Photosystem I Integration in Natural, Two-Electrode, Gel-Based Dye-Sensitized Solar Cells
Joshua Passantino a, Kody Wolfe b, Keiann Simon a, David Cliffel c, Kane Jennings a
a Vanderbilt University - Department of Chemical and Biomolecular Engineering, Nashville, United States
b Vanderbilt University - Interdisciplinary Materials Science & Engineering Program, Nashville, United States
c Vanderbilt University - Department of Chemistry, Nashville, United States
Proceedings of International Online Conference on Bio-hybrid Approaches to Solar Energy Conversion (Biohybrid)
Online, Spain, 2020 October 27th - 29th
Organizers: Jenny Zhang, Vincent Friebe and Lars Jeuken
Poster, Joshua Passantino, 061
Publication date: 8th October 2020
ePoster: 

The Photosystem I (PSI) protein complex is known to enhance bioelectrode performance for many liquid-based photoelectrochemical cells. A hydrogel as the electrolyte media allows for simpler fabrication of more robust and practical solar cells in comparison to liquid-based devices. This manuscript reports a natural, gel-based dye-sensitized solar cell that integrates PSI to improve device efficiency. TiO2-coated FTO slides, dyed by blackberry anthocyanin, act as a photoanode while a film of PSI deposited onto copper comprises the photocathode. Ascorbic acid (AscH) and 2,6-dichlorophenolindophenol (DCPIP) are the redox mediator couple inside an agarose hydrogel, enabling PSI to produce excess oxidized species near the cathode to improve device performance. A comparison of performance at low pH and neutral pH was performed to test the pH-dependent properties of the AscH/DCPIP couple. Devices at neutral pH performed better than those at lower pH. The PSI film enhanced photovoltage by 75 mV to a total photovoltage of 0.45 V per device and provided a mediator concentration-dependent photocurrent enhancement over non-PSI devices, reaching an instantaneous power conversion efficiency of 0.30% compared to 0.18% without PSI, a 1.67-fold increase. At steady state, power conversion efficiencies for devices with and without PSI were 0.042% and 0.028%, respectively.

We gratefully acknowledge support from the National Science Foundation (DMR-1507505 and 156014), the NSF Graduate Research Fellowship Program (DGE-1445197 and DGE-1937963), and the U.S. Department of Agriculture (2019-67021-29857). We also thank the Vanderbilt Institute of Nanoscale Science and Engineering (VINSE) for their assistance.

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