Laboratory of Photonics and Interfaces, Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology (EPFL) , Station 6, 1015 Lausanne, Switzerland.
Nano Lett. 2014 Dec 10;14(12):6991-6. doi: 10.1021/nl503279x. Epub 2014 Nov 20.
As the photovoltaic performance of a device is strongly influenced by the morphology of perovskite, achieving precise control over the crystal formation of organic-inorganic halide perovskites synthesized in the ambience of chloride ions has garnered much attention. Although the resulting morphology dictates the performance of the device considerably, the understanding of the role of chloride ions has been scant. To unravel this mystery, we investigated three different organic-inorganic halide perovskite materials grown from the chloride-containing precursors under different but optimized conditions. Despite the presence of chloride ions in the reaction mixture, scanning transmission electron microscopy- energy dispersive spectroscopy (STEM-EDS) reveals that the CH3NH3PbI3 perovskites formed are chloride-free. Moreover bright field transmission electron microscopy indicates that chloride ions effect the growth of the CH3NH3PbI3.
由于器件的光伏性能强烈受到钙钛矿形态的影响,因此精确控制在氯离子环境中合成的有机-无机卤化物钙钛矿的晶体形成引起了广泛关注。尽管所得形态对器件性能有很大影响,但对氯离子作用的理解却很少。为了解开这个谜团,我们研究了三种不同的有机-无机卤化物钙钛矿材料,这些材料是从含有氯的前体中在不同但优化的条件下生长而成的。尽管反应混合物中存在氯离子,但扫描透射电子显微镜-能量色散光谱(STEM-EDS)表明形成的 CH3NH3PbI3 钙钛矿是无氯的。此外,明场透射电子显微镜表明,氯离子会影响 CH3NH3PbI3 的生长。