Bay-Functionalized Perylene Diimide Derivative Cathode Interfacial Layer for High-Performance Organic Solar Cells

被引:21
|
作者
Zhou, Dan [1 ]
Han, Liangjing [1 ,2 ]
Hu, Lin [2 ]
Yang, Shu [4 ]
Shen, Xingxing [4 ]
Li, Yubing [1 ]
Tong, Yongfen [1 ]
Wang, Fang [1 ]
Li, Zaifang [2 ]
Chen, Lie [3 ]
机构
[1] Nanchang Hangkong Univ, Key Lab Jiangxi Prov Persistent Pollutants Contro, 696 Fenghe South Ave, Nanchang 330063, Peoples R China
[2] Jiaxing Univ, China Australia Inst Adv Mat & Mfg IAMM, 899 Guangqiong Ave, Jiaxing 314001, Peoples R China
[3] Nanchang Univ, Inst Polymers & Energy Chem IPEC, 999 Xuefu Ave, Nanchang 330031, Peoples R China
[4] Hebei Normal Univ Sci & Technol, Coll Chem Engn, Qinhuangdao 066004, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
organic solar cells; small molecules; cathode interfacial layer; perylene diimide; bay functionalization; EFFICIENCY; ENERGY; INTERLAYERS; ABSORPTION; ELECTRODES; ACCEPTOR; DENSITY; VOLTAGE; DESIGN;
D O I
10.1021/acsami.2c22069
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The field of organic solar cells (OSCs) has acquired rapid progress with the development of nonfullerene acceptors. Interfacial engineering is also significant for the enhancement of the power conversion efficiency (PCE) in OSCs. Among the cathode interfacial materials (CIMs), perylene diimide (PDI) small molecules are promising owing to the excellent electron affinity and electron mobility. Although the well-known PDINN molecule has excellent properties, it has a high planarity formed by an extensive rigid pi-conjugated backbone. Because the PDI molecular backbone has a strong tendency to aggregate, it causes the problem of excessive molecular aggregation and stacking, which directly leads to excessive crystallinity. Proper accumulation is beneficial for charge transport, but oversized crystals formed by overaggregation will hinder charge transport, ultimately affecting the film morphology and charge transport efficiency. Modifying the bay position of PDINN is an effective strategy to reduce the planarity, modulate the molecular aggregation, optimize the morphology, and enhance the charge-collecting efficiency. Therefore, PDINN-S was synthesized from PDINN by substituting the hydrogen with thiophene. The optimal PCE in the PM6:Y6 active layer was 16.18% and remained at 80% of the initial value after 720 h in a glovebox. This provides some guidance for exploring CIMs and preparing large-scale OSCs in the future.
引用
收藏
页码:8367 / 8376
页数:10
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