Issue 94, 2014
From the journal:

Chemical Communications

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

Meng Zhang,a   Li-Juan Yu,a   Yi-Fan Huang,a   Jia-Wei Yan,a   Guo-Kun Liu,a   De-Yin Wu,*a   Zhong-Qun Tiana  and  Bing-Wei Mao*a  

* Corresponding authors

a State Key Laboratory of Physical Chemistry of Solid Surfaces and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China
E-mail: bwmao@xmu.edu.cn, dywu@xmu.edu.cn

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

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Article information

DOI
https://doi.org/10.1039/C4CC06269H
Article type
Communication
Submitted
10 Aug 2014
Accepted
06 Oct 2014
First published
06 Oct 2014

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

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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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