Phosphor-converted white light-emitting diodes (pc-WLEDs) are efficient light sources used in lighting, high-tech displays, and electronic devices. One of the most significant challenges of pc-WLEDs is the thermal quenching, in which the phosphor suffers from emission loss with increasing temperature during high-power LED operation. Here, we report a blue-emitting NaSc(PO):xEu phosphor (λ = 453 nm) that does not exhibit thermal quenching even up to 200 °C. This phenomenon of zero thermal quenching originates from the ability of the phosphor to compensate the emission losses and therefore sustain the luminescence with increasing temperature. The findings are explained by polymorphic modification and possible energy transfer from electron-hole pairs at the thermally activated defect levels to the Eu 5d-band with increasing temperature. Our results could initiate the exploration of phosphors with zero thermal quenching for high-power LED applications.

Organolead halide perovskites have emerged as a promising optoelectronic material for lighting due to its high quantum yield, color-tunable, and narrow emission. Despite their unique properties, toxicity has intensified the search for ecofriendly alternatives through partial or complete replacement of lead. Herein, we report a roomtemperature synthesized Mn 2+ -substituted 3D-organolead perovskite displacing ∼90% of lead, simultaneously retaining its unique excitonic emission, with an additional orange emission of Mn 2+ via energy transfer. A high Mn solubility limit of 90% was attained for the first time in lead halide perovskites, facilitated by the flexible organic cation (CH 3 NH 3 ) + network, preserving the perovskite structure. The emission intensities of the exciton and Mn were influenced by the halide identity that regulates the energy transfer to Mn. Homogeneous emission and electron spin resonance characteristics of Mn 2+ indicate a uniform distribution of Mn. These results suggest that low-toxicity 3D-CH 3 NH 3 Pb 1−x Mn x Br 3−(2x+1) Cl 2x+1 nanocrystals may be exploited as magnetically doped quantum dots with unique optoelectronic properties.

A moisture-stable, red-emitting fluoride phosphor with an organic hydrophobic skin is reported. A simple strategy was employed to form a metal-free, organic, passivating skin using oleic acid (OA) as a hydrophobic encapsulant via solvothermal treatment. Unlike other phosphor coatings that suffer from initial efficiency loss, the OA-passivated KSiF:Mn (KSF-OA) phosphor exhibited the unique property of stable emission efficiency. Control of thickness and a highly transparent passivating layer helped to retain the emission efficiency of the material after encapsulation. A moisture-stable KSF-OA phosphor could be synthesized because of the exceptionally hydrophobic nature of OA and the formation of hydrogen bonds (F···H) resulting from the strong interactions between the fluorine in KSF and hydrogen in OA. The KSF-OA phosphor exhibited excellent moisture stability and maintained 85% of its emission intensity even after 450 h at high temperature (85 °C) and humidity (85%). As a proof-of-concept, this strategy was used for another moisture-sensitive SrSiON:Eu phosphor which showed enhanced moisture stability, retaining 85% of emission intensity after 500 h under the same conditions. White light-emitting devices were fabricated using surface-passivated KSF and YAlO:Ce which exhibited excellent color rendering index of 86, under blue LED excitation.

In the past decades, solid-state lighting based on phosphors as energy converters has been a fast-growing industry. Phosphorconverted white light-emitting diodes (pc-wLEDs) enable high-power applications and miniaturization; for this, the phosphor must have good stability and high efficiency. In order to satisfy this demand, phosphor plates have been proposed instead of conventional organic-based phosphor binders. In this review, such phosphor plates are categorized according to their synthesis methods, and the advantages and disadvantages of each category are detailed. In addition, we describe the major aspects of phosphor plates that require improvement for applications in high-power devices. For the fabrication of high-power LEDs, the phosphor configuration, color purity, porosity, and particle size of glass powders are key properties to enhance the luminescence efficiency and reduce the generation of heat inside wLED packages, thereby improving thermal stability. The advent of authentic, energy-efficient lighting in the home and workplace significantly affected the modern way of life. Beginning with the mass production of incandescent light bulbs, and with the subsequent evolution of fluorescence lights, lighting technology has developed rapidly in the last few decades. Since Edison's incandescent bulb in 1879, 1 artificial lighting has been developed to increase power output and decrease the size of the system. The development of red light-emitting diodes (LEDs) in 1962 2 and blue LEDs in 1993 3 allowed innovation in lighting and display. In particular, combinations of blue LEDs and yellow phosphors are used for many applications because they can realize cheap and efficient white solid-state lighting with several advantages including long lifetimes, eco-friendly behavior, and the capacity of miniaturization. 4-6In phosphor-converted white LEDs (pc-wLEDs), the phosphor converter dispersed in silicon resin (phosphor-in-silicon; PiS) is directly packed on a blue InGaN chip.7 When driven by a bias current, the emitted blue light absorbed by the phosphor is emitted as yellow light; together with the transmitted blue light, this constitutes white luminescence. However, this method lacks a red component, which entails the drawbacks of a poor color rendering index (CRI) and limited correlated color temperature (CCT). To overcome these drawbacks, one proposed method mixes yellow phosphors with phosphors having green to red emissions under blue excitation. 8 In pc-wLEDs, the color is primarily determined by the ratio of the blue emission from the LED chip to the yellow to red emission from the phosphor. However, the efficacy and brightness are determined by the converted yellow to red emission, as it contributes the bulk of lumens. In this configuration, the heat generated from the LED chip and phosphor cannot be efficiently dissipated because of the poor thermal stability and weak thermal conductivity of the resin, which causes luminous decay and color shifting in white light-emitting diodes (wLEDs).9 When the tempe...

Zero-dimensional (0D) inorganic perovskites have recently emerged as an interesting class of material owing to their intrinsic Pb2+ emission, polaron formation, and large exciton binding energy. They have a unique quantum-confined structure, originating from the complete isolation of octahedra exhibiting single-molecule behavior. Herein, we probe the optical behavior of single-molecule-like isolated octahedra in 0D Cesium lead halide (Cs4PbX6, X = Cl, Br/Cl, Br) nanocrystals through isovalent manganese doping at lead sites. The incorporation of manganese induced phase stabilization of 0D Cs4PbX6 over CsPbX3 by lowering the symmetry of PbX6 via enhanced octahedral distortion. This approach enables the synthesis of CsPbX3 free Cs4PbX6 nanocrystals. A high photoluminescence quantum yield for manganese emission was obtained in colloidal (29%) and solid (21%, powder) forms. These performances can be attributed to structure-induced confinement effects, which enhance the energy transfer from localized host exciton states to Mn2+ dopant within the isolated octahedra.