Pal Provas, Saha Sujoy, Banik Ananya, Sarkar Arka, Biswas Kanishka
New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Jakkur P.O., Bangalore, India.
Chemistry. 2018 Feb 6;24(8):1811-1815. doi: 10.1002/chem.201705682. Epub 2018 Jan 16.
All-inorganic and hybrid perovskite type halides are generally synthesized by solution-based methods, with the help of long chain organic capping ligands, complex organometallic precursors, and high boiling organic solvents. Herein, a room temperature, solvent-free, general, and scalable all-solid-state mechanochemical synthesis is demonstrated for different inorganic perovskite type halides, with versatile structural connectivity in three (3D), two (2D), and zero (0D) dimensions. 3D CsPbBr , 2D CsPb Br , 0D Cs PbBr , 3D CsPbCl , 2D CsPb Cl , 0D Cs PbCl , 3D CsPbI , and 3D RbPbI have all been synthesized by this method. The all-solid-state synthesis is materialized through an inorganic retrosynthetic approach, which directs the decision on the solid-state precursors (e.g., CsX and PbX (X=Cl/Br/I) with desired stoichiometric ratios. Moreover, post-synthetic structural transformations from 3D to 2D and 0D perovskite halides were performed by the same mechanochemical synthetic approach at room temperature.
全无机和杂化钙钛矿型卤化物通常借助长链有机封端配体、复杂有机金属前驱体和高沸点有机溶剂,通过基于溶液的方法合成。在此,展示了一种室温、无溶剂、通用且可扩展的全固态机械化学合成方法,用于合成具有三维(3D)、二维(2D)和零维(0D)多种结构连接性的不同无机钙钛矿型卤化物。3D CsPbBr₃、2D Cs₂PbBr₄、0D Cs₄PbBr₆、3D CsPbCl₃、2D Cs₂PbCl₄、0D Cs₄PbCl₆、3D CsPbI₃和3D RbPbI₃均已通过该方法合成。全固态合成通过无机逆合成方法实现,该方法指导对具有所需化学计量比的固态前驱体(例如CsX和PbX₂(X = Cl/Br/I))的选择。此外,在室温下通过相同的机械化学合成方法进行了从3D到2D和0D钙钛矿卤化物的合成后结构转变。