Nonfullerene acceptors based on extended fused rings flanked with benzothiadiazolyl-methylenemalononitrile for polymer solar cells

被引:92
作者
Bai, Huitao [1 ,2 ]
Wu, Yao [1 ]
Wang, Yifan [2 ,4 ]
Wu, Yang [3 ]
Li, Rong [1 ]
Cheng, Pei [2 ,4 ]
Zhang, Mingyu [1 ]
Wang, Jiayu [1 ]
Ma, Wei [3 ]
Zhan, Xiaowei [1 ]
机构
[1] Peking Univ, Coll Engn, Dept Mat Sci & Engn, Key Lab Polymer Chem & Phys,Minist Educ, Beijing 100871, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Key Lab Organ Solids, Beijing 100190, Peoples R China
[3] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, Xian 710049, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
OPEN-CIRCUIT-VOLTAGE; NON-FULLERENE; PHOTOVOLTAIC PERFORMANCE; QUANTUM EFFICIENCY; ELECTRON-ACCEPTORS; SMALL MOLECULES; DONOR; DIKETOPYRROLOPYRROLE; INDACENODITHIOPHENE; ABSORPTION;
D O I
10.1039/c5ta05901a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two novel A-D-A type molecules IDT-2BM and IDTT-2BM with extended fused-ring indacenodithiophene (IDT) or indacenodithienothiophene (IDTT) units as cores and strong electron-withdrawing unit 2-(benzo[c][1,2,5]thiadiazol-4-ylmethylene)malononitrile (BM) as the end-capping group were synthesized and investigated as electron acceptors in solution-processed polymer solar cells (PSCs). IDT-2BM and IDTT-2BM exhibited strong and broad absorption from 300 to 800 nm, and appropriate LUMO (-3.8 eV) and HOMO (-5.5 to -5.6 eV) levels matching with the classical polymer donor PBDTTT-C-T. IDT-2BM and IDTT-2BM films exhibited intrinsic electron mobilities of about 3.7 x 10(-6) and 1.0 x 10(-5) cm(2) V-1 s(-1), respectively. Fullerene-free PSCs employing PBDTTT-C-T as the donor and IDT-2BM or IDTT-2BM as the acceptor afforded power conversion efficiencies of 4.26% and 4.81%, respectively.
引用
收藏
页码:20758 / 20766
页数:9
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