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通过通用交联策略实现机械强度和形态稳定性同时提高的本征可拉伸有机太阳能电池。

Intrinsically Stretchable Organic Solar Cells with Simultaneously Improved Mechanical Robustness and Morphological Stability Enabled by a Universal Crosslinking Strategy.

作者信息

Wang Zhenye, Zhang Di, Xu Meichen, Liu Junfeng, He Jiayi, Yang Lvpeng, Li Zhilin, Gao Yerun, Shao Ming

机构信息

Wuhan National Laboratory for Optoelectronics, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.

Optics Valley Laboratory, Wuhan, 430074, P. R. China.

出版信息

Small. 2022 Jul;18(26):e2201589. doi: 10.1002/smll.202201589. Epub 2022 May 31.

DOI:10.1002/smll.202201589
PMID:35638221
Abstract

Developing intrinsically stretchable organic solar cells (OSCs) with excellent mechanical robustness and long-term operation stability is highly demanded for practical applications. Here, the representative PM6/Y6 active layer film, crosslinked by a photo-crosslinkable small molecule 2,6-bis(4-azidobenzylidene)cyclohexanone (BAC) containing azide groups, exhibits a significantly enhanced stretchability of 18% and toughness of 6.94 MJ m , compared to non-crosslinked film (stretchability of 4.5% and toughness of 0.75 MJ m ). It is found that controlling the crosslinking density, including crosslinker concentration and crosslinking time, plays a vital impact on the stretchability and mechanical toughness of active layer film. The resulting intrinsically stretchable OSCs achieve a high power conversion efficiency (PCE) of 13.4% and retain 80% of its performance even under the large strain of 20%. To date, this is the highest PCE for intrinsically stretchable OSCs based on small molecular acceptors. Moreover, crosslinking of active layer film suppresses the crystallization of PM6 polymer chains and avoids the excessive aggregation of small molecular acceptors under thermal heating or light illumination, leading to a stabilized film morphology and significantly improved device stability. Overall, these results provide a universal strategy to simultaneously enhance the mechanical properties and stability of OSCs without sacrificing their photovoltaic performance.

摘要

开发具有优异机械鲁棒性和长期运行稳定性的本征可拉伸有机太阳能电池(OSCs)对于实际应用具有迫切需求。在此,通过含有叠氮基团的光可交联小分子2,6-双(4-叠氮基亚苄基)环己酮(BAC)交联的代表性PM6/Y6活性层薄膜,与未交联薄膜(拉伸率为4.5%,韧性为0.75 MJ/m)相比,展现出显著增强的18%拉伸率和6.94 MJ/m的韧性。研究发现,控制交联密度,包括交联剂浓度和交联时间,对活性层薄膜的拉伸率和机械韧性起着至关重要的影响。由此得到的本征可拉伸OSCs实现了13.4%的高功率转换效率(PCE),并且即使在20%的大应变下仍保留其性能的80%。迄今为止,这是基于小分子受体的本征可拉伸OSCs的最高PCE。此外,活性层薄膜的交联抑制了PM6聚合物链的结晶,并避免了小分子受体在热加热或光照下的过度聚集,从而导致稳定的薄膜形态并显著提高了器件稳定性。总体而言,这些结果提供了一种通用策略,可在不牺牲其光伏性能的情况下同时增强OSCs的机械性能和稳定性。

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