Asymmetric 9,9′-bifluorenylidene-based small molecules as the non-fullerene acceptors for organic photovoltaic cells

Three new asymmetric 9,9′-bifluorenylidene-based derivatives, 2,7-dibutoxyl-3′,6′-bis(5-methylenemalononitrile-3-octylthiophen-2-yl)-9,9′-bifluorenylidene (BF-TDCN2), 2,7-dibutoxyl-3′,6′-bis(5-(methylene-indene-1,3-dione)-3-octylthiophen-2-yl)-9,9′-bifluorenylidene (BF-TID2) and 2,7-dibutoxyl-3′,6′-...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Dyes and pigments 2020-06, Vol.177, p.108233, Article 108233
Hauptverfasser: Zhang, Tong, Yu, Tianzhi, Zhao, Yuling, Wei, Chengjin, Ma, Hailin, Li, Yanmei, Zhang, Hui
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Three new asymmetric 9,9′-bifluorenylidene-based derivatives, 2,7-dibutoxyl-3′,6′-bis(5-methylenemalononitrile-3-octylthiophen-2-yl)-9,9′-bifluorenylidene (BF-TDCN2), 2,7-dibutoxyl-3′,6′-bis(5-(methylene-indene-1,3-dione)-3-octylthiophen-2-yl)-9,9′-bifluorenylidene (BF-TID2) and 2,7-dibutoxyl-3′,6′-bis(5-(2-methylene-3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile)-3-octylthiophen-2-yl)-9,9′-bifluorenylidene (BF-TDCI2), were successfully synthesized by grafting different electron-withdrawing groups (malononitrile (DCN), 1H-indene-1,3(2H)-dione (ID) and 2-(3-oxo-2,3-dihydro-1H-inden-1-ylidene)malononitrile (DCI)), which were used as the electron acceptors for organic photovoltaic cells. By changing the electron-withdrawing ability of the terminal group, the molecular energy level and band gap can be easily adjusted. The optical bandgaps of the three compounds in the thin films decreased with increasing the electron-withdrawing ability of the terminal group. Besides, the lateral chains of alkoxy groups located at the asymmetric end also play a certain influence on the solubility, molecular aggregation and the miscibility with polymer donor. Among these electron acceptors, the photovoltaic cell fabricated PBDB-T:BF-TDCI2 exhibited a maximum power conversion efficiency of 4.85% with an open-circuit voltage of 0.88 V and a low energy loss of 0.62 eV. By investigating different processing processes, the results showed that the power conversion efficiency can be improved by 20% with simple solvent annealing treatment. Through further study on the morphology and photophysical properties of the active layers, it was found that the processed device had better phase separation size and morphology, which was favorable to enhancing the intermolecular interaction, thus improving exciton separation and charge transfer in the active layer. Three asymmetric 9,9′-BF-based derivatives were synthesized by grafting different electron-withdrawing groups for organic photovoltaic cell. Among them, the highest power conversion efficiency (PCE) of the device fabricated from 9,9′-BF-based derivative containing 1,1-dicyanomethylene-3-indanone was 4.85%. [Display omitted] •Three asymmetric 9,9′-BF-based derivatives were synthesized for organic photovoltaic cell.•The compound exhibits good solubility in common organic solvents.•The highest PCE of 4.85% was obtained.
ISSN:0143-7208
1873-3743
DOI:10.1016/j.dyepig.2020.108233