Relationship of the different Ca sites in the matrix with luminescence properties of orange‒red emitting Li0.04Ca0.96-xSiO3:Smx phosphors

Li_0.04Ca_0.96-xSiO₃:Sm_x orange?red emitting phosphors were synthesized using the sol-gel method. X-ray diffraction, Rietveld refinement of XRD patterns, Fourier transform infrared spectroscopy and ?uorescence spectrophotometry were used to characterize the crystal structure, sites of cationic Ca and luminescence properties of the prepared phosphors. The relationship of the different Ca sites in the matrix with the luminescence properties was analysed. The results indicate that the prepared phosphors reveal a β-CaSiO₃ phase with a monoclinic crystal structure and space Group P21/a. As the Sm³⁺ concentration increases, the unit cell volume of phosphors and the Ca–O band lengths of different Ca sites decrease due to substitution of Ca²⁺ by smaller Sm³⁺ ions. By excitation at 404 nm, Li_0.04Ca_0.96-xSiO₃:Sm_x phosphors exhibit warm orange?red light, corresponding to the electron transitions from ⁴G_5/2 → ⁶H_5/2 (567 nm), ⁴G_5/2 → ⁶H_7/2 (605 nm) and ⁴G_5/2 → ⁶H_9/2 (651 nm) of Sm³⁺. The concentration quenching phenomenon appears at Sm³⁺ concentrations beyond 0.02. The refinement results demonstrate that three cationic Ca sites, named Ca1, Ca2 and Ca3, exist in the β-CaSiO₃ host lattice. The Ca²⁺ ions at Ca1 and Ca2 sites are coordinated with six oxygen ions, leading to the same coordination number (CN). The Ca²⁺ ion located at Ca3 site has seven coordination numbers. The Ca1 site possesses a smaller lattice distortion and better symmetry than those of Ca2 and Ca3 sites. However, the Ca3 site exhibits the largest lattice distortion and poor symmetry. The Sm³⁺ present in symmetric Ca1 sites in the matrix illustrates the strong emission intensity, long luminescence lifetimes and good thermal stability.     

Spectroscopic and photoluminescence characteristics of Sm3+ doped calcium aluminozincate phosphor for applications in w-LED

Monophase Calcium Aluminozincate (Ca₃Al₄ZnO₁₀) phosphor doped with Sm³⁺ ions by varying concentrations have been prepared at 1300 °C using conventional solid state reaction technique. The crystal structure and phase analysis of the as-prepared phosphor has been carried out by X-ray Diffraction (XRD) studies. Morphology and functional groups present in the phosphor have been investigated thoroughly by using Scanning Electron Microscope (SEM) and Fourier Transform Infrared (FT-IR) spectral measurements, respectively. Under 401 nm excitation, the as-prepared phosphor exhibit intense visible orange emission at 601 nm. It has been observed that 1.0 mol% of Sm³⁺ ions concentration is optimum to give intense visible orange emission. The PL analysis reveals that the dipole-dipole interaction is primarily responsible for the concentration quenching observed beyond 1.0 mol% of Sm³⁺ ions. The TR-PL study reveals a bi-exponential behavior of decay curves with an average lifetime of the order of microseconds. The CIE coordinates (x=0.574 and y=0.424) measured for the optimized phosphor are very close to the intense orange emission coordinates specified by Nichia Corporation developed Amber LED NSPAR 70BS (0.570, 0.420). The spectroscopic, PL and TR-PL studies suggest the potential use of Sm³⁺ doped calcium aluminozincate phosphors for display and white light emitting devices.     

Photoluminescence properties and thermal stability of samarium-doped barium phosphate phosphors

In this paper, Sm³⁺-doped Ca₆BaP₄O₁₇ phosphors were synthesized via a conventional solid-state reaction method. Orange-red emission was observed from these phosphors under near-ultraviolet (UV) excitation at 405 nm. The luminescence properties of the obtained phosphors were characterized. The Ca₆BaP₄O₁₇:Sm³⁺ phosphor can be efficiently excited by near-UV and blue light, and their emission spectrum consists of three emission peaks, at 567, 602, and 650 nm, respectively. The thermal stability of Ca₆BaP₄O₁₇:Sm³⁺ phosphors was investigated systematically and corresponding mechanisms were proposed. Based on the results, the as-prepared Ca₆BaP₄O₁₇:Sm³⁺ phosphors are promising orange-red-emitting phosphors for near-UV-based white light-emitting diodes.     

