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Syntheses of planar 1,5,2,4,6,8-dithiotetrazocine derivatives and thermodynamic study on intermolecular charge transfer for developing efficient organic solar cell

A series of planar 1,5,2,4,6,8-dithiotetrazocine derivatives were synthesized for study on charge transfer at donor/acceptor interface. The fluorescence quenching spectra, and the highest occupied molecular orbital (−6.10 ∼ −6.25 eV) and the lowest unoccupied molecular orbital (−3.45 ∼ −3.58 eV) ene...

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Published in:Materials chemistry and physics 2016-07, Vol.177, p.463-471
Main Authors: Zhang, Chao-Zhi, Shen, Dan, Yuan, Yang, Song, Ming-Xia, Li, Shi-Juan, Cao, Hui
Format: Article
Language:English
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Summary:A series of planar 1,5,2,4,6,8-dithiotetrazocine derivatives were synthesized for study on charge transfer at donor/acceptor interface. The fluorescence quenching spectra, and the highest occupied molecular orbital (−6.10 ∼ −6.25 eV) and the lowest unoccupied molecular orbital (−3.45 ∼ −3.58 eV) energy levels of these 1,5,2,4,6,8-dithiotetrazocine derivatives show that they would be potential acceptor materials. Based on theoretical calculations, thermodynamic study on charge transfer at donor/acceptor interface was carried out. The results of experiments and theoretical calculations show that the electrons could transfer spontaneously from poly(3-hexylthiophene) to these acceptors. The percentages of fluorescence quenching increase with negative Gibbs free energy values increasing in the charge transfer procedures. Therefore, short circuit current values of organic solar cells would increase with the Gibbs free energy values increasing. This paper suggests a useful way for developing efficient organic solar cells. [Display omitted] •Syntheses of planar 1,5,2,4,6,8-dithiotetrazocine derivatives for develop effective acceptor.•Electrons at excited state in P3HT could transfer spontaneously to these acceptors.•Thermodynamic study on charge transfer at donor/acceptor interface.•Short circuit currents would be predicted by Gibbs free energy in procedure of charge transfer.
ISSN:0254-0584
1879-3312
DOI:10.1016/j.matchemphys.2016.04.055