材料科学
铋
锡
合金
钒
氧化钒
碳化钒
氧化物
电催化剂
无机化学
过渡金属
冶金
催化作用
电化学
物理化学
电极
化学
生物化学
作者
Jiaye Zhu,Guorong Zhou,Yun Tong,Lu Chen,Pengzuo Chen
标识
DOI:10.1002/adfm.202420177
摘要
Abstract The electrocatalytic conversion of carbon dioxide (CO 2 ) 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 (VO x ) clusters decorated Bi‐Sn alloy (BiSn(VO x )) catalyst. Theoretical and in situ spectral studies confirm the simultaneously improved kinetics of CO 2 activation and subsequent protonation via VO x clusters mediated water dissociation process, thereby optimizing the electrocatalytic activity and selectivity of CO 2 to formate. Remarkably, this BiSn(VO x ) 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(VO x ) 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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