Issue 45, 2020

In situ surface-enhanced electronic and vibrational Raman scattering spectroscopy at metal/molecule interfaces

Abstract

SERS signals from nanostructured surfaces of Au, covered with thiol monolayers, were monitored under application of various electrochemical potentials over a wide Raman-shift range of both the Stokes and anti-Stokes branches. The background continuum in the SERS spectra varied in intensity with apparent correlations with breaking of Au–S bond or evolution of Au–O. This clearly indicates that the origin of the background can be ascribed to non-resonant electronic Raman scattering, which is sensitive to the electronic density at the surface. Using the property of the electronic Raman scattering, full information on the electric double layer at both sides of the metal/dielectric interface was analysed. In the low Raman-shift region below 200 cm−1, moreover, the evolution and disappearance of collective motions of thiol assembly was able to be monitored in situ, which is hardly obtainable with other vibrational absorption spectroscopies.

Graphical abstract: In situ surface-enhanced electronic and vibrational Raman scattering spectroscopy at metal/molecule interfaces

Supplementary files

Article information

Article type
Paper
Submitted
25 ส.ค. 2563
Accepted
29 ก.ย. 2563
First published
30 ก.ย. 2563

Nanoscale, 2020,12, 22988-22994

In situ surface-enhanced electronic and vibrational Raman scattering spectroscopy at metal/molecule interfaces

M. Inagaki, K. Motobayashi and K. Ikeda, Nanoscale, 2020, 12, 22988 DOI: 10.1039/D0NR06150F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements