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Monte Carlo modeling of geminate recombination in polymer-polymer photovoltaic devices.

机译:聚合物-聚合物光伏器件中锗化合物重组的蒙特卡洛模型。

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摘要

A Monte Carlo model is used to examine geminate pair dissociation in polymer-polymer photovoltaic devices. It is found that increasing one or both carrier mobilities aids geminate separation yield ηGS particularly at low fields. This, in turn, leads to improved maximum power output from polymer-polymer blend photovoltaics, even when carrier mobilities are unbalanced by a factor of 10. The dynamic behaviors of geminate charges that eventually separate and recombine are examined for the first time. It is shown that geminate pairs in a bilayer become effectively free when separated by ∼4nm, which is far smaller than the thermal capture radius of 16nm here. This may lead one to expect that ηGS would not be limited by the separation allowed by the morphology once the domain size has increased above 4nm. In fact it is found that ηGS in a blend improves continuously as the average domain size increases from 4to16nm. We show that although a small degree of separation may be available in a blend, the limited number of possible routes to further separation makes charge pairs in blends more susceptible to recombination than charge pairs in a bilayer.
机译:蒙特卡洛模型用于检查聚合物-聚合物光伏器件中的成对对解离。发现增加一种或两种载流子迁移率特别是在低场下有助于叠氮化物分离产率ηGS。反过来,即使载流子迁移率不平衡10倍,这也可以提高聚合物-聚合物共混光伏产品的最大功率输出。首次检查了最终分离和复合的双电荷的动态行为。结果表明,双层中的双峰对相隔约4nm时实际上变得自由了,这远小于这里的16nm的热捕获半径。这可能导致人们期望,一旦畴尺寸增加到4nm以上,ηGS便不会受到形态学允许的分离的限制。实际上,发现随着平均畴尺寸从4nm增大到16nm,共混物中的ηGS不断提高。我们表明,尽管在共混物中可以使用小程度的分离,但进一步分离的可能途径数量有限,使得共混物中的电荷对比双层中的电荷对更易于重组。

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  • 年度 2008
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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