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无机钙钛矿型卤化物的全固态机械化学合成及合成后转化

All-Solid-State Mechanochemical Synthesis and Post-Synthetic Transformation of Inorganic Perovskite-type Halides.

作者信息

Pal Provas, Saha Sujoy, Banik Ananya, Sarkar Arka, Biswas Kanishka

机构信息

New Chemistry Unit, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Jakkur P.O., Bangalore, India.

出版信息

Chemistry. 2018 Feb 6;24(8):1811-1815. doi: 10.1002/chem.201705682. Epub 2018 Jan 16.

Abstract

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.

摘要

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。

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