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Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS)
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 t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710363/ https://www.ncbi.nlm.nih.gov/pubmed/31482089 http://dx.doi.org/10.3389/fchem.2019.00582 |
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author | Kim, Jayeong Jang, Yujin Kim, Nam-Jung Kim, Heehun Yi, Gyu-Chul Shin, Yukyung Kim, Myung Hwa Yoon, Seokhyun |
author_facet | Kim, Jayeong Jang, Yujin Kim, Nam-Jung Kim, Heehun Yi, Gyu-Chul Shin, Yukyung Kim, Myung Hwa Yoon, Seokhyun |
author_sort | Kim, Jayeong |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6710363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67103632019-09-03 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 Front Chem Chemistry 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. Frontiers Media S.A. 2019-08-20 /pmc/articles/PMC6710363/ /pubmed/31482089 http://dx.doi.org/10.3389/fchem.2019.00582 Text en Copyright © 2019 Kim, Jang, Kim, Kim, Yi, Shin, Kim and Yoon. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Kim, Jayeong Jang, Yujin Kim, Nam-Jung Kim, Heehun Yi, Gyu-Chul Shin, Yukyung Kim, Myung Hwa Yoon, Seokhyun Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS) |
title | Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS) |
title_full | Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS) |
title_fullStr | Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS) |
title_full_unstemmed | Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS) |
title_short | Study of Chemical Enhancement Mechanism in Non-plasmonic Surface Enhanced Raman Spectroscopy (SERS) |
title_sort | study of chemical enhancement mechanism in non-plasmonic surface enhanced raman spectroscopy (sers) |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710363/ https://www.ncbi.nlm.nih.gov/pubmed/31482089 http://dx.doi.org/10.3389/fchem.2019.00582 |
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