电催化CO的气态和液态产品的反应路径规则2 在吸附剂相互作用下减少
Feng Hu1,2, Xiaoqian Xu1, Yajie Sun1
1Jiangsu Key Laboratory of Electrochemical Energy Storage Technologies, College of Materials Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing, 210016, P. R. China.
Angewandte Chemie (International ed. in English)
|December 9, 2024
概括
对Ag-Cu纳米结构的受控化使得选择性电化学CO2降解成为气态CO或液态产品,如酸盐和乙醇. 在CO2RR催化中的这一突破揭示了用于提高效率的路径切换机制.
科学领域:
- 电化学 电化学 电化学
- 催化剂是一种催化剂.
- 材料科学 材料科学 材料科学
背景情况:
- 电化学二氧化碳还原反应 (CO2RR) 的性能通过过渡金属上的化离子吸附得到增强.
- 对选择性CO2RR途径的反应机制尚不清楚.
研究的目的:
- 在受控化的Ag-Cu纳米结构上揭示气态 (CO) 和液态产品 (格式,乙醇) 之间的明显路径切换.
- 了解化在 CO2RR 中调中间体和反应通路中的作用.
主要方法:
- 精确定义的Ag-Cu纳米结构的合成与控制的化.
- 使用流电池设置的电化学二氧化碳减少.
- 在现场红外光谱和理论计算.
主要成果:
- 通过调整AgCl层厚度来调整Ag/AgCl上的CO2转化为CO,实现高选择性.
- 优化的Cl-Ag/Cu系统将二氧化碳转化为甲酸盐和乙醇,具有近100%的法拉第效率和高电流密度.
- 通过减少吉布斯自由能量障碍,确定*OCHO中间体对于促进CO和形成途径至关重要.
结论:
- 化在指导Ag-Cu催化剂上的CO2RR路径方面发挥着关键作用.
- 侧向吸附效应,特别是*OCHO,对于确定产品选择性至关重要.
- 这项研究提供了对控制CO2RR选择性的基本见解,以产生有价值的产品.
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