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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 biocathode 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.

Ultraslow response, on the order of minutes, of the interfacial tension to the change in the phase-boundary potential at the interface between water and a room-temperature ionic liquid, trioctylmethylammonium bis(nonafluorobutanesulfonyl)amide, has been demonstrated. This ultraslow relaxation, which is not observed at the interface between two immiscible electrolyte solutions made of molecular organic solvents, is likely to be due to the long-range and collective ordering of ions of the electrical double layer on the ionic liquid side of the interface.

A membraneless direct electron transfer (DET)-type dihydrogen (H2)/air-breathing biofuel cell without any mediator was constructed wherein bilirubin oxidase from Myrothecium verrucaria (BOD) and membrane-bound [NiFe] hydrogenase from Desulfovibrio vulgaris Miyazaki F (MBH) were used as biocatalysts for the cathode and the anode, respectively, and Ketjen black-modified water proof carbon paper (KB/WPCC) was used as an electrode material. The KB/WPCC surface was modified with 2-aminobenzoic acid and p-phenylenediamine, respectively, to face the positively charged electron-accepting site of BOD and the negatively charged electron-donating site of MBH to the electrode surface. A gas-diffusion system was employed for the electrodes to realize high-speed substrate supply. As result, great improvement in the current density of O2 reduction with BOD and H2 reduction with MBH were realized at negatively and postively charged surfaces, repectively. Gas diffusion system also supressed the oxidative inactivation of MBH at high electrode potentials. Finally, based on the impoved bioanode and biocathode, a dual gas-diffusion membrane-and mediatorless H2/air-breathing biofuel cell was constructed. The maximum power density reached 6.1 mW cm −2 (at 0.72 V), and the open circuit voltage was 1.12 V using 1 atm of H2 gas as a fuel at room temperature and under passive and quiescent conditions.

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H2/O2biofuel cells utilizing hydrogenases and multicopper oxidases as bioelectrocatalysts are clean, sustainable, and environmentally friendly power devices.

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A new gas-diffusion-type biocathode was constructed for carbon dioxide (CO 2) reduction. In this work, tungsten-containing formate dehydrogenase (FoDH1), which is a promising enzyme for interconversion of formate and CO 2 , was used as a catalyst and was absorbed on a Ketjen Black (KB)-modified electrode. We used 1,1'-trimethylene-2,2'-bipyridinium dibromide as a mediator, and the hydrophobicity of the FoDH1-absorbed electrode was optimized according to the weight ratio of the polytetrafluoroethylene binder to KB. We achieved cathodic current densities of about 20 mA cm −2 under mild and quiescent conditions (neutral pH, atmospheric pressure, and room temperature).