A pyrroloquinolinequinone-dependent glucose dehydrogenase (PQQ-GDH)-electrode with direct electron transfer based on polyaniline modified carbon nanotubes for biofuel cell application

被引:66
|
作者
Schubart, Ivo W. [1 ]
Goebel, Gero [1 ]
Lisdat, Fred [1 ]
机构
[1] Wildau Tech Univ Appl Sci, D-15745 Wildau, Germany
关键词
Biofuel cell; Glucose dehydrogenase; Direct electron transfer; Polyaniline; Carbon nanotubes; MWCNT-MODIFIED GOLD; BILIRUBIN OXIDASE; ACINETOBACTER-CALCOACETICUS; SULFONATED POLYANILINE; CONDUCTING POLYMERS; PQQ; ENZYME; BIOSENSORS; ELECTROCHEMISTRY; RECONSTITUTION;
D O I
10.1016/j.electacta.2012.03.128
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this study we present a pyrroloquinolinequinone-dependent glucose dehydrogenase [(PQQ)-GDH] electrode with direct electron transfer between the enzyme and electrode. Soluble pyrroloquinolinequinone-dependent glucose dehydrogenase from Acinetobacter calcoaceticus is covalently bound to an electropolymerized polyaniline copolymer film on a multi-walled carbon nanotube (MWCNT)-modified gold electrode. The pulsed electropolymerization of 2-methoxyaniline-5-sulfonic acid (MASA) and m-aminobenzoic acid (ABA) is optimized with respect to the efficiency of the bioelectrocatalytic conversion of glucose. The glucose oxidation starts at -0.1 V vs. Ag/AgCl and current densities up to 500 mu A/cm(2) at low potential of +0.1 V vs. Ag/AgCl can be achieved. The electrode shows a glucose sensitivity in the range from 0.1 mM to 5 mM at a potential of +0.1 V vs. Ag/Ag/Cl. The dynamic range is extended to 100 mM at +0.4V vs. Ag/AgCl. The electron transfer mechanism is studied and buffer effects are investigated. The developed enzyme electrode is examined for bioenergetic application by assembling of a membrane-less biofuel cell. For the cathode a bilirubin oxidase (BOD) based MWCNT-modified gold electrode with direct electron transfer (DET) is used. The biofuel cell exhibits a cell potential of 680 +/- 20 mV and a maximum power density of up to 65 mu W/cm(2) at 350 mV vs. Ag/AgCl. (C) 2012 Published by Elsevier Ltd.
引用
收藏
页码:224 / 232
页数:9
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