Non-fused nonfullerene acceptors based on thieno[2',3':4,5]thieno[3,2-b] indole for efficient organic solar cells

被引:2
|
作者
Wu, Zeguang [1 ,2 ]
Yi, Lifei [2 ]
Meng, Yongdie [3 ]
Zhang, Ning [2 ]
Xiao, Manjun [3 ]
Liu, Yiyi [2 ]
Zhao, Xiaomei [2 ]
Cao, Jiamin [2 ]
机构
[1] Hunan Univ Sci & Technol, Sch Resource & Environm & Safety Engn, Xiangtan 411201, Peoples R China
[2] Hunan Univ Sci & Technol, Sch Chem & Chem Engn, Key Lab Theoret Organ Chem & Funct Mol, Minist Educ, Xiangtan 411201, Peoples R China
[3] Xiangtan Univ, Coll Chem, Key Lab Environm Friendly Chem & Applicat, Minist Educ, Xiangtan 411105, Peoples R China
关键词
Organic solar cells; Non-fullerene acceptors; Thieno[2',3':4,5]thieno[3,2-b]indole; Non-fused; ELECTRON-ACCEPTORS; POLYMER; ABSORPTION; UNIT;
D O I
10.1016/j.synthmet.2023.117454
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Thieno[3,2-b]indole (TI) has attracted more and more attention in organic electronics. Herein, thieno[2',3':4,5] thieno[3,2-b]indole (TTI), as a tetracyclic derivative of TI, was been developed by fused another thiophene unit. Furtherly, two non-fused NFAs TTI-2F and TTI-2Cl based on TTI have been synthesized via simple and easy synthetic routes. TTI-2F and TTI-2Cl both exhibited excellent thermal stability, low optical bandgaps of-1.5 eV, nearly planar molecular geometries, and suitable energy levels. As a result, PM6:TTI-2F solar cells afforded a decent PCE of 10.67 %, with an VOC of 0.935 V, a J(SC) of 19.21 mA/cm(2) and a FF of 59.40 %, which was due to the suitable intermolecular interactions, higher HOMO energy level, better exciton dissociation, suppressed trapassisted recombination, and balanced charge carrier mobilities. As comparison, PM6:TTI-2Cl cell exhibited much lower PCE of 8.34 %. These results demonstrated that NFAs based on TTI are promising for industrialized organic photovoltaic applications due to the simple synthesis and decent photovoltaic performance.
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页数:8
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