首页> 外文期刊>Journal of Polymer Research >Theoretical studies on the electronic structures and optical properties of the thiophene oligomer containing 2-(trifluoromethyl) thieno [3, 4-b] thiophene moiety and the CF3 end-caps
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Theoretical studies on the electronic structures and optical properties of the thiophene oligomer containing 2-(trifluoromethyl) thieno [3, 4-b] thiophene moiety and the CF3 end-caps

机译:含2-(三氟甲基)噻吩并[3,4-b]噻吩部分和CF3 端帽的噻吩低聚物的电子结构和光学性质的理论研究

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摘要

Structural, electronic, and optical properties of a series of π-conjugated thiophene oligomers P1-P3 and CF 3 P1-CF 3 P3 have been theoretically investigated. P1-P3 contain the 2- (trifluoromethyl) thieno [3, 4-b] thiophene moiety as the centre and 1–3 repeating thiophene units adjacent to its two sides respectively, while their corresponding derivatives CF 3 P1-CF 3 P3 with the CF3 as end-caps. The geometric structures of the oligomers in the ground and excited state were optimized by PBE1PBE and CIS methods with 6–31G (d) basis sets, respectively. All the oligomers exhibit zigzag arrangements. The absorptions and emissions were calculated by the time-dependent density functional theory method (TD-PBE1PBE). The lowest-lying absorptions of all the oligomers can be characterized as π-π* electron transition. For each series of oligomers, there is a progressive lowering in HOMO-LUMO gap with the increase of the repeating unit, being consistent with the red-shifted trend in the lowest-lying absorption and fluorescence from P1 to P3 and CF 3 P1 to CF 3 P3. To compare the P- and corresponding CF 3 P-oligomers, the end-cap CF3 group causes the slight blue shifts in absorption and emission spectra. The ionization potentials (IPS), electron affinities (EAs), and reorganization energies (λ) as well as the hole/electron extraction energies (HEP/EEP) of the oligomers were explored and those of the corresponding polymer were obtained by extrapolation method. The IP and HEP of P-polymer are lower than those of CF 3 P-polymer, indicating that the P-polymer is more suitable for hole transport than CF 3 P-polymer, while the higher EA and EEP for CF 3 P-polymer suggest the better electron transfer property. For CF3 end-caps, the CF 3 P-polymer exhibits the equal reorganization energy between electron and hole, which is a precondition for the charge transfer balance.
机译:从理论上研究了一系列π共轭噻吩低聚物P1-P3和CF 3 P1-CF 3 P3的结构,电子和光学性质。 P1-P3分别以2-(三氟甲基)噻吩并[3,4-b]噻吩部分为中心,并在其两侧分别包含1-3个重复的噻吩单元,而它们的相应衍生物CF 3 3 P3,其中CF3 为端盖。通过PBE1PBE和CIS方法分别用6–31G(d)基集优化了低聚物在基态和激发态的几何结构。所有的低聚物均表现出之字形排列。通过时变密度泛函理论方法(TD-PBE1PBE)计算吸收和发射。所有低聚物中最低的吸收可以表征为π-π* 电子跃迁。对于每个系列的低聚物,HOMO-LUMO间隙都随着重复单元的增加而逐渐降低,这与从P1到P3和CF 3 P1到CF 3 P3。为了比较P-和相应的CF 3 P-低聚物,封端CF3 基团在吸收和发射光谱中引起了轻微的蓝移。探索了低聚物的电离势(IPS ),电子亲和力(EA)和重组能(λ)以及空穴/电子提取能(HEP / EEP),并获得了相应聚合物的电离能通过外推法。 P聚合物的IP和HEP低于CF 3 P聚合物,这表明P聚合物比CF 3 P聚合物更适合空穴传输,而EA较高CF 3 P聚合物的EEP和EEP均表明电子转移性能更好。对于CF3 端盖,CF 3 P聚合物在电子和空穴之间具有相等的重组能,这是电荷转移平衡的前提。

著录项

  • 来源
    《Journal of Polymer Research》 |2012年第10期|p.1-10|共10页
  • 作者单位

    State Key Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun, 130023, People’s Republic of China;

    State Key Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun, 130023, People’s Republic of China;

    State Key Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun, 130023, People’s Republic of China;

    State Key Laboratory of Theoretical and Computational Chemistry, Institute of Theoretical Chemistry, Jilin University, Changchun, 130023, People’s Republic of China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Conjugated polymer; Absorption; Fluorescence; Electronic structure;

    机译:共轭聚合物;吸收;荧光;电子结构;

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