Admittance as a useful tool for investigation of solute-solvent interactions at the double layer

被引:1
|
作者
Krishnan, Chirakkal [1 ,2 ,3 ]
Garnett, Merrill [2 ]
Chu, Benjamin [1 ,3 ]
机构
[1] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
[2] Garnett McKeen Lab Inc, Bohemia, NY 11716 USA
[3] Stonybrook Technol & Appl Res, Stony Brook, NY 11794 USA
关键词
Electric double layer; Admittance; Impedance; Potential induced and water structure-enforced ion pair; ELECTRICAL DOUBLE-LAYER; AQUEOUS SODIUM-CHLORIDE; SELF-ASSEMBLY PROCESS; SPATIOTEMPORAL OSCILLATIONS; BIOLOGICAL MOLECULES; IMPEDANCE MEASUREMENTS; STRONG ELECTROLYTES; PARKINSONS-DISEASE; SOLUTION INTERFACE; HYDROGEN-PEROXIDE;
D O I
10.1016/j.elecom.2009.09.037
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The application of admittance measurements, an often neglected topic in impedance spectroscopy, to further our understanding of solute-solvent interactions at the double layer is presented by comparing aqueous solutions of sodium acetate and protonated lidocaine acetate. Unlike impedance, the overlap of concentration-dependent hydration cospheres and the potential- and frequency-dependent orientation effects of water molecules around the ions at or near the double layer could be manifested in admittance data. Admittance, but not impedance, also allows identification of interactions between two dipoles, such as amino and carbonyl groups, by changing frequencies and applied potentials. The effects manifest themselves by exhibiting cathodic and anodic shifts with frequency changes. All the admittance data could be reasonably explained by utilizing the concept of "potential induced and water structure-enforced ion-pair formation". (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2229 / 2232
页数:4
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