卤化物
纳米晶
量子产额
钙钛矿(结构)
光致发光
材料科学
分散性
金属卤化物
金属
产量(工程)
铜
无机化学
离子键合
纳米技术
化学工程
化学
结晶学
离子
有机化学
光电子学
荧光
冶金
物理
高分子化学
量子力学
工程类
作者
Chang‐Xu Li,Seung-Bum Cho,Dong‐Hwan Kim,Il‐Kyu Park
标识
DOI:10.1021/acs.chemmater.2c01318
摘要
Lead-free copper-based perovskite Cs3Cu2X5 nanocrystals (NCs) have attracted a great deal of attention as novel active materials in optoelectronic devices because of their high emission stability, unique self-trap exciton emission, and high quantum yield, as well as their relatively low toxicity and earth-abundant constituents. On the contrary, despite the widespread interest in Cs3Cu2X5 bulk or thin-film structures, the synthesis of highly crystalline and uniform Cs3Cu2X5 NCs in high yield has rarely been reported on the basis of the conventional growth kinetics because of our insufficient understanding of their formation mechanism. We report a strategy for increasing the yield and controlling the size of Cs3Cu2X5 NCs by utilizing the metal halide additive to adjust the thermodynamic equilibrium and chemical potential. Monodisperse Cs3Cu2I5 nanocubes with a photoluminescence quantum yield of 72.4% could be obtained because of the unique properties of MnI2, which can form multiple ionic salts and promote the reaction of CuI with a ligand to form Cu oleate-rich conditions for the assembly of NCs. Therefore, the metal halide additive plays a critical role in increasing the synthesis yield and controlling the size of copper-based Cs3Cu2I5 NCs based on precise mechanistic studies.
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