Luminescence properties of Ca2GdNbO6: Sm3+, Eu3+ red phosphors with high quantum yield and excellent thermal stability for WLEDs

A series of Ca₂GdNbO₆: xSm³⁺ (0.01 ≤ x ≤ 0.15) and Ca₂GdNbO₆: 0.03Sm³⁺, yEu³⁺ (0.05 ≤ y ≤ 0.3) phosphors were synthesized by the traditional solid-state sintering process. XRD and the corresponding refinement results indicate that both Sm³⁺ and Eu³⁺ ions are doped successfully into the lattice of Ca₂GdNbO₆. The micro-morphology shows that the elements of Ca₂GdNbO₆: 0.03Sm³⁺, 0.2Eu³⁺ phosphor are evenly distributed in the sample, and the particle size is about 2 μm. The optical properties and fluorescence lifetime of Ca₂GdNbO₆: 0.03Sm³⁺, Eu³⁺ phosphors were detailedly studied. The emission peak at ⁵D₀→⁷F₂ (614 nm) is the strongest and emits red light under 406 nm excitation. The increase of Eu³⁺ concentration causes the energy transfers from Sm³⁺ to Eu³⁺ ions, and the transfer efficiency reaches 28.6%. Ca₂GdNbO₆: 0.03Sm³⁺, 0.2Eu³⁺ phosphor has a quantum yield of about 82.7%, and thermal quenching activation energy is of 0.312 eV. The color coordinate (0.646, 0.352) of Ca₂GdNbO₆: 0.03Sm³⁺, 0.2Eu³⁺ phosphors is located in the red area. The LED device fabricated based on the above phosphor emit bright white light, and CCT = 5400 K, Ra = 92.8. The results present that Ca₂GdNbO₆: 0.03Sm³⁺, Eu³⁺ phosphors potentially find use in the future.     

Optical transition and luminescence properties of Sm3+-doped YNbO4 powder phosphors

A series of YNbO₄: Sm³⁺ powder phosphors with different doping concentrations were synthesized by a traditional high-temperature solid-state reaction method. The crystal structure of the obtained samples was characterized by means of X-ray diffraction. Concentration quenching, energy-transfer mechanism, and luminescence thermal stability of YNbO₄: Sm³⁺ samples were studied through the fluorescence spectra and decays. It was concluded that electric dipole-dipole interaction was the dominant energy-transfer mechanism between Sm³⁺ ions according to both Van Uitert's model and Dexter's model. Using the Arrhenius model, crossover process was proven to be responsible for the luminescence thermal quenching of Sm³⁺. Moreover, a novel approach for evaluating the optical transition properties of Sm³⁺ ion in YNbO₄ powders using the diffuse-diffraction spectrum and fluorescence decay was examined in the framework of Judd-Ofelt (J-O) theory. It was confirmed that the J-O parameters Ω_λ (λ = 2, 4, 6) of Sm³⁺ in YNbO₄ powder were reliable by comparing the radiation transition rate with the measured emission results.     

Thermal stability and luminescence of novel garnet-type yafsoanite Ca3Zn3(TeO6)2:Sm3+ phosphors for white LEDs

In this study, novel garnet-type yafsoanite tellurate Ca₃Zn₃(TeO₆)₂:Sm³⁺ phosphors are successfully synthesized using the traditional high-temperature solid-state reaction. The phase purity of the obtained phosphors is analyzed by X-ray diffraction and Rietveld refinement studies. Morphological variations are also observed with the different concentrations of Sm³⁺ ions substitution, which is analyzed using Scanning Electron Microscopy (SEM). The photoluminescent properties of the phosphors are systematically investigated. Results show that the samples display the strongest emission peak at 612 nm under the near-ultraviolet (n-UV) 409 nm excitation. This peak can be ascribed to the ⁴G_5/2 → ⁶H_7/2 transition of Sm³⁺. The Ca₃Zn₃(TeO₆)₂:Sm³⁺ phosphor shows a high color purity, exhibits excellent thermal stability and good color drifting resistance. Furthermore, red and white light-emitting diodes have been successfully prepared. The white light-emitting diodes (w-LEDs) demonstrates a high color rendering index (CRI, R_a) and low correlated color temperature (CCT). This study introduces a new orange-red-emitting phosphor and discusses its application in herb-growth w-LEDs.     

