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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Photophysics of Charge Generation in Organic Photovoltaic Materials: Kinetic Studies of Geminate and Free Polarons in a Model Donor/ Acceptor System
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Photophysics of Charge Generation in Organic Photovoltaic Materials: Kinetic Studies of Geminate and Free Polarons in a Model Donor/ Acceptor System

机译:有机光伏材料中电荷产生的光物理性质:模型供体/受体系统中双键和自由极化子的动力学研究

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摘要

Photoinduced charge generation is studied in a model donor/acceptor blended system, consisting of bulk-heterojunction blends of the conjugated polymer regioregular poly(3-hexylthiophene) (P3HT) and the dye molecule phthalocyanine (PC). Excitation at 780 nm, into the PC NIR absorption band, creates excitons in PC domains without populating the P3HT excited state. The kinetics of geminate polaron pairs (GPP) and free polarons can then be followed without the interference from the signatures of directly created polarons, energy transfer, or significant exciton migration.The donor/ acceptor film morphology has a significant impact on the ratio of free polarons and GPP that are formed: increased phase segregation leads to a pronounced increase on the fraction of free polarons formed directly. Unlike the free polaron population, GPPs are affected by fast recombination directly to the ground state, occurring with a time constant of 170 ps. Both GPP and free polarons are formed at the P3HT/PC interfaces. Free polarons are, however, able to migrate from these interfaces into the bulk, quasi-crystalline P3HT regions. Finally, the results obtained with our model system were compared with the photoinduced charge generation in P3HT/PCBM 1:1 blend films. Indication for free polaron formation yield following electron transfer of ~100% was obtained; no GPP formation was observed. This is in agreement with previous studies of both the photophysics and OPV device characterization based on these blends.
机译:在模型供体/受体共混体系中研究了光诱导电荷的产生,该体系由共轭聚合物区域规则的聚(3-己基噻吩)(P3HT)和染料分子酞菁(PC)的本体-异质结共混物组成。在780 nm处激发到PC NIR吸收带中,在PC域中产生激子,而没有填充P3HT激发态。然后可以追踪双极化极化子对(GPP)和自由极化子的动力学,而不受直接产生的极化子的签名,能量转移或大量激子迁移的干扰。施主/受主薄膜的形态对游离比率具有重大影响形成的极化子和GPP:增加的相偏析会导致直接形成的游离极化子的比例明显增加。与自由极化子种群不同,GPP受直接重组为基态的快速重组的影响,时间常数为170 ps。 GPP和自由极化子都在P3HT / PC接口处形成。但是,自由极化子能够从这些界面迁移到块状准P3HT区域。最后,将我们的模型系统获得的结果与P3HT / PCBM 1:1混合膜中的光诱导电荷产生进行了比较。指示电子转移后游离极化子的形成产率为〜100%;没有观察到GPP形成。这与基于这些混合物的光物理和OPV器件表征的先前研究相一致。

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