Department of Polymer Science and Engineering, University of Massachusetts, Amherst, Massachusetts 01003, USA.
Nano Lett. 2011 Feb 9;11(2):561-7. doi: 10.1021/nl103482n. Epub 2010 Dec 21.
Controlling thin film morphology is key in optimizing the efficiency of polymer-based photovoltaic (PV) devices. We show that morphology and interfacial behavior of the multicomponent active layers confined between electrodes are strongly influenced by the preparation conditions. Here, we provide detailed descriptions of the morphologies and interfacial behavior in thin film mixtures of regioregular poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl C61-butyric acid methyl ester (PCBM), a typical active layer in a polymer-based PV device, in contact with an anode layer of PEDOT-PSS and either unconfined or confined by an Al cathode during thermal treatment. Small angle neutron scattering and electron microscopy show that a nanoscopic, bicontinuous morphology develops within seconds of annealing at 150 °C and coarsens slightly with further annealing. P3HT and PCBM are shown to be highly miscible, to exhibit a rapid, unusual interdiffusion, and to display a preferential segregation of one component to the electrode interfaces. The ultimate morphology is related to device efficiency.
控制薄膜形态是优化基于聚合物的光伏(PV)器件效率的关键。我们表明,受限在电极之间的多组分活性层的形态和界面行为强烈受到制备条件的影响。在这里,我们详细描述了在典型的聚合物基 PV 器件的活性层中,与 PEDOT-PSS 阳极层接触的、由未受限或受限的 Al 阴极热退火的、旋涂的聚(3-己基噻吩)(P3HT)和[6,6]-苯基 C61-丁酸甲酯(PCBM)的薄膜混合物的形态和界面行为。小角中子散射和电子显微镜表明,在 150°C 退火几秒钟内就会形成纳米级双连续形态,并且随着进一步退火略微粗化。P3HT 和 PCBM 表现出高度的混溶性,表现出快速、不寻常的互扩散,并且表现出一种向电极界面优先分离的倾向。最终的形态与器件效率有关。