Two-way rushing travel: Cathodic-anodic coupling of Bi2O3-SnO@CuO nanowires, a bifunctional catalyst with excellent CO2RR and MOR performance for the efficient production of formate

被引:19
作者
Tang, Zheng [1 ]
Wang, Yu [1 ]
Qian, Wenxuan [1 ]
Piao, Zhe [1 ]
Wang, Honggui [1 ]
Zhang, Ya [1 ]
机构
[1] Yangzhou Univ, Sch Environm Sci & Engn, Yangzhou 225127, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dioxide reduction reaction; Methanol oxidation reaction; Formate; Coupled electrolysis; Cu foam; CARBON-DIOXIDE; AT-C; ELECTROREDUCTION; NANOPARTICLES; CONVERSION; REDUCTION; OXIDATION; SURFACE;
D O I
10.1016/j.jcis.2023.08.196
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrocatalytic carbon dioxide reduction reaction (CO2RR) generates high value-added products and simultaneously reduces excess atmospheric CO2 concentrations, is regarded as a potential approach to achieve carbon neutrality. However, the kinetic process of the anode oxygen evolution reaction (OER) is slow, resulting in a poor electrochemical efficiency of CO2RR. It is a breakthrough to replace OER with methanol oxidation reaction (MOR), which has more advantageous reaction kinetics. Herein, this work proposed a bifunctional catalyst Bi2O3-SnO modified CuO nanowires (Bi2O3-SnO@CuO NWs) with excellent CO2RR and MOR performance. For CO2RR, Bi2O3-SnO@CuO NWs achieved more than 90% formate selectivity at wide potential windows from -0.88 to -1.08 V (vs. reversible hydrogen electrode (RHE)), peaking at 96.6%. Meanwhile, anodic Bi2O3SnO@CuO NWs achieved 100 mA cm-2 at a low potential of 1.53 V (vs. RHE), possessing nearly 100% formate selectivity ranging from 1.6 to 1.8 V (vs. RHE). Impressively, by coupling cathodic CO2RR and anodic MOR, the integrated electrolytic cell realized co-production of formate (cathode: 94.7% and anode: 97.5%), minimizing the energy input by approximately 69%, compared with CO2RR. This work provided a meaningful perspective for the design of bifunctional catalysts and coupling reaction systems in CO2RR.
引用
收藏
页码:1653 / 1664
页数:12
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