Zhang Meng, Yu Li-Juan, Huang Yi-Fan, Yan Jia-Wei, Liu Guo-Kun, Wu De-Yin, Tian Zhong-Qun, Mao Bing-Wei
State Key Laboratory of Physical Chemistry of Solid Surfaces and Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Chem Commun (Camb). 2014 Dec 7;50(94):14740-3. doi: 10.1039/c4cc06269h.
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.
我们首次采用壳层隔离纳米粒子增强策略，将拉曼光谱研究扩展到离子液体中的单晶电极表面，并结合密度泛函理论（DFT）计算来阐明基于咪唑鎓的离子液体-金单晶电极界面的结构细节。
