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Proceedings ArticleDOI

Effect of meso substituent on Optoelectronic Properties in BODIPY based donor acceptor Copolymers

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TLDR
In this paper, two copolymers of Boron dipyrromethane (BODIPY) and Fluorene are designed, synthesized and their optoelectronics properties is reported.
Abstract
In this work two novel copolymers of Boron dipyrromethane (BODIPY) and Fluorene are designed, synthesized and their optoelectronics properties is reported. The polymers were designed to study the effect of the substituent at the meso position of BODIPY on the optoelectronic properties of the polymer. Changing the methyl group on the phenyl group at the meso position in the BODIPY subunit to trifluoromethyl group not only lowers the LUMO energy value but also improves the electron transport in the polymer. The polymers have also been used as electron transport material to fabricate all polymer solar cell and polymer photodetectors.

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References
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Journal ArticleDOI

Bodipy-backboned polymers as electron donor in bulk heterojunction solar cells

TL;DR: Bodipy-based polymers, which possess a high absorption coefficient with a bandgap of approximately 1.6 eV, have been used as electron donor in solution-processed bulk heterojunction (BHJ) solar cells containing PCBM as acceptor.
Journal ArticleDOI

Tetraphenylethylene-BODIPY aggregation-induced emission luminogens for near-infrared polymer light-emitting diodes

TL;DR: In this article, a new class of emitters based on 4,4-difluoro-4-bora-3 a,4 a -diaza- s -indacene (BODIPY), functionalized at different positions with tetraphenylethylene (TPE), was presented.
Journal ArticleDOI

Role of intermolecular interactions involving organic fluorine in trifluoromethylated benzanilides

TL;DR: In this paper, a comparison of the experimental molecular conformation with that obtained from DFT theoretical calculations delineates the significant role of the trifluoromethyl group on the phenyl ring, which results in variations in conformational flexibility associated with the molecule.
Journal ArticleDOI

Synthesis, Optoelectronic, and Transistor Properties of BODIPY- and Cyclopenta[c]thiophene-Containing π-Conjugated Copolymers

TL;DR: In this paper, three low-band-gap copolymers were synthesized by fusing dipyrromethene difluoroborane (BODIPY) as acceptor and thiophene-capped 5,5-bis(hexyloxymethyl)-5,6-dihydro-4H-cyclopenta[c]-thiophene (CPT) as the donor (D).
Journal ArticleDOI

The relationship between intermolecular interactions and charge transport properties of trifluoromethylated polycyclic aromatic hydrocarbons

TL;DR: In this article, a series of polycyclic aromatic hydrocarbons (PAHs) derivatives with different intermolecular interactions were studied by both band-like model and hopping model to obtain a better understanding of structure property relationships.
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