了解溶液分子掺杂的驱动力

A. Moulé, Tucker L. Murrey, Ian E. Jacobs, Z. I. Bedolla-Valdez, J. Saska, Goktug Gonel, Alice S. Fergerson, Nichole L. Yacoub, Rachel M. Talbot, Nikolay Shevchenko, M. Mascal, A. Salleo, Camila Cendra
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引用次数: 0

摘要

顺序溶液掺杂是一种加工技术,它允许从不会溶解聚合物的溶剂中掺杂共轭聚合物薄膜。本文提出了一种用溶液浓度来预测cm-3薄膜掺杂水平的方法。我们用四种聚合物和三种不同的新合成的掺杂剂证明了可以用简单的朗缪尔等温线来模拟掺杂水平。此外,紫外/可见光谱分析显示了态密度的填充。在相同的空穴密度下,具有更锐利带边缘的聚合物表现出更高的导电性。我们分析了一系列的DPP聚合物,并展示了聚合物的顺序如何随着掺杂水平的变化而变化。最近的第二个发现是,顺序掺杂薄膜中的阴离子可以在掺杂后与另一个阴离子交换。这意味着用于掺杂聚合物的反应性分子可以被移除,并用不具有反应性的不同离子代替。我们提出了一个多离子Langmuir等温线模型,并证明混合离子溶液中的薄膜掺杂水平也可以预测。
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Understanding the driving force for solution molecular doping
Sequential solution doping is a processing technique that allows a conjugated polymer film to be doped from a solvent that will not dissolve the polymer. We present here a method to predict the film doping level in cm-3 from the solution concentration used to dope the film. We show using four polymers and three different and newly synthesized dopants that the doping level can me modeled using a simple Langmuir isotherm. In addition, analysis of the UV/vis spectra shows filling of the density of states. Polymers with a sharper band edge demonstrate much high conductivity for the same hole density. We analyze a series of DPP polymers and show how the polymer order changes as a function of the doping level. A second recent discovery is that the anion in sequentially doped films can be exchanged with another anion after doping. This means that the reactive molecule used to doped the polymer can be removed and replaced with a different ion that is not reactive. We present a multi-ion Langmuir isotherm model and show that the film doping level in mixed ion solutions can also be predicted.
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