Modulating and probing the dynamic intermolecular interactions in plasmonic molecule-pair junctions

被引:15
作者
Ma, Tao [1 ,2 ]
Guo, Jing [2 ]
Chang, Shuai [1 ]
Wang, Xuewen [2 ]
Zhou, Jianghao [1 ,2 ]
Liang, Feng [1 ]
He, Jin [2 ,3 ]
机构
[1] Wuhan Univ Sci & Technol, Sch Chem & Chem Engn, Sch Met & Mat, State Key Lab Refractories & Met, Wuhan 430081, Hubei, Peoples R China
[2] Florida Int Univ, Dept Phys, Miami, FL 33199 USA
[3] Florida Int Univ, Biomol Sci Inst, Miami, FL 33199 USA
基金
美国国家科学基金会;
关键词
ENHANCED RAMAN-SCATTERING; 4-MERCAPTOBENZOIC ACID; SINGLE; SERS; AG; SPECTROSCOPY; FABRICATION; SILVER;
D O I
10.1039/c9cp02030f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Reversible intermolecular interactions play critical roles in nature. However, it is still challenging to monitor the dynamic intermolecular interactions at the single-molecule level in aqueous solution. Here, we studied the dynamic changes of intermolecular interactions at the carboxyl/carboxyl interfaces between a pair of molecules trapped in a plasmonic nanocavity formed between a gold nanoparticle (GNP) and a gold nanoelectrode (GNE). The development of intermolecular interactions, including the appearance of hydrogen bonds (h-bonds), during and after single GNP collision events on the GNE, was monitored by time-resolved surface-enhanced Raman spectroscopy at a tens of milliseconds time resolution. Spectral fingerprints of the carboxyl group corresponding to non-specific intermolecular interactions and h-bonds are identified. Furthermore, we demonstrated that the strength of intermolecular interaction could be mechanically modulated by changing the applied bias at the GNE, which resulted in small and controllable changes in the nanogap distance. Unlike non-specific intermolecular interactions, the intermolecular h-bonds can only be formed stochastically and are more sensitive to the gap distance modulation. This report demonstrates a new approach to modulate and probe intermolecular interactions within nanogaps.
引用
收藏
页码:15940 / 15948
页数:9
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