White Light Emission from Sr2LiSiO4F:Sm3+,Tb3+ Phosphors Under Near‐UV Light Excitation

The Tb³⁺/Sm³⁺ codoped Sr₂LiSiO₄F white emitting phosphors were synthesized by a solid‐state reaction technique at high temperature. The X‐ray diffraction patterns, photoluminescence properties, and decay behaviors have been investigated. The Tb³⁺ emissions (blue and green) and Sm³⁺ emissions (orange) are both observed in the codoped samples Sr₂LiSiO₄F: 0.05Sm³⁺, xTb³⁺ by near‐UV light (370 nm) exciting. The white emission has been obtained by adjusting Tb³⁺ doping concentration at 5% (x = 0.05). These luminescent powders are expected to be a potential candidate as white emitting phosphor for near‐ultraviolet InGaN‐based white light‐emitting diodes.     

Near-ultraviolet light–induced dazzling red emission in CaGd2(MoO4)4:2xSm3+ compounds for phosphor-converted WLEDs

The Sm³⁺-activated CaGd₂(MoO₄)₄ phosphors were prepared through a sol-gel reaction route. From the results of excitation spectrum, three-dimensional emission spectra and contour lines, it was confirmed that the near-ultraviolet (NUV) light was the proper excitation light source for the synthesized phosphors. Under 405 nm irradiation, the luminescent behaviors of the studied samples were revealed to be dependent on the Sm³⁺ ion concentration and its optimal value of 0.03 mol was obtained. Through theoretical analysis, it is evident that the dipole-dipole interaction can be responsible for the involved concentration quenching mechanism in the final products and the critical distance was 39.7 Å. Moreover, the temperature-dependent emission spectra demonstrated that the studied samples had admirable thermal stability and the activation energy was decided to be 0.21 eV. Furthermore, the internal quantum efficiency of the Sm³⁺-activated CaGd₂(MoO₄)₄ phosphors was found to be 21.6%. Finally, to explore the practical applications of obtained compounds for indoor illumination, a white light-emitting diode (WLED) device which contained a NUV chip, prepared phosphors, and commercial blue-emitting and green-emitting phosphors was packaged. The packaged WLEDs device can emit dazzling white light with satisfied color coordinate of (0.305, 0.318), proper color rendering index (82.6), and correlated color temperature (7069 K).     

Sites occupancy preference of Bi3+ and white light emission through co‐doped Sm3+ in LiGd5P2O8

Bi³⁺, Sm³⁺‐activated LiGd₅P₂O₈ (LGPO) phosphors were prepared through high‐temperature solid‐state method. In LGPO host, there are 5 types of Gd crystallographic sites, named as Gd(1)/Gd(2)/Gd(3)/Gd(4), and Gd(5). Bi³⁺‐activated LGPO phosphors exhibit 1 broad excitation band from 250 to 320 nm centered at 293 nm and a broad asymmetric emission band ranging from 350 to 600 nm with the maximum value approximately at 409 nm. It can be concluded from dual‐emission spectra that Bi³⁺ may occupy 2 Gd sites and an obvious spectral blue‐shift appeared with increasing Bi³⁺ content, which is caused by the intensity of crystal field of Bi³⁺ is decreased. Notably, through the calculation of each Gd‐O chemical parameter, the environmental factor (h_e) value of each Gd site can be obtained and it can be further inferred that 2 emission bands centered at 409/461 nm are ascribed to Bi³⁺ ions which occupies Gd(3) and Gd(4) sites, respectively. Energy transfer from Bi³⁺ to Sm³⁺ ions in Bi³⁺/Sm³⁺ co‐doped LGPO samples occurred and it realizes the color‐tunable emission from cyan to yellow including white‐light emission, through controlling Sm³⁺ content. Moreover, energy transfer mechanism between Bi³⁺ and Sm³⁺ ions is verified to be dipole‐dipole interaction by analyzing the spectroscopic experimental results and the critical distance between them is calculated to be 8.22 Å by concentration quenching method. Finally, it is illustrated that Bi³⁺ and Sm³⁺ co‐doped LGPO phosphors will be a promising candidate for n‐UV chip pumped w‐LEDs.     

