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Fluorination effects on bithiophene unit in benzodithiophene-4,8-dione based D–A type alternating copolymers for highly efficient polymer solar cells

In this study, two D–A polymers consisting of benzodithiophene-4,8-dione and tetrathiophene with or without fluorination were synthesized to reveal the photovoltaic properties of fluorination effect on the polymer backbone. Polymer PDFTB with two fluorine atoms substituted on the backbone exhibits a...

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Detalles Bibliográficos
Autores principales: Chen, Yunxiang, Chen, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756423/
https://www.ncbi.nlm.nih.gov/pubmed/36545117
http://dx.doi.org/10.1039/d2ra05925h
Descripción
Sumario:In this study, two D–A polymers consisting of benzodithiophene-4,8-dione and tetrathiophene with or without fluorination were synthesized to reveal the photovoltaic properties of fluorination effect on the polymer backbone. Polymer PDFTB with two fluorine atoms substituted on the backbone exhibits an enhanced π–π stacking effect, deeper HOMO energy level and better backbone planarity than PDTB without fluorine atom substitution. Devices based on PDFTB:ITIC show a power conversion efficiency of 4.39%, which is 15% higher than that of PDTB-based devices due to the higher hole mobility, optimized surface morphology and homogeneous phase separation of the active layer. These results suggest that the fluorination strategy is a facile way to design polymeric donors for solvent-processed polymer solar cells.