电催化剂
纳米颗粒
纳米尺度
材料科学
纳米技术
粒子(生态学)
降级(电信)
理论(学习稳定性)
电化学发光
化学发光
化学工程
化学
电极
电化学
计算机科学
物理化学
海洋学
地质学
电信
机器学习
工程类
作者
Zhouzhou Zhu,Xiangfu Hu,Ying Wei,Jiahao Pan,Zhenda Lu
标识
DOI:10.1021/acs.jpclett.4c03226
摘要
Understanding the stability of single nanoparticles is crucial for optimizing their performance in various applications, including catalysis. In this study, we employed electrochemiluminescence (ECL) imaging to investigate the temporal stability of individual Au and Pt nanoparticles within precisely engineered arrays. Our results reveal significant differences in the stability of Au and Pt NPs. While both exhibit initial decay due to diffusion limitations, Au NPs undergo more rapid degradation, attributed to surface oxidation and detachment. In contrast, Pt NPs demonstrate much better stability with little surface oxidation. This study provides valuable insights into the fundamental behavior of single-NP electrocatalysis and highlights the potential of ECL imaging as a powerful tool for unraveling the complex dynamics of nanoscale systems.
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