Hybrid Cycloalkyl-Alkyl Chain-Based Symmetric/Asymmetric Acceptors with Optimized Crystal Packing and Interfacial Exciton Properties for Efficient Organic Solar Cells

被引:70
作者
Xiao, Cong [1 ]
Wang, Xunchang [1 ,2 ]
Zhong, Tian [1 ]
Zhou, Ruixue [1 ]
Zheng, Xufan [1 ]
Liu, Yirui [1 ]
Hu, Tianyu [1 ]
Luo, Yixuan [1 ,3 ]
Sun, Fengbo [1 ,3 ]
Xiao, Biao [1 ]
Liu, Zhitian [1 ,3 ]
Yang, Chunming [1 ,4 ]
Yang, Renqiang [1 ]
机构
[1] Jianghan Univ, Minist Educ, Sch Optoelect Mat & Technol, Key Lab Optoelect Chem Mat & Devices, Wuhan 430056, Peoples R China
[2] Jianghan Univ, State Key Lab Fine Blasting, Wuhan 430056, Peoples R China
[3] Wuhan Inst Technol, Hubei Engn Technol Res Ctr Optoelect & New Energy, Wuhan 430205, Peoples R China
[4] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
基金
中国国家自然科学基金;
关键词
asymmetric small molecule acceptors; crystal packing; organic solar cells; side-chain engineering; POLYMER;
D O I
10.1002/advs.202206580
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hybrid cycloalkyl-alkyl side chains are considered a unique composite side-chain system for the construction of novel organic semiconductor materials. However, there is a lack of fundamental understanding of the variations in the single-crystal structures as well as the optoelectronic and energetic properties generated by the introduction of hybrid side chains in electron acceptors. Herein, symmetric/asymmetric acceptors (Y-C10ch and A-C10ch) bearing bilateral and unilateral 10-cyclohexyldecyl are designed, synthesized, and compared with the symmetric acceptor 2,2 '-((2Z,2 ' Z)-((12,13-bis(2-butyloctyl)-3,9 bis(ethylhexyl)-12,13-dihydro-[1,2,5]thiadiazolo[3,4-e]thieno[2 '',3 ''':4 ',5 ']thieno[2 ',3 ':4,5] pyrrolo[3,2-g]thieno[2 ',3 ':4,5]thieno[3,2-b]indole-2,10- diyl)bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (L8-BO). The stepwise introduction of 10-cyclohexyldecyl side chains decreases the optical bandgap, deepens the energy level, and enables the acceptor molecules to pack closely in a regular manner. Crystallographic analysis demonstrates that the 10-cyclohexyldecyl chain endows the acceptor with a more planar skeleton and enforces more compact 3D network packing, resulting in an active layer with higher domain purity. Moreover, the 10-cyclohexyldecyl chain affects the donor/acceptor interfacial energetics and accelerates exciton dissociation, enabling a power conversion efficiency (PCE) of >18% in the 2,2 '-((2Z,2 ' Z)-((12,13-bis(2-ethylhexyl)-3,9-diundecyl12,13-dihydro-[1,2,5]thiadiazolo[3,4-e]thieno[2 '',3 ''':4 ',5 ']thieno[2 ',3 ':4,5]pyrrolo[3,2-g]thieno[2 ',3 ':4,5]thieno[3,2-b]indole-2,10-diyl)bis(methanylylidene))bis(5,6-difluoro-3-oxo-2,3-dihydro-1H-indene-2,1-diylidene))dimalononitrile (Y6) (PM6):A-C10ch-based organic solar cells (OSCs). Importantly, the incorporation of Y-C10ch as the third component of the PM6:L8-BO blend results in a higher PCE of 19.1%. The superior molecular packing behavior of the 10-cyclohexyldecyl side chain is highlighted here for the fabrication of high-performance OSCs.
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页数:12
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