Issue 94, 2014

Extending the shell-isolated nanoparticle-enhanced Raman spectroscopy approach to interfacial ionic liquids at single crystal electrode surfaces

Abstract

We employ, for the first time, a shell-isolated nanoparticle-enhancement strategy to extend Raman spectroscopy studies to single crystal electrode surfaces in ionic liquids, and combine density functional theory (DFT) calculations to elucidate the structural details of the imidazolium-based ionic liquid–Au single crystal electrode interfaces.

Graphical abstract: Extending the shell-isolated nanoparticle-enhanced Raman spectroscopy approach to interfacial ionic liquids at single crystal electrode surfaces

Supplementary files

Article information

Article type
Communication
Submitted
10 Aug 2014
Accepted
06 Oct 2014
First published
06 Oct 2014

Chem. Commun., 2014,50, 14740-14743

Author version available

Extending the shell-isolated nanoparticle-enhanced Raman spectroscopy approach to interfacial ionic liquids at single crystal electrode surfaces

M. Zhang, L. Yu, Y. Huang, J. Yan, G. Liu, D. Wu, Z. Tian and B. Mao, Chem. Commun., 2014, 50, 14740 DOI: 10.1039/C4CC06269H

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