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The study on phosphors‐converted white light‐emitting diodes (pc‐WLEDs) using lead‐free double perovskites (DPs) as single‐component white phosphors is widely concerned. However, the photoluminescence quantum yields (PLQY) of white luminescence and color rendering index (CRI) of WLED are not satisfactory. Herein, a new Sb/Ho: Cs2Na0.9Ag0.1(In/Bi)Cl6 single‐component white phosphor with the highest PLQY of 93% and a record CRI of 97.4 is reported. Experimental data and theoretical calculations evidence that in addition to broadband yellow emission of the self‐trapped exciton (STE) recombination, the material also exhibits blue emission from Sb3+: 3P1→1S0 transition and red one assigned to Ho3+: 5F5→5I8 transition. Steady‐state and time‐resolved PL spectra verify the existence of two energy transfer channels from both Sb3+ and STE to Ho3+ dopants. As a demo, Sb/Ho: Cs2Na0.9Ag0.1(In/Bi) Cl6‐based WLED is constructed, showing excellent comprehensive optical performance with specially improved saturation red index R9 and blue one R12. This work provides a novel single‐component rare‐earth doped DP white phosphor for high CRI full‐spectrum solid‐state lighting. [ABSTRACT FROM AUTHOR]

Lead halide perovskite quantum dots (PeQDs) have garnered increasing attention due to their extraordinary optoelectronic properties. In recent years, femtosecond (fs) laser direct writing shows to be an effective way of inducing localized crystallization of PeQDs inside glass matrix while remaining their structural stability and optical performance. This article reviews the research progress on fs laser irradiation‐induced nucleation/growth of PeQDs in glass and discusses the latest advancements in the use of the technology for optical data storage, micrometer‐scale light‐emitting diode (LED), information security protection, and other related fields. It offers novel insights and perspectives for exploring new functionality and device application of fs laser‐printed PeQDs glass composite structures. [ABSTRACT FROM AUTHOR]

Eu2+‐doped phosphors have attracted the great attention of researchers in the past decade. However, Eu2+ dopant in inorganic hosts often suffers from the self‐oxidation effect, therefore causing the attenuated emission intensity and quantum efficiency. In this regard, developing Eu2+ doped phosphors with the prohibited self‐oxidation effect of Eu2+ and increased thermal stability is urgently required. Herein, an innovative cyan‐light emitting Li2CaSiO4:Eu2+/Eu3+, Lu3+ (LCSO) phosphor is designed. Both experimental results and theoretical calculations demonstrate that adding Lu3+ restricts the self‐oxidation of Eu2+ into Eu3+, thus improving the emission of Eu2+. Meanwhile, the Lu3+ introduction brings out excellent thermal stability. Finally, an efficient WLED with a color temperature (CCT) of 4573 K and a high color rendering index (Ra) of 84.2 is obtained using the as‐prepared phosphor due to the perfect compensation of the cyan light. As the introduction of Lu3+ improves the stability of Eu2+, a much greater difference in PL decay rate between Eu2+ and Eu3+ in LCSO is reached, thereby improving their sensitivity in temperature sensing. The strategy of Lu3+ introduction for prohibiting the self‐oxidation of Eu2+ for efficient and stable Eu2+ emission may stimulate some new ideas in designing high‐performance phosphors for more diverse applications. [ABSTRACT FROM AUTHOR]

Halogen‐mixed CsPb(Br/I)3 perovskite quantum dots (PeQDs) embedded glass can address the issue of stability, but suffers from low photoluminescence quantum yields (PLQYs) for the hindered in situ nucleation/growth inside the robust glass network. Uncovering the exact mechanism is highly desirable to develop high‐performance CsPb(Br/I)3@glass for commercial applications, but the topic remains unexplored. Here, based on femtosecond transient (fs‐TA) absorption, temperature‐dependent PL spectra, and theoretical calculations, a comprehensive understanding on heat‐treatment (HT) temperature‐induced modification of microstructures and carrier dynamics in the CsPb(Br/I)3@glass is build. It is evidenced that high‐temperature HT will promote more I− ions diffusion from glass matrix into CsPb(Br/I)3 lattice, leading to the retarded hot carrier (HC) cooling, and improved exciton recombination. This is attributed to the synergistic effect of the reduced effect carrier mass, the weakened carrier‐phonon coupling, the inhibited Klemens channel, and the eliminated defect states. Revealing these underlying mechanisms will empower to exert precise control and optimize PLQY of CsPb(Br/I)3@glass up to near unity. [ABSTRACT FROM AUTHOR]

Next‐generation high‐brightness lighting faces a big challenge in developing laser‐drivable color‐converting materials with effective thermal management. Herein, a new material architecture of Al2O3‐Y3Al5O12: Ce3+ (YAG: Ce) transparent composite ceramics coated with Al film (TCC@Al) is proposed. The as‐prepared material shows the highest thermal conductivity (29.3 W m−1 K−1) among YAG: Ce‐related transparent ceramics (TC) ever reported owing to the combination role of short‐range thermal conduction of Al2O3 microcrystals and long‐range thermal conduction of Al film. Temperature‐dependent photoluminescence (PL) spectra and femtosecond transient absorption (fs‐TA) spectra evidence the importance of thermal management, whereby the luminescent loss of TCC@Al is only 8.92% at 450 K and is far smaller than TC counterpart (15.86%). Importantly, no obvious luminescence saturation is detected upon 20 W mm−2 blue laser irradiation and the inhomogeneous angular color distribution is suppressed by the scatter of Al2O3 microcrystals, yielding uniform white light with ultra‐high luminous flux (LF) of 4294 lm@20 W mm−2 and luminous efficacy (LE) of 215 lm W−1. As a consequence, the present TCC@Al‐converted laser‐driven lighting prototype exhibits much better optical performance than the commercial TC‐based one. [ABSTRACT FROM AUTHOR]

