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Bulk heterojunction morphology of polymer:fullerene blends revealed by ultrafast spectroscopy

机译:超快光谱显示聚合物:富勒烯共混物的本体异质结形态

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摘要

Morphology of organic photovoltaic bulk heterojunctions (BHJs) – a nanoscale texture of the donor and acceptor phases – is one of the key factors influencing efficiency of organic solar cells. Detailed knowledge of the morphology is hampered by the fact that it is notoriously difficult to investigate by microscopic methods. Here we all-optically track the exciton harvesting dynamics in the fullerene acceptor phase from which subdivision of the fullerene domain sizes into the mixed phase (2–15 nm) and large (>50 nm) domains is readily obtained via the Monte-Carlo simulations. These results were independently confirmed by a combination of X-ray scattering, electron and atomic-force microscopies, and time-resolved photoluminescence spectroscopy. In the large domains, the excitons are lost due to the high energy disorder while in the ordered materials the excitons are harvested with high efficiency even from the domains as large as 100 nm due to the absence of low-energy traps. Therefore, optimizing of blend nanomorphology together with increasing the material order are deemed as winning strategies in the exciton harvesting optimization.
机译:有机光伏本体异质结(BHJ)的形态(施主和受主相的纳米级织构)是影响有机太阳能电池效率的关键因素之一。众所周知,很难用显微镜方法进行研究,这妨碍了对形态学的详细了解。在这里,我们全光跟踪富勒烯受体相中的激子收获动力学,通过蒙特卡洛模拟可以轻松地将富勒烯畴尺寸细分为混合相(2-15 nm)和大(> 50 nm)畴。这些结果通过X射线散射,电子和原子力显微镜检查以及时间分辨光致发光光谱学的组合得到独立确认。在大范围内,激子由于高能紊乱而损失,而在有序材料中,由于不存在低能阱,即使在100 nm的范围内,激子也能高效收获。因此,在激子收获优化中,优化掺混物纳米形态与增加材料顺序是获胜策略。

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