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用于与 Y 型最先进的受体在二元共混物中进行配对的具有挑战性的 PM6 类似给体聚合物,用于体异质结太阳能电池。

Challenging PM6-like donor polymers for pairing with a Y-type state-of-the-art acceptor in binary blends for bulk heterojunction solar cells.

机构信息

Department of Chemistry and Bioscience, Aalborg University, Fredrik Bajers Vej 7H, Aalborg East, DK-9220, Denmark.

College of Polymer Science and Engineering, State Key Laboratory of Polymer Materials Engineering, Sichuan University, Chengdu, 610065, China.

出版信息

Phys Chem Chem Phys. 2023 Jan 27;25(4):2916-2925. doi: 10.1039/d2cp05414k.

Abstract

Being fluorine-free and a high performance material as a small organic acceptor molecule, BTP-eC9 has been well mixed with BDT-based PM6 donor polymers for providing satisfactory photovoltaic properties, especially towards future large scale/large area solar cell production. However, as one of the key electrical outputs from such binary active layer materials, the open circuit voltage () was limited to 0.84 V, which needs to be further improved for BTP-eC9 to have a bright future. This paper focuses on the molecular design of alkylthio- and alkoxy-phenyl flanked benzo[1,2-:4,5-']dithiophene-based conjugated polymers (PBDT-PS-ttTPD or P10 for short and PBDT-PO-ttTPD or P11), which were successfully synthesized and applied as donor materials for pairing with BTP-eC9 in organic photovoltaic (OPV) devices. By fine-tuning the side chains of the benzodithiophene (BDT) moiety, such non-fullerene OPV devices with normal configuration demonstrate an attractively high open circuit voltage () of 0.89 and 0.87 V in P10/BTP-eC9 and P11/BTP-eC9 based binary single bulk heterojunction OPV devices, while still maintaining an excellent of 22.7 and 20.0 mA cm with a final power conversion efficiency (PCE) of 12.93% and 9.37%, respectively. The alkylthio-phenyl chain substituted BDT polymer exhibits better photovoltaic performance in all aspects than the alternative with alkoxy chains due to the synergistic effect of the alkylthio-phenyl flanked BDT, TPD, and π-bridge (thieno[3,2-]thiophene).

摘要

作为一种无氟的高性能小分子有机受体材料,BTP-eC9 已与基于 BDT 的 PM6 给体聚合物很好地混合,为提供令人满意的光伏性能,尤其是在未来的大规模/大面积太阳能电池生产方面。然而,作为这种二元活性层材料的关键电输出之一,开路电压()被限制在 0.84V,这需要进一步提高 BTP-eC9 的性能,使其拥有光明的未来。本文专注于烷基硫代和烷氧基苯基侧翼的苯并[1,2-b:4,5-b']二噻吩基共轭聚合物(PBDT-PS-ttTPD 或简称 P10 和 PBDT-PO-ttTPD 或 P11)的分子设计,这些聚合物已成功合成并作为供体材料应用于与 BTP-eC9 配对的有机光伏(OPV)器件中。通过精细调整苯并二噻吩(BDT)部分的侧链,具有正常结构的非富勒烯 OPV 器件在 P10/BTP-eC9 和 P11/BTP-eC9 二元单体内层异质结 OPV 器件中展示了引人注目的高开路电压()为 0.89 和 0.87V,同时仍保持优异的 22.7 和 20.0mAcm,最终功率转换效率(PCE)分别为 12.93%和 9.37%。由于烷基硫代苯基侧翼的 BDT、TPD 和π桥(噻吩[3,2-b]噻吩)的协同效应,烷基硫代苯基取代的 BDT 聚合物在各个方面都表现出比具有烷氧基链的替代物更好的光伏性能。

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