White light‐emitting diodes (WLEDs) with high color‐rendering index (CRI, >90) are important for backlight displays and solid‐state lighting applications. Although the well‐developed colloidal quantum dots (QDs) based on heavy metals such as cadmium and lead are promising candidates for WLEDs, the low CRI still remains a significant limitation. In addition, the severe toxicity of heavy metals greatly limits their widespread use. Herein, the study demonstrates low‐cost and environmentally friendly carbon quantum dots (CQDs)‐based WLEDs that exhibit a high CRI of 94.33, surpassing that of conventional cadmium/lead‐containing QD‐based WLEDs. This achievement is attained through the employment of a binary host‐induced exciplex strategy. The high hole/electron mobility and suitable energy levels of the donor and acceptor give rise to a broadband orange–yellow emission stemming from the exciplex. As the host, the binary exciplex is capable of contributing blue and orange–yellow emission components while efficiently mitigating the aggregation‐induced quenching of CQDs. Meanwhile, CQDs effectively address the deep‐red emission gap, enabling the realization of CQDs‐based WLEDs with high CRI. These WLEDs also exhibit a remarkably low turn‐on voltage of 2.8 V, a maximum luminance exceeding 2000 cd m−2, a correlated color temperature of 4976 K, and Commission Internationale de l'Eclairage coordinates of (0.34, 0.32). [ABSTRACT FROM AUTHOR]

Developing violet‐light‐excitable deep‐red (650–660 nm) Eu2+‐activated phosphor is essential for full‐spectrum lighting. However, the related phosphors with facile synthesis, excellent optical performance, and superior thermal stability are scarce. Herein, a new class of (Sr,Ba)Lu2O4: Eu2+ deep‐red phosphor (660 nm) excitable by violet light via Ba2+‐induced local structure engineering is reported. Impressively, tunable emission from 615 to 682 nm, accompanied by significant improvement of thermal stability (81%@423 K), is achieved by partially substituting Sr2+ by Ba2+ in SrLu2O4: Eu2+. Crystal field analysis, density functional theory calculations, and thermoluminescence spectra confirm that the strong distortion and enhanced covalency of [EuO6] octahedron are responsible for spectral tunability, and the formation of shallow trapping states is beneficial for electron compensation to inhibit thermal quenching in the Sr0.85Ba0.15Lu2O4: Eu2+ phosphor. Finally, a white light‐emitting diode prototype fabricated by coupling of the Sr0.85Ba0.15Lu2O4: Eu2+ deep‐red phosphor and commercial blue/green phosphors with violet chip can yield sunlight‐like white light with an ultra‐high color rendering index (Ra = 95.2, R9 = 97.0) and an appropriate correlated color temperature of 4121 K, verifying its significant application potential in full‐spectrum solid‐state lighting. [ABSTRACT FROM AUTHOR]

Lead halide perovskite quantum dots (PeQDs) generally show slow hot carrier (HC) cooling because of the retarded relaxation of longitudinal optical (LO) phonons induced by hot phonon bottleneck effect. Although the feature is beneficial for designing photovoltaic devices beyond Schottky–Queisser limitation by manipulating HC excess energy, it would be hostile toward light‐emitting applications where fast HC cooling is preferred. Herein, a Ni2+ doping strategy is reported to effectively boost HC cooling in CsPbI3 PeQDs and inhibit Auger recombination, giving rise to near unity photoluminescent quantum yield (PLQY) for the Ni: CsPbI3 sample. Femtosecond transient (fs‐TA) absorption, temperature‐dependent PL spectra and theoretical calculations evidence that Ni2+ doping results in the enhancement of electron‐LO phonon coupling, the introduction of extra energy states at band edges, the increasement of effective carrier mass, and the modification of phonon dispersion spectra as well as density of states (DOS) of LO phonon modes. These synergistic roles ensure efficient Klemens decay within Ni: CsPbI3, which facilitates fast decay of hot phonons and break hot phonon bottleneck. These findings provide a valid route to tackle HC dynamics and pave a way for PeQDs‐based efficient light‐emitting applications. [ABSTRACT FROM AUTHOR]

Perovskite quantum dots (PeQDs) are seen as the credible alternative to traditional QDs ascolor converter in liquid crystal display (LCD). Unfortunately, PeQDs sufferfrom instability and color separation, and the prepared PeQDs enhanced films(PQDFs) need the protection of expensive barrier layers, which significantly increases price and limits their application. Herein, large‐area yellow monolithic PQDF is fabricated with both green CsPbBr3 and red CsPbBr1I2QDs encapsulated in the dual matrices of inorganic glass and polypropylene (PP) via an industrialized melt extruding & rolling method. The PQDF shows high photoluminescence quantum yield (PLQY) of 92% and narrow full width at half maximum (FWHM) of 19 nm (green) and 33 nm (red). Importantly, the bare PQDF without barrier layers can pass harsh aging test at 85 °C/85% RH and reach anoperating T90 lifetime over 1000 h. Finally, a white backlit unit is designed by coupling yellow monolithic PQDF with blue light guide panel, and the constructed prototype display shows superior color rendering performance forits narrow green/red emissions, reaching a color gamut of 110% National Television System Committee (NTSC). This work provides a novel and easy‐to‐industrialize route to prepare PQDFs to realize their commercial application in backlit display. [ABSTRACT FROM AUTHOR]

