罗丹明6G
纳米结构
拉曼散射
材料科学
等离子体子
纳米技术
拉曼光谱
胶体金
纳米颗粒
光电子学
光学
物理
荧光
作者
Yoshiki Suganami,Tomoya Oshikiri,Hideyuki Mitomo,Keiji Sasaki,Yen-En Liu,Xu Shi,Yasutaka Matsuo,Kuniharu Ijiro,Hiroaki Misawa
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-02-01
卷期号:18 (6): 4993-5002
被引量:6
标识
DOI:10.1021/acsnano.3c10959
摘要
We developed a substrate that enables highly sensitive and spatially uniform surface-enhanced Raman scattering (SERS). This substrate comprises densely packed gold nanoparticles (d-AuNPs)/titanium dioxide/Au film (d-ATA). The d-ATA substrate demonstrates modal ultrastrong coupling between localized surface plasmon resonances (LSPRs) of AuNPs and Fabry–Pérot nanocavities. d-ATA exhibits a significant enhancement of the near-field intensity, resulting in a 78-fold increase in the SERS signal for crystal violet (CV) compared to that of d-AuNP/TiO2 substrates. Importantly, high sensitivity and a spatially uniform signal intensity can be obtained without precise control of the shape and arrangement of the nanoscale AuNPs, enabling quantitative SERS measurements. Additionally, SERS measurements of rhodamine 6G (R6G) on this substrate under ultralow adsorption conditions (0.6 R6G molecules/AuNP) show a spatial variation in the signal intensity within 3%. These findings suggest that the SERS signal under modal ultrastrong coupling originates from multiple plasmonic particles with quantum coherence.
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