Synthesis and characterization of triphenylamine flanked thiazole-based small molecules for high performance solution processed organic solar cells

被引:60
作者
Dutta, Pranabesh [1 ]
Yang, Wooseung [1 ]
Eom, Seung Hun [1 ]
Lee, Soo-Hyoung [1 ]
机构
[1] Chonbuk Natl Univ, Sch Semicond & Chem Engn, Jeonju 561756, South Korea
基金
新加坡国家研究基金会;
关键词
Donor-acceptor; Conjugated small molecules; Suzuki coupling; Thiazole derivatives; Organic solar cells; Power conversion efficiency; FIELD-EFFECT TRANSISTORS; OPEN-CIRCUIT VOLTAGE; PHOTOVOLTAIC PROPERTIES; CONVERSION EFFICIENCY; BAND-GAP; POLYMER; COPOLYMERS; THIAZOLOTHIAZOLE; CORE; OLIGOTHIOPHENES;
D O I
10.1016/j.orgel.2011.11.016
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Two new small molecules, 5,5-bis(2-triphenylamino-3-decylthiophen-2-yl)-2,2-bithiazole (M1) and 2,5-bis(2-triphenylamino-3-decylthiophen-2-yl) thiazolo[5,4-d]thiazole (M2) based on an electron-donor triphenylamine unit and electron-acceptor thiophene-thiazolothiazole or thiophene-bithiazole units were synthesized by a palladium(0)-catalyzed Suzuki coupling reaction and examined as donor materials for application in organic solar cells. The small molecules had an absorption band in the range of 300-560 nm, with an optical band gap of 2.22 and 2.25 for M1 and M2, respectively. As determined by cyclic voltammetry, the highest occupied molecular orbital and lowest unoccupied molecular orbital energy levels of M1 were -5.27 eV and -3.05 eV, respectively, which were 0.05 eV and 0.02 eV greater than that of M2. Photovoltaic properties of the small molecules were investigated by constructing bulk-heterojunction organic solar cell (OSC) devices using M1 and M2 as donors and fullerene derivatives, 6,6-phenyl-C61-butyric acid methyl ester (PC61BM) and 6,6-phenyl-C71-butyric acid methyl ester (PC71BM) as acceptors with the device architecture ITO/PEDOT:PSS/M1 or M2:PCBM/LiF/Al. The effect of the small molecule/fullerene weight ratio, active layer thickness, and processing solvent were carefully investigated to improve the performance of the OSCs. Under AM 1.5 G 100 mW/cm(2) illumination, the optimized OSC device with M1 and PC71BM at a weight ratio of 1: 3 delivered a power conversion efficiency (PCE) of 1.30%, with a short circuit current of 4.63 mA/cm(2), an open circuit voltage of 0.97 V, and a fill factor of 0.29. In contrast, M2 produced a better performance under identical device conditions. A PCE as high as 2.39% was recorded, with a short circuit current of 6.49 mA/cm(2), an open circuit voltage of 0.94 V, and a fill factor of 0.39. (C) 2011 Elsevier B. V. All rights reserved.
引用
收藏
页码:273 / 282
页数:10
相关论文
共 69 条
[1]   Synthesis, physical properties, and field-effect transistors of novel thiophene/thiazolothiazole co-oligomers [J].
Ando, S ;
Nishida, J ;
Inoue, Y ;
Tokito, S ;
Yamashita, Y .
JOURNAL OF MATERIALS CHEMISTRY, 2004, 14 (12) :1787-1790
[2]   Marked Alkyl- vs Alkenyl-Substitutent Effects on Squaraine Dye Solid-State Structure, Carrier Mobility, and Bulk-Heterojunction Solar Cell Efficiency [J].
Bagnis, Diego ;
Beverina, Luca ;
Huang, Hui ;
Silvestri, Fabio ;
Yao, Yan ;
Yan, Henry ;
Pagani, Giorgio A. ;
Marks, Tobin J. ;
Facchetti, Antonio .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (12) :4074-+
[3]   Processable Low-Bandgap Polymers for Photovoltaic Applications [J].
Boudreault, Pierre-Luc T. ;
Najari, Ahmed ;
Leclerc, Mario .
CHEMISTRY OF MATERIALS, 2011, 23 (03) :456-469
[4]  
Brabec CJ, 2002, ADV FUNCT MATER, V12, P709, DOI 10.1002/1616-3028(20021016)12:10<709::AID-ADFM709>3.0.CO
[5]  
2-N
[6]   Tailored merocyanine dyes for solution-processed BHJ solar cells [J].
Buerckstuemmer, Hannah ;
Kronenberg, Nils Michael ;
Gsaenger, Marcel ;
Stolte, Matthias ;
Meerholz, Klaus ;
Wuerthner, Frank .
JOURNAL OF MATERIALS CHEMISTRY, 2010, 20 (02) :240-243
[7]   Polymer solar cells with enhanced open-circuit voltage and efficiency [J].
Chen, Hsiang-Yu ;
Hou, Jianhui ;
Zhang, Shaoqing ;
Liang, Yongye ;
Yang, Guanwen ;
Yang, Yang ;
Yu, Luping ;
Wu, Yue ;
Li, Gang .
NATURE PHOTONICS, 2009, 3 (11) :649-653
[8]   Development of Novel Conjugated Donor Polymers for High-Efficiency Bulk-Heterojunction Photovoltaic Devices [J].
Chen, Junwu ;
Cao, Yong .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (11) :1709-1718
[9]   Synthesis of annulated thiophene perylene bisimide analogues: their applications to bulk heterojunction organic solar cells [J].
Choi, Hyunbong ;
Paek, Sanghyun ;
Song, Juman ;
Kim, Chulwoo ;
Cho, Nara ;
Ko, Jaejung .
CHEMICAL COMMUNICATIONS, 2011, 47 (19) :5509-5511
[10]   Novel Silafluorene-Based Conjugated Polymers with Pendant Acceptor Groups for High Performance Solar Cells [J].
Duan, Chunhui ;
Cai, Wanzhu ;
Huang, Fei ;
Zhang, Jie ;
Wang, Ming ;
Yang, Tingbin ;
Zhong, Chengmei ;
Gong, Xiong ;
Cao, Yong .
MACROMOLECULES, 2010, 43 (12) :5262-5268