Currently, narrowband light‐convertor is critically urgent for preeminent color representation in lighting and display fields, however, the development of target materials still remains challenging. Herein, glass ceramic (GC) composite based on in situ glass crystallization, where the condense glass network structure acts as effective obstructors for long distance ion diffusion, is elaborately designed to inhibit activators' multi‐sites occupation for acquiring narrowband emitting. Following this strategy, an unprecedented narrowband blue emission of Eu2+‐activators with a peak at 447 nm and full‐width of half maximum (FWHM) of ≈30 nm is developed in a new type of Sr5(PO4)3Cl (SPOCl) GC composite. The Eu2+‐activators' hindered diffusion inside the GC composite makes preferential and limit occupation of the [Sr1O9] sites, enabling narrowband blue luminescence. Furthermore, the GC composite highlights remarkable performance in high‐power violet‐excitable full‐spectrum lighting and transparent display (TD) prototype fields, due to its high color purity (≈98.1%), photoluminescence quantum field (PLQY, ≈80.5%) and thermal stability (≈82.1%@150 °C). This work not only promotes the profound understanding of the relationship between light manipulation and glass crystallization, but also paves the way toward the implementation of high‐quality lighting and display of GC composites. [ABSTRACT FROM AUTHOR]

Orthogonal three‐color luminescence materials designed based on lanthanide doping multi‐component nano‐systems have exhibited great potential in volume display technology. Previous studies devoted to integrate the different color emitters within a single core‐shell nanoparticle, which suffers complexity in synthesis and difficulty in repeatability. In this work, an alternative is proposed. Three kinds of upconversion nanocrystals (UCNCs) with relatively simple configurations are prepared separately. Each kind of nanocrystals takes charge of emit a specific color upon one particular excitation (i.e., 808, 980, and 1540 nm pumps). Luminescent property of the mixture containing these nanocrystals are investigated. Excitation wavelength driven orthogonal three‐color luminescence property is found in this mixture. With the combination excitation, the emission color can be modulated, covering a gamut with its aera of 110% sRGB, superior to the previous reports. In addition, a quantized strategy to evaluate the orthogonality of the luminescence is also proposed, which will be useful for the further investigation and development of remote‐type controlled luminescent materials. Finally, the demonstration of colored 3D display application is conducted and presented in this work. [ABSTRACT FROM AUTHOR]

Laser‐driven projection display puts forward urgent demand for color converter materials to simultaneously achieve balanced‐spectrum properties and strong heat dissipation. Herein, this work develops a novel optofunctional composite by coupling Y3Al5O12:Ce3+ transparent ceramics (TC) with CaAlSiN3:Eu2+ phosphor‐in‐glass film (PiGF) for the first time. Remarkably, this new material architecture design enables a balance between the spectrum properties and heat dissipation ability, and can yield high‐quality white light with brightness of over 2500 lm, luminous efficacy (LE) of over 200 lm W−1, correlated color temperature (CCT) of 3700–4100 K, and improved color rendering index (CRI) of 60–70. Furthermore, the PiGF@TC‐converted laser projection system is also successfully designed, showing natural and real color restoration. Additionally, the combined action of thermal quenching and optical excitation intensity quenching is confirmed for the luminescence saturation upon high‐power blue laser driven. The main mechanism of optical quenching is identified to be energy upconversion dominated by second‐order nonlinear processes. The findings described here suggest a step toward developing the admirable laser‐driven color converters for next‐generation lighting sources. [ABSTRACT FROM AUTHOR]

Robust amorphous glass protected CsPbBr3 (CsPbBr3@glass) perovskite quantum dots (PeQDs) with ultra‐pure green emission and superior long‐term stability are highly desirable for developing wide‐color‐gamut liquid crystal displays. However, most of the reported CsPbBr3@glass nanocomposites are subject to low external quantum efficiency (EQE). This work demonstrates that ZrO2 additive has an "accumulation" effect on the borosilicate glass network structure to promote in situ nucleation/growth of PeQDs inside glass rather than self‐crystallization. This effect is beneficial in reducing surface defects, improving the quality of PeQDs, and thus boosting radiative recombination of excitons. As a consequence, the as‐prepared CsPbBr3@glass shows a record EQE of up to 75% and can pass the accelerated aging tests at 85 °C/85% RH for 1000 h and blue light irradiation over 2000 h. Finally, a prototype display using CsPbBr3@glass‐based straight‐down backlit unit is designed and gains more favorable responses in blind selection tests for its high brightness of 2647 cd m−2 and high color purity of 88%. The findings will pave the way for realizing the commercial application of CsPbBr3@glass nanocomposite in PeQDs‐converted backlit display. [ABSTRACT FROM AUTHOR]

The complex and high‐precision patterning of perovskite quantum dots (PeQDs) is of vital importance for exploring their new functionalities and device applications. In this work, a strategy based on the combination femtosecond (fs) laser‐irradiation and humidity‐control is reported to construct patterns of cyan CsPb(Cl/Br)3 PeQDs in a transparent glass medium. Benefiting from their ionic crystal feature and low formation energy, CsPb(Cl/Br)3 PeQDs can be locally crystallized and decomposed via fs laser irradiation without further heat‐treatment. More notably, it is found that a water molecule is able to affect the growth of CsPb(Cl/Br)3 PeQDs in glass. By modulation of relative humidity in air, the selectively decomposed perovskite structure is spontaneously regenerated, and the highly emissive CsPb(Cl/Br)3 PeQDs can be in situ manufactured in the confined glass region. This allows for reversible luminescence from the same patterns of laser printing‐erasing‐recovering, and the process can be repeated for multiple cycles without destruction of optical performance and robustness. The results provide a flexible method to develop new encryption/decryption technology for information security and anti‐counterfeiting. [ABSTRACT FROM AUTHOR]

