Issue 12, 2016

2,1,3-Benzooxadiazole, thiophene and benzodithiophene based random copolymers for organic photovoltaics: thiophene versus thieno[3,2-b]thiophene as π-conjugated linkers

Abstract

Three conjugated random copolymers comprising benzodithiophene and thiophene as the donor units and benzooxadiazole as the acceptor unit, spaced with thiophene and thieno[3,2-b]thiophene π-bridges, were designed and synthesized. The effects of different linkers on the optical and electrochemical properties were investigated. The polymer containing a thieno[3,2-b]thiophene π-bridge revealed a red shifted absorption compared to its thiophene analogue. Morphological and photovoltaic properties of a polymer:fullerene blend film were investigated. The blend of one of the random copolymers (P2) and PC71BM ([6,6]-phenyl-C71-butyric acid methyl ester) revealed a photovoltaic performance efficiency of 5.17% due to the high short-circuit current density and fill factor.

Graphical abstract: 2,1,3-Benzooxadiazole, thiophene and benzodithiophene based random copolymers for organic photovoltaics: thiophene versus thieno[3,2-b]thiophene as π-conjugated linkers

Article information

Article type
Paper
Submitted
08 Aug 2016
Accepted
17 Oct 2016
First published
18 Oct 2016

New J. Chem., 2016,40, 10455-10464

2,1,3-Benzooxadiazole, thiophene and benzodithiophene based random copolymers for organic photovoltaics: thiophene versus thieno[3,2-b]thiophene as π-conjugated linkers

S. Goker, G. Hizalan, E. Aktas, S. Kutkan, A. Cirpan and L. Toppare, New J. Chem., 2016, 40, 10455 DOI: 10.1039/C6NJ02469F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements