Decoding Upconversion-Emitting Phase in Complex Composites Through Single-Particle-Level Upconversion Imaging and Density Functional Theory Calculations.

The crystal structure and phase stability of a host lattice plays an important role in efficient upconversion phenomena. In stable hosts, lanthanides doping should not generally change the crystal structure of the host itself. But when phase of a system drastically changes after lanthanide doping resulting in multiple phases, accurate identification of upconverting phase remains a challenge. Herein, an attempt to synthesize lanthanide-doped NiMoO4 by microwave hydrothermal method produced MoO3/Yb2Mo4O15/NiMoO4 micro-nano composite upconversion phosphor. A combined approach of density functional theory (DFT) calculations and single-particle-level upconversion imaging has been employed to elucidate the phase stability of different phases and upconversion properties within the composite. Through single-particle-level imaging under 980 nm excitation, an unprecedented resolution in visualizing individual emitting and non-emitting regions within the composite has been achieved, thereby allowing to accurately assign the Yb2Mo4O15 as a sole upconversion emitting phase in the composite. Result of the DFT calculation further shows that the Yb2Mo4O15 phase is the most thermodynamically preferred over other lanthanide-doped phases in the composite. This comprehensive understanding not only advances the knowledge of upconversion emission from composite materials but also holds promise for tailoring optical properties of materials for various applications, including bioimaging, sensing, and photonics, where controlled light emission is crucial.

Current status on synthesis, properties and applications of CsPbX3(X = Cl, Br, I) perovskite quantum dots/nanocrystals.

The quantum confinement effect and interesting optical properties of cesium lead halide (CsPbX3; X = Cl, Br, I) perovskite quantum dots (QDs) and nanocrystals (NCs) have given a new horizon to lighting and photonic applications. Given the exponential rate at which scientific results on CsPbX3NCs are published in the last few years, it can be expected that the research in CsPbX3NCs will further receive increasing scientific interests in the near future and possibly lead to great commercial opportunities to realize these materials based practical applications. With the rapid progress in the single-photon emitting CsPbX3QDs and NCs, practical applications of the quantum technologies such as single-photon emitting light-emitting diode, quantum lasers, quantum computing might soon be possible. But to reach at cutting edge of stable perovskite QDs/NCs, the study of fundamental insight and theoretical aspects of crystal design is yet insufficient. Even more, it has aroused many unanswered questions related to the stability, optical and electronic properties of the CsPbX3QDs. Aim of the present review is to illustrate didactically a precise study of recent progress in the synthesis, properties and applications of CsPbX3QDs and NCs. Critical issues that currently restrict the applicability of these QDs will be identified and advanced methodologies currently in the developing queue, to overcome the roadblock, will be presented. And finally, the prospects for future directions will be provided.

Ho-SiAlON Ceramics as Green Phosphors under Ultra-Violet Excitations.

In most inorganic phosphors, increasing the concentration of activators inevitably causes the concentration quenching effect, resulting in reduced emission intensity at a high level of activator doping and the conventional practice is to limit the activator concentration to avoid the quenching. In contrast, SiAlON ceramics preserve their chemical composition over a very wide range of doping of activator ions, which favors the adjustment and optimization of the luminescence properties avoiding concentration quenching. Here, we investigate the photoluminescence properties of Ho-doped SiAlON (Ho-SiAlON) ceramics phosphors prepared by the hot-press method. Ho-SiAlON ceramics show strong green visible (554 nm) as well as infrared (2046 nm) broadband downshifting emissions under 348 nm excitation. It is shown that there is no concentration quenching, even at a very high level of Ho doping. The emission intensity of the 554 nm band increased two-fold when the Ho concentration is doubled. The results show that the Ho-SiAlON ceramics can be useful for efficient green phosphors.