Currently, lanthanide (Ln3+) doped Pb‐free double perovskites (DPs) suffer from competitive emissions of the self‐trapped exciton (STE) and Ln3+. Herein, a new type of Nd3+‐doped Cs2AgInCl6 DPs with Na+/Bi3+ co‐alloying is developed. Benefiting from Na+/Bi3+‐induced local structural modification, both STE broadband visible luminescence and Nd3+ near‐infrared (NIR) emissions are boosted via free exciton sensitization. Specifically, a total 648‐fold enhancement in emitting intensities compared to the Na+/Bi3+‐free counterpart is realized, with a significantly improved NIR photoluminescence quantum yield (PLQY) from 0.16% to 30.3%. First‐principles density functional theory calculations, Raman spectra, and steady/transient‐state PL spectra verify the modification of local site symmetry, breakdown of parity‐forbidden absorption, and reduction of electron‐phonon coupling via Na+/Bi3+ doping. Finally, a compact vis–NIR broadband light‐emitting diode (LED) is designed by coupling the Na/Bi/Nd: Cs2AgInCl6 DP with a commercial ultraviolet LED chip, which shows promising applications in spectroscopic analyses and multifunctional lighting. [ABSTRACT FROM AUTHOR]

Laser‐driven projector puts forward urgent demand for light‐conversion materials to achieve high‐quality image display. Herein, a composite structure phosphor‐in‐glass film (PiGF) is fabricated via screen‐printing YAG:Ce and low‐melting glass on the alumina substrate. Benefited from well‐retained optical properties of YAG:Ce in amorphous glass and high thermal conductivity of substrate, PiGF can produce desirable luminous flux of 7169 lm and luminous efficiency of 192 lm W−1 at saturation threshold of 13.25 W mm−2. Furthermore, it is demonstrated that thermal management by using a cool fan with aluminum heat sink is essential to reduce heat aggregation and improve white‐light stability of PiGF‐based laser lighting source operated in a reflective mode. Accordingly, a PiGF‐converted laser projection system is successfully designed for the first time, showing more vivid and brighter display feature benefited from high laser‐driven luminance of LCD screen (2180 cd m−2). This work highlights the practical application of PiGF@alumina‐substrate composite as an efficient laser‐driven color converter in high‐brightness projection display. [ABSTRACT FROM AUTHOR]

High‐quality backlit display puts forward urgent demand for color‐converting materials. Recently, metal halide perovskites (MHPs) with full spectral tunability, high photoluminescence quantum yields (PLQYs), and high color purity have found potential application in wide‐color‐gamut display. Regrettably, naked MHPs suffer from long‐term instable issue and cannot pass harsh stability tests. Herein, amorphous‐glass‐protected green/red CsPbX3 quantum dots (QDs) are prepared by elaborately optimizing glass structure, perovskite concentration, and in situ crystallization. PLQYs of green CsPbBr3@glass and red CsPbBr1.5I1.5@glass reach 94% and 78%, respectively, which are the highest ones of CsPbX3@glass composites reported so far and comparable to colloidal counterparts. Benefited from complete isolation of QDs from external environment by glass network, CsPbX3@glass can endure harsh commercial standard aging tests of 85 °C/85%RH and blue‐light‐irradiation, which are applied to construct white light‐emitting diodes (wLEDs) with high external quantum efficiency of 13.8% and ultra‐high luminance of 500 000 cd m−2. Accordingly, the perovskite wLED arrays‐based backlit unit and a prototype display device are designed for the first time, showing more vivid and wide‐color‐gamut feature benefited from narrowband emissions of CsPbX3 QDs. This work highlights practical application of CsPbX3@glass composite as an efficient and stable light color converter in backlit display. [ABSTRACT FROM AUTHOR]

Laser‐driven projection display puts forward urgent demand for color converter materials to achieve wide‐color‐gamut and high‐quality image presentation. In this study, a hierarchical structure quantum dots‐in‐glass film (QiGF) is fabricated via co‐sintering stable green/red‐emitting CsPbX3@glass (X3 = Br3, Br1.5I1.5) and commercial low‐melting glass on the sapphire substrate. Benefiting from the well‐retained optical properties of CsPbX3 quantum dots in amorphous glass and high thermal conductivity, QiGF succeeded in inhibiting luminescence saturation after 20 W mm−2 blue laser irradiation. A brand‐new white‐lighting source designed by coupling a blue laser with a pattern "QiGF wheel" produced ultra‐narrow blue/green/red tri‐color emissions and total luminous flux of 146 lm. Accordingly, a QiGF‐converted laser projection system is successfully designed for the first time, showing more natural and real color restoration for its wide color gamut display feature (157% of conventional light‐emitting diode projection and 107% of NTSC standard). The present study highlights the practical application of CsPbX3 quantum dots composite as an efficient laser‐driven color converter in projection display. [ABSTRACT FROM AUTHOR]

New antiviral influenza treatments can effectively alleviate illness while reducing viral shedding. However, how such effects can translate into lower population infections of seasonal influenza in China remains unknown. To shed light on the public health impacts of novel antiviral agents for influenza, we constructed a dynamic transmission model to simulate the seasonal influenza epidemics in China. Two antivirus treatments, baloxavir and oseltamivir, were evaluated by estimating their impacts on the incidences of influenza infection in a single flu season. In the base‐case analysis of a 10% antiviral treatment uptake rate, 2760 and 3420 per 10 000 persons contracted influenza under the treatment of baloxavir and oseltamivir, respectively. These incidence rates amounted to an 18.90% relative risk reduction (RRR) of infection associated with baloxavir in relation to oseltamivir. The corresponding RRR was 82.16% when the antiviral treatment uptake rate was increased to 35%. In addition, the peak of the prevalence of infected individuals per 10 000 persons under the baloxavir treatment was 177 (range: 93–274) fewer than that of oseltamivir. Our analyses suggest that the baloxavir treatment strategy reduces the incidence of influenza in China compared with oseltamivir in the setting of a seasonal flu epidemic. Also, increasing the uptake rate of antiviral treatment can potentially prevent millions of infections during a single flu season. [ABSTRACT FROM AUTHOR]

