White Light-emitting Diode Device Research Articles

Supramolecular Sequential Light-Harvesting Systems for Constructing White LED Device and Latent Fingerprint Imaging.

The fabrication of supramolecular light-harvesting systems (LHS) with sequential energy transfer is of significance in utilizing light energy. In this study, we report the non-covalent self-assembly of a sequential LHS by pillar[5]arene-based host-guest interaction in water and its applications in white light-emitting diode (LED) device and latent fingerprint imaging. The host-guest complex WP5⸧G self-assembles into nanoparticles in water and shows enhanced aggregation-induced emission (AIE) effect. The nanoparticles can be further used to construct sequential LHS with fluorescent dyes 4,7-di(2-thienyl)-benzo[2,1,3]thiadiazole (DBT) and sulforhodamine 101 (SR101). Impressively, the system shows white-light emission when the molar ratio of WP5⸧G/DBT/SR101 is 1100/2/16. The material can be coated on a LED bulb to achieve white-light emission. In addition, the sequential LHS exhibit color-tunable fluorescence including red emission, which have been successfully applied to high-resolution imaging of latent fingerprints. Therefore, we demonstrated a general strategy for the construction of sequential LHS in water based on macrocyclic host-guest interaction and explored its multi-functional applications in white-light LED device and imaging of latent fingerprints, which will promote future development and application of supramolecular LHSs.

Efficiently green-emitting and ultra-stable CsPbBr3@SiO2 nanocomposites for white light-emitting diodes

Inorganic oxide especially SiO2 encapsulation strategy is an effective way to improve the stability of all-inorganic cesium lead halide perovskite (CsPbX3, X = Cl, Br, I) nanocrystals (NCs). However, when CsPbX3 NCs are encapsulated in SiO2 by in situ tetraethyl orthosilicate (TEOS) hydrolysis, the unavoidable by-products (water and ethanol) of TEOS hydrolysis commonly damage the structural and optical properties of the CsPbX3 NCs. Herein, TDPA-CsPbBr3 NCs with the dense tetradecylphosphonic acid (TDPA) passivation were pre-prepared and subsequently encapsulated into SiO2 via in situ TEOS hydrolysis. Benefitting from the dense phosphonic passivation layer capable of resisting the erosion of polar by-products generated by TEOS hydrolysis, the obtained TDPA-CsPbBr3@SiO2 nanocomposites maintain the excellent optical properties of the colloidal CsPbBr3 NCs, showing near-unity photoluminescence quantum yield (PLQY) and ultra-narrow full width at half maximum (FWHM). Furthermore, the TDPA-CsPbBr3@SiO2 nanocomposites exhibit outstanding stability against ethanol, UV light, and heating treatment due to the dual protection of dense phosphonate ligand layers and inorganic SiO2 matrix. The white light-emitting diodes (WLED) device was fabricated by sequentially depositing green-emitting TDPA-CsPbBr3@SiO2 nanocomposites and red-emitting K2SiF6:Mn on blue-emitting GaN LED chip. The obtained WLED exhibits excellent luminous performances with standard white emission of CIE Coordinates (0.33, 0.33), a color gamut 138 % of the NTSC and 103 % of Rec. 2020, respectively. This study demonstrates that TDPA-CsPbBr3@SiO2 nanocomposites have a potential application in solid-state lighting and backlight displays.

Development of thermally stable red-emitting lead-free double-perovskite phosphors with an internal PLQY approaching 100.

White light-emitting diode (WLEDs), acting as a new generation of solid-state lighting, play a critical role in energy conservation. Red-emitting phosphors with high efficiency could effectively improve the quality of WLED devices. In this report, Eu3+-doped Ca2ScTaO6 luminescent materials have been successfully synthesized by a high-temperature solid-state method. Its crystal structure was confirmed to be a monoclinic lead-free double-perovskite material system with the space group P21/n by the X-ray diffraction patterns. The strongest emission peak was about 614 nm distributed to the 5D0 → 7F2 electric-dipole transition. Additionally, the optimal doping concentration was found to be 40 mol%, and the concentration quenching mechanism is assigned to d-d interactions. The Ca2ScTaO6:Eu3+ phosphors exhibited an ultrahigh internal quantum yield (about 100%) with good thermal stability (81.5% at 423 K compared with the emission intensity at 303 K). Furthermore, a WLED with a suitable correlated color temperature (4201 K) and a color rendering index (87.62) was fabricated. The phosphor-based polydimethylsiloxane light-emitting flexible film exhibited good luminescence, which is suitable to be utilized in flexible displays. The obtained results suggest that the high-efficiency red-emitting Ca2ScTaO6:Eu3+ phosphors are promising commercial candidates for use in near-ultraviolet-excited WLEDs.

