Optimized Photoemission from Organic Molecules in 2D Layered Halide Perovskites
Muhammad S. Muhammad, Dilruba A. Popy, Hamza Shoukat, John M. Lane, Neeraj Rai, Vojtech Vanecek, Zdeneek Remes, Romana Kucerkova, Vladimir Babin, Chenjia Mi, Yitong Dong, Mark D. Smith, Novruz G. Akhmedov, Daniel T. Glatzhofer, and Bayram Saparov

TL;DR
This paper reports the design and synthesis of new organic-inorganic hybrid 2D layered perovskites with high photoluminescence efficiency originating from organic molecules, showing potential for optoelectronic and radiation detection applications.
Contribution
It introduces novel hybrid perovskite materials with organic components as the primary source of photoemission, achieving record-high quantum yields and demonstrating their stability and practical potential.
Findings
Photoluminescence quantum yields up to 50.83% and 26.60%.
Emission originates from organic cations confirmed by spectroscopy and DFT.
Materials exhibit high environmental and thermal stability.
Abstract
In recent years, hybrid organic-inorganic metal halides have been at the forefront of materials research. Typically, the functional (e.g., optoelectronic) properties of hybrid halides are derived from the inorganic structural part, whereas the organic structural units can add extra advantages in terms of stability, rigidity, and processability. Here, we report the design, synthesis, and characterization of two new hybrid materials in which the outstanding photophysical properties originate from the organic structural part. The new compounds, (C15H16N)2CdCl4 and ((Br)C15H15N)2CdCl4, have 2D layered Ruddlesden-Poppertype perovskite structures. These hybrids are blue-white light emitters just like their corresponding pure organic salts, but with much improved emission efficiencies. Optical spectroscopy and density functional theory (DFT) studies confirm that photoemission comes from the…
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Taxonomy
TopicsPerovskite Materials and Applications · Luminescence and Fluorescent Materials · Covalent Organic Framework Applications
