4.6 Article

Aqueous-soluble bipyridine cobalt(ii/iii) complexes act as direct redox mediators in photosystem I-based biophotovoltaic devices

期刊

RSC ADVANCES
卷 11, 期 18, 页码 10434-10450

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0ra10221k

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资金

  1. CSUB
  2. NSME Dean's office
  3. NIH R25 Award [R25GM086761]
  4. Gibson Family Foundation
  5. Tennessee Plant Research Center
  6. Dr Donald L. Akers Faculty Enrichment Fellowship
  7. National Science Foundation [DGE-0801470, EPS 1004083]
  8. Army Research Laboratory (ARL) [W91 1NF-11-2-0029]

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This study characterizes synthetic cobalt complexes as redox mediators for PSI-based biophotovoltaic devices and demonstrates their stability and effectiveness in organic solvents. The research shows evidence of direct electron transfer from cobalt complexes to PSI, leading to photocurrent generation. The findings suggest the potential for fine-tuning redox active species to interact with biological partners for the development of low cost, carbon-neutral energy production in the future.
Sustainable energy production is critical for meeting growing worldwide energy demands. Due to its stability and reduction potential, photosystem I (PSI) is attractive as the photosensitizer in biophotovoltaic devices. Herein, we characterize aqueous and organic solvent soluble synthetic bipyridine-based cobalt complexes as redox mediators for PSI-based biophotovoltaics applications. Cobalt-based complexes are not destructive to protein and have appropriate midpoint potentials for electron donation to PSI. We report on PSI stability in organic solvents commonly used in biophotovoltaics. We also show the effects of a mixed organic solvent phase on PSI reduction kinetics, slowing reduction rates approximately 8-38 fold as compared to fully aqueous systems, with implications for dye regeneration rates in PSI-based biophotovoltaics. Further, we show evidence of direct electron transfer from cobalt complexes to PSI. Finally, we report on photocurrent generation from Co mediator-PSI biophotovoltaic devices. Taken together, we discuss the development of novel Co complexes and our ability to fine-tune their characteristics via functional groups and counteranion choice to drive interaction with a biological electron acceptor on multiple levels from redox midpoints, spectral overlap, and solvent requirements, among others. This work suggests that fine-tuning of redox active species for interaction with a biological partner is possible for the creation and improvement of low cost, carbon-neutral energy production in the future.

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