Dual emission quaternary alloyed quantum dots for white light-emitting diodes with high color-rendering index

We report the synthesis of manganese doped Ag–Zn–In–S(AZIS)/ZnS QDs for the facile fabrication of white light-emitting diodes (WLEDs). By controlling the ratio of Mn/(Zn + In), dual emission Mn:AZIS/ZnS QDs with different relative proportion of host emission and Mn2+-related emission were prepared. With proper doping, the emission of Mn: AZIS/ZnS QDs covers most of the visible spectrum. Based on the as prepared Mn:AZIS/ZnS QDs, a warm WLED device exhibited a highest color rendering index (CRI) of 92.5 companied by a correlated color temperature (CCT) of 3162 K. With the increasing of Mn2+ concentration, the corresponding WLED devices shown warmer CCT values and lower luminous efficiencies (LEs). The color-conversion efficiency of the QDs decreasing with the increasing of Mn2+ concentration may be responsible partly for the variation of device LEs. With further deep investigation on the mechanism of color-conversion between the exciting light and QDs, and the energy transfer from the host material to the manganese dopant, WLEDs based on the dual emission Mn:AZIS/ZnS QDs with better device performances are excepted to find diverse application in lighting fields.

New green garnet-type phosphor LuMgAl5SiO12:Ce3+ for filling cyan gap to achieve full-spectrum and high colour-rendering-index white light-emitting diodes

Phosphors with simple preparation, high luminous efficiency and excellent thermal stability are highly desirable for commercial white light-emitting diodes (W-LED). In the paper, a new garnet-type green phosphor LuMgAl5SiO12:Ce3+ (LMASO:Ce3+) has been successfully prepared by a high-temperature solid-state reaction. The crystal structure and photoluminescence properties were investigated in detail. X-ray diffraction and the Rietveld refinement demonstrated the crystal structure of LMASO belongs to cubic systems with an Ia 3¯ d (230) space group. The unit cell parameters of LMASO:0.08Ce3+ phosphor were found to be a = 11.90418 Å and V = 1686.935 Å3. LMASO:Ce3+ phosphors have two excitation bands with peaks at 340 and 436 nm, attributed to the 4f → 5d transition of Ce3+ ions. Under excitation at 436 nm, LMASO:0.08Ce3+ phosphor exhibits a broad and asymmetric emission band in the 450–700 nm range. Notably, a W-LED device was created by combining a 455 nm blue LED chip with the obtained green sample and the commercially available red CaAlSiN3:Eu3+ phosphor. The device emitted a bright warm white light with a low correlated color temperature of 3584 K and a high color rendering index of 96.0 at a drive current of 40 mA. The article indicates that LMASO:Ce3+ samples can serve as a potential green phosphor for W-LEDs, and offers a new strategy for designing efficient phosphors.

Insight into the optical evaluation of sunlike LED devices with full-visible spectrum emission based on ultra-low melting tin fluorophosphate glass for human centric lighting

