电合成
等离子体子
纳米颗粒
电化学
电子转移
纳米技术
电催化剂
材料科学
等离子纳米粒子
化学物理
银纳米粒子
化学
电极
光化学
物理化学
光电子学
作者
Zerong Liang,Wei Xu,Jian Li,Chuhong Lin,Wenmin Zhang,Wensheng Liu,Xing‐Hua Xia,Yi‐Ge Zhou
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-11-13
卷期号:23 (23): 10871-10878
被引量:3
标识
DOI:10.1021/acs.nanolett.3c03091
摘要
Plasmon-enhanced electrochemistry (PEEC) has been observed to facilitate energy conversion systems by converting light energy to chemical energy. However, comprehensively understanding the PEEC mechanism remains challenging due to the predominant use of ensemble-based methodologies on macroscopic electrodes, which fails to measure electron-transfer kinetics due to constraints from mass transport and the averaging effect. In this study, we have employed nanoparticle impact electrochemistry (NIE), a newly developed electroanalytical technique capable of measuring electrochemical dynamics at a single-nanoparticle level under optimal mass transport conditions, along with microscopic electron-transfer theory for data interpretation. By investigating the plasmon enhanced hydrogen evolution reaction (HER) at individual silver nanoparticles (AgNPs), we have clearly revealed the previously unknown influence of solvent effects within the PEEC mechanism. This finding suggests an additional approach to optimize plasmon-assisted electrocatalysis and electrosynthesis systems.
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