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Updated: Sep 4, 2025

Low Pressure Vapor-assisted Solution Process for Tunable Band Gap Pinhole-free Methylammonium Lead Halide Perovskite Films
Published on: September 8, 2017
Highly stable halide perovskites for photocatalysis via multi-dimensional structure design and in situ phase
Yiqin Gong1, Fan Ye2, Qiliang Zhu1
1Shanghai Engineering Research Centre of Hierarchical Nanomaterials, Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China. jianhuashen@ecust.edu.cn.
Abstract:
Lead halide perovskite CsPbBr3 quantum dots (QDs) possess several desirable features which enable them to be promising candidates for photocatalysis. However, the instability caused by their inherent liquid-like ionic properties hampers their further development. Herein, this work employs the surficial molecular modification strategy and a multi-dimensional structure design to ease the instability issue. The additive 2-phenylethanamine bromide (PEABr) can serve as a ligand to compensate for stripping the amine ligands and passivate the surficial bromide vacancy defects of CsPbBr3 QDs in photocatalysis. In addition, PEABr acts as a reactant to form 2D and quasi-2D perovskite nanosheets. The addition of a small amount of these nanosheets into QDs can enhance their general stability due to their unique layered structures. Moreover, PEABr can trigger the phase transition of cubic CsPbBr3 into tetragonal CsPb2Br5. The newly formed Z-scheme homologous heterojunctions further improve the catalytic performance. Simulated photocatalytic dynamics reveals that our multi-dimensional structure favors decreasing the reaction barrier energy and then facilitating the photocatalytic reaction. Therefore, the electron consumption rate of our multi-dimensional perovskites doubles that of pristine CsPbBr3 QDs and also has superior long-term stability.
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