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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Sprache:eng
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Zusammenfassung: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.
ISSN:1476-4687