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Thermodynamic constants for excimer formation and dissociation in oxidized poly(9,9-dioctylfluorene) (PFO)

机译:用于氧化聚(9,9-二辛基氟烯)(PFO)中的准分子形成和解离的热力学常数

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We have studied the temperature-dependent photoluminescence (PL) characteristics of oxidised PFO thin films at temperatures above 298K. We find the relative strength of the green emission band (g-band) to increase greatly at temperatures corresponding to the onset of crystallisation. Based on the proposal that the g-band arises from a fluorenone-based excimer, this finding would seem to indicate that a close approach of neighbouring fluorenone-containing segments may be energetically favourable. Finally, by successfully identifying diffusion-limited and dynamic equilibrium regimes within the temperature dependence of the ratio R=ID/IM, we extract an activation energy for excimer formation of ~ 0.05 eV and an excimer binding energy of ~ 0.51 eV. This is a relatively high binding energy for an excimer and lends credibility to the notion of an energetically favourable fluorenone:fluorenone coupling configuration, perhaps as a result of the considerable ground state dipole moments associated with the ketone group.
机译:我们研究了在298K以上温度的温度下依赖于氧化PFO薄膜的光致发光(PL)特性。我们发现绿色发射带(G频带)的相对强度在对应于结晶开始的温度下大大增加。基于G频带由氟核酮的准分机产生的提议,该发现似乎表明含有相邻的含氟酮段的密切方法可能是能量有利的。最后,通过成功地识别在比率r = ID / Im的温度依赖性内的扩散限制和动态平衡制度,我们提取激活能量,用于准分子形成约0.05eV和〜0.51eV的准结合能量。这是一种相对高的准备能量,适用于准分子,并利用能量有利的氟烯酮的概念的可信度:芴酮偶联构型,也许是与与酮组相关的相当大的地位偶极偶联矩。

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