在阴极极化过程中诱导Au的结构演变
Yu-Qi Wang1,2, Jiaju Fu1, Yue Feng1,2
1CAS Key Laboratory of Molecular Nanostructure and Nanotechnology, CAS Research/Education Center for Excellence in Molecular Sciences, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Journal of the American Chemical Society
|September 26, 2024
概括
金属离子对电催化二氧化碳的减少有很大影响. 像Cs+这样的较大离子会促进黄金表面的粗,从而形成增强CO2RR效率的活性位点.
科学领域:
- 电化学
- 材料科学
- 表面科学
背景情况:
- 电催化减排 (CO2RR) 对于可持续能源至关重要.
- 电解质中的金属 (AM+) 影响CO2RR活性.
- 对于AM+影响的确切机制仍有争议.
研究的目的:
- 调查AM+在Au上的CO2RR中的作用.
- 阐明AM+对催化活性影响的机制.
- 将表面结构变化与CO2RR性能相关联.
主要方法:
- 电化学扫描道显微镜 (EC-STM) 用于现场表面观测.
- 在各种AM+电解质中,Au{111}的阴极极化.
- 电化学CO2RR性能测量
主要成果:
- 在阴极极化过程中在AM+电解质中观察到Au(111) 的表面粗化.
- 表面粗的顺序为Cs+ > Rb+ > K+ > Na+ > Li+ 对于临界电位和面积.
- 较高的表面粗度与增强的CO2RR催化活性相关.
- 对于诱导表面粗和形成活性位点来说,AM+是必不可少的.
结论:
- 在CO2RR过程中,AM+离子对Au的表面结构演变起着至关重要的作用.
- 由AM+引起的表面粗导致高度活跃的低协调的Au位点的形成.
- 这种机制解释了更大的AM+电解质中的增强CO2RR.
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