Hydrangea-like Superstructured Micro/Nanoreactor of Topotactically Converted Ultrathin Bismuth Nanosheets for Highly Active CO2 Electroreduction to Formate

被引:60
|
作者
Peng, Chan-Juan [1 ,2 ]
Zeng, Guang [1 ]
Ma, Dong-Dong [1 ]
Cao, Changsheng [1 ,2 ]
Zhou, Shenghua [1 ,2 ]
Wu, Xin-Tao [1 ,3 ]
Zhu, Qi-Long [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Fujian Sci & Technol Innovat Lab Optoelect Inform, Fuzhou 350108, Peoples R China
基金
中国国家自然科学基金;
关键词
bismuth oxide formate; superstructures; bismuth nanosheets; electrocatalytic CO2 reduction; formate; REDUCTION SELECTIVITY; EFFICIENT; GRAPHENE; ENERGY;
D O I
10.1021/acsami.1c03871
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
An electrocatalytic carbon dioxide reduction reaction (CO2RR) is an appealing route to obtain the value-added feedstocks and alleviate the energy crisis. However, how to achieve high-performance electrocatalysts for CO2 reduction to formate is challenging owing to the poor intrinsic activity, insufficient conductivity, and low surface density of active sites. Herein, we fabricated an extremely active and selective hydrangealike superstructured micro/nanoreactor of ultrathin bismuth nanosheets through an in situ electrochemical topotactic transformation of hierarchical bismuth oxide formate (BiOCOOH). The resulted bismuth nanosheet superstructure is in the form of three-dimensional intercrossed networks of ultrathin nanosheets, forming an ordered open porous structure through self-assembly, which can be used as a micro/nanoreactor to enable a large electrochemically active surface area as well as high atomic utilization. Such a distinctive nanostructure endows the material with high electrocatalytic performances for CO2 reduction to formate with near-unity Faradaic selectivity (>95%) in a wide potential window from -0.78 to -1.18 V. Furthermore, this micro/nanoreactor can give the high current densities over 300 mA cm(-2) at low applied potentials without compromising selectivity in a flow cell reactor. Density functional theory (DFT) and in situ attenuated total reflection-infrared spectroscopy (in situ ATR-IR) were further conducted to interpret the CO2RR mechanisms.
引用
收藏
页码:20589 / 20597
页数:9
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