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Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS)
- Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS)
- Kim, Jayeong; Jang, Yujin; Kim, Nam-Jung; Kim, Heehun; Yi, Gyu-Chul; Shin, Yukyung; Kim, Myung Hwa; Yoon, Seokhyun
- Ewha Authors
- SCOPUS Author ID
- Issue Date
- Journal Title
- FRONTIERS IN CHEMISTRY
- FRONTIERS IN CHEMISTRY vol. 7
- surface enhanced Raman scattering; chemical enhancement; enhancement mechanism; charge transfer; semiconductor microstructure
- FRONTIERS MEDIA SA
- SCIE; SCOPUS
- Document Type
- 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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