Control of luminescence by tuning of crystal symmetry and local structure in Mn4+-activated narrow band fluoride phosphors

This work was supported by the Ministry of Science and Technology of Taiwan (Contract Nos. MOST 104-2113-M-002-012-MY3 and MOST 104-2923-M-002-007-MY3) and National Center for Research and Development Poland Grant (No. PL-TW2/8/2015). Y Jin thanks the National Nature Science Foundation of China (No. 11104366), Chongqing Research Program of Basic Research and Frontier Technology (No. cstc2014jcyjA50018), and the Scientific and Technological Research Program of Chongqing Municipal Education Commission (No. KJ1500913). T. Lesniewski would like to acknowledge the support of University of Gdansk Research Grant 538-5200-B468-17.Mn4+-doped fluoride phosphors have been widely used in wide-gamut backlighting devices because of their extremely narrow emission band. In this study, solid solutions of Na2(SixGe1-x)F6:Mn4+ and Na2(GeyTigros)F6:Mn4+ have been successfully synthesized to elucidate the behavior of zero-phonon line (ZPL) in different structures because of the sensitivity of ZPL intensity to the local coordinated environment. The structures of the products are examined by X-ray diffraction and Rietveld refinement. The ratio between ZPL and the highest emission intensity υ6 phonon sideband exhibits a strong relationship with luminescent decay rate. First-principles calculations are conducted to model the variation in the structural and electronic properties of the prepared solid solutions as a function of the composition. The calculated results are consistent with the experimentally determined structural parameters. To compensate for the limitations of Rietveld refinement, electron paramagnetic resonance and high-resolution steady-state emission spectra are used to prove the diverse local environment for Mn4+ in the structure. Finally, the spectral luminous efficacy of radiation (LER) is used to reveal the important role of ZPL in practical application.PostprintPeer reviewe

Growth and EPR properties of ErVO4 single crystals

Single crystals of ErVO4 were grown by the Czochralski method under ambient pressure in a nitrogen atmosphere. Obtained crystals were transparent with strong pink coloring. Electron paramagnetic resonance (EPR) spectra were recorded as a function of the applied magnetic field. Temperature and angular dependences of the EPR spectra of the samples in the 3–300 K temperature range were analyzed applying both Lorentzian––Gauss approximation for diluted medium and Dyson for dense magnetic medium. EPR-NMR program was done to find local symmetry and spin Hamiltonian parameters of erbium ions

Antimicrobial properties of pristine and Pt-modified titania P25 in rotating magnetic field conditions

Effective and cheap water purification is one of the most important tasks facing humanity. Among various methods of water treatment, heterogeneous photocatalysis is probably most recommended. However, the application of artificial sources of irradiation results in high investment and operating costs. Accordingly, either vis-responsive photocatalysts or different ways of photocatalyst activation should be developed. In the present study, rotating magnetic field (RMF) has been tested to inactivate gram-positive (Staphylococcus epidermidis) and gram-negative (Escherichia coli) bacteria in the presence of pristine and Pt-modified titania P25 photocatalyst. Liquid cultures of the bacteria have been exposed to the titania and RMF (RMF frequency of 1–50 Hz, RMF magnetic induction of ca. 19.92 mT, 180 min exposure time, temperature of incubation at 37 °C). It has been found that highly active titania photocatalyst might also work in the absence of photoirradiation but under RMF. Moreover, its modification with platinum besides highly improved photocatalytic activity (tested for two model reactions of oxidative decomposition of acetic acid and anaerobic dehydrogenation of methanol under UV/vis irradiation) results in significant enhancement of antimicrobial effect under RMF. Additionally, photocatalysts with larger content of oxidized forms of platinum show higher antimicrobial activity, and thus it is proposed that platinum oxides are more active than zero-valent platinum under RMF. This study provides evidence of antimicrobial effect of titania without photoirradiation, indicating that RMF might efficiently activate photocatalyst

A Long Cycle-Life High-Voltage Spinel Lithium-Ion Battery Electrode Achieved by Site-Selective Doping

© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Spinel LiNi0.5Mn1.5O4 (LNMO) is a promising cathode candidate for the next-generation high energy-density lithium-ion batteries (LIBs). Unfortunately, the application of LNMO is hindered by its poor cycle stability. Now, site-selectively doped LNMO electrode is prepared with exceptional durability. In this work, Mg is selectively doped onto both tetrahedral (8a) and octahedral (16c) sites in the Fd (Formula presented.) m structure. This site-selective doping not only suppresses unfavorable two-phase reactions and stabilizes the LNMO structure against structural deformation, but also mitigates the dissolution of Mn during cycling. Mg-doped LNMOs exhibit extraordinarily stable electrochemical performance in both half-cells and prototype full-batteries with novel TiNb2O7 counter-electrodes. This work pioneers an atomic-doping engineering strategy for electrode materials that could be extended to other energy materials to create high-performance devices

Ultra-Broadband Phosphors Converted Near-Infrared Light Emitting Diode with Efficient Radiant Power for Spectroscopy Applications

Copyright © 2019 American Chemical Society. Narrowing the size of near-infrared (NIR) spectrometers has gained substantial interest among researchers in both scientific and nonscientific communities due to the inherent usage in the nondestructive investigations, especially for foodstuff evaluation and human health monitoring. The immense size and deteriorating accessibility of traditional NIR light sources make the phosphor-converted NIR light-emitting diode (pc-NIR LED) with high radiant flux an alternative growing light source. In this work, the crystal structure of La3GaGe5O16 is solved for the actual crystallographic sites through a joint Rietveld refinement tool (X-ray diffraction and high-resolution neutron powder diffraction) and reporting for the ultrabroadband NIR luminescence (650-1050 nm) by doping with Cr3+ with the hyper-radiant power of 43.1 mW. It is noteworthy that the possible benchmarking radiant power of 65.2 mW is achieved by the chemical substitution of Gd3+ and Sn4+. The presence of multiple excited behavior states (multiple luminescent centers) of Cr3+ due to its intermediate crystal field resulted in broadening of the emission spectrum along with increased intensity. The nonexponential decay character of the R-line and broadband luminescence further confirms the observation of the multiple excited state. The findings of this work are discussed based on structural characterization and spectroscopic studies at different measurement environments, and the potentials of the phosphors are also demonstrated by the prototype pc-NIR LED packaging

Pentavalent Manganese Luminescence: Designing Narrow-Band Near-Infrared Light-Emitting Diodes as Next-Generation Compact Light Sources

Manganese in the pentavalent state (Mn5+) is both rare and central in materials exhibiting narrow-band near-infrared (NIR) emission and is highly sought after for phosphor-converted light-emitting diodes as promising candidates for future miniature solid-state NIR light source. We develop the Ca14Zn6Ga10-xMnxO35 (x = 0.3, 0.5, 1.0, 1.25, 1.5, and 3.0) series that exhibit simultaneous Mn4+ (650-750 nm) and Mn5+ (1100-1250 nm) luminescence. We reveal a preferential occupancy of Mn in regular octahedral and tetrahedral environments, with the short bond length between these responsible for luminescence. We present a theoretical spin-orbital interaction model in which breaking the spin selection rule permits the luminescence of Mn4+ and Mn5+. A total photon flux of 87.5 mW under a 7 mA driving current demonstrates its potential for real-time application. This work pushes our understanding of achieving Mn5+ luminescence and opens the way for the design of Mn5+-based narrow-band NIR phosphors