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首页> 外文期刊>ACS applied materials & interfaces >Introduction of Siloxane-Terminated Side Chains into Semiconducting Polymers To Tune Phase Separation with Nonfullerene Acceptor for Polymer Solar Cells
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Introduction of Siloxane-Terminated Side Chains into Semiconducting Polymers To Tune Phase Separation with Nonfullerene Acceptor for Polymer Solar Cells

机译:将硅氧烷封端的侧链引入半导体聚合物中,以曲调聚合物太阳能电池的非氟氯橡胶的相分离

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In this work, five PTB7-Th-based conjugated polymers (PTB7-Th, PTBSi20, PTBSi25, PTBSi33, and PTBSi100) with different contents of siloxane-terminated pentyl side chain were synthesized, and properties of corresponding blend films with narrow band gap nonfullerene IEICO-4F acceptor were extensively investigated. According to the contact angle testing, the PTB7-Th with 100% alkyl side chain and PTBSi100 100% siloxane-terminated side chain on the benzodithiophene unit showed surface energy values of 40.04 and 34.52 mJ/m(2), respectively. The results demonstrate that relative to alkyl side chain in PTB7-Th, the siloxane-terminated side chain could effectively reduce the surface energy of a resulting polymer. Based on Flory-Huggins interaction parameter estimations, the miscibility between the polymer and IEICO-4F would vary in an order of PTB7-Th > PTBSi20 > PTBSi25 > PTBSi33 > PTBSi100, suggesting that siloxane-terminated side chain would afford a tunable driving force for phase separation. Transmission electron microscopy and Raman mapping could confirm large bulk domains inside the PTBSi100:IEICO-4F blend film. In polymer solar cells, the blend film of the PTBSi100 with the lowest miscibility to IEICO-4F showed an undesirable power conversion efficiency (PCE) of 8.52%, which was significantly lower than that of 11.23% for PTB7-Th, suggesting that too large phase separation driving force is not beneficial for the device performance. Side-chain random copolymers PTBSi20, PTBSi25, and PTBSi33 for fine tuning could display PCEs of 11.94, 12.61, and 11.80%, respectively, all higher than that of PTB7-Th. Our results not only reveal the big surface energy difference between the siloxane-terminated side chain and the common alkyl side chain but also provide a guideline for side chain engineering of conjugated polymer donors with tunable morphology and optimal matching with a nonfullerene acceptor.
机译:在这项工作中,合成了具有不同硅氧烷封端的戊酰侧链的五种基于PTB7-,PTBSI20,PTBSI25,PTBSI33和PTBSI100),以及具有窄带间隙非含量的相应混合物膜的性质IEICO-4F受体被广泛调查。根据接触角测试,PTB7-含有100%烷基侧链和苯并二噻吩单元上的PTBSI100 100%硅氧烷封端的侧链分别显示出40.04和34.52mJ / m(2)的表面能值。结果表明,相对于PTB7-TH中的烷基侧链,硅氧烷封端的侧链可以有效地降低所得聚合物的表面能。基于血管 - Huggins相互作用参数估计,聚合物和IEICO-4F之间的混合物将以PTB7-TN> PTBSI20> PTBSI25> PTBSI33> PTBSI100的顺序变化,表明硅氧烷封端的侧链将提供可调谐驱动力相分离。透射电子显微镜和拉曼映射可以确认PTBSI100内部的大型散装域:IEICO-4F共混膜。在聚合物太阳能电池中,具有最低混溶性的PTBSI100的共混膜具有最低的IEICO-4F,显示出8.52%的不期望的功率转化效率(PCE),其PTB7-TH显着低于11.23%,表明太大了相分离驱动力对设备性能无利可图。用于微调的侧链随机共聚物PTBSI20,PTBSI25和PTBSI33可分别显示11.94,12.61和11.80%的PTBE,全部高于PTB7 -TH。我们的结果不仅揭示了硅氧烷封端的侧链和常见的烷基侧链之间的大表面能差,还提供了具有可调谐形态的共轭聚合物供体的侧链工程准则和与非氟联受体的最佳匹配。

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