An efficient rare-earth free deep red-emitting GdGeSbO6:Mn4+ phosphor for white light-emitting diodes.

Red phosphors play an important role in improving the light quality and color rendering index of white light-emitting diodes (WLEDs) for lighting. In this paper, we report the transition ion Mn4+-activated deep red phosphor GdGeSbO6:x%Mn4+ and analyze its crystal structure, composition and luminescence behavior in detail. Its optimal doping concentration of Mn4+ is 0.3%. Under ultraviolet (UV) excitation, GdGeSbO6:0.3%Mn4+ produces a narrow emission peak centred at 682 nm in the range of 650-800 nm with a full width at half maximum (FWHM) of 25 nm, which is attributed to the spin-prohibited 2Eg → 4A2g transition of Mn4+ ions. Notably, the optimal phosphor GdGeSbO6:0.3%Mn4+ has a high internal quantum efficiency (IQE ≈ 65%) and excellent thermal stability performance (I423 K/I303 K ≈ 62%). The synthesis of high-performance warm WLEDs and full-spectrum WLEDs was achieved by combining and coating GdGeSbO6:0.3%Mn4+ phosphors with commercial phosphors on the surface of a 365 nm UV chip.

Temperature-controlled tunable emission of Bi3+-doped Rb2SnCl6 all-inorganic vacancy ordered lead-free perovskite for advanced anticounterfeiting.

At present, tuning the luminescence characteristics of phosphors by external physical stimuli such as temperature and pressure has attracted the interest of researchers. However, the emission-tunable luminescence processes by temperature or pressure in lead-free perovskite with ordered vacancy materials have not been systematically studied. In this study, Bi3+-doped Rb2SnCl6 crystals were successfully synthesized using a simple precipitation method, and these crystals demonstrated a remarkable enhancement of luminescence intensity compared with the unannealed ones at 140-200 °C, and with a red-shift in the emission peak from 450 to 500 nm. It was found that the annealing treatment increased the Bi-Cl bond length leading to emission red-shift and achieved the change in the emission intensity due to the band gap modulation of the material. Furthermore, a candidate material for the color-changing optical security strategies was obtained by combining the Bi3+-doped Rb2SnCl6 phosphor and printing ink. This work is a valuable reference for the rational design of luminescent perovskites with promising new functionalities and stimulates the great potential of luminescent perovskites in developing promising phosphors for advanced anticounterfeiting.

A new dual-ligand DUT-52-type metal-organic framework for ratiometric luminescence detection of aqueous-phase Cu2+ and Cr2O72.

Metal-organic frameworks (MOFs) are a unique class of multifunctional hybrid crystals that have been successfully utilized in diverse ranges of applications. However, since MOFs are prone to aqueous degradation, the development of stable luminescent MOF platforms in aqueous media is still a huge challenge. Here, a novel dual-ligand Eu3+/DUT-52-COOH composite is prepared based on the luminescent DUT-52 prototype structure via a dual-ligand strategy and a post-synthetic modification (PSM) method. The functionalized Eu3+/DUT-52-COOH material exhibits dual emission and good photothermal stability in aqueous media. Thus, Eu3+/DUT-52-COOH is developed as a ratiometric luminescent sensor to achieve highly selective and sensitive detection of Cu2+ and Cr2O72- in aqueous solutions and has a low detection limit of 3.43 µM and 25.7 nM, respectively. This work is one of the few cases of detecting Cu2+ and Cr2O72- in aqueous media based on a DUT-52, and the detection signals can be observed by the bare eye without using sophisticated analytical instruments. The possible sensing mechanism is discussed in detail. The results obtained in this project may provide broad prospects for developing smart sensing systems to accomplish highly efficient, easily operable and quantitative intelligent recognition of Cu2+ and Cr2O72-.

Excitation-Dependent Tunable White Light of ns2 Ions Doped Rb2SnCl6 Vacancy Ordered Double Perovskite.

Single-matrix white light-emitting diodes are still a challenge. Achieving tunable white light emission from lead-free perovskites attracts much attention. Herein, nanoscale Rb2SnCl6 (RSC) vacancy ordered double perovskite were synthesized by an optimized precipitation method. Further, using ns2 ions (Bi3+, Te4+, and Sb3+) doped RSC vacancy ordered double perovskite to obtain broadband blue, yellow-green, and orange-red emission. The color temperature adjustable high-quality white light emission based on the codoping strategy is obtained by controlling the doping ratio of Bi3+ and Te4+. Additionally, the white light-emitting diodes encapsulated by this single matrix white luminescent material exhibit excellent stability. Combined with theoretical calculations, it is elucidated that these high-efficiency emissions are not only derived from the unique electronic transition of ns2 ions but also related to the energy band properties and the crystal field. This work shows that ns2 ions doped RSC vacancy ordered double perovskite can meet the needs of different luminous colors and color temperature tunable white light emission. Meanwhile, it is a strong competitor to replace the lead-based perovskite.

An unusual red-to-brown colorimetric sensing method for ultrasensitive silver(I) ion detection based on a non-aggregation of hyperbranched polyethylenimine derivative stabilized gold nanoparticles.

Here we have developed a facile and rapid colorimetric method for the sensitive and selective detection of Ag(+) based on the non-aggregation of gold nanoparticles (Au NPs) capped with hyperbranched polyethylenimine derivatives. In the detection process, an unusual colour change from red to brown was observed due to the formation of Au-Ag core-shell nanoparticles, which was more sensitive than that of the usual colorimetric assays (red to blue) based on the aggregation of Au NPs. After the colour changed, the non-aggregation-based Au-Ag core-shell nanomaterials did not aggregate further and could remain stable for a long time, which was convenient to record, detect and observe. The sensing probe exhibited a drastically long observing time for detecting Ag(+) owing to the stability of the Au-Ag core-shell non-aggregates, high sensitivity with a low detection limit of 8.76 nM by the naked eye and 1.09 nM by using a UV-vis spectrophotometer and a good linear relationship within the range from 1.09 to 109 nM. The colour change of the system is very fast, occurring within 1 to 2 minutes. Moreover, the proposed method also showed a remarkably high selectivity toward Ag(+) and was successfully used in tap water and drinking water samples. Therefore, this unusual colorimetric assay based on the non-aggregation of Au NPs has a great potential as a simple, rapid, sensitive and selective detection method for the detection of Ag(+).