Miniature direct electron transfer based sulphite/oxygen enzymatic fuel cells

被引:21
作者
Zeng, T. [1 ]
Pankratov, D. [2 ,3 ]
Falk, M. [2 ]
Leimkuehler, S. [1 ]
Shleev, S. [2 ,3 ]
Wollenberger, U. [1 ]
机构
[1] Univ Potsdam, Inst Biochem & Biol, D-14476 Potsdam, Germany
[2] Malmo Univ, S-20506 Malmo, Sweden
[3] Kurchatov Inst, Natl Res Ctr, Kurchatov NBIC Ctr, Moscow 123182, Russia
基金
俄罗斯科学基金会;
关键词
Enzymatic fuel cell; Microscale electrode; Direct electron transfer; Sulphite oxidase; Bilirubin oxidase; HUMAN SULFITE OXIDASE; BIOFUEL CELLS; BILIRUBIN OXIDASE; GOLD ELECTRODES; CYTOCHROME-C; REDUCTION; ENZYMES; B(5);
D O I
10.1016/j.bios.2014.10.080
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A direct electron transfer (DET) based sulphite/oxygen biofuel cell is reported that utilises human sulphite oxidase (hSOx) and Myrothecium verrucaria bilirubin oxidase (MvBOx) and nanostructured gold electrodes. For bioanode construction, the nanostructured gold microelectrodes were further modified with 3,3'-dithiodipropionic acid di(N-hydroxysuccinimide ester) to which polyethylene imine was covalently attached. hSOx was adsorbed onto this chemically modified nanostructured electrode with high surface loading of electroactive enzyme and in presence of sulphite high anodic bioelectrocatalytic currents were generated with an onset potential of 0.05 V vs. NHE. The biocathode contained MyBOx directly adsorbed to the deposited gold nanoparticles for cathodic oxygen reduction starting at 0.71 V vs. NHE. Both enzyme electrodes were integrated to a DET-type biofuel cell. Power densities of 8 and 1 mu W cm(-2) were achieved at 0.15 V and 0.45 V of cell voltages, respectively, with the membrane based biodevices under aerobic conditions. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 42
页数:4
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