Hydrogen is one of the most promising alternatives for fossil fuels. However, the power output of hydrogen/oxygen fuel cells is often restricted by mass transport limitations of the substrate. Here, we present a dual-gas breathing H2/air biofuel cell that overcomes these limitations. The cell is equipped with a hydrogen-oxidizing redox polymer/hydrogenase gas-breathing bioanode and an oxygen-reducing bilirubin oxidase gas-breathing biocathode (operated in a direct electron transfer regime). The bioanode consists of a two layer system with a redox polymer-based adhesion layer and an active, redox polymer/hydrogenase top layer. The redox polymers protect the biocatalyst from high potentials and oxygen damage. The bioanodes show remarkable current densities of up to 8 mA cm-2. A maximum power density of 3.6 mW cm-2 at 0.7 V and an open circuit voltage of up to 1.13 V were achieved in biofuel cell tests, representing outstanding values for a device that is based on a redox polymer-based hydrogenase bioanode.

In the development of biofuel cells great effort is dedicated to achieving outstanding figures of merit, such as high stability, maximum power output, and a large open circuit voltage. Biofuel cells with immobilized redox mediators, such as redox polymers with integrated enzymes, show experimentally a substantially higher open circuit voltage than the thermodynamically expected value. Although this phenomenon is widely reported in the literature, there is no comprehensive understanding of the potential shift, the high open circuit voltages have not been discussed in detail, and hence they are only accepted as an inherent property of the investigated systems. We demonstrate that this effect is the result of a Nernstian shift of the electrode potential when catalytic conversion takes place in the absence or at very low current flow. Experimental evidence confirms that the immobilization of redox centers on the electrode surface results in the assembled biofuel cell delivering a higher power output because of charge storage upon catalytic conversion. Our findings have direct implications for the design and evaluation of (bio)fuel cells with pseudocapacitive elements.

Hydrogenases with Ni- and/or Fe-based active sites are highly active hydrogen oxidation catalysts with activities similar to those of noble metal catalysts. However, the activity is connected to a sensitivity towards high-potential deactivation and oxygen damage. Here we report a fully protected polymer multilayer/hydrogenase-based bioanode in which the sensitive hydrogen oxidation catalyst is protected from high-potential deactivation and from oxygen damage by using a polymer multilayer architecture. The active catalyst is embedded in a low-potential polymer (protection from high-potential deactivation) and covered with a polymer-supported bienzymatic oxygen removal system. In contrast to previously reported polymer-based protection systems, the proposed strategy fully decouples the hydrogenase reaction form the protection process. Incorporation of the bioanode into a hydrogen/glucose biofuel cell provides a benchmark open circuit voltage of 1.15 V and power densities of up to 530 µW cm−2 at 0.85 V.

We report a prototype air‐breathing carbon cloth‐based electrode that was fabricated starting from a commercially available screen‐printed electrode equipped with a transparent ITO working electrode (DropSens, ref. ITO10). The fabrication of the air‐breathing electrodes is straightforward, shows satisfactory reproducibility and a good electrochemical response as evaluated by means of [Fe(CN)6]3−/4− voltammetry. The gas‐diffusion electrodes were successfully modified with the O2 reducing enzyme bilirubin oxidase from Myrothecium verrucaria in a direct electron transfer regime. The enzyme modified electrodes showed a remarkable high current density for O2 reduction in passive air‐breathing mode of up to 5 mA cm−2. Moreover, the enzyme modified electrodes were applied as O2 reducing biocathodes in a glucose/air enzymatic biofuel cell in combination with a high current density glucose oxidase/redox polymer bioanode. The biofuel cell provides a high maximum power density of (0.34±0.02) mW cm−2 at 0.25 V. The straightforward design, low cost and the high reproducibility of these electrodes are considered as basis for standardized measurements under gas‐breathing conditions and for high throughput screening of gas converting (bio‐)catalysts.

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Ein besonderes Augenmerk bei der Entwicklung von Biobrennstoffzellen liegt im Erreichen von herausragenden Kennzahlen, wie extreme Langlebigkeit, hohe Maximalleistung oder hohe Leerlaufspannung. Dabei werden für Biobrennstoffzellen, die ein pseudokapazitives Element in Form immobilisierter Redoxmediatoren aufweisen, wie sie z. B. in Redoxpolymer/Enzymelektroden vorhanden sind, in der Praxis erhöhte Leerlaufspannungen beobachtet, die sich deutlich von den theoretisch zu erwartenden Werten unterscheiden. Obwohl dieser Effekt in der Literatur dokumentiert ist, wurde dem genauen Verständnis dieses Phänomens wenig oder kaum Beachtung geschenkt und als inhärenter Bestandteil des zu Grunde liegenden Systems akzeptiert. Dieser Beitrag zeigt, dass dieser Effekt auf einer Nernstverschiebung des Elektrodenpotentials beruht, der durch das Eintreten der biokatalytischen Umsetzung eines entsprechenden Substrats durch den Biokatalysator, bei Abwesenheit oder bei nur geringem Stromflusses induziert wird. Unsere Ergebnisse zeigen, dass durch die Verwendung von auf der Elektrodenoberfläche immobilisierten Redoxmediatoren, eine entsprechende Biobrennstoffzelle eine deutlich höhere Leerlaufspannung aufweist, die auf einer durch die Enzymreaktion induzierten Ladungsspeicherung innerhalb der Redoxpolymermatrix, beruht. Somit ergibt sich ein völlig neuer Gesichtspunkt für das Design und die Evaluierung von auf pseudokapazitiven Elementen basierenden (Bio‐)Brennstoffzellen.