Mapping the capacitance of self-assembled monolayers at metal/electrolyte interfaces at the nanoscale by in-liquid scanning dielectric microscopy

被引:17
作者
Millan-Solsona, Ruben [1 ,2 ]
Checa, Marti [1 ]
Fumagalli, Laura [3 ,4 ]
Gomila, Gabriel [1 ,2 ]
机构
[1] Barcelona Inst Sci & Technol, Inst Bioenginyeria Catalunya IBEC, C Baldiri Reixac 11-15, Barcelona 08028, Spain
[2] Univ Barcelona, Dept Engn Elect & Biomed, C Marti i Franques 1, Barcelona 08028, Spain
[3] Univ Manchester, Dept Phys & Astron, Manchester M13 9PL, Lancs, England
[4] Univ Manchester, Natl Graphene Inst, Manchester M13 9PL, Lancs, England
基金
欧洲研究理事会; 欧盟地平线“2020”; 英国工程与自然科学研究理事会;
关键词
IMPEDANCE SPECTROSCOPY; FORCE MICROSCOPY; CHAIN-LENGTH; CONSTANT; STRESS; LAYER; GOLD;
D O I
10.1039/d0nr05723a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic self-assembled monolayers (SAMs) at metal/electrolyte interfaces have been thoroughly investigated both from fundamental and applied points of view. A relevant figure of merit of metal/SAM/electrolyte interfaces is the specific capacitance, which determines the charge that can be accumulated at the metal electrode. Here, we show that the specific capacitance of non-uniform alkanethiol SAMs at gold/electrolyte interfaces can be quantitatively measured and mapped at the nanoscale by in-liquid scanning dielectric microscopy in force detection mode. We show that sub-100 nm spatial resolution in ultrathin (<1 nm) SAMs can be achieved, largely improving the performance of current sensing characterization techniques. The present results provide access to study the dielectric properties of metal/SAM/electrolyte interfaces at scales that have remained unexplored until now.
引用
收藏
页码:20658 / 20668
页数:11
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