纳米柱
材料科学
表面等离子共振
拉曼散射
带隙
半导体
拉曼光谱
光致发光
共振(粒子物理)
紫外线
光电子学
蓝移
分子
纳米技术
纳米结构
光学
纳米颗粒
原子物理学
化学
有机化学
物理
作者
Zhijun Wu,Zheng Chunfang,Qi Lin,Qun Fu,Huaping Zhao,Yong Lei
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2024-02-18
卷期号:35 (21): 215501-215501
标识
DOI:10.1088/1361-6528/ad2a5a
摘要
Abstract We observed a unique interpillar gap-related surface-enhanced Raman scattering (SERS) behavior of p -aminothiophenol (PATP) molecules from periodic TiO 2 nanopillar arrays with three gap sizes of 191, 297 and 401 nm, which is completely different from that on Ag and Ni nanopillar arrays. Especially, the gap-size-dependent charge-transfer (CT) resonance enhancement from TiO 2 /Ni has been indicated through comparisons of variation trend of SERS intensities with inter-pillar gap size between TiO 2 /Ni and Ag/TiO 2 /Ni as well as Ni nanoarrays, and been confirmed by spectra of ultraviolet–visible absorption and photoluminescence. Results demonstrate that the CT resonance enhancement is more susceptible to the change of the gap size compared with the surface plasmon resonance (SPR) enhancement in TiO 2 /Ni nanoarrays. Hence, SPR and CT enhancement showing different variation trend and rate with the gap size that leads to a different relative contribution of CT resonance to the overall SERS enhancement as gap size changes, and consequently results in a unique gap-related SERS behavior for TiO 2 /Ni nanoarrays. The present study is not only helpful for investigating SERS mechanism for semiconductors but also providing a method to design and optimize periodic metal/semiconductor SERS substrates in a controllable way.
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