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Geminate charge pair recombination in sensitized photoconducting polymer

机译:敏化光电导聚合物中的双键电荷对重组

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摘要

Recombination kinetics of the geminate charge pairs, generated by photoexcitation of charge transfer (CT) complexes in sensitized poly-N-epoxypropylcarbazole, have been investigated by transient absorption and time-resolved fluorescence techniques and modeled by Monte Carlo method. The quantitative agreement of simulations with experimental data is obtained by assuming the distance between the thermalized charge pairs to be several times longer than the typical distance between electron donor and acceptor in CT complexes. Faster recombination is observed in the films with higher sensitizer concentrations and explained by assuming that electron acceptor molecules act as scattering centers for hole motion during thermalization, thus reducing the thermalization distance. The dynamical blue shift of the fluorescence band and comparison of hole density with fluorescence kinetics suggest that heterogeneity of CT complexes results in different radiative probabilities and in distribution of the initial charge pair separation distances.
机译:通过瞬态吸收和时间分辨荧光技术研究了敏化聚N-环氧丙基咔唑中电荷转移(CT)配合物的光激发产生的双电荷对的重组动力学,并通过蒙特卡洛方法进行了建模。通过假定热化电荷对之间的距离比CT络合物中电子供体与受体之间的典型距离长几倍,从而获得与实验数据的模拟定量一致性。在具有较高敏化剂浓度的薄膜中观察到更快的复合,并通过假设电子受体分子在热化过程中充当空穴运动的散射中心来解释,从而缩短了热化距离。荧光带的动态蓝移以及空穴密度与荧光动力学的比较表明,CT络合物的异质性导致不同的辐射概率和初始电荷对分离距离的分布。

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