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Polarization Energies at Organic–Organic Interfaces: Impact on the Charge Separation Barrier at Donor–Acceptor Interfaces in Organic Solar Cells

机译:有机-有机界面的极化能:对有机太阳能电池供体-受体界面处电荷分离势垒的影响

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摘要

We probe the energetic landscape at a model pentacene/fullerene-C60 interface to investigate the interactions between positive and negative charges, which are critical to the processes of charge separation and recombination in organic solar cells. Using a polarizable force field, we find that polarization energy, i.e. the stabilization a charge feels due to its environment, is larger at the interface than in the bulk for both a positive and a negative charge. The combination of the charge being more stabilized at the interface and the Coulomb attraction between the charges, results in a barrier to charge separation at the pentacene-C60 interface that can be in excess of 0.7 eV for static configurations of the donor and acceptor locations. However, the impact of molecular motions, i.e., the dynamics, at the interface at room temperature results in a distribution of polarization energies and in charge separation barriers that can be significantly reduced. The dynamic nature of the interface is thus critical, with the polarization energy distributions indicating that sites along the interface shift in time between favorable and unfavorable configurations for charge separation.
机译:我们在模型并五苯/富勒烯-C60界面上探索高能景观,以研究正电荷和负电荷之间的相互作用,这对于有机太阳能电池中电荷分离和重组的过程至关重要。利用可极化的力场,我们发现极化能量,即电荷由于其环境而感觉到的稳定,在正电荷和负电荷下在界面处都比在体中更大。电荷在界面处更稳定以及电荷之间的库仑吸引力的组合导致并五苯-C60界面电荷分离的障碍,对于供体和受体位置的静态构型可能超过0.7 eV。但是,室温下界面处的分子运动即动力学的影响导致极化能量的分布和电荷分离势垒的显着降低。因此,界面的动态性质至关重要,极化能量分布表明沿界面的位点在时间上在电荷分离的有利和不利构型之间移动。

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