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Improvement of the optoelectronic and photovoltaic properties of a cyanopyrid-2,6-dione-based donor via molecular engineering

journal contribution
posted on 2024-11-01, 23:08 authored by Amanpreet Hundal, Anubha Agarwal, Mohammed Jameel, Jing-Yu Chen, Jing-Liang Li, Lathe JonesLathe Jones, Navneet Kaur, Steven Langford, Akhil Gupta
Through the molecular engineering of cyanopyrid-2,6-dione functionality, herein we report the design and synthesis of a novel, small molecule electron donor, (Z)-5-((5'-(4-(diphenylamino)phenyl)-[2,2′-bithiophen]-5-yl)methylene)-1-(4-(hexyloxy)phenyl)-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine-3-carbonitrile (coded as CP2), which exhibits improved optoelectronic and photovoltaic properties when compared with its structural analogue (E)-5-((5'-(4-(diphenylamino)phenyl)-[2,2′-bithiophen]-5-yl)methylene)-1-(2-ethylhexyl)-4-methyl-2,6-dioxo-1,2,5,6-tetrahydropyridine-3-carbonitrile (coded as CP1). The molecular engineering helps to achieve more desirable energy levels together with bathochromic shift in the absorption spectrum, which improves the short-circuit current density. A high conversion efficiency of 6.28% was obtained in simple devices (CP2: PC61BM 1: 1) which is one of the best results in the current literature for cyanopyrid-2,6-dione-based small molecule donors.

Funding

Supramolecular assembly of chromophores:the effects of nucleation kinetics on their molecular packing, fibre structure and light harvesting efficiency

Australian Research Council

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History

Related Materials

  1. 1.
    DOI - Is published in 10.1016/j.dyepig.2019.107661
  2. 2.
    ISSN - Is published in 01437208

Journal

Dyes and Pigments

Volume

170

Number

107661

Issue

170

Start page

1

End page

7

Total pages

7

Publisher

Elsevier

Place published

United Kingdom

Language

English

Copyright

© 2019 Elsevier Ltd. All rights reserved.

Former Identifier

2006093826

Esploro creation date

2020-06-22

Fedora creation date

2019-09-06

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