Currently, advanced optical security techniques are imminent in response to the increasingly rampant counterfeit and pirated goods on a global scale. Herein, hexagonal Na(NdxY1−x)F4 (x = 0–1) solid‐solution nanocrystals (NCs) embedded glasses are successfully fabricated via in situ glass crystallization. Benefited from the protection of inorganic glass, Na(NdxY1−x)F4 NCs exhibit superior long‐term stability and can endure high‐power 808 nm laser irradiation. Importantly, opposite variations between near‐infrared (NIR) luminescence and laser‐induced temperature can be detected for the nanocomposites, which are sensitive to Nd3+ doping concentration. As a proof‐of‐concept experiment, Nd3+ concentration dependent anti‐counterfeiting patterns with high‐concealment and high‐precision are designed and show bright emission and dimmish thermal images in Nd3+‐tenuous composites under the irradiation of 808 nm laser, while opposite displays can be achieved in Nd3+‐enriched one. This kind of information encryption triggered by a commercial single light source to achieve dual opposing displays in one material can effectively improve security in anti‐counterfeiting. [ABSTRACT FROM AUTHOR]

Elaborate engineering of emitting wavelength of green down‐converter in the spectral range of ≈525–535 nm with narrow full‐width at half‐maximum (fwhm < 25 nm) is an essential prerequisite for faithfully reproducing colors in the quantum dot (QD)‐based backlit display. Herein, different from the previous complex synthesis for green films, FAPbBr3 perovskite QDs films are fabricated by a dual‐additive assisted in situ growth strategy. Both C6H5CH2CH2NH3+ and 1,4,7,10,13,16‐hexaoxacyclooctadecane additives are introduced to synergistically tune green emitting (≈525–535 nm) with the narrowest fwhm down to 21 nm and the highest photoluminescence quantum yield (PLQY) up to 99%. Improved nanocomposite film with excellent long‐term stability is used to construct a prototype liquid crystal display (LCD) with a wide color gamut (118% National Television System Committee and 88% Recommendation BT 2020), a high saturation, and a remarkable color rendition. The performance is superior to that of the commercial white‐LED‐based LCD, showing a great potential of the present green film for high‐definition display application in the future. [ABSTRACT FROM AUTHOR]

Currently, exploiting luminescent materials with super thermal stability and high luminous efficiency are highly urgent to meet the needs of fast developing high‐power solid‐state lighting (SSL). Glass ceramic (GC) bulk material is an optimal medium with rigid glass network structure and controllable glass crystallization. Herein, an in situ glass crystallization strategy combined with self‐reduced Eu2+ is developed to fabricate Eu2+ doped NaAlSiO4 (NASO) GC composites in air. Structural and spectroscopic characterizations verify that the in situ precipitated NASO nanocrystals with high crystallization density can accommodate Eu2+ emitting centers in the same glass region, which facilitates the separation of Eu2+ dopants from glass into crystalline lattice without the requirement of long‐distance ionic diffusion and provides strong crystal‐field environment for Eu2+ 5d‐4f transition. Particularly, the present composites can produce intense greenish‐yellow emission with apparent photoluminescence quantum yield (PLQY) of ≈70%, intrinsic PLQY of ≈100%, superior thermal stability with 90% PL remained at 150 °C and excellent water‐resistance. Employing NSAO: Eu2+ GC as a color converter, the performance of constructed light‐emitting diode (LED)/laser diode (LD) lighting devices is extraordinary and stable during long‐term working. These findings would expand the application of GC composites and open up new avenues for exploration of novel GC materials and glass crystallization strategies. [ABSTRACT FROM AUTHOR]

Aims: The present study aimed to evaluate the cost‐effectiveness of the 5‐day remdesivir regimen compared with standard of care among severe COVID‐19 patients in China, the evidence on which is essential to inform the necessity of securing access to remdesivir. Methods: A dynamic transmission model that extended the susceptible–exposed–infected–recovered framework by incorporating asymptomatic, presymptomatic and waiting‐to‐be‐diagnosed patients was constructed to conduct the cost‐effectiveness analysis from the healthcare system perspective. To estimate epidemic parameters, the model was first calibrated to the observed epidemic curve in Wuhan from 23 January to 19 March 2020. Following the calibration, the infected compartment was replaced by 3 severity‐defined health states to reflect differential costs and quality of life associated with disease gravity. Costs and quality‐adjusted life year (QALY) outcomes of 9 million simulated people were accrued across time to evaluate the incremental cost‐effectiveness ratio of remdesivir. As robustness checks, an alternative modelling technique using decision tree, additional epidemic scenarios representing different epidemic intensities, and 1‐way parameter variations were also analysed. Results: Remdesivir treatment cost CN¥97.93 million more than standard of care. Also, the net QALY gain from 5‐day remdesivir treatment was 6947 QALYs. As such, the incremental cost‐effectiveness ratio was CN¥14 098/QALY, substantially lower than the gross domestic product per capita threshold. The peak daily number of severe cases was 19% lower in the remdesivir treatment strategy. Overall, results were robust in alternative scenarios and sensitivity analyses. Conclusion: Given the cost‐effectiveness profile, access to remdesivir for severe COVID‐19 patients in China should be considered. [ABSTRACT FROM AUTHOR]

