2024, Vol. 626 Issue 7997, p86-91, 6p
Publication Year :
2024

Abstract

Electrolysis that reduces carbon dioxide (CO<subscript>2</subscript>) to useful chemicals can, in principle, contribute to a more sustainable and carbon-neutral future1–6. However, it remains challenging to develop this into a robust process because efficient conversion typically requires alkaline conditions in which CO<subscript>2</subscript> precipitates as carbonate, and this limits carbon utilization and the stability of the system7–12. Strategies such as physical washing, pulsed operation and the use of dipolar membranes can partially alleviate these problems but do not fully resolve them11,13–15. CO<subscript>2</subscript> electrolysis in acid electrolyte, where carbonate does not form, has therefore been explored as an ultimately more workable solution16–18. Herein we develop a proton-exchange membrane system that reduces CO<subscript>2</subscript> 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<subscript>2</subscript> 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<subscript>2</subscript> at a current density of 600 mA cm<superscript>−2</superscript> 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.We develop a proton-exchange membrane system that reduces CO<subscript>2</subscript> to formic acid at a catalyst that is derived from waste lead–acid batteries and in which a lattice carbon activation mechanism contributes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00280836
Volume :
626
Issue :
7997
Database :
Complementary Index
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
175248125
Full Text :
https://doi.org/10.1038/s41586-023-06917-5