Chemically Interrogating N-Heterocyclic Carbenes at the Single-Molecule Level Using Tip-Enhanced Raman Spectroscopy

被引:0
|
作者
Li, Linfei [1 ]
Mahapatra, Sayantan [1 ]
Schultz, Jeremy F. [1 ]
Zhang, Xu [2 ]
Jiang, Nan [1 ,3 ]
机构
[1] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[2] Calif State Univ, Dept Phys & Astron, Northridge, CA 91330 USA
[3] Univ Illinois, Dept Phys, Chicago, IL 60607 USA
基金
美国国家科学基金会;
关键词
N-heterocyclic carbenes; Raman spectroscopy; TERS; STM; Ag(111); NANOSCALE; MODES;
D O I
10.1021/acsnano.4c10942
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
N-heterocyclic carbenes (NHCs) have been established as powerful modifiers to functionalize metal surfaces for a wide variety of energy and nanoelectronic applications. To fundamentally understand and harness NHC modification, it is essential to identify suitable methods to interrogate NHC surface chemistry at the spatial limit. Here, we demonstrate tip-enhanced Raman spectroscopy (TERS) as a promising tool for chemically probing the surface properties of NHCs at the single-molecule scale. We show that with subnanometer resolution, TERS measurements are capable of not only unambiguously identifying the chemical structure of individual NHCs by their vibrational fingerprints but also definitively determining the binding mode of NHCs on metal surfaces. In particular, by investigating low-temperature NHC adsorption on Ag(111), our TERS studies provide insights into the temperature dependence of the adsorption properties of NHCs. This work suggests the potential of single-molecule vibrational spectroscopy for investigations of NHC surface modification at the most fundamental level.
引用
收藏
页码:32118 / 32125
页数:8
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