Spectroscopic characterization of new polymer donor FO6-T for large area and semi-transparent OPVs
Keren Ai a, Lucy Hart a, James Durrant a
a Department of Chemistry and Centre for Processable Electronics, Imperial College London, London, W12 0BZ, UK
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV23)
London, United Kingdom, 2023 June 12th - 14th
Organizers: Tracey Clarke, James Durrant and Trystan Watson
Poster, Keren Ai, 291
Publication date: 30th March 2023

The potential of organic photovoltaics (OPVs) in large-area, indoor and semi-transparent applications has been rapidly growing. So far, the efficiency of OPV has seen a significant boost of over 19% due to the progress in non-fullerene acceptors (NFAs) and conjugated polymer donors. Nevertheless, the limitations of synthetic complexities, high processing cost, and their long-term stability have served as a deterrent to the development of OPV commercialisation, due to the lack of complete understanding in material photophysics and design rules.  

In this study, we plan to study the potential of FO6-T in large-scale and semi-transparent applications via multiple spectroscopy techniques. FO6-T is a new low-cost donor polymer, which requires only two synthesis steps. When blended it with NFA L8BO, devices achieved over 15% efficiency.  

We observed the red-shift absorption spectrum in FO6-T compared with current donor materials, indicating its great potential in semi-transparent devices. Femtosecond transient absorption spectroscopy (TAS) was employed and we observed the charge generation and charge transfer states in both neat and blended FO6-T systems. We investigated long-lived charge carriers in neat FO6-T films in both femtosecond and micro-second TAS, which suggests a possible free charge generation process. Furthermore, we studied the role of long-lived charge carriers in FO6-T:L8BO organic solar cells by photoluminescence and fluence-dependent TAS techniques.  

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