Full spectrum sunlike light-emitting diode (LED) devices in the wavelength range of 380–670 nm have received much attention for their applications in human centric lighting. Herein, the inorganic color converter of the sunlike phosphor-in-glass (PiG) has been developed by embedding the green-emitting (Lu3-xYxAl5O12: Ce3+) and red-emitting (Sr0.6Ca0.4AlSiN3: Eu2+) phosphor powders in ultra-low melting tin fluorophosphate glass. Notably, the sunlike PiG exhibits the full spectrum in the wavelength range of 380–670 nm under the excitation of a near-ultraviolet (NUV) chip. Tunable color temperature (2785 K–5806 K) and high color rendering index (Ra = 95) were obtained by varying the mix ratio of the red-emitting component in the glass matrix. Further, the full visible spectrum emission was regulated by adjusting the Lu/Y ratio of the green phosphor Lu3-xYxAl5O12: Ce3+ and the color quality was further optimized (Ra = 97). The color quality of white light-emitting diode (WLED) was systematically investigated using Illuminating Engineering Society (IES) of North America evaluation systems and the LED devices exhibit fidelity index (Rf) and gamut index (Rg) close to sunlight (Rf = 95, Rg = 101). Compared with the traditional phosphor-in-silicone (PiS), the sunlike PiG based WLED exhibits a low working temperature of ∼37 °C for high power LED. Therefore, the WLED devices based on sunlike-PiG can be regarded as promising candidates for ultra-high color rendering index light sources because of the adjustable color temperature, high color quality, low-efficiency loss, excellent thermal properties and water stability.

A highly thermal-stable red-emitting tantalate phosphor for WLED and multiple-mode optical temperature sensor dual-applications

Recently, more and more attention has been concentrated on luminescence materials activated with rare-earth ions for white light-emitting diodes (WLEDs) or optical thermometers. However, due to their opposite requirements for thermal response, it is hard to realize the above dual applications in the same material. Herein, a red-emitting tantalate phosphor, Gd3TaO7:Eu3+, was designed and prepared to solve the problem. The emission of Eu3+ in the phosphor was surprisingly observed to be different from that in most of the reported red phosphors activated with Eu3+, that is, the emissions coming from the f - f transitions of Eu3+ exhibit severe splitting, and the intensities of several strong transitions are not very different. According to the structural and spectral analyses, the reasons may be the highly covalent and polarized lattice environments of Eu3+ in this material. When excited with 393 nm, the temperature-dependent photoluminescence (TDPL) of Gd3TaO7:Eu3+ presents a normal thermal quenching and the integrated intensity at 500 K keeps 90.8 % compared to that at 300 K. Whereas the TDPL presents an edge abnormal thermal quenching phenomenon upon the excitation of 330 nm. Taking advantage of the special TDPL characteristics, a WLED device and a multiple-mode optical thermometer are successfully realized in this material. The former has excellent performances with high Ra of 88.8 and low CCT of 3882 K, and the latter includes one type of excitation intensity ratio and two types of fluorescence intensity ratio with the maximal relative temperature sensitivities of 0.92 % K−1, 0.97 % K−1 and 0.92 % K−1, respectively. The results reveal that Gd3TaO7:Eu3+ phosphor has a great prospect in WLED and multiple-mode optical temperature sensor dual-applications, and this work may provide a new and effective strategy for developing multifunctional optical materials.

Antimony-Triggered Tunable White Light Emission in Lead-Free Zero-Dimensional Indium Halide with Ultrastable CCT of White Light Emitting Diodes.

A highly efficient and easily tunable luminescence is significant for solid-state luminescent (SSL) materials. However, achieving a photoluminescence quantum yield (PLQY) close to unity and tuning the emission remain challenging tasks. Metal doping strategies enable resolution of these issues. Herein, we report the preparation of a novel organic-inorganic lead-free indium-based metal halide hybrid (MP)3InCl6•EtOH (MP = C4H10ON) with a typical zero-dimension structure. When excited at 320 nm, (MP)3InCl6•EtOH exhibits a dual emission band at 420 and 600 nm, which originates from the organic cation [MP] and the [InCl6]3- octahedral unit. The photoluminescence can be significantly enhanced through Sb3+ doping, resulting in an increase in PLQY from 0.78% to near unity. Multiple emission color tunings have been achieved by regulating the Sb doping level and the radiation wavelength, resulting in a change in emission color from blue → white → orange. Optical characterizations reveal that the significantly enhanced emission centered at 600 nm can be attributed to more efficient absorption, closely associated with an additional 1S0 → 3P1 transition in the inorganic octahedron [In(Sb)Cl6]3- due to Sb3+ doping. With its excellent optical performance, a white light emitting diode (WLED) has been successfully fabricated by coating the mixture of (MP)3InCl6•EtOH:15%Sb3+ with blue phosphor BaMgAl10O17:Eu2+ onto a UV LED chip. The WLED device exhibits perfect white light emission with regard to the International Commission on Illumination (CIE) coordinates of (0.36, 0.34). Significantly, the WLED device maintains a stable correlated color temperature (CCT) range of 4119-4393 K and CIE coordinates (x: 0.37-0.34, y: 0.35-0.33) as the driven current varies from 20 to 200 mA, demonstrating outstanding stability across different power levels. This work not only presents a novel system for achieving remarkably enhanced luminescent performance and tuning emission bands in 0D metal halides but also represents a significant step toward achieving resistance to color drifting for stable WLEDs.

