纳米片
双金属片
材料科学
电化学
催化作用
可逆氢电极
法拉第效率
化学工程
格式化
氧化还原
密度泛函理论
电极
无机化学
纳米技术
化学
工作电极
物理化学
冶金
计算化学
生物化学
工程类
作者
Wenbo Wu,Jiaye Zhu,Yun Tong,Shuangfei Xiang,Pengzuo Chen
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-11-24
卷期号:17 (5): 3684-3692
被引量:43
标识
DOI:10.1007/s12274-023-6269-7
摘要
Regulating the electronic structure of Bi-based materials by alloying engineering is promising to promote the electrocatalytic activity, but it remains some challenges to be solved. In this study, a facile electrochemical co-deposition strategy is developed to synthesize the bimetallic Bi9Cu1 alloy nanosheet on carbon cloth (Bi9Cu1/CC), which represents a novel self-supporting electrode for the electrocatalytic carbon dioxide (CO2) reduction reaction (CO2RR). The Bi9Cu1/CC catalyst has achieved a remarkable catalytic performance with high Faradaic efficiencies (FE) of over 90% for formate at wide potentials from −0.7 to −1.2 V vs. reversible hydrogen electrode (RHE). Moreover, the reversible Zn-CO2 battery can be driven by Bi9Cu1/CC cathode with a largest power density of 1.4 mW·cm−2, and superior operating stability. The systematic characterizations and electrochemical results confirm that the improved catalytic active sites, the enhanced mass/charge transport and the optimal reaction kinetics of Bi nanosheet are realized for CO2RR by Cu alloying. In situ attenuated total reflection infrared (ATR-IR) result confirms the bimetallic Bi-Cu active sites prefer to follow the ⋆OCHO conversion pathway. The density functional theory (DFT) calculations suggest that the Cu alloying contributes to the increased density of states near the Fermi surface of Bi and the optimized adsorption of ⋆OCHO intermediates on the Bi sites, resulting in the excellent catalytic performance.
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