Issue 11, 2013

Anthradithiophene-benzothiadiazole-based small molecule donors for organic solar cells

Abstract

A new A–D–A small molecule involving anthradithiophene as a donor and benzothiadiazole as an acceptor unit has been synthesized by Stille coupling reaction. Its thermal, optical and electronic properties, hole mobility and photovoltaic properties have been fully characterized. The resulting material shows a broad absorption range (300–750 nm), a low band gap (1.59 eV) and a moderate hole mobility (8.81 × 10−4 cm2 V−1 s−1). We used the new small molecule blended with PC71BM as the active layer to fabricate solution-processed organic solar cells (OSCs), and employed a variety of post-treatment methods to optimize the device performance. With the help of polar solvent exposure, the highest power conversion efficiency (PCE) of 0.55% was obtained. These results would supply useful information to understand the relationship between molecular structure and photovoltaic properties of anthradithiophene/benzothiadiazole-based OSCs.

Graphical abstract: Anthradithiophene-benzothiadiazole-based small molecule donors for organic solar cells

Article information

Article type
Paper
Submitted
25 Jul 2013
Accepted
11 Aug 2013
First published
12 Aug 2013

New J. Chem., 2013,37, 3627-3633

Anthradithiophene-benzothiadiazole-based small molecule donors for organic solar cells

Q. Liu, Y. Liu, Y. Wang, L. Ai, X. Ouyang, L. Han and Z. Ge, New J. Chem., 2013, 37, 3627 DOI: 10.1039/C3NJ00824J

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