Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin film
Phthalocyanines are frequently used as probing molecules in the field of single-molecule surface-enhanced Raman spectroscopy (SERS) and tip-enhanced Raman spectroscopy (TERS). In this work, we systematically compare the SERS and TERS spectra from a thin cobalt phthalocyanine (CoPc) film that is depo...
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doaj-6a7cbeecfb5c4d0ea997f1e8b238fc9f2021-05-02T20:49:39ZengDe GruyterNanophotonics2192-86142019-07-01891533154610.1515/nanoph-2019-0100nanoph-2019-0100Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin filmChen Yu-Ting0Pan Lin1Horneber Anke2van den Berg Marius3Miao Peng4Xu Ping5Adam Pierre-Michel6Meixner Alfred J.7Zhang Dai8Institute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen and LISA+, Tübingen, GermanyInstitute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen and LISA+, Tübingen, GermanyInstitute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen and LISA+, Tübingen, GermanyInstitute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen and LISA+, Tübingen, GermanyInstitute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen and LISA+, Tübingen, GermanyMIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, ChinaLight, Nanomaterials and Nanotechnologies (L2n), Institut Charles Delaunay, CNRS, Université de Technologie de Troyes, Troyes, FranceInstitute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen and LISA+, 72076 Tübingen, GermanyInstitute of Physical and Theoretical Chemistry, Eberhard Karls University of Tübingen and LISA+, 72076 Tübingen, GermanyPhthalocyanines are frequently used as probing molecules in the field of single-molecule surface-enhanced Raman spectroscopy (SERS) and tip-enhanced Raman spectroscopy (TERS). In this work, we systematically compare the SERS and TERS spectra from a thin cobalt phthalocyanine (CoPc) film that is deposited on a Au film. The contributions from electromagnetic (EM), resonance, and charge-transfer enhancements are discussed. Radially and azimuthally polarized vector beams are used to investigate the influences of molecular orientation and the localized surface plasmon resonance (SPR). Furthermore, two different excitation wavelengths (636 and 532 nm) are used to study the resonant excitation effect as well as the involvement of the charge-transfer processes between CoPc and the Au substrate. It is shown that the Raman peaks of CoPc are mostly enhanced by 636 nm excitation through a combination of resonant excitation, high EM enhancement, and chemical enhancement via charge transfer from the metal to the molecule. At 532 nm excitation, however, the SERS and TERS spectra are dominated by photoluminescence, which originates from a photo-induced charge-transfer process from the optically excited molecule to the metal. The contributions of the different enhancement mechanisms explain the optical contrasts seen in the TERS images of Au nanodisks covered by the CoPc film. The insight achieved in this work will help to understand the optical contrast in sub- or single-molecule TERS imaging and apply SERS or TERS in the field of photocatalysis.http://www.degruyter.com/view/j/nanoph.2019.8.issue-9/nanoph-2019-0100/nanoph-2019-0100.xml?format=INTTERSSERSphthalocyaninescharge transferphotoluminescence |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chen Yu-Ting Pan Lin Horneber Anke van den Berg Marius Miao Peng Xu Ping Adam Pierre-Michel Meixner Alfred J. Zhang Dai |
spellingShingle |
Chen Yu-Ting Pan Lin Horneber Anke van den Berg Marius Miao Peng Xu Ping Adam Pierre-Michel Meixner Alfred J. Zhang Dai Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin film Nanophotonics TERS SERS phthalocyanines charge transfer photoluminescence |
author_facet |
Chen Yu-Ting Pan Lin Horneber Anke van den Berg Marius Miao Peng Xu Ping Adam Pierre-Michel Meixner Alfred J. Zhang Dai |
author_sort |
Chen Yu-Ting |
title |
Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin film |
title_short |
Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin film |
title_full |
Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin film |
title_fullStr |
Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin film |
title_full_unstemmed |
Charge transfer and electromagnetic enhancement processes revealed in the SERS and TERS of a CoPc thin film |
title_sort |
charge transfer and electromagnetic enhancement processes revealed in the sers and ters of a copc thin film |
publisher |
De Gruyter |
series |
Nanophotonics |
issn |
2192-8614 |
publishDate |
2019-07-01 |
description |
Phthalocyanines are frequently used as probing molecules in the field of single-molecule surface-enhanced Raman spectroscopy (SERS) and tip-enhanced Raman spectroscopy (TERS). In this work, we systematically compare the SERS and TERS spectra from a thin cobalt phthalocyanine (CoPc) film that is deposited on a Au film. The contributions from electromagnetic (EM), resonance, and charge-transfer enhancements are discussed. Radially and azimuthally polarized vector beams are used to investigate the influences of molecular orientation and the localized surface plasmon resonance (SPR). Furthermore, two different excitation wavelengths (636 and 532 nm) are used to study the resonant excitation effect as well as the involvement of the charge-transfer processes between CoPc and the Au substrate. It is shown that the Raman peaks of CoPc are mostly enhanced by 636 nm excitation through a combination of resonant excitation, high EM enhancement, and chemical enhancement via charge transfer from the metal to the molecule. At 532 nm excitation, however, the SERS and TERS spectra are dominated by photoluminescence, which originates from a photo-induced charge-transfer process from the optically excited molecule to the metal. The contributions of the different enhancement mechanisms explain the optical contrasts seen in the TERS images of Au nanodisks covered by the CoPc film. The insight achieved in this work will help to understand the optical contrast in sub- or single-molecule TERS imaging and apply SERS or TERS in the field of photocatalysis. |
topic |
TERS SERS phthalocyanines charge transfer photoluminescence |
url |
http://www.degruyter.com/view/j/nanoph.2019.8.issue-9/nanoph-2019-0100/nanoph-2019-0100.xml?format=INT |
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