Schaefer C, Michels J J, van der Schoot P
Dutch Polymer Institute, P.O. Box 902, 5600 AX Eindhoven, The Netherlands.
Theory of Polymers and Soft Matter, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, The Netherlands.
Macromolecules. 2017 Aug 8;50(15):5914-5919. doi: 10.1021/acs.macromol.7b01224. Epub 2017 Jul 18.
Solution-cast, thin-film polymer composites find a wide range of applications, such as in the photoactive layer of organic solar cells. The performance of this layer crucially relies on its phase-separated morphology. Efficient charge-carrier extraction requires each of the components to preferentially wet one of the two electrodes. It is often presumed that the experimentally observed surface enrichment required for this is caused by specific interactions of the active ingredients with each surface. By applying a generalized diffusion model, we find the dynamics to also play an important role in determining which component accumulates at which surface. We show that for sufficiently fast evaporation the component with the smallest cooperative diffusivity accumulates at the free interface. Counterintuitively, depending on the interactions between the various components, this may be the smaller solute. Our comprehensive numerical and analytical study provides a tool to predict and control phase-separated morphologies in thin-film polymer composites.
溶液浇铸的薄膜聚合物复合材料有广泛的应用,比如在有机太阳能电池的光活性层中。该层的性能关键取决于其相分离形态。高效的电荷载流子提取要求每个组分优先润湿两个电极之一。人们常常推测,实验观察到的为此所需的表面富集是由活性成分与每个表面的特定相互作用引起的。通过应用广义扩散模型,我们发现动力学在决定哪个组分在哪个表面积累方面也起着重要作用。我们表明,对于足够快的蒸发,具有最小协同扩散率的组分在自由界面处积累。与直觉相反,根据各组分之间的相互作用,这可能是较小的溶质。我们全面的数值和分析研究提供了一种预测和控制薄膜聚合物复合材料相分离形态的工具。