4.8 Article

Rational Design of a Photosystem I Photoanode for the Fabrication of Biophotovoltaic Devices

Journal

ADVANCED ENERGY MATERIALS
Volume 11, Issue 47, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202102858

Keywords

biophotovoltaics; electrode materials; gas-diffusion electrodes; Langmuir-Blodgett films; photosystem I; redox polymers

Funding

  1. Deutsche Forschungsgemeinschaft (DFG) [390677874]
  2. European Union [813006]
  3. China Scholarship Council (CSC)
  4. Research Training Group 2341 MiCon (Microbial Substrate Conversion)
  5. Projekt DEAL
  6. Marie Curie Actions (MSCA) [813006] Funding Source: Marie Curie Actions (MSCA)

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Photosystem I (PSI) has the potential for fabrication of light-driven semi-artificial bioelectrodes, with Langmuir monolayers and specially designed redox polymers enabling efficient electron transfer for advanced biophotoanodes. The developed bioelectrode can generate substantial photocurrents and even operate at low potentials, surpassing the performance of comparable devices. When combined with a gas-breathing biocathode, the assembly forms a biophotovoltaic cell that delivers considerable power outputs, showcasing the potential for advanced biophotovoltaic device development.
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 mu A 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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