High-performance luminescence of europium ion-activated Na2O-CaO-SiO2 system glass-ceramics through component regulation and crystallization process optimization strategies

Luminescent glass-ceramics has garnered significant attention within the research community owing to its exceptional characteristics, including robust chemical stability, outstanding thermal stability, and efficient thermal conductivity. However, persistent challenges include issues related to suboptimal luminous efficiency and color rendering index. In the context of this research endeavor, we have achieved a noteworthy achievement by successfully fabricating a novel variant of glass-ceramics doped with both Eu2+ and Eu3+ ions within the Na2O-CaO-SiO2 system glass. This innovative glass-ceramics composition encompassed Na4Ca4Si6O18 crystals, characterized by grain sizes <110 nm. Our investigations, featuring comprehensive optical spectra analysis and detailed morphological examinations, have provided substantial evidence indicating the preferential occupation of Eu3+ ions in the Ca2+ sites residing within the Na4Ca4Si6O18 crystal lattice, conversely, it is possible that the distribution of Eu2+ ions occurred within the glass matrix. Additionally, it is worth noting that this glass-ceramic material demonstrated a heightened excitation efficiency when subjected to 464 nm blue light, surpassing its performance with 393 nm violet light. Detailed fluorescence spectral analysis unveiled the impressive internal quantum efficiency of the glass-ceramics, reaching an impressive 80.27%, and this glass-ceramics exhibited remarkable fluorescence thermal stability at 150 °C, preserving approximately ∼75% of its luminescent intensity at room temperature. Furthermore, we have encapsulated the white light-emitting diode (W-LED) device, integrated with a 460 nm LED chip, optimized glass-ceramics, and YAG: Ce3+ phosphor. The outcomes were characterized by the warm white-light emission, suitable chromaticity coordinates, a high color rendering index (approximately 85.4), and impressive luminous efficiency (up to 112.47 lm/W). In summary, these findings unequivocally underscore the substantial potential of glass-ceramics in the realm of high-power W-LED lighting applications.

Temperature-dependent photoluminescent behavior of millimeter-scale Cs4PbBr6/CsPbBr3 bulk crystals and their application to white light-emitting diodes

The zero-dimensional perovskite composite Cs4PbBr6/CsPbBr3 has attracted significant attention for its remarkable photoluminescence (PL), which remains highly effective even in solid state. This work presents a detailed analysis of the steady-state and time-resolved PL (TRPL) behavior of millimeter-scale Cs4PbBr6/CsPbBr3 crystals over a temperature range of 80 to 360 K, which covers exciton binding energy, phonon energy, and PL peak energy shifting with increasing temperature. According to the results, Cs4PbBr6/CsPbBr3 exhibits high exciton binding energy and phonon energy, with calculated values of 358.7 and 94.8 meV, respectively. Specifically, when the temperature is below ∼235 K, thermal expansion dominates to influence the TRPL and peak energy, whereas electron-phonon interaction becomes the dominant factor as temperature rises from 235 to 325 K. It is found that Cs4PbBr6/CsPbBr3 has a PL behavior similar to CsPbBr3, and characterization and TRPL results demonstrate that nanometer-scale CsPbBr3 crystals embed in the Cs4PbBr6 bulk matrix. Meanwhile, a white light-emitting diode (WLED) device based on Cs4PbBr6/CsPbBr3 with luminous efficiency of 64.56 lm/W is fabricated, and its color coordinate is measured as (0.34, 0.31) under 20 mA, which is in close proximity to the standard white color coordinate. Moreover, the color gamut of the device is measured as 128.66% of the National Television Systems Committee (NTSC). The WLED electroluminescence (EL) spectra show high Correlated Color Temperature (CCT) stability for the working current varying from 5 to 100 mA, and after continuous operation for 12 h, the EL intensity decreases and stabilizes at ∼70% of the initial EL intensity. These findings suggest that Cs4PbBr6/CsPbBr3 crystals are a promising candidate for WLEDs.

