Zhao Jun, Swinnen Ann, Van Assche Guy, Manca Jean, Vanderzande Dirk, Van Mele Bruno
Department of Physical Chemistry and Polymer Science, Faculty of Engineering Sciences, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium.
J Phys Chem B. 2009 Feb 12;113(6):1587-91. doi: 10.1021/jp804151a.
In this work, the phase diagram of poly(3-hexyl thiophene) (P3HT) and [6,6]-phenyl C61-butyric acid methyl ester (PCBM) blends is measured by means of standard and modulated temperature differential scanning calorimetry. Blends were made by solvent-casting from chlorobenzene, as blends cast from toluene or 1,2-dichlorobenzene prove to retain effects of phase segregation during casting, hindering the determination of the phase diagram. The film morphology of P3HT/PCBM blends cast from chlorobenzene results from a dual crystallization behavior, in which the crystallization of each component is hindered by the other component. A single glass transition is observed for all compositions. The glass transition temperature (Tg) increases with increasing concentration of PCBM: from 12.1 degrees C for pure P3HT to 131.2 degrees C for pure PCBM. The observed Tg defines the operating window for the thermal annealing and explains the long-term instability of both the morphology and the photovoltaic performance of the P3HT/PCBM solar cells.
在本工作中,通过标准温度和调制温度差示扫描量热法测量了聚(3 - 己基噻吩)(P3HT)与[6,6]-苯基C61 - 丁酸甲酯(PCBM)共混物的相图。共混物通过从氯苯中溶液浇铸制成,因为从甲苯或1,2 - 二氯苯中浇铸的共混物在浇铸过程中会保留相分离的影响,从而妨碍相图的测定。从氯苯中浇铸的P3HT/PCBM共混物的薄膜形态源于双重结晶行为,其中各组分的结晶受到另一组分的阻碍。所有组成均观察到单一玻璃化转变。玻璃化转变温度(Tg)随PCBM浓度的增加而升高:从纯P3HT的12.1℃升至纯PCBM的131.2℃。观察到的Tg定义了热退火的操作窗口,并解释了P3HT/PCBM太阳能电池的形态和光伏性能的长期不稳定性。