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首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Pathways for photoinduced charge separation and recombination at donor-acceptor heterojunctions: The case of oligophenylenevinylene-perylene bisimide complexes
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Pathways for photoinduced charge separation and recombination at donor-acceptor heterojunctions: The case of oligophenylenevinylene-perylene bisimide complexes

机译:供体-受体异质结处光诱导电荷分离和重组的途径:低聚亚苯基亚乙烯基-per双酰亚胺配合物的情况

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摘要

Semiempirical Hartree-Fock techniques have been applied to assess the molecular parameters governing the efficiency of photoinduced charge generation and recombination processes in donor/acceptor complexes involving a three-ring oligophenylenevinylene as donor and perylene bisimide as acceptor. The corresponding rates have been estimated in the framework of the Marcus-Levich-Jortner formalism for different geometries of the complexes. The results indicate that dissociation pathways involving the lowest two charge transfer excited states contribute significantly to the dynamics of the whole process. The rates are found to be strongly sensitive to the relative position of the donor and acceptor units and can be rationalized in terms of symmetry arguments applied to relevant electronic levels.
机译:半经验Hartree-Fock技术已用于评估分子参数,这些参数控制着以三环低聚亚苯基亚乙烯基为施主,and双酰亚胺为受主的供体/受体复合物中光诱导电荷产生和重组过程的效率。在配合物的不同几何形状的Marcus-Levich-Jortner形式主义的框架中,估计了相应的比率。结果表明,涉及最低的两个电荷转移激发态的离解途径对整个过程的动力学有显着贡献。发现速率对供体和受体单元的相对位置非常敏感,并且可以根据应用于相关电子水平的对称性参数进行合理化。

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