A perylenediimide dimer containing an asymmetric π-bridge and its fused derivative for fullerene-free organic solar cells. Issue 10 (28th February 2018)

• Record Type: Journal Article
• Authors: Chen, Fan; Ding, Guodong; Tang, Ailing; Xiao, Bo; Li, Jianfeng; Zhou, Erjun
• Is Part Of: Journal of materials chemistry. Volume 6:Issue 10(2018)
• Page Start: 2580
• Page End: 2587
• Publication Date: 2018-02-28
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Optical materials -- Research -- Periodicals; Electronics -- Materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c8tc00089a
• Languages: English
• ISSNs: 2050-7526

Abstract

Abstract : Recent success stories of perylenediimide (PDI) derivatives have stimulated tremendous interest. Abstract : Recent success stories of perylenediimide (PDI) derivatives have stimulated tremendous interest. They are under intense investigation to replace fullerenes as the electron acceptor in organic solar cells. In priciple, the strategy of linking two PDI rings to get a PDI dimer could efficiently suppress the excessive π–π stacking tendency and avoid the large phase separation. However, almost all the reported PDI dimers are symmetric structures, asymmetric building blocks as the π-bridge are rare. Here, we used an asymmetric 6-(thiophen-2-yl)benzo[ b ]thiophene (T-BTh) group as the π-bridge to connect two PDI units, affording compoundA101 . Through annulation ofA101, we further synthesized the fused PDI dimer ofA102 . FusedA102 shows increased effective π-conjugation and reduced twist angle between the two PDI subplanes, resulting in a favorable morphology and strong π–π stacking. As a result, A102 showed an improved power conversion efficiency of 5.65% in comparison with that ofA101 (3.57%), due to the higher open-circuit voltage ( V OC ) and short-circuit current ( J SC ). The higher V OC results from the higher lowest unoccupied molecular orbital (LUMO) level ofA102 and the higher J SC can be explained on the basis of better charge carrier mobilities. These results provide important information and open a new way to design novel PDI-based or other small molecular electron acceptors.