Several randomized clinical trials (RCTs) that investigated the effectiveness of remdesivir for the treatment of coronavirus disease‐2019 (COVID‐19) have generated inconsistent evidence. The present study aimed to synthesize available RCT evidence using network meta‐analyses (NMAs). Both blinded and open‐label RCTs in PubMed database from inception to 7 June 2020 that contained "remdesivir", "Covid‐19", and "trial" in the abstracts conducted on hospitalized COVID‐19 persons were identified and screened. The studies must have at least one remdesivir arm and evaluated one of the pre‐specified outcomes. The outcomes were clinical improvement between days 10 to 15 after randomization and clinical recovery during the follow‐up period. The identified literature was supplemented with relatively recent studies that were known to the researchers if not already included. Frequentist NMAs with random effects were conducted. Both 10‐day and 5‐day remdesivir regimens were associated with higher odds of clinical improvement (odds ratio [OR] of 10‐day regimen: 1.35, 95% confidence interval [CI], 1.09‐1.67); OR of 5‐day regimen: 1.81, 95% CI, 1.32‐2.45, and higher probabilities of clinical recovery (relative risk [RR] of 10‐day regimen: 1.24, 95% CI, 1.07‐1.43; RR of 5‐day regimen: 1.47, 95% CI, 1.16‐1.87 compared with placebo. Remdesivir may have clinical benefits among hospitalized COVID‐19 persons. Highlights: Remdesivir has benefit of clinical improvement and clinical recovery among hospitalized Covid‐19 patients. Remdesivir may be recommended among hospitalized Covid‐19 patients. Evidence on mortality benefit and safety profiles of remdesivir is needed in future. [ABSTRACT FROM AUTHOR]

Owing to the conventional phosphor‐converted white LEDs (pc‐WLEDs) generally suffer from blue‐green cavity, thus, developing an appropriate phosphors covering both the blue and green regions in their emission spectra are very urgent. Herein, a novel Sc silicate phosphor, KBaScSi2O7:Eu2+ (KBSS:Eu2+), has been successfully designed and prepared via a solid‐state reaction. The crystal structure, luminescent properties, thermal quenching, quantum efficiency as well as its application in UV‐pumped WLEDs have been investigated systematically. The KBSS:Eu2+ phosphor exhibits a strong and broad excitation band ranging from 290 to 450 nm, and gives a sufficient cyan emission of 488 nm with a full‐width half‐maximum (FWHM) of 70 nm, which filled the blue‐green cavity. Importantly, the optimized KBSS:Eu2+ phosphor possesses an ultrahigh quantum efficiency (QE) up to 91.3% and an excellent thermal stability retaining 90% at 423 K with respect to that measured at room temperature. Finally, the as‐fabricated UV‐based WLEDs device, with only coupled the mixture of KBSS:Eu2+ cyan phosphor and CaAlSiN3:Eu2+ red ones to a commercial 365nm UV chip, exhibits a satisfactory color‐rendering index (Ra = 88.6), correlated color temperature (CCT = 3770K), and luminous efficiency (LE = 21 lm/W). [ABSTRACT FROM AUTHOR]

Abstract: Yb/Er doped hexagonal β‐NaLnF4 (Ln = Gd, Y, Lu) are regarded as the most efficient green upconversion (UC) materials. Unfortunately, β‐NaLnF4 is quite difficult to grow as monocrystal owing to cubic‐to‐hexagonal phase transition during cooling. As an alternative, herein a nanocrystallization controllable strategy to synthesize monodisperse whole‐family β‐NaLnF4 (from NaLaF4 to NaLuF4) embedded bulky glass ceramics is reported. A series of structural and spectroscopic characterizations indicate that Na content and Al/Si ratio are the most important factors to determine phase‐selective NaLnF4 crystallization in the aluminosilicate oxyfluoride glasses. Impressively, such nanocomposites are evidenced to be ideal hosts for upconversion luminescence of Yb3+/Er3+ dopants and as the proof‐of‐concept experiments, their applications in a random laser and incoherent LED‐excitable upconverting device as emitting media are demonstrated. It is expected that this study will provide a deep understanding for controllable crystallization in glass and extend the practical applications of glass ceramics in optoelectronic fields. [ABSTRACT FROM AUTHOR]

Transparent glass-ceramics containing Ce3+: Y3Al5O12 phosphors and Eu3+ ions were successfully fabricated by a low-temperature co-sintering technique to explore their potential application in white light-emitting diodes (WLEDs). Microstructure of the sample was studied using a scanning electron microscope equipped with an energy dispersive X-ray spectroscopy. The impact of co-sintering temperature, Ce3+: Y3Al5O12 crystal content and Eu3+ doping content on optical properties of glass-ceramics were systematically studied by emission, excitation spectra, and decay curves. Notably, the spatial separation of these two different activators in the present glass-ceramics, where Ce3+ ions located in YAG crystalline phase while the Eu3+ ones stayed in glass matrix, is advantageous to the realization of both intense yellow emission assigned to Ce3+: 5 d→4 f transition and red luminescence originating from Eu3+: 4 f→4 f transitions. As a result, the quantum yield of the glass-ceramic reached as high as 93%, and the constructed WLEDs exhibited an optimal luminous efficacy of 122 lm/W, correlated color temperature of 6532 K and color rendering index of 75. [ABSTRACT FROM AUTHOR]