Extensive emission tuning and characterization of highly efficient CuInS2 quantum dots for white light-emitting diodes.

Whole visible range emitting CuInS2/ZnS QDs were obtained with broad band-width and high luminous efficiency by altering the Cu/In ratio and coating ZnS layer. 1-Dodecanethiol (DDT) as a sulfur source in the ZnS coating process can inhibit the lattice defects caused by Zn2+ inter-diffusion, thus increasing the photoluminescence quantum yield (PL QY). Then the stability and lighting performance of white light-emitting diodes (WLEDs) based on these CuInS2/ZnS QDs were characterized. The optimized WLED device exhibited a moderate luminous efficacy (LE) (70.33 lm·W-1) and ultrahigh color qualities (CRI Ra = 92.7, R9 = 95.9, R13 = 96.3) with warm white at a correlated color temperature (CCT) of 4052 K.

Highly efficient blue‐emitting phosphor via charge compensation strategy and its application for white LED lighting

AbstractHighly efficient phosphors are indispensable for near‐ultraviolet (n‐UV) pumped white light emitting diodes (WLEDs). In this work, a novel blue emitting Sr6GdSc(BO3)6:0.08Ce3+ phosphor was synthesized, exhibiting a broadband blue emission (full width at half‐maximum (FWMH) = 133 nm) excited by 375 nm. Furthermore, the blue emission of Sr6GdSc(BO3)6:0.08Ce3+ was enhanced by 3.9 times through codoping Na+ ions due to the influence of charge compensation and micromorphology and size of phosphor particles. At the same time, the internal quantum efficiency was improved from 45.4% to 98.6% and the external quantum efficiency up to 75.0%. Finally, the 365 nm excited two WLED devices were constructed by integrating Sr6GdSc(BO3)6:0.08Ce3+, Sr6GdSc(BO3)6:0.08Ce3+,0.08Na+, commercial green and red phosphors with high color rendering index. These results reveal that the phosphors have prospective application in high‐quality warm white lighting.

Broadband emission characteristics and WLED application of self-activated YMZn3AlO7 (M=Ca, Sr, Ba) phosphors

In this study, a non-activated ion-doped full-spectrum emission phosphor for white light-emitting diode (WLED) lighting is proposed using oxygen defect engineering. The YMZn3AlO7 (M = Ca, Sr, Ba) phosphors with "114″ structure were prepared via a high-temperature solid-state reaction. Under excitation with 373 nm ultraviolet (UV) light, YSrZn3AlO7 in YMZn3AlO7 (M = Ca, Sr, Ba) exhibited the highest emission intensity and formed a wide yellow emission band centred at 563 nm. The full width at half maximum of the YSrZn3AlO7 phosphor was 172.6 nm. A theoretical model based on the designed oxygen vacancies was proposed to determine the self-activated luminescence mechanism. Density functional theory calculations revealed that oxygen vacancies lead to the generation of new energy levels. Electron paramagnetic resonance experiments further confirmed that the luminescence originated from oxygen vacancies. Eventually, a warm WLED device ((x, y) = (0.4057, 0.4359)) with a correlated color temperature of 3814 K and a relative color rendering index of 83 was successfully prepared using the YSrZn3AlO7 phosphor and a 365 nm UV LED chip. These results suggest that YSrZn3AlO7 is a promising WLED phosphor and provide new insights into the application of self-activated phosphors in WLED.

High-Efficiency Narrow-Band Green-Emitting Manganese(II) Halide for Multifunctional Applications.

