TY - JOUR
T1 - Enzyme-based glucose fuel cell using Vitamin K3-immobilized polymer as an electron mediator
AU - Sato, Fuyuki
AU - Togo, Makoto
AU - Islam, Mohammed Kamrul
AU - Matsue, Tomokazu
AU - Kosuge, Junichi
AU - Fukasaku, Noboru
AU - Kurosawa, Satoshi
AU - Nishizawa, Matsuhiko
N1 - Funding Information:
This work was partly supported by a Health and Labor Sciences Research Grant for Research on medical devices for analyzing, supporting and replacing the function of the human body from the Ministry of Health, Labor and Welfare of Japan. The authors express appreciation to F. Mizutani (AIST, Tsukuba) for the kind donation of the PDMS emulsion.
PY - 2005/7
Y1 - 2005/7
N2 - To create an enzyme-based biological fuel cell generating electricity from glucose and O2, 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 K3; 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 μW/cm2 at 0.36 V in an air-saturated phosphate buffered saline solution (pH 7.0) at 37 °C containing 0.5 mM NADH and 10 mM glucose. Although its performance deteriorated to ca. 4 μW/cm2 over 4 days, the cell subsequently maintained this power density for more than 2 weeks.
AB - To create an enzyme-based biological fuel cell generating electricity from glucose and O2, 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 K3; 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 μW/cm2 at 0.36 V in an air-saturated phosphate buffered saline solution (pH 7.0) at 37 °C containing 0.5 mM NADH and 10 mM glucose. Although its performance deteriorated to ca. 4 μW/cm2 over 4 days, the cell subsequently maintained this power density for more than 2 weeks.
KW - Diaphorase
KW - Fuel cell
KW - Glucose dehydrogenase
KW - Naphthoquinone
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U2 - 10.1016/j.elecom.2005.04.015
DO - 10.1016/j.elecom.2005.04.015
M3 - Article
AN - SCOPUS:20344399650
SN - 1388-2481
VL - 7
SP - 643
EP - 647
JO - Electrochemistry Communications
JF - Electrochemistry Communications
IS - 7
ER -