Fused Tris(thienothiophene)-Based Electron Acceptor with Strong Near-Infrared Absorption for High-Performance As-Cast Solar Cells

被引:362
作者
Li, Tengfei [1 ]
Dai, Shuixing [1 ]
Ke, Zhifan [2 ]
Yang, Langxuan [1 ]
Wang, Jiayu [1 ]
Yan, Cenqi [1 ]
Ma, Wei [2 ]
Zhan, Xiaowei [1 ]
机构
[1] Peking Univ, Minist Educ, Key Lab Polymer Chem & Phys, Dept Mat Sci & Engn,Coll Engn, Beijing 100871, Peoples R China
[2] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
near-infrared absorption; nonfullerene acceptors; organic solar cells; semitransparent; tris(thieno[3; 2-b]thiophene); POLYMER; EFFICIENCY; LAYER; GAP;
D O I
10.1002/adma.201705969
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A fused tris(thienothiophene) (3TT) building block is designed and synthesized with strong electron-donating and molecular packing properties, where three thienothiophene units are condensed with two cyclopentadienyl rings. Based on 3TT, a fused octacylic electron acceptor (FOIC) is designed and synthesized, using strong electron-withdrawing 2-(5/6-fluoro-3-oxo-2,3-dihydro-1H-inden-1-ylidene)-malononitrile as end groups. FOIC exhibits absorption in 600-950 nm region peaked at 836 nm with extinction coefficient of up to 2 x 10(5)m(-1) cm(-1), low bandgap of 1.32 eV, and high electron mobility of 1.2 x 10(-3) cm(2) V-1 s(-1). Compared with its counterpart ITIC3 based on indacenothienothiophene core, FOIC exhibits significantly upshifted highest occupied molecular orbital level, slightly downshifted lowest unoccupied molecular orbital level, significantly redshifted absorption, and higher mobility. The as-cast organic solar cells (OSCs) based on blends of PTB7-Th donor and FOIC acceptor without additional treatments exhibit power conversion efficiencies (PCEs) as high as 12.0%, which is much higher than that of PTB7-Th: ITIC3 (8.09%). The as-cast semitransparent OSCs based on the same blends show PCEs of up to 10.3% with an average visible transmittance of 37.4%.
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页数:7
相关论文
共 47 条
[1]  
Baran D, 2017, NAT MATER, V16, P363, DOI [10.1038/NMAT4797, 10.1038/nmat4797]
[2]   11.4% Efficiency non-fullerene polymer solar cells with trialkylsilyl substituted 2D-conjugated polymer as donor [J].
Bin, Haijun ;
Gao, Liang ;
Zhang, Zhi-Guo ;
Yang, Yankang ;
Zhang, Yindong ;
Zhang, Chunfeng ;
Chen, Shanshan ;
Xue, Lingwei ;
Yang, Changduk ;
Xiao, Min ;
Li, Yongfang .
NATURE COMMUNICATIONS, 2016, 7
[3]   An Efficient Triple-Junction Polymer Solar Cell Having a Power Conversion Efficiency Exceeding 11% [J].
Chen, Chun-Chao ;
Chang, Wei-Hsuan ;
Yoshimura, Ken ;
Ohya, Kenichiro ;
You, Jingbi ;
Gao, Jing ;
Hong, Zirou ;
Yang, Yang .
ADVANCED MATERIALS, 2014, 26 (32) :5670-+
[4]   A Wide-Bandgap Donor Polymer for Highly Efficient Non-fullerene Organic Solar Cells with a Small Voltage Loss [J].
Chen, Shangshang ;
Liu, Yuhang ;
Zhang, Lin ;
Chow, Philip C. Y. ;
Wang, Zheng ;
Zhang, Guangye ;
Ma, Wei ;
Yan, He .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (18) :6298-6301
[5]   Dithienocyclopentathieno[3,2-b]thiophene Hexacyclic Arene for Solution-Processed Organic Field-Effect Transistors and Photovoltaic Applications [J].
Cheng, Yen-Ju ;
Chen, Chiu-Hsiang ;
Lin, Tai-Yen ;
Hsu, Chain-Shu .
CHEMISTRY-AN ASIAN JOURNAL, 2012, 7 (04) :818-825
[6]   Synthesis of Conjugated Polymers for Organic Solar Cell Applications [J].
Cheng, Yen-Ju ;
Yang, Sheng-Hsiung ;
Hsu, Chain-Shu .
CHEMICAL REVIEWS, 2009, 109 (11) :5868-5923
[7]   Quantification of Geminate and Non-Geminate Recombination Losses within a Solution-Processed Small-Molecule Bulk Heterojunction Solar Cell [J].
Credgington, Dan ;
Jamieson, Fiona C. ;
Walker, Bright ;
Thuc-Quyen Nguyen ;
Durrant, James R. .
ADVANCED MATERIALS, 2012, 24 (16) :2135-2141
[8]   Improvement of open-circuit voltage and photovoltaic properties of 2D-conjugated polymers by alkylthio substitution [J].
Cui, Chaohua ;
Wong, Wai-Yeung ;
Li, Yongfang .
ENERGY & ENVIRONMENTAL SCIENCE, 2014, 7 (07) :2276-2284
[9]   Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells [J].
Dai, Shuixing ;
Zhao, Fuwen ;
Zhang, Qianqian ;
Lau, Tsz-Ki ;
Li, Tengfei ;
Liu, Kuan ;
Ling, Qidan ;
Wang, Chunru ;
Lu, Xinhui ;
You, Wei ;
Zhan, Xiaowei .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2017, 139 (03) :1336-1343
[10]   Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells [J].
Deng, Dan ;
Zhang, Yajie ;
Zhang, Jianqi ;
Wang, Zaiyu ;
Zhu, Lingyun ;
Fang, Jin ;
Xia, Benzheng ;
Wang, Zhen ;
Lu, Kun ;
Ma, Wei ;
Wei, Zhixiang .
NATURE COMMUNICATIONS, 2016, 7