Zero-dimensional (0D) Mn2+-based metal halides used as luminescent materials and scintillators have become a research hotspot in the field of photoelectric materials and devices due to their unique composition, structure, and fluorescence properties. It is of great value to explore new Mn2+-based metal halides to achieve multifunctional applications. Herein, the novel 0D Mn2+-based metal halide single crystal (BPTP)2MnBr4 is synthesized by a simple solvent-antisolvent recrystallization method. Under excitation at 468 nm, the (BPTP)2MnBr4 single crystal shows a pronounced narrow-band green luminescence centered at 515 nm derived from the d-d transition of the Mn2+ ion. This emission has a relatively narrow full width at half maximum of 43 nm and a high photoluminescence quantum yield (PLQY) of 82%. In addition, (BPTP)2MnBr4 exhibits good thermal stability at 393 K with a retention of 79% of the initial photoluminescence intensity at 298 K. Benefiting from its strong blue light excitation, high PLQY, and good thermal stability, we manufacture an ideal white light-emitting diode (LED) device using a 460 nm blue LED chip, green-emitting (BPTP)2MnBr4, and commercial K2SiF6:Mn4+ red phosphor. Under 20 mA drive current, the LED shows a high luminous efficiency of 112 lm/W and a wide color gamut of 110.8%, according to the National Television System Committee standard. In addition, (BPTP)2MnBr4 crystals show a strong X-ray absorption. Based on the commercial Lu3Al5O12:Ce3+ scintillator, the calculated light yield of (BPTP)2MnBr4 reaches up to about 136,000 photons/MeV and the detection limit reaches 0.282 μGyair s-1. Additionally, a melt quenching approach is used to construct a (BPTP)2MnBr4 clear glass scintillation screen, realizing a spatial resolution of 10.1 lp/mm. The proper performances of (BPTP)2MnBr4 as phosphor-converted LED materials and the X-ray scintillator with the addition of eco-friendly, low-cost solution processability make 0D Mn2+-based metal halides potential luminescent materials for multifunctional applications.

Synthesis, crystal structure, and characterizations of Eu3+-activated Ca2LnHf2(AlO4)3 (ln = Lu, Y and Gd) red-emitting phosphors for phosphors-converted white LEDs

High-brightness red-emitting Ca2LnHf2Al3O12:Eu3+ (Ln = Lu, Y and Gd) garnet phosphors with high photoluminescence efficiency are demonstrated for application in white light-emitting diodes (LEDs), and they have been successfully prepared using a high-temperature solid-state method. X-ray diffraction, field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, elemental mapping, photoluminescence excitation and photoluminescence spectra, decay lifetimes, photoluminescence quantum yield and temperature-dependent emission spectra have been used to characterize these samples. Under near-ultraviolet excitation into the 7F0→5L6 transition of Eu3+ at 394 nm, the Ca2LnHf2Al3O12:Eu3+ (Ln = Lu, Y and Gd) samples produce the characteristic red emissions of Eu3+ ions with peaks around 591, 611, 656, and 709 nm, corresponding to the 5D0→7F1, 5D0→7F2, 5D0→7F3, and 5D0→7F4 transitions. These samples exhibit significant concentration-dependent luminescence behaviors, and the highest emission intensity is achieved at 50 mol% Eu3+ doping concentration owing to the concentration quenching effect caused by the dipole-dipole interaction between neighboring Eu3+ activators. The CIE color coordinates of these optimal Ca2LnHf2Al3O12:50%Eu3+ (Ln = Lu, Y and Gd) phosphors are (0.6339, 0.3654), (0.6341, 0.3653), and (0.6343, 0.3651), along with respective color purity of 92.4%, 92.6%, and 92.6%. The photoluminescence quantum yields of Ca2LnHf2Al3O12:50%Eu3+ are determined to be 39.2%, 56.6%, and 53.3% for Ln = Lu, Y, Gd, respectively. A white LED device has been fabricated through utilizing the Ca2YHf2Al3O12:50%Eu3+ phosphor as red-emitting color converter, which generates bright warm-white light with high color rendering index (80.8), low correlated color temperature (3920 K), CIE chromaticity coordinates (0.3827, 0.3742), and high luminous efficacy (11.56 lmW−1) under 40 mA driving current.

