Plasma induced grain boundaries to boost electrochemical reduction of CO2 to formate

被引:0
|
作者
Wang, Guan [1 ]
Zhong, Shengtao [1 ]
Xiong, Xiaoqian [1 ]
Li, Jing [1 ]
Wang, Fangyuan [1 ]
Huo, Li [1 ]
Wu, Daoxiong [1 ]
Han, Xingqi [1 ]
Wang, Zhitong [1 ]
Chen, Qi [1 ]
Tian, Xinlong [1 ]
Deng, Peilin [1 ]
机构
[1] Hainan Univ, Sch Marine Sci & Engn, State Key Lab Marine Resource Utilizat South China, Haikou 570228, Hainan, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
CO; 2; electroreduction; Bi nanosheet; Grain boundary; Unsaturation Bi atoms; MEA device; TOTAL-ENERGY CALCULATIONS; SALT-TEMPLATED SYNTHESIS; BISMUTH; ELECTROREDUCTION; NANOSHEETS;
D O I
10.1016/j.jechem.2024.04.026
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Bismuth-based catalysts are highly promising for the electrochemical carbon dioxide reduction reaction (eCO(2)RR) to formate product. However, achieving high activity and selectivity towards formate and ensuring long-term stability remains challenging. This work reports the oxygen plasma inducing strategy to construct the abundant grain boundaries of Bi/BiOx on ultrathin two-dimensional Bi nanosheets. The oxygen plasma-treated Bi nanosheet (OP-Bi) exhibits over 90% Faradaic efficiency (FE) for formate at a wide potential range from -0.5 to -1.1 V, and maintains a great stability catalytic performance without significant decay over 30 h in flow cell. Moreover, membrane electrode assembly (MEA) device with OP-Bi as catalyst sustains the robust current density of 100 mA cm(-2) over 50 h, maintaining a formate FE above 90%. In addition, rechargeable Zn-CO2 battery presents the peak power density of 1.22 mW cm(-2) with OP-Bi as bifunctional catalyst. The mechanism experiments demonstrate that the high-density grain boundaries of OP-Bi provide more exposed active sites, faster electron transfer capacity, and the stronger intrinsic activity of Bi atoms. In situ spectroscopy and theoretical calculations further elucidate that the unsaturated Bi coordination atoms between the grain boundaries can effectively activate CO2 molecules through elongating the C-O bond, and reducing the formation energy barrier of the key intermediate (*OCOH), thereby enhancing the catalytic performance of eCO(2)RR to formate product.
引用
收藏
页码:636 / 643
页数:8
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