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The impact of thermal treatment on the performance of benzo[1,2-b:4,5-b′]difuran-based organic solar cells

The new low bandgap benzo[1,2-b:4,5-b′]difuran (BDF)-based organic small molecule, namely B1, was synthesized by Stille coupling polymerization reactions. B1 was found to be soluble in common organic solvents such as chloroform, toluene and chlorobenzene with excellent film forming properties. The s...

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Detalles Bibliográficos
Autores principales: Liu, Bo, Wang, Xiaobo, Li, Lang, Wang, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057403/
https://www.ncbi.nlm.nih.gov/pubmed/35515412
http://dx.doi.org/10.1039/d0ra07415b
Descripción
Sumario:The new low bandgap benzo[1,2-b:4,5-b′]difuran (BDF)-based organic small molecule, namely B1, was synthesized by Stille coupling polymerization reactions. B1 was found to be soluble in common organic solvents such as chloroform, toluene and chlorobenzene with excellent film forming properties. The structure of B1 was verified by (1)H NMR, GC-MS and elemental analysis. The B1 films exhibit broad absorption bands from 300 to 750 nm. The hole mobility of B1 : PC(61)BM (1 : 1, w/w) blend film reached up to 7.7 × 10(−2) cm V(−1) s(−1) after thermal annealing by the space-charge-limited current method. BHJ organic solar cells (OSCs) were fabricated with a device structure of ITO/PEDOT : PSS/B1 : C(61)BM/LiF/Al. When the active layer was thermally annealed at 120 °C, B1 showed the best photovoltaic performance, with a PCE up to 5.0%. We also studied the connection between the morphologies of the active layers and the photovoltaic performance by AFM, PL, etc. Our observation will guide future design for even better small molecules for highly efficient OSCs.