Shuhei Yamamoto

Quinoxaline-based π-conjugated donor polymer for highly efficient organic thin-film solar cells

A quinoxaline-based π-conjugated donor polymer, poly[2,7-(9,9-dioctylfluorene)-alt-5,5-(5′,8′-di-2-thienyl-2′,3′-diphenylquinoxaline)] (N-P7), was synthesized to achieve a high power conversion efficiency (PCE) of bulk heterojunction (BHJ)-based solar cells. The optical band-gap and highest occupied molecular orbital level of N-P7 were 1.95 and −5.37 eV, respectively. BHJ-based solar cells using N-P7 as a donor and phenyl C71 butyric acid methyl ester as an acceptor gave a PCE as high as 5.5% under AM 1.5G 100 mW/cm2 illumination. We also investigated the effects of substituent groups of quinoxaline-based polymers on the morphology of the BHJ layer.

Thermally stable, highly efficient, ultraflexible organic photovoltaics

Significance We have developed an ultraflexible organic photovoltaic (OPV) that achieves sufficient thermal stability of up to 120 °C and a high power conversion efficiency of 10% with a total thickness of 3 μm. By combining an inherently stable donor:acceptor blend as the active layer and ultrathin substrate and barriers with excellent thermal capability, we were able to overcome the trade-offs between efficiency, stability, and device thickness. The ultraflexible and thermally stable OPV can be easily integrated into textiles through the commercially available hot-melt process without causing performance degradation, thereby presenting great potential as a ubiquitous and wearable power source in daily life. Flexible photovoltaics with extreme mechanical compliance present appealing possibilities to power Internet of Things (IoT) sensors and wearable electronic devices. Although improvement in thermal stability is essential, simultaneous achievement of high power conversion efficiency (PCE) and thermal stability in flexible organic photovoltaics (OPVs) remains challenging due to the difficulties in maintaining an optimal microstructure of the active layer under thermal stress. The insufficient thermal capability of a plastic substrate and the environmental influences cannot be fully expelled by ultrathin barrier coatings. Here, we have successfully fabricated ultraflexible OPVs with initial efficiencies of up to 10% that can endure temperatures of over 100 °C, maintaining 80% of the initial efficiency under accelerated testing conditions for over 500 hours in air. Particularly, we introduce a low-bandgap poly(benzodithiophene-cothieno[3,4-b]thiophene) (PBDTTT) donor polymer that forms a sturdy microstructure when blended with a fullerene acceptor. We demonstrate a feasible way to adhere ultraflexible OPVs onto textiles through a hot-melt process without causing severe performance degradation.