电场
纳米技术
纳米结构
催化作用
曲率
材料科学
化学
物理
有机化学
几何学
数学
量子力学
作者
Shenming Wang,Xiaohui Liu,Lin Yang,Wenxuan Yang,Zhenzhen Feng,Guangyong Qin,Tongtao Yue,Hua He,Jingbin Zeng
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-03-27
卷期号:25 (14): 5663-5671
被引量:9
标识
DOI:10.1021/acs.nanolett.4c06399
摘要
The catalytic performance of plasmonic nanostructures is strongly influenced by surface morphology. While the antenna effect in tip regions has received considerable attention, the role of gap morphology has been largely overlooked. Comprehending morphology-regulated catalysis at the subparticle level remains constrained by morphology heterogeneity and imaging resolution limitations, hindering rational nanocatalyst design. Here, we develop a single-particle catalytic activity assay by coupling single-molecule fluorescence (SMF) imaging with plasmon-enhanced fluorescence, enabling the probing of catalytic dynamics of plasmonic Au nanostructures and their correlation with local electric fields. Using this approach, we demonstrate that nanospine formation with nanoscale gaps on Au nanostructures significantly enhances catalytic activity. Further investigations using SMF imaging, electric field simulations, and molecular dynamics simulations reveal that the gap-enhanced catalytic activity is driven by amplified electric fields and increased substrate adsorption at negatively curved sites. This study provides valuable insights into designing plasmonic nanocatalysts through surface morphology engineering.
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