拉曼光谱
纳米颗粒
原位
催化作用
材料科学
氢氧化物
纳米技术
化学工程
光谱学
金属
氧化物
化学
有机化学
工程类
物理
冶金
光学
量子力学
作者
Jing Liu,Han‐Liang Zhong,Xiangyu Li,Mufei Yue,Weimin Yang,Xueqiu You,Jing‐Hua Tian,Yaohui Wang,Jian‐Feng Li
出处
期刊:Nano Research
[Springer Nature]
日期:2023-02-04
卷期号:17 (6): 4687-4692
被引量:6
标识
DOI:10.1007/s12274-023-5473-9
摘要
The composition and evolution of interfacial species play a key role during electrocatalytic process. Unveiling the structural evolution and intermediate during catalytic process by in situ characterization can shed new light on the electrocatalytic reaction mechanism and develop highly efficient catalyst. However, directly probing the interfacial species is extremely difficult for most spectroscopic techniques due to complicated interfacial environment and ultra-low surface concentration. Herein, electrochemical core-shell nanoparticle enhanced Raman spectroscopy is utilized to probe the composition and evolution processes of interfacial species on Au@Pt, Au@Co, and Au@PtCo core—shell nanoparticle surfaces. The spectral evidences of interfacial intermediates including hydroxide radical (OH*), superoxide ion (O 2 − ), as well as metal oxide species are directly captured by in situ Raman spectroscopy, which are further confirmed by the both isotopic experiment and density functional theory calculation. These results provide a mechanistic guideline for the rational design of highly efficient electrocatalysts.
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