混溶性
材料科学
聚合物
微观结构
弹性模量
旋节分解
复合材料
聚合物混合物
相(物质)
共聚物
有机化学
化学
作者
Kangkang Zhou,Kaihu Xian,Qingchun Qi,Mengyuan Gao,Zhongxiang Peng,Junwei Liu,Yang Liu,Saimeng Li,Youdi Zhang,Yanhou Geng,Long Ye
标识
DOI:10.1002/adfm.202201781
摘要
Abstract The rapid development of low bandgap polymer acceptors has promoted the efficiency up to ≈17% for all‐polymer solar cells (all‐PSCs). Nevertheless, the polymeric blend film, core to the photoelectric conversion of all‐PSCs, has not been thoroughly understood in terms of the influence and regulatory factors of mechanical properties, which hinders the advances in flexible and wearable applications. Herein, a range of characterization methods is combined to investigate the mechanical properties, miscibility, and film microstructure of the blends based on several representative polymer donors (PTzBI‐Si, PTVT‐T, PM6 and PTQ10) and a benchmark polymer acceptor N2200, and to further reveal the miscibility‐property relationships of the miscibility property. The results stress that fracture behaviors and elastic moduli of these blends with varied compositions show different changing trends, which are affected by molecular interactions and aggregated structure of the blends. The elastic moduli of the four all‐polymer blends can be nicely predicted by different models that are deduced from macromolecular mechanics. Most crucially, the correlations between elastic modulus, morphology, and miscibility of all‐polymer blends are elucidated for the first time. The derived relationships is validated with another high‐efficiency blend and will be the key to the successful fabrication of mechanically robust and stretchable all‐PSCs with high efficiency.
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