Spontaneous modification of carbon surface with neutral red from its diazonium salts for bioelectrochemical systems

被引:31
|
作者
Guo, Kun [1 ,2 ]
Chen, Xin [3 ]
Freguia, Stefano [1 ]
Donose, Bogdan C. [1 ]
机构
[1] Univ Queensland, Adv Water Management Ctr, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Ctr Microbial Electrosynth, Brisbane, Qld 4072, Australia
[3] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
来源
关键词
Neutral red; Aryl diazonium salts; Spontaneous modification; Extracellular electron transfer; Bioelectrochemical systems; HARVESTING ENERGY; POLY(NEUTRAL RED); KINETIC ACTIVITY; ORGANIC LAYERS; REDUCTION; ANODE; ANTHRAQUINONE; ELECTRICITY; ELECTRODES; CELL;
D O I
10.1016/j.bios.2013.02.051
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This study introduces a novel and simple method to covalently graft neutral red (NR) onto carbon surfaces based on spontaneous reduction of in situ generated NR diazonium salts. Immobilization of neutral red on carbon surface was achieved by immersing carbon electrodes in NR-NaNO2-HCl solution. The functionalized electrodes were characterized by cyclic voltammetry (CV), atomic force microscope (AFM), and X-ray photoelectron spectroscopy (XPS). Results demonstrated that NR attached in this way retains high electrochemical activity and proved that NR was covalently bound to the carbon surface via the pathway of reduction of aryl diazonium salts. The NR-modified electrodes showed a good stability when stored in PBS solution in the dark. The current output of an acetate-oxidising microbial bioanode made of NR-modified graphite felts were 3.63 +/- 0.36 times higher than the unmodified electrodes, which indicates that covalently bound NR can act as electron transfer mediator to facilitate electron transfer from bacteria to electrodes. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:184 / 189
页数:6
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