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Enzyme-based glucose fuel cell using Vitamin K3-immobilized polymer as an electron mediator
被引:90
作者:
Sato, F
Togo, M
Islam, MK
Matsue, T
Kosuge, J
Fukasaku, N
Kurosawa, S
Nishizawa, M
机构:
[1] Tohoku Univ, Grad Sch Engn, Dept Bioengn & Robot, Aoba Ku, Sendai, Miyagi 9808579, Japan
[2] Tohoku Univ, Grad Sch Engn, Dept Biomol Chem, Aoba Ku, Sendai, Miyagi 9808579, Japan
[3] Daiichi Pure Chem Co Ltd, Naka, Ibaraki 3191182, Japan
关键词:
fuel cell;
diaphorase;
glucose dehydrogenase;
naphthoquinone;
D O I:
10.1016/j.elecom.2005.04.015
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
To create an enzyme-based biological fuel cell generating electricity from glucose and O-2, we modified a glassy carbon electrode with a bi-layer polymer membrane, the inner layer containing diaphorase (Dp) and the outer, glucose dehydrogenase (GDH, an NAD(+)-dependent enzyme). The Dp membrane was formed from a newly synthesized 2-methyl-1,4-naphthoquinone (Vitamin K-3; VK3)-based polymer. This polymer showed reversible redox activity at a potential close to that of free VK3 (-0.25 V vs. Ag/AgCl sat. KCl), and served as an electron mediator of Dp for the electrocatalytic oxidation of NADH to NAD(+). The addition of Ketjenblack into the Dp/VK3 film enhanced the generation of NAD(+). The outer GDH membrane oxidized glucose continuously using NAD(+) generated at the inner Dp film. To construct the glucose/O-2 biological fuel cell, we coupled the enzyme-modified anode with a polydimethylsiloxane-coated Pt cathode. The cell's open circuit voltage was 0.62 V and its maximum power density was 14.5 mu W/cm(2) at 0.36 V in an air-saturated phosphate buffered saline solution (pH 7.0) at 37 degrees C containing 0.5 mM NADH and 10 mM glucose. Although its performance deteriorated to ca. 4 mu W/cm(2) over 4 days, the cell subsequently maintained this power density for more than 2 weeks. (C) 2005 Elsevier B.V. All rights reserved.
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页码:643 / 647
页数:5
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