Functional design and implementation of multilayer Ce:YAG/Cr:YAG composite transparent ceramics by tape casting for white LEDs/LDs

The shortage of red-light emission in Ce3+:Y3Al5O12 (Ce:YAG) luminescent ceramics is a bottleneck problem to realize the key applications of ceramics based white light-emitting diode (LED) and laser diode (LD) devices. However, the energy band-gap engineering for Ce3+ ion via host substitution or red-emission ions co-doping always leads to its decrease of luminescence efficiency (LE), while a spectrum overlay strategy would be simple and effective. In this study, multilayer composite structure Ce:YAG/Cr:YAG transparent ceramics (TCs) with high color rendering index (CRI) were fabricated by tape casting and vacuum sintering. An organic tape casting protocol with low toxicity and environmental protection was developed and the amounts of dispersants, binders, and plasticizers were systematically optimized to produce good quality tapes with no defects. The transmittance of ceramic reached 78% at 800 nm. By using a 455 nm blue chip, the CRI of the Ce:YAG/Cr:YAG TCs based LED device was increased from 26.7 to 77.5, and the LE was decreased from 181.5 to 10.4 lm/W. Additionally, the optimized LE and CRI for LD device were 130.2 lm/W and 78.1, respectively. Therefore, this research displays that the design and implementation of ceramic functional layer to achieve the essential enhancement of CRI in TC based white lighting is a promising method through the tape casting forming technology.

High-color-quality blue-light-pumped full-spectrum white-light-emitting diodes realized by efficient green-emitting CaY2HfScAl3O12:Ce3+ phosphors

Rare-earth doped inorganic phosphors are critical for solid-state white lighting. Particularly, efficient broadband, blue-light-excitable, green-emitting phosphors are highly needed for fabricating full-spectrum white-light-emitting diodes (WLEDs) with high-color-quality. Herein, we describe a new efficient blue-light-excited CaY2HfScAl3O12:Ce3+ green phosphor with high quantum efficiency (QE) and broad emission bandwidth. X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectrometer, excitation and emission spectra, CIE color coordinates, QE values, and temperature-dependent emission spectra have been used to characterize the samples. Rietveld refinement reveals that the CaY2HfScAl3O12 garnet compound has a cubic structure with lattice parameters of a = b = c = 12.38(13) Å, α = β = γ = 90°, and V = 1897.85(6) Å3. Impressively, the Ce3+ ions in the CaY2HfScAl3O12 host exhibit broadband excitation bands in the 300–500 nm spectral range with a maximum at 450 nm. Upon 450 nm excitation, the optimal phosphor doped with 2 mol% Ce3+ shows a broad green emission band in the wavelength range of 460–750 nm peaking around 532 nm, along with full width at half maximum of 121 nm as well as high internal QE of 78.9% and external QE of 46.6%. Ce3+ concentration-dependent luminescence properties and thermal stability at elevated temperature have been comprehensively studied. Finally, a WLED device is fabricated by utilizing CaY2HfScAl3O12:Ce3+ green phosphor, CaAlSiN3:Eu2+ red phosphor and a 450 nm blue LED chip, which generates bright full-spectrum warm-white light with ultrahigh color rendering index (Ra = 98.0, R9 = 97.5) and low correlated color temperature of 3602 K under 180 mA drive current. This work provides new insights into designing and developing efficient green phosphors for full-spectrum LED lighting.

Preparation and luminescence properties of Ba0.92-xSrxAl2Si2O8:0.08Eu2+ blue-cyan phosphors for white light LEDs

