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首页> 外文期刊>ACS applied materials & interfaces >Bispentafluorophenyl-Containing Additive: Enhancing Efficiency and Morphological Stability of Polymer Solar Cells via Hand-Grabbing-Like Supramolecular Pentafluorophenyl-Fullerene Interactions
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Bispentafluorophenyl-Containing Additive: Enhancing Efficiency and Morphological Stability of Polymer Solar Cells via Hand-Grabbing-Like Supramolecular Pentafluorophenyl-Fullerene Interactions

机译:含双氟苯基的添加剂:通过手工抓住类似的超分子五氟苯基 - 富勒烯相互作用提高聚合物太阳能电池的效率和形态稳定性

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摘要

A new class of additive materials bis(pentafluorophenyl) diesters (BFEs) where the two pentafluorophenyl (C6F5) moieties are attached at the both ends of a linear aliphatic chain with tunable tether lengths (BFS, BF7, and BF13) were designed and synthesized. In the presence of BF7 to restrict the migration of fullerehe by hand-grabbing-like supramolecular interactions induced between the C6F5 groups and the surface of fullerene, the P3HT:PC61BM:BF7 device showed stable device characteristiCs after thermal heating at 150 degrees C for 25, 'IL The morphologies Of the active layers were systematically investigated by optical microscopy, grazing-incidence small-angle X-ray scattering (GISAXS), and atomic force microscopy. The tether length between the two C6F5 groups plays a pivotal role in controlling the intermolecular attractions. BF13 with a long and flexible tether might form a BF13-fullerene sandwich complex that fails to prevent fullerene's movement and aggregation, while BF5 with too short tether length decreases the possibility of interactions between the C6F5 groups and the fullerenes. BF7 with the optimal tether length has the best ability to stabilize the morphology. In sharp contrast, the nonfluorinated BP7 analogue without C6F5-C-60 physical interactions does not have the capability of morphological stabilization, unambiguously revealing the necessity of the C6F5 group. Most importantly, the function of BF7 can be also applied to the high-performance PffBT4BT-20D:PC71BM system, which exhibited an original PCE of 8.80%. After thermal heating at 85 degrees C for 200 h, the efficiency of the Pffi3T4BT-20D:PC71BM:BF7 device only decreased slightly to 7.73%, maintaining 88% of its original efficiency. To the best of our knowledge, this is the first time that the thermabdriven morphological evolution of the high-performance PffBT4BT-20D polymer has been investigated, and its morphological stability in the inverted device can be successfully preserved by the incorporation of BF7. This research also demonstrates that BF7 is not only effective with PC61BM but also to PC71BM.
机译:一种新的添加剂材料BIS(五氟苯基)二酯(BFE),其中设计并合成了两个五氟苯基(C6F5)部分,其中两个五氟苯基(C6F5)部分附着在线性脂族链的两端(BFS,BF7和BF13)。在BF7的存在下,通过在C6F5基团和富勒烯表面诱导的手工抓取的超分子相互作用,P3HT:PC61BM:BF7器件在150摄氏度下热加热后显示出稳定的装置特性,25 “IL通过光学显微镜系统地研究了活性层的形态学,从而掠入 - 发生小角X射线散射(吉即)和原子力显微镜。两个C6F5基团之间的系绳长度在控制分子间吸引力方面发挥了枢转作用。 BF13具有长且柔性的系绳可以形成BF13-富勒烯夹心复合物,不能防止富勒烯的运动和聚集,而具有太短系绳长度的BF5降低C6F5组和富勒烯之间相互作用的可能性。 BF7具有最佳系绳长度具有稳定形态的最佳能力。在鲜明的对比度下,没有C6F5-C-60物理相互作用的非氟化BP7类似物没有形态稳定化的能力,明确地揭示C6F5组的必要性。最重要的是,BF7的功能也可以应用于高性能PFFBT4BT-20D:PC71BM系统,其呈现为8.80%的原始PCE。在85℃下热加热200小时后,PFFI3T4BT-20D:PC71BM的效率:BF7器件仅略微下降至7.73%,维持其原始效率的88%。据我们所知,这是第一次研究了高性能PFFBT4BT-20D聚合物的热工形态演化,并且通过掺入BF7,可以成功地保留倒置装置的形态稳定性。该研究还表明BF7不仅对PC61BM有效,而且还对PC71BM有效。

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