In-situ electrochemical transformation of F-modified metallic bismuth for highly-efficient CO2 electroreduction and Zn-CO2 battery

被引:7
作者
Wu, Wenbo [1 ]
Tong, Yun [1 ]
Ye, Yutong
Zhou, Guorong [1 ]
He, Jinfeng [1 ]
Zhu, Jiaye [1 ]
Ren, Xuhui [1 ]
Zhang, Nan [2 ]
Wang, Huigang [3 ]
Chen, Pengzuo [1 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Chem & Chem Engn, Key Lab Surface & Interface Sci Polymer Mat Zhejia, Hangzhou 310018, Zhejiang, Peoples R China
[2] SINOPEC Shanghai Res Inst Petrochem Technol Co Ltd, Shanghai 201208, Peoples R China
[3] Zhejiang Normal Univ, Hangzhou Inst Adv Studies, 1108 Gengwen Rd, Hangzhou 311231, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
F; -modification; Bismuth catalyst; CO2; Electroreduction; Co -production of formate; Zn-CO2; Battery; REDUCTION;
D O I
10.1016/j.cej.2024.153105
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electrocatalytic CO2 reduction (ECO2R) to produce formate is one of the essential routes for CO2 upgrading. Herein, the bismuth oxyfluoride (BiOF) material is firstly rationally designed as a precursor to derive the F-modified Bi catalyst (FD-Bi) for ECO2R. The FD-Bi catalyst achieves more than 90 % Faradaic efficiency of formate (FEformate) over a wide potential range of -0.5 similar to -1.2 V vs. RHE. By coupling in-situ Raman and infrared spectroscopy, the transformation of BiOF to FD-Bi and the formation of key *OCHO intermediates have been revealed. Density functional theory (DFT) calculations further confirm the optimized electronic structure and the favorable adsorption energies of intermediates on F-modified Bi catalyst. In a coupled system for the co-production of formate, a high FEformate of 159.1 % can be realized at a small cell voltage of 1.9 V. In addition, Zn-CO2 battery equipped with FD-Bi delivers a high power density of 2.68 mW<middle dot>cm(-2) and superior stability.
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页数:9
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