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Influence of Crystallinity and Energetics on Charge Separation in Polymer–Inorganic Nanocomposite Films for Solar Cells

机译:结晶度和能量对太阳能电池用聚合物-无机纳米复合薄膜中电荷分离的影响

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摘要

The dissociation of photogenerated excitons and the subsequent spatial separation of the charges are of crucial importance to the design of efficient donor-acceptor heterojunction solar cells. While huge progress has been made in understanding charge generation at all-organic junctions, the process in hybrid organic:inorganic systems has barely been addressed. Here, we explore the influence of energetic driving force and local crystallinity on the efficiency of charge pair generation at hybrid organic:inorganic semiconductor heterojunctions. We use x-ray diffraction, photoluminescence quenching, transient absorption spectroscopy, photovoltaic device and electroluminescence measurements to demonstrate that the dissociation of photogenerated polaron pairs at hybrid heterojunctions is assisted by the presence of crystalline electron acceptor domains. We propose that such domains encourage delocalization of the geminate pair state. The present findings suggest that the requirement for a large driving energy for charge separation is relaxed when a more crystalline electron acceptor is used.
机译:光生激子的离解和电荷的随后空间分离对于有效的供体-受体异质结太阳能电池的设计至关重要。尽管在了解所有有机连接处的电荷产生方面已取得了巨大进展,但有机,无机混合系统中的过程仍未得到解决。在这里,我们探讨了高能驱动力和局部结晶度对杂化有机:无机半导体异质结处电荷对生成效率的影响。我们使用X射线衍射,光致发光猝灭,瞬态吸收光谱,光伏设备和电致发光测量来证明在杂化异质结处光生极化子对的离解是由晶体电子受体域的存在辅助的。我们建议这样的域鼓励双联状态的离域。本发现表明,当使用结晶度更高的电子受体时,放宽了电荷分离所需的大驱动能量的要求。

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