Porphyrin dimers as donors for solution-processed bulk heterojunction organic solar cells. Issue 65 (23rd June 2016)

• Record Type: Journal Article
• Authors: Hsu, Fang-Chi; Hsieh, Ming-Kuang; Kashi, Chiranjeevulu; Yeh, Chen-Yu; Lin, Tai-Yuan; Chen, Yang-Fang
• Is Part Of: RSC advances. Volume 6:Issue 65(2016)
• Page Start: 60626
• Page End: 60632
• Publication Date: 2016-06-23
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6ra04746g
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : We synthesize a novel class of porphyrin dimers consisting of two zinc-metalated porphyrin units covalently linked through ethynyl or butadiyne group as electron donors for the fabrication of organic bulk heterojunction (BHJ) solar cells. Abstract : We synthesize a novel class of porphyrin dimers consisting of two zinc-metalated porphyrin units covalently linked through ethynyl (KC1) or butadiyne (KC2) group as electron donors blended with [6, 6]-phenyl C70 butyric acid methyl ester (PC70 BM) as electron acceptor for the fabrication of organic bulk heterojunction (BHJ) solar cells. The solution processed BHJ solar cells with porphyrin dimers:PC70 BM show superior performance than those based on their parent monomer due to much broader light absorption spectra. It is found that devices with KC2 : PC70 BM blend in the weight ratio of 1 : 4 exhibit higher power conversion efficiency (PCE) over those with KC1:PC70 BM blend. When the KC2:PC70 BM blend is processed from solvent containing 3% v/v 1-chloronaphathalene (CN), the PCE of the solar cell is improved to 2.03% from 1.73%. The superior performance and the performance improvement of the solar cells with KC2:PC70 BM are due to the high short circuit current density ( J sc ) resulting from a higher effective device mobility and a lower series resistance. The study provides a useful guideline for designing porphyrin based donor materials for optoelectronic device application.