等离子体子
表面增强拉曼光谱
拉曼光谱
分子
纳米技术
材料科学
化学气相沉积
表面等离子共振
基质(水族馆)
化学物理
化学
拉曼散射
光电子学
纳米颗粒
有机化学
光学
海洋学
物理
地质学
作者
Jayeong Kim,Yujin Jang,Nam-Jung Kim,Heehun Kim,Gyu‐Chul Yi,Yukyung Shin,Myung Hwa Kim,Seokhyun Yoon
标识
DOI:10.3389/fchem.2019.00582
摘要
Surface enhanced Raman spectroscopy (SERS) has been intensively investigated during the past decades for its enormous electromagnetic field enhancement near the nanoscale metallic surfaces. Chemical enhancement of SERS, however, remains rather elusive despite intensive research efforts, mainly due to the relatively complex enhancing factors and inconsistent experimental results. To study details of chemical enhancement mechanism, we prepared various low dimensional semiconductor substrates such as ZnO and GaN that were fabricated via metal organic chemical vapor deposition process. We used three kinds of molecules (4-MPY, 4-MBA, 4-ATP) as analytes to measure SERS spectra under non-plasmonic conditions to understand charge transfer mechanisms between a substrate and analyte molecules leading to chemical enhancement. We observed that there is a preferential route for charge transfer responsible for chemical enhancement, that is, there exists a dominant enhancement process in non-plasmonic SERS. To further confirm our idea of charge transfer mechanism, we used a combination of 2-dimensional transition metal dichalcogenide substrates and analyte molecules. We also observed significant enhancement of Raman signal from molecules adsorbed on 2-dimensional transition metal dichalcogenide surface that is completely consistent with our previous results. We also discuss crucial factors for increasing enhancement factors for chemical enhancement without involving plasmonic resonance.
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