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一种用于高性能聚合物供体材料的具有成本效益的α-氟化联噻吩苯并二噻吩单元

A Cost-Effective Alpha-Fluorinated Bithienyl Benzodithiophene Unit for High-Performance Polymer Donor Material.

作者信息

Zhang Wenqing, Sun Chenkai, Qin Shucheng, Shang Ziya, Li Shaman, Zhu Can, Yang Guang, Meng Lei, Li Yongfang

机构信息

College of Chemistry, and Green Catalysis Center, Zhengzhou University, Zhengzhou 450001, China.

Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.

出版信息

ACS Appl Mater Interfaces. 2021 Nov 24;13(46):55403-55411. doi: 10.1021/acsami.1c15278. Epub 2021 Nov 10.

Abstract

To reduce synthetic cost of the classic fluorinated bithienyl benzodithiophene (BDTT-F) unit, here, an alpha-fluorinated bithienyl benzodithiophene unit, namely, α-BDTT-F (F atom in the α position of the lateral thiophene unit), is developed by the isomerization strategy of exchanging the positions of the F atom and flexible alkyl chain on the lateral thiophene unit of the BDTT-F unit. The α-BDTT-F unit was synthesized with less synthetic steps, higher synthetic yield, and less purification times from the same raw materials as those of the BDTT-F unit, thus with low synthetic cost. Theoretical calculation indicates that the α-BDTT-F unit possesses a similar twisted conformation and electronic structures as those of the BDTT-F unit. The α-BDTT-F-based polymer α-PBQ10 exhibits similar light absorption and energy levels as those of the corresponding BDTT-F-based polymer PBQ10 but marginally increased molecular aggregation and stronger hole transport than PBQ10. In consequence, the α-PBQ10:Y6-based polymer solar cell demonstrates a slightly enhanced power conversion efficiency (PCE) of 16.26% compared with that of the PBQ10:Y6-based device (PCE = 16.23%). Also, the PCE is further improved to 16.77% through subtle microscopic morphology regulation of the photoactive layer with the fullerene derivative indene-C60 bisadduct as the third component. This work provides new ideas for the design of low-cost and high-efficiency photovoltaic molecules.

摘要

为降低经典氟化联噻吩苯并二噻吩(BDTT-F)单元的合成成本,在此,通过将BDTT-F单元侧链噻吩单元上的氟原子与柔性烷基链的位置进行交换的异构化策略,开发了一种α-氟化联噻吩苯并二噻吩单元,即α-BDTT-F(氟原子位于侧链噻吩单元的α位)。与BDTT-F单元相比,α-BDTT-F单元由相同的原料合成,合成步骤更少,合成产率更高,纯化次数更少,因此合成成本较低。理论计算表明,α-BDTT-F单元具有与BDTT-F单元相似的扭曲构象和电子结构。基于α-BDTT-F的聚合物α-PBQ10表现出与相应的基于BDTT-F的聚合物PBQ10相似的光吸收和能级,但分子聚集略有增加,空穴传输比PBQ10更强。因此,基于α-PBQ10:Y6的聚合物太阳能电池的功率转换效率(PCE)为16.26%,相比基于PBQ10:Y6的器件(PCE = 16.23%)略有提高。此外,通过以富勒烯衍生物茚-C60双加合物作为第三组分对光活性层进行精细的微观形态调控,PCE进一步提高到16.77%。这项工作为低成本、高效率光伏分子的设计提供了新思路。

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