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Hydroquinone redox mediator enhances the photovoltaic performances of chlorophyll-based bio-inspired solar cells.


ABSTRACT: Chlorophyll (Chl) derivatives have recently been proposed as photoactive materials in next-generation bio-inspired solar cells, because of their natural abundance, environmental friendliness, excellent photoelectric performance, and biodegradability. However, the intrinsic excitation dynamics of Chl derivatives remain unclear. Here, we show sub-nanosecond pump-probe time-resolved absorption spectroscopy of Chl derivatives both in solution and solid film states. We observe the formation of triplet-excited states of Chl derivatives both in deoxygenated solutions and in film samples by adding all-trans-β-carotene as a triplet scavenger. In addition, radical species of the Chl derivatives in solution were identified by adding hydroquinone as a cation radical scavenger and/or anion radical donor. These radical species (either cations or anions) can become carriers in Chl-derivative-based solar cells. Remarkably, the introduction of hydroquinone to the film samples enhanced the carrier lifetimes and the power conversion efficiency of Chl-based solar cells by 20% (from pristine 1.29% to 1.55%). This enhancement is due to a charge recombination process of Chl-A+/Chl-D-, which is based on the natural Z-scheme process of photosynthesis.

SUBMITTER: Duan S 

PROVIDER: S-EPMC9814249 | biostudies-literature | 2021 Aug

REPOSITORIES: biostudies-literature

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Hydroquinone redox mediator enhances the photovoltaic performances of chlorophyll-based bio-inspired solar cells.

Duan Shengnan S   Uragami Chiasa C   Horiuchi Kota K   Hino Kazuki K   Wang Xiao-Feng XF   Sasaki Shin-Ichi SI   Tamiaki Hitoshi H   Hashimoto Hideki H  

Communications chemistry 20210811 1


Chlorophyll (Chl) derivatives have recently been proposed as photoactive materials in next-generation bio-inspired solar cells, because of their natural abundance, environmental friendliness, excellent photoelectric performance, and biodegradability. However, the intrinsic excitation dynamics of Chl derivatives remain unclear. Here, we show sub-nanosecond pump-probe time-resolved absorption spectroscopy of Chl derivatives both in solution and solid film states. We observe the formation of triple  ...[more]

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