1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Double perovskite Cs 2AgInCl 6:Cr 3+: broadband and near-infrared luminescent materials

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          A Cr 3+-doped halide double perovskite Cs 2AgInCl 6:Cr 3+ is first reported which exhibits a broad near-infrared emission ranging from 850 to 1350 nm centered at 1010 nm with a FWHM of 180 nm.

          Abstract

          Searching for high performance and broader applications of inorganic halide perovskites has drawn extensive attention. In this work, a Cr 3+-doped halide perovskite, Cs 2AgInCl 6:Cr 3+, which exhibits broadband near-infrared (NIR) emission is first obtained via the traditional high temperature solid-state reaction. A broad emission band ranging from 850 to 1350 nm centered at 1010 nm with a full-width at half-maximum (FWHM) of 180 nm is assigned to the spin-allowed 4T 24A 2 transition of octahedrally coordinated Cr 3+ ions in a very weak crystal-field environment. The excitation bands centered at 353, 565 and 800 nm can be attributed to the absorption of the Cs 2AgInCl 6 host, the Cr 3+ d–d transitions of 4A 24T 1 and 4A 24T 2, respectively. Upon 760 nm excitation, the photoluminescence quantum yield (PLQY) of Cs 2AgIn 0.9Cl 6:0.1Cr 3+ is about ∼22.03%. Cs 2AgInCl 6:Cr 3+ phosphors with such broadband NIR emission have potential in phosphor converted light emitting diodes (pc-LEDs) which have applications in bioimaging and biomonitoring.

          Related collections

          Most cited references50

          • Record: found
          • Abstract: found
          • Article: not found

          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.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Crystal Growth of the Perovskite Semiconductor CsPbBr3: A New Material for High-Energy Radiation Detection

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Sunlight-activated long-persistent luminescence in the near-infrared from Cr(3+)-doped zinc gallogermanates.

              Visible-light persistent phosphors are being widely used as self-sustained night-vision materials because of their sufficiently strong and long afterglow (>10 h) and their ability to be excited by sunlight as well as room light. In contrast, persistent phosphors for near-infrared (NIR) wavelengths are lacking. Here we report a series of Cr(3+)-doped zinc gallogermanate NIR persistent phosphors that exhibit strong emission at 650-1,000 nm, extending beyond the typical 690-750 nm, and with a super-long afterglow of more than 360 h. These new NIR persistent phosphors are all-weather materials that can be rapidly, effectively and repeatedly charged by natural sunlight in almost all kinds of outdoor environment. Seconds to minutes of sunlight activation can result in more than two weeks of persistent NIR light emission. This new series of NIR persistent materials have potential applications in night-vision surveillance, solar energy utilization and in vivo bio-imaging.
                Bookmark

                Author and article information

                Contributors
                Journal
                ICFNAW
                Inorganic Chemistry Frontiers
                Inorg. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1553
                December 3 2019
                2019
                : 6
                : 12
                : 3621-3628
                Affiliations
                [1 ]The Beijing Municipal Key Laboratory of New Energy Materials and Technologies
                [2 ]School of Materials Sciences and Engineering
                [3 ]University of Science and Technology Beijing
                [4 ]Beijing 100083
                [5 ]China
                Article
                10.1039/C9QI00905A
                bdea274a-0e65-4089-a968-e9620233b3c4
                © 2019

                http://rsc.li/journals-terms-of-use

                History

                Comments

                Comment on this article