Dimeric Giant Molecule Acceptors Featuring N-type Linker: Enhancing Intramolecular Coupling for High-Performance Polymer Solar Cells

被引:1
|
作者
Fu, Hongyuan [1 ]
Wang, Qingyuan [1 ]
Chen, Qi [1 ]
Zhang, Yaogang [2 ]
Meng, Shixin [1 ]
Xue, Lingwei [3 ]
Zhang, Chunfeng [4 ]
Yi, Yuanping [2 ]
Zhang, Zhi-Guo [1 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, CAS Key Lab Organ Solids, Beijing 100190, Peoples R China
[3] Pingdingshan Univ, Yaoshan Lab, Pingdingshan 467000, Henan, Peoples R China
[4] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Sch Phys, Natl Lab Solid State Microstruct, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymer solar cells; acceptor; intramolecular coupling; linker; Knoevenagel condensation; ORGANIC PHOTOVOLTAICS; CHARGE-TRANSPORT; MOBILITIES; EFFICIENT;
D O I
10.1002/anie.202403005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Giant molecular acceptors (GMAs) are typically designed through the conjugated linking of individual small molecule acceptors (SMAs). This design imparts an extended molecular size, elevating the glass transition temperature (Tg) relative to their SMA counterparts. Consequently, it effectively suppresses the thermodynamic relaxation of the acceptor component when blended with polymer donors to construct stable polymer solar cells (PSCs). Despite their merits, the optimization of their chemical structure for further enhancing of device performance remains challenge. Different from previous reports utilizing p-type linkers, here, we explore an n-type linker, specifically the benzothiadiazole unit, to dimerize the SMA units via a click-like Knoevenagel condensation, affording BT-DL. In comparison with B-DL with a benzene linkage, BT-DL exhibits significantly stronger intramolecular super-exchange coupling, a desirable property for the acceptor component. Furthermore, BT-DL demonstrates a higher film absorption coefficient, redshifted absorption, larger crystalline coherence, and higher electron mobility. These inherent advantages of BT-DL translate into a higher power conversion efficiency of 18.49 % in PSCs, a substantial improvement over the 9.17 % efficiency observed in corresponding devices with B-DL as the acceptor. Notably, the BT-DL based device exhibits exceptional stability, retaining over 90 % of its initial efficiency even after enduring 1000 hours of thermal stress at 90 degrees C. This work provides a cost-effective approach to the synthesis of n-type linker-dimerized GMAs, and highlight their potential advantage in enhancing intramolecular coupling for more efficient and durable photovoltaic technologies. Giant molecular acceptors are typically designed with different linkers to tune their intermolecular and intramolecular interactions. Unlike prior approaches using p-type linkers, here we explore an n-type linker, notably the benzothiadiazole unit, affording BT-DL via a click-like Knoevenagel condensation. It exhibits stronger intramolecular super-exchange coupling compared to its benzene-linked counterpart, leading to better device efficiency.+ image
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页数:10
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