Surface properties of self-assembled monolayer films of tetra-substituted cobalt, iron and manganese alkylthio phthalocyanine complexes

被引:15
作者
Akinbulu, Isaac Adebayo [1 ]
Khene, Samson [1 ]
Nyokong, Tebello [1 ]
机构
[1] Rhodes Univ, Dept Chem, ZA-6140 Grahamstown, South Africa
基金
新加坡国家研究基金会;
关键词
Phthalocyanine; Self-assembled monolayer; Electrochemical impedance spectroscopy; Atomic force microscopy; Carbofuran; ELECTROCATALYTIC REDUCTION; GOLD ELECTRODES; VOLTAMMETRIC CHARACTERIZATION; ASSESSING NONLINEARITY; GRAPHITE-ELECTRODES; MOLECULAR FILMS; OXIDATION; ELECTROCHEMISTRY; ELECTROOXIDATION; DIOXYGEN;
D O I
10.1016/j.electacta.2010.06.065
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Self-assembled monolayer (SAM) films of iron (SAM-1), cobalt (SAM-2) and manganese (SAM-3) phthalocyanine complexes, tetra-substituted with diethylaminoethanethio at the non-peripheral positions, were formed on gold electrode in dimethylformamide (DMF). Electrochemical, impedimentary and surface properties of the SAM films were investigated. Cyclic voltammetry was used to investigate the electrochemical properties of the films. Ability of the films to inhibit common faradaic processes on bare gold surface (gold oxidation, solution redox chemistry of [Fe(H2O)(6)](3+)/[Fe(H2O)(6)](2+) and underpotential deposition (UDP) of copper) was investigated. Electrochemical impedance spectroscopy (EIS), using [Fe(CN)(6)](3-/4-) redox process as a probe, offered insights into the electrical properties of the films/electrode interfaces. Surface properties of the films were probed using atomic force microscopy (AFM) and scanning electron microscopy (SEM). The films were employed for the electrocatalytic oxidation of the pesticide, carbofuran. Electrocatalysis was evidenced from enhanced current signal and less positive oxidation potential of the pesticide on each film, relative to that observed on the bare gold electrode. Mechanism of electrocatalytic oxidation of the pesticide was studied using rotating disc electrode voltammetry. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7085 / 7093
页数:9
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