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Vanadium Oxide Clusters Mediated Bismuth-Tin Alloy for Accelerated Dynamics of Electrocatalytic CO2 Conversion
被引:4
|作者:
Zhu, Jiaye
[1
]
Zhou, Guorong
[1
]
Tong, Yun
[1
]
Chen, Lu
[2
]
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] Univ Cambridge, Yusuf Hamied Dept Chem, Cambridge CB2 1EW, England
基金:
中国国家自然科学基金;
关键词:
BiSn alloy;
CO2;
electroreduction;
formate product;
vanadium oxide clusters;
Zn-CO2;
battery;
ELECTROREDUCTION;
TRANSFORMATION;
REDUCTION;
D O I:
10.1002/adfm.202420177
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
The electrocatalytic conversion of carbon dioxide (CO2) to formate is significant for carbon neutrality. How to improve the reaction kinetics of electrocatalysts is one of the important challenges. An innovative electrodeposition strategy is presented herein to rationally synthesize the vanadium oxide (VOx) clusters decorated Bi-Sn alloy (BiSn(VOx)) catalyst. Theoretical and in situ spectral studies confirm the simultaneously improved kinetics of CO2 activation and subsequent protonation via VOx clusters mediated water dissociation process, thereby optimizing the electrocatalytic activity and selectivity of CO2 to formate. Remarkably, this BiSn(VOx) catalyst achieves high Faradic efficiency (FE) of formate over 90% within wide potential window of 800 mV and excellent stability over 100 h at -0.6 V versus RHE. Moreover, the BiSn(VOx) cathode integrated rechargeable Zn-CO(2 )battery realizes the largest power density of 3.8 mW cm(-2), while the assembled co-electrolysis electrolyzer delivers a total FE of formate over 182% at a cell voltage of 0.6 V, outperforming the highest value so far. The work provides a promising way to develop advanced electrocatalysts for electrolysis.
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页数:8
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