Electrical and SERS detection of disulfide-mediated dimerization in single-molecule benzene-1,4-dithiol junctions

被引:67
作者
Zheng, Jueting [1 ]
Liu, Junyang [1 ]
Zhuo, Yijing [1 ]
Li, Ruihao [1 ]
Jin, Xi [1 ]
Yang, Yang [1 ]
Chen, Zhao-Bin [1 ]
Shi, Jia [1 ]
Xiao, Zongyuan [1 ]
Hong, Wenjing [1 ]
Tian, Zhong-qun [1 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Pen Tung Sah Inst Micronano Sci & Technol,iChEM, Coll Chem & Chem Engn,Graphene Ind & Engn Res Ins, Xiamen 361005, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金; 中国博士后科学基金;
关键词
SURFACE-ENHANCED RAMAN; CONTROLLABLE BREAK JUNCTION; METAL JUNCTIONS; CONDUCTANCE; 1,4-BENZENEDITHIOL; SCATTERING; BENZENEDITHIOL; ELECTRODES; SILVER; SWITCH;
D O I
10.1039/c8sc00727f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We applied a combination of mechanically controllable break junction (MCBJ) and in situ surface enhanced Raman spectroscopy (SERS) methods to investigate the long-standing single-molecule conductance discrepancy of prototypical benzene-1,4-dithiol (BDT) junctions. Single-molecule conductance characterization, together with configuration analysis of the molecular junction, suggested that disulfide-mediated dimerization of BDT contributed to the low conductance feature, which was further verified by the detection of S-S bond formation through in situ SERS characterization. Control experiments demonstrated that the disulfide-mediated dimerization could be tuned via the chemical inhibitor. Our findings suggest that a combined electrical and SERS method is capable of probing chemical reactions at the single-molecule level.
引用
收藏
页码:5033 / 5038
页数:6
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