After coating 20 Yb/2 Er:NaGdF4 core nanocrystals with a NaYbF4 shell, upconversion emission of the rare earth ions weakens. So far, the exact reason for this phenomenon is still unclear due to lack of the direct evidence. In this report, a core@shell@shell sandwich-like structure is designed and fabricated to investigate this phenomenon. We find that high Yb3+ concentration in the shell has mainly two adverse impacts: it promotes not only the deleterious back energy transfer from Er3+ in the core to Yb3+ in the shell but also the energy transfer from Yb3+ in the core to Yb3+ in the shell. To obtain nanocrystals with high upconversion efficency, appropriate Yb3+ concentration should be introduced into the shell or the transition layer. [ABSTRACT FROM AUTHOR]

The requirement of using ultraviolet light to stimulate afterglow luminescence has seriously restricted indoors/outdoors applications of most persistent materials developed hitherto. Herein, efficient blue-light-activated Ce3+, Pr3+: YAGG phosphors, showing optimized long-persistent luminescence lasting for 1 h, were prepared and investigated in detail with the aid of X-ray diffraction refinement, steady-state/persistent photoluminescence spectra, room/low-temperature persistent decay curves, and three-dimensional thermo-luminescence spectra. Notably, the afterglow properties were found highly dependent on the Ga content which greatly alters both the host band gap energy and the Ce3+: 5 d level structure and thus is beneficial to the electrons' photoionization and trapping processes. Moreover, Pr3+ additive was found not only prolonged the afterglow lifetime of Ce3+ through improving concentration of carriers captured at the trap, but also served as the red-emissive centers for color tuning. The persistent energy transfer from Ce3+ to Pr3+ was experimentally demonstrated for the first time. [ABSTRACT FROM AUTHOR]

Cr3+-doped SrGa12O19 is demonstrated to be a broadband near-infrared (650-950 nm) long-persistent phosphor whose luminescence can last for more than 2 h after ultraviolet irradiation is stopped. Detailed analysis of the photoluminescence and thermoluminescence spectra and of the persistent decay behavior of the Cr3+-doped SrGa12O19 samples indicate that the persistent energy transfer from the SrGa12O19 host to the Cr3+ ions and the filling and release of electrons into and from the shallow and deep traps through the conduction band is responsible for the long-persistent phosphorescence. [ABSTRACT FROM AUTHOR]

Upon introducing Ca2+ dopants into the grain lattices by substituting Gd3+ ions, irregular Yb/Er:NaGdF4 nanocrystals prepared through a simple solvothermal route convert into highly uniform nanorods. Meanwhile, their upconversion luminescence intensifies by about 200 times, probably due to a modification of the crystal structure of NaGdF4 and an improvement in the crystallinity of the nanophase. [ABSTRACT FROM AUTHOR]

Currently, the major commercial white light-emitting diode (WLED) is the phosphor-converted LED made of the InGaN blue-emitting chip and the Ce3+:Y3Al5O12 (Ce:YAG) yellow phosphor dispersed in organic epoxy resin or silicone. However, the organic binder in high-power WLED may age easily and turn yellow due to the accumulated heat emitted from the chip, which adversely affects the WLED properties such as luminous efficacy and color coordination, and therefore reduces its long-term reliability as well as lifetime. Herein, an innovative luminescent material: transparent Ce:YAG phosphor-in-glass (PiG) inorganic color converter, is developed to replace the conventional resin/silicone-based phosphor converter for the construction of high-power WLED. The PiG-based WLED exhibits not only excellent heat-resistance and humidity-resistance characteristics, but also superior optical performances with a luminous efficacy of 124 lm/W, a correlated color temperature of 6674 K and a color rendering index of 70. This easy fabrication, low-cost and long-lifetime WLED is expected to be a new-generation indoor/outdoor high-power lighting source. [ABSTRACT FROM AUTHOR]

In situ growth of CsPbX3 (X = Cl, Br, I) perovskite quantum dots (PeQDs) in inorganic glass can address their stability issue for wide‐color‐gamut full‐color backlit displays. However, most of the reported CsPbX3 precipitated in glass are limited by low absorption and low external quantum efficiency (EQE). This work demonstrates that CaO additive can adjust the polymerization of borosilicate glass network, and promote the precipitation of whole‐family CsPbX3 PeQDs in glass with a record absorption efficiency above 75%. As a result, the as‐prepared green and red CsPbX3@glass (X3 = Br3, Br1I2) exhibit high EQEs of 75% and 67%, and can pass harsh stability tests after immersing water, irradiating by intensive blue light and experiencing 85 °C/85%RH aging over 1000 h owing to effective protection of PeQDs from external environment with the help of robust glass matrix. As a proof of concept, a white backlit module is fabricated by coupling a single‐layer yellow PeQDs enhanced film (PQDF) with blue light guide panel, and the designed prototype display device with wide color gamut of 115% of the NTSC 1953 exhibits a more realistic and vivid color images. This work will pave the way for the realization of commercial application of ultra‐stable CsPbX3@glass in QD‐backlight displays. [ABSTRACT FROM AUTHOR]

Next‐generation high‐brightness laser lighting confronts a key challenge in preparing static color‐converting materials with remarkable luminescence saturation. Herein, a novel architecture of transmissive Y3Al5O12: Ce3+ (YAG) phosphor‐in‐glass film (PiGF) with double‐sided sapphires, i.e., a sandwich structured sapphire@PiGF@sapphire (S@PiGF@S) composite, is designed and fabricated by a thermocompression sintering technology. This kind of material can tolerate high laser power density (LPD) for the efficient double‐sided thermal channels and the high‐energy laser spot away from the PiGF emitting layer. As a consequence, the optimized S@PiGF@S color converter yields white light with a high luminous flux (LF) of 7602 lm at a record luminescence saturation threshold of 46.47 W·mm−2 benefiting from its low working temperature of merely 284 °C, which is 6.3 times that of traditional PiGF@sapphire color converter (1205 lm@10.89 W·mm−2). These findings verify that the developed S@PiGF@S color converter enables preferably optical‐thermal performances for promising applications in high‐brightness laser lighting. [ABSTRACT FROM AUTHOR]

