Fluorescence Emission Is Highly Structure-Dependent in Hybrid Lead Halides

Abstract

Hybrid lead halide perovskites have received extensive scientific attention owing to their great potential in the field of fluorescent displays and light-emitting diodes. Currently, most luminescent materials contain functional molecular and rareearth metal ion parts. However, the mechanism of photoluminescence property in two-dimensional hybrid lead halide perovskites with different layered inorganic skeletons has been reported rarely. To better understand the effect of an inorganic skeleton on the fluorescence property, here, we report three organic−inorganic hybrid materials with different layered inorganic frameworks: (MACH) 2 •PbBr 4 (Prv-1, MACH = cyclohexylmethylammonium), (2-MPQ)•PbBr 4 (Prv-2, 2-MPQ = 2-methylpiperazinium), and (TMBA) 4 •Pb 3 Br 10 (Prv-3, TMBA = N′N′N′trimethylbenzylammonium). Among them, Prv-1 is a (100)-oriented perovskite, Prv-2 belongs to the (110)-oriented perovskite, and the inorganic framework of Prv-3 possesses [Pb 3 Br 10 ] units. Interestingly, Prv-1 has a strong blue-violet fluorescence emission, while the luminescence effect of Prv-2 is very weak; notably, Prv-3 emits a charming bright-orange light. Meanwhile, results of theoretical computational studies also reveal that the electronic structure of all three compounds is highly dependent on structurally distorted [PbBr 6 ] octahedra, and the frontier molecular orbital (FMO) analysis further suggests that HOMO and LUMO of Prv-3 are contributed by inorganic and organic components, respectively. In addition, all three materials belong to direct band gap semiconductors, and the band gaps are 2.79, 2.97, and 2.76 eV, respectively. Significantly, there are obvious differences in conduction bands. Based on the above analysis, the photoluminescence mechanism of three hybrid materials is explained from the electronic levels. Consequentially, this work might provide practical strategies and perspectives for exploring novel structure-related properties.