The development of O2 tolerant glucose sensors based on the highly active and robust enzyme glucose oxidase is still a major challenge because of the competition between the natural electron acceptor O2 and free‐diffusing or polymer‐bound artificial electron acceptors. We report the fabrication of a glucose oxidase based bioanode that operates under ambient conditions. Combination of this bioanode with a bilirubin oxidase based biocathode enabled the fabrication of a glucose/O2 powered biofuel cell as integrated power source for a self‐powered device. Glucose oxidase at the anode was electrically wired via a low‐potential redox polymer, i. e. a Toluidine Blue‐modified poly(methacrylate) based polymer, that ensures a high open‐circuit voltage of the biofuel cell but also catalytically reduces O2 and hence requires a protection shield for measurements under ambient conditions. The sensing layer was deposited by means of potential pulse‐assisted co‐deposition of glucose oxidase within the redox polymer and was protected from O2 by a newly proposed lactate oxidase/catalase based O2 removal layer that was immobilized within a hydrophilic redox‐silent polymer on top of the sensing layer. The protection layer was powered by lactate, a natural component in human blood. The biofuel cell exhibited an OCV of ca. 650 mV and the power output was dependent on the glucose concentration without any interference from oxygen providing that lactate was available in the analyte solution.
Photosystem I (PSI), a robust and abundant biomolecule capable of delivering high‐energy photoelectrons, has a great potential for the fabrication of light‐driven semi‐artificial bioelectrodes. Although possibilities have been explored in this regard, the true capabilities of this technology have not been achieved yet, particularly for their use as bioanodes. Here, the use of PSI Langmuir monolayers and their electrical wiring with specifically designed redox polymers is shown, ensuring an efficient mediated electron transfer as the basis for the fabrication of an advanced biophotoanode. The bioelectrode is rationally implemented and optimized for enabling the generation of substantial photocurrents of up to 17.6 µA cm−2 and is even capable of delivering photocurrents at potentials as low as −300 mV vs standard hydrogen electrode, surpassing the performance of comparable devices. To highlight the applicability of the developed light‐driven bioanode, a biophotovoltaic cell is assembled in combination with a gas‐breathing biocathode. The assembly operates in a single compartment cell and delivers considerable power outputs at large cell voltages. The implemented biophotoanode constitutes an important step toward the development of advanced biophotovoltaic devices.
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