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      Origin of Luminescence in Sb 3+- and Bi 3+-Doped Cs 2SnCl 6 Perovskites: Excited State Relaxation and Spin–Orbit Coupling

      1 , 1
      The Journal of Physical Chemistry Letters
      American Chemical Society (ACS)

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          Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides

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            Efficient and stable emission of warm-white light from lead-free halide double perovskites

            Lighting accounts for one-fifth of global electricity consumption1. Single materials with efficient and stable white-light emission are ideal for lighting applications, but photon emission covering the entire visible spectrum is difficult to achieve using a single material. Metal halide perovskites have outstanding emission properties2,3; however, the best-performing materials of this type contain lead and have unsatisfactory stability. Here we report a lead-free double perovskite that exhibits efficient and stable white-light emission via self-trapped excitons that originate from the Jahn-Teller distortion of the AgCl6 octahedron in the excited state. By alloying sodium cations into Cs2AgInCl6, we break the dark transition (the inversion-symmetry-induced parity-forbidden transition) by manipulating the parity of the wavefunction of the self-trapped exciton and reduce the electronic dimensionality of the semiconductor4. This leads to an increase in photoluminescence efficiency by three orders of magnitude compared to pure Cs2AgInCl6. The optimally alloyed Cs2(Ag0.60Na0.40)InCl6 with 0.04 per cent bismuth doping emits warm-white light with 86 ± 5 per cent quantum efficiency and works for over 1,000 hours. We anticipate that these results will stimulate research on single-emitter-based white-light-emitting phosphors and diodes for next-generation lighting and display technologies.
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              State of the Art and Prospects for Halide Perovskite Nanocrystals

              Metal-halide perovskites have rapidly emerged as one of the most promising materials of the 21st century, with many exciting properties and great potential for a broad range of applications, from photovoltaics to optoelectronics and photocatalysis. The ease with which metal-halide perovskites can be synthesized in the form of brightly luminescent colloidal nanocrystals, as well as their tunable and intriguing optical and electronic properties, has attracted researchers from different disciplines of science and technology. In the last few years, there has been a significant progress in the shape-controlled synthesis of perovskite nanocrystals and understanding of their properties and applications. In this comprehensive review, researchers having expertise in different fields (chemistry, physics, and device engineering) of metal-halide perovskite nanocrystals have joined together to provide a state of the art overview and future prospects of metal-halide perovskite nanocrystal research.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                The Journal of Physical Chemistry Letters
                J. Phys. Chem. Lett.
                American Chemical Society (ACS)
                1948-7185
                1948-7185
                October 21 2021
                October 07 2021
                October 21 2021
                : 12
                : 41
                : 10002-10008
                Affiliations
                [1 ]Department of Chemistry, Indian Institute of Science Education and Research (IISER), Pune, 411008, India
                Article
                10.1021/acs.jpclett.1c02973
                34618471
                1fe20d86-6466-4cb6-a90b-4cbd4f6ae5e5
                © 2021

                https://doi.org/10.15223/policy-029

                https://doi.org/10.15223/policy-037

                https://doi.org/10.15223/policy-045

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