Improvement of a direct electron transfer-type fructose/dioxygen biofuel cell with a substrate-modified biocathode

被引:95
作者
So, Keisei [1 ]
Kawai, Shota [1 ]
Hamano, Yasuyuki [1 ]
Kitazumi, Yuki [1 ]
Shirai, Osamu [1 ]
Hibi, Makoto [2 ]
Ogawa, Jun [1 ]
Kano, Kenji [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Appl Life Sci, Sakyo Ku, Kyoto 6068502, Japan
[2] Kyoto Univ, Grad Sch Agr, Lab Ind Microbiol, Sakyo Ku, Kyoto 6068502, Japan
关键词
BLUE COPPER OXIDASE; FRUCTOSE DEHYDROGENASE; BILIRUBIN OXIDASE; DIFFUSION BIOCATHODE; FUEL-CELLS; REDUCTION; IMMOBILIZATION; PURIFICATION; PERFORMANCE; OXIDATION;
D O I
10.1039/c3cp54888k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The fructose/dioxygen biofuel cell, one of the direct electron transfer (DET)-type bioelectrochemical devices, utilizes fructose dehydrogenase (FDH) on the anode and multi-copper oxidase such as bilirubin oxidase (BOD) on the cathode as catalysts. The power density in the literature is limited by the biocathode performance. We show that the DET-type bio-cathode performance is greatly improved, when bilirubin or some related substances are adsorbed on electrodes before the BOD adsorption. Several data show that the substrate modification induces the appropriate orientation of BOD on the electrode surface for the DET. The substrate-modification method has successfully been applied to air-breathing gas-diffusion-type biocathodes. We have also optimized the conditions of the FDH adsorption on carbon cryogel electrodes. Finally, a one-compartment DET-type biofuel cell without separators has been constructed, and the maximum power density of 2.6 mW cm(-2) was achieved at 0.46 V of cell voltage under quiescent (passive) and air atmospheric conditions.
引用
收藏
页码:4823 / 4829
页数:7
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