光激发
光电流
离解(化学)
材料科学
富勒烯
有机太阳能电池
激发态
光化学
偶极子
光电子学
化学
原子物理学
物理化学
复合材料
物理
有机化学
聚合物
作者
Xixiang Zhu,Guichuan Zhang,Jia Zhang,Hin‐Lap Yip,Bin Hu
出处
期刊:Joule
[Elsevier BV]
日期:2020-10-08
卷期号:4 (11): 2443-2457
被引量:42
标识
DOI:10.1016/j.joule.2020.09.005
摘要
This paper reports self-stimulated dissociation occurring at donor:acceptor interfaces in non-fullerene solar cells to completely separate electron-hole pairs toward developing high-efficiency photovoltaic actions. By monitoring in situ, the dissociation at D:A (PM6:Y6) interfaces with magnetic field effects of the photocurrent, it was observed that, as the excitons are increased by gradually increasing photoexcitation intensity, the dissociation at D:A interfaces becomes surprisingly easier, once the non-fullerene Y6 molecules are optically excited. This presents a self-stimulated dissociation phenomenon identified by gradually increasing light illumination, while monitoring the dissociation with magnetic field effects of the photocurrent. Our photoexcitation-dependent magneto-capacitance at 1 MHz found that optically exciting the Y6 molecules generates a dipolar polarization signal, leading to a light-induced bulk polarization in the PM6:Y6 system. Essentially, the self-stimulated dissociation is enabled by optically excited non-fullerene Y6 molecules with photoinduced dipolar polarization to completely separate electron-hole pairs at D:A interfaces toward developing high-efficiency photovoltaics in non-fullerene organic solar cells.
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