Durable CO2 conversion in the proton-exchange membrane system

被引:118
|
作者
Fang, Wensheng [1 ]
Guo, Wei [1 ]
Lu, Ruihu [2 ]
Yan, Ya [3 ]
Liu, Xiaokang [4 ]
Wu, Dan [4 ]
Li, Fu Min [1 ]
Zhou, Yansong [1 ]
He, Chaohui [1 ]
Xia, Chenfeng [1 ]
Niu, Huiting [1 ]
Wang, Sicong [4 ]
Liu, Youwen [5 ,6 ]
Mao, Yu [2 ]
Zhang, Chengyi [2 ]
You, Bo [1 ]
Pang, Yuanjie [7 ]
Duan, Lele [8 ,9 ]
Yang, Xuan [1 ]
Song, Fei [10 ]
Zhai, Tianyou [5 ,6 ]
Wang, Guoxiong [11 ]
Guo, Xingpeng [1 ]
Tan, Bien [1 ]
Yao, Tao [4 ]
Wang, Ziyun [2 ]
Xia, Bao Yu [1 ]
机构
[1] Huazhong Univ Sci & Technol, Minist Agr, State Key Lab Mat Proc & Die & Mould Technol, Key Lab Mat Chem Energy Convers & Storage,Hubei Ke, Wuhan, Peoples R China
[2] Univ Auckland, Sch Chem Sci, Auckland, New Zealand
[3] Chinese Acad Sci SICCAS, Shanghai Inst Ceram, CAS Key Lab Mat Energy Convers, Shanghai, Peoples R China
[4] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei, Peoples R China
[5] Huazhong Univ Sci & Technol, State Key Lab Mat Proc & Die & Mould Technol, Wuhan, Peoples R China
[6] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, Wuhan, Peoples R China
[7] Huazhong Univ Sci & Technol, Sch Opt & Elect Informat, Wuhan Natl Lab Optoelect, Wuhan, Peoples R China
[8] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China
[9] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen, Peoples R China
[10] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai Synchrotron Radiat Facil, Shanghai, Peoples R China
[11] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian Natl Lab Clean Energy, Dalian, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
TECHNOECONOMIC ANALYSIS; REDUCTION; ELECTROLYSIS; SELECTIVITY;
D O I
10.1038/s41586-023-06917-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Electrolysis that reduces carbon dioxide (CO2) to useful chemicals can, in principle, contribute to a more sustainable and carbon-neutral future(1,2,3,4,5,6). However, it remains challenging to develop this into a robust process because efficient conversion typically requires alkaline conditions in which CO2 precipitates as carbonate, and this limits carbon utilization and the stability of the system(7,8,9,10,11,12). Strategies such as physical washing, pulsed operation and the use of dipolar membranes can partially alleviate these problems but do not fully resolve them(11,13,14,15). CO2 electrolysis in acid electrolyte, where carbonate does not form, has therefore been explored as an ultimately more workable solution(16,17,18). Herein we develop a proton-exchange membrane system that reduces CO2 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 CO2 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 CO2 at a current density of 600 mA cm(-2) 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.
引用
收藏
页码:86 / +
页数:10
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