Flexible regulation of local chemistry and band gap of perovskite quantum dots (PeQDs) is crucial for exploring their new functionalities and device applications. In this work, a strategy based on the combination of femtosecond (fs) laser‐irradiation and thermal treatment to effectively manipulate chemical composition and emitting wavelength of PeQDs in amorphous glass, is reported. The engineering of ultrafast laser‐induced thermal effect enables to induce in situ nucleation/growth of dual‐phase PeQDs within an individual glass matrix. By elevating heat‐treatment (HT) temperature, I− ions are driven to surmount the diffusion barrier into the PeQDs lattice, leading to a tunable emission wavelength ranging from 613 to 647 nm. Besides, it is verified that the temperature‐dependent diffusion rate of I− ions plays a pivotal role in affecting luminescent efficiency and color of the dual‐phase glass. Finally, fs laser direct writing of multi‐color patterns is presented, which provides a flexible method to develop new encryption/decryption technology for information security and anti‐counterfeiting. [ABSTRACT FROM AUTHOR]

Recently, Mn2+‐doped CsPb(Cl/Br)3 perovskite nanocrystals (NCs), showing the advantages of dual‐color emissions via exciton‐to‐dopant energy transfer and reduced usage of toxic Pb2+ heavy metal ions by nontoxic Mn2+ substitution, are widely explored. However, photoluminescence quantum yields (PLQYs) for Mn2+‐doped CsPb(Cl/Br)3 NCs still need to be further improved. Here, a halogen‐hot‐injection strategy is developed to prepare Mn:CsPb(Cl0.6Br0.4)3 NCs with the maximal PLQY of 65%. With this method, intense blue narrowband emission from excitonic recombination and orange broadband emission from Mn2+ 4T1 → 6A1 transition can be simultaneously achieved. The competitive luminescence between perovskite NCs and Mn2+ dopants is systematically investigated by controlling the injected halogen types and ratios. As a proof‐of‐concept experiment, the present Mn2+‐doped CsPb(Cl/Br)3 perovskite NCs with highly efficient dual‐color emissions are demonstrated to be applicable as color converter in UV‐excitable solid‐state lighting. [ABSTRACT FROM AUTHOR]

The commonly used automotive head‐up display (HUD) technology is confronted with the problems of poor stability in organic resin counterpart and the unsatisfactory display effect of projection lighting source. To solve these issues, developing state‐of‐the‐art materials and designing new HUD schemes with a wide color gamut is of necessity. Herein, a series of pure red/green/blue (R/G/B) upconverting (UC) nano‐glass‐ceramics (GCs) containing lanthanide‐doped NaLuF4 nanocrystals (NCs) are synthesized in a cost‐effective, environment‐friendly, and scalable manner, simultaneously achieving high crystallinity (≈45.44%) and high transparency (>80%). Yb3+ is chosen as the sensitizer to Tm3+ (blue UC)/Ho3+ (green UC), due to its large absorption cross section from ground state 2F7/2 to excited state 2F5/2; meanwhile Er3+, Tm3+ co‐doped into NCs can obtain pure red UC emission via promoting the population of Er3+ red‐emitting 4F9/2 state. Consequently, the as‐prepared materials exhibit high R/G/B color purity of > 80% owing to the energy transfer between different lanthanide ions (Yb3+, Tm3+, Ho3+, and Er3+) upon 980 nm near‐infrared (NIR) laser excitation, and possess superior thermal reversibility/water resistivity. Remarkably, two unprecedented HUD prototypes are constructed to demonstrate the application feasibility of developed pure R/G/B UC GCs. [ABSTRACT FROM AUTHOR]

Review: 80 refs. [ABSTRACT FROM AUTHOR]

SrGa12O19:Cr3+x (x = 0.0005-0.02) are fabricated by calcination of stoichiometric amounts of SrCO3, Ga2O3, and Cr2O3 in air (1. [ABSTRACT FROM AUTHOR]

The title phosphor is synthesized by solid state reaction of a stoichiometric mixture of CaCO3, Ga2O3, GeO2, Cr2O3, Tm2O3, and Yb2O3 (900 °C for 2 h in air followed by calcination at 1180 °C for 6 h in air). [ABSTRACT FROM AUTHOR]

Eu2+-doped (0.03 mol.%) SrMg1-xMnxP2O7 (x = 0-1) yellow-red emitting phosphors are prepared by a solid state reaction of appropriate amounts of SrCO3, MgO, NH4H2PO4, Eu2O3, and MnCO3 (5% H2/N2 reducing atmosphere, alumina crucible, 1000°C, 5 h). [ABSTRACT FROM AUTHOR]

Lanthanoid-doped Na3Zr(Hf)F7 nanocrystals are prepared solvothermally from EtOH solutions containing MOCl2 (M: Zr, Hf), Ln(NO3)3 (Ln: La-Lu), NH4F, sodium oleate, oleic acid, oleylamine, and H2O (autoclave, 130 °C, 12 h). [ABSTRACT FROM AUTHOR]

The title nanocrystals are solvothermally synthesized from mixtures of Ln(NO3)3 (Ln: La-Lu, Y), Ba(NO3)2, NH4F, NaOH, EtOH, oleic acid, and H2O (autoclave, 180 °C, 24 h). [ABSTRACT FROM AUTHOR]