Currently, there is a cyan gap in white light-emitting diodes (LEDs) manufactured by combining near-ultraviolet (NUV) chips with tricolour (blue/green/red) phosphors, resulting in a poor colour rendering index (Ra). Broadband blue-cyan phosphors contain blue, cyan and green luminescent components that complement the cyan gap. In this paper, feldspar-structured Ba0.92-xSrxAl2Si2O8:0.08Eu2+ (x = 0–0.5) phosphors were prepared by a high-temperature solid-phase method and a cation substitution strategy. A phase transition was achieved by varying the concentration of x, which resulted in the formation of two luminescent centres and a 10.33-fold enhancement of the luminescence intensity for Ba0.92Al2Si2O8:0.08Eu2+. The colour of the emission changed from the original green to blue-cyan, and the strongest emission peak with a half-height width of 94.5 nm was observed at a Sr2+ concentration of 0.3 (30%) and covered the blue, cyan and green wavelength ranges (390–600 nm). The experimental value of the optical band of the substrate is 5.71 eV, and the luminous intensity of the Ba0.62Sr0.3Al2Si2O8:0.08Eu2+ sample at 150 °C was 91.3% of that at room temperature. Ba0.62Sr0.3Al2Si2O8:0.08Eu2+, (Ca, Sr) AlSiN3:Eu2+ and 365 nm NUV chips were successfully packaged into white LED devices. The colour rendering index (Ra) of the prepared white LED devices was 87, R9 was 89, the colour coordinates were (0.3763, 0.3382), and the colour temperature was 3759 K, which effectively solves the problem of the lack of cyan luminescent components in white LED devices and simplifies the manufacturing process of white LEDs.

Large-Scale Synthesis of Tunable Fluorescent Carbon Dots Powder for Light-Emitting Diodes and Fingerprint Identification.

The emergence and fast development of carbon dots (CDs) provide an unprecedented opportunity for applications in the field of photoelectricity, but their practicability still suffers from complicated synthesis procedures and the substrate dependence of solid-state fluorescence. In this study, we design a unique microwave-assisted solid-phase synthesis route for preparing tunable fluorescent CD powders with yellow, orange, and red fluorescence (Y-CDs, O-CDs, R-CDs) by simply adjusting the mass ratio of reactants, a method which is suitable for the large-scale synthesis of CDs. The Y-/O-/R-CDs were systematically characterized using physics and spectroscopy techniques. Based on the perfect solid-state fluorescence performance of the proposed fluorescent CD powders, the Y-/O-/R-CDs were successfully applied for the construction of multi-color and white light-emitting diode devices at low cost. Furthermore, the Y-CDs displayed much higher yield and luminous efficiency than the O-CDs and R-CDs and were further used for fingerprint identification on the surfaces of glass sheets and tinfoil. In addition, the R-CD aqueous solution fluorescence is sensitive to pH, suggesting its use as a pH indicator for monitoring intracellular pH fluctuations. The proposed series of fluorescent powders composed of CDs may herald a new era in the application of optical components and criminal investigation fields.

Improving the quality of red light emitting from Eu3+ by Co-doping Tb3+ in LuBa3(BO3)3

The red light emitting from phosphors activated with Eu3+ is of great significance for optimizing the comprehensive performances of white light-emitting diodes (WLEDs) for solid-state lighting. Herein, LuBa3(BO3)3:Eu3+ and LuBa3(BO3)3:Tb3+,Eu3+ phosphors are synthesized via the high temperature solid-state reaction to investigate the effects of the doping concentration of Eu3+ and the co-doping of Tb3+ on the quality of red emission from Eu3+ in the host. Under the excitation of 392 nm light, the dominant emission peak of LuBa3(BO3)3:xEu3+ gradually shifts from 593 nm to 610 nm when the doping concentration of Eu3+ is increased from 0.02 to 0.10, and the quality of red light emitting from Eu3+ in the host is found to be further improved with increasing the co-doping concentration of Tb3+, both of which are explained with the Judd-Ofelt theory. The calculated results indicate that the enhancement of red emission is attributed to the decrease of the environment symmetry of Eu3+ by increasing the concentration of Eu3+ in LuBa3(BO3)3:Eu3+ or co-doping Tb3+ ions. The color purity of the emission from LuBa3(BO3)3:0.10 Tb3+,0.10Eu3+ is 94.11%, and the luminescent intensity of the phosphor at 425 K is 69% of that at room temperature. Moreover, a WLED device with the high color rendering index of 91.1 is obtained by fabricating LuBa3(BO3)3:0.10 Tb3+,0.10Eu3+ and other phosphors with a 365 nm LED chip. The good comprehensive performances suggest that LuBa3(BO3)3:Tb3+,Eu3+ has a great application prospect as a red phosphor in the field of high-quality solid lighting.