Synthesis and luminescence properties of reddish-orange-emitting Ca2GdNbO6:Sm3+ phosphors with good thermal stability for high CRI white applications

Novel reddish-orange-emitting Ca₂GdNbO₆:Sm³⁺ phosphors based on the emission of ⁴G_5/2 → ⁶H_9/2 transition at 651 nm with the chromatic coordinate of (0.633, 0.366) were synthesized. The crystal structure and chemical purity were identified in detail. Under the 407 nm excitation, the optimum concentration of Sm³⁺ ion was found to be 5 mol% dominated by the dipole-dipole interaction in the Ca₂GdNbO₆ host material. The color purity of the sample with optimum doping was estimated to be about 78.38%. Besides, the thermal stability was also studied, and it was further found that the emission intensity remained 65.32% at 423 K. The packaged white LED device exhibited excellent CRI and CCT values of 92.43 and 4896 K. Finally, the polydimethylsiloxane film with a stable structure and flexible property was prepared. These above results reveal that novel reddish-orange-emitting Ca₂GdNbO₆:Sm³⁺ phosphors can be applied in high CRI white communication and flexible display applications.     

Abnormal thermal quenching behavior and optical properties of a novel apatite-type NaCa3Bi(PO4)3F:Sm3+ orange-red-emitting phosphor for w-LED applications

Novel apatite-type NaCa₃Bi(PO₄)₃F:xSm³⁺ (0.01 ≤ x ≤ 0.30) orange-red-light phosphors were synthesized through the solid-state method at high temperature. The crystal structure, energy band structure, density of state, phase purity, particle morphology, photoluminescence properties, thermostability, and luminescence decay of the phosphors were comprehensively characterized. When λ_ex = 404 nm, the optimal NaCa₃Bi(PO₄)₃F:0.05 S m³⁺ phosphor showed the orange-red emission (597 nm). The NaCa₃Bi(PO₄)₃F:Sm³⁺ phosphors exhibited abnormal thermal quenching properties as their emission intensity increased by about 2.57% from 300 to 380 K. Their intensity at 440 K was still 1.01-fold stronger than that at room temperature. The abnormal thermal quenching mechanisms were well explained via the coordinate configuration scheme. The thermal activation energy (E_a) was calculated to be 0.79 eV. The color purity of all the phosphors reached 99.9%. Ultimately, a white light-emitting diode (w-LED) was fabricated based on the tri-color RGB method. The color rendering index and the chromaticity coordinates of the fabricated w-LED were 89 and (0.310, 0.319), respectively. Thus, these high thermostability NaCa₃Bi(PO₄)₃F:Sm³⁺ orange-red phosphors can be potentially used in w-LED applications.     

Synthesis and spectroscopic analysis of Sm3+ doped CeO2 ceramic powders for the application of white LEDs

Orange-red light-emitting Sm³⁺-doped cerium oxide (CeO₂) ceramic powder with various concentrations of Sm³⁺ ions was prepared through a sol-gel process. X-ray diffraction and Rietveld analysis confirmed the formation of a purely cubic structure with a space group of $\mathit{Fm}\stackrel{?}{3}m$. The lattice parameters and unit cell volumes of the CeO₂:Sm³⁺ powder increased with the concentration of Sm³⁺ ions. The energy-dispersive X-ray spectra and corresponding mapping images confirmed the elemental composition and adequate dispersion of all elements in the CeO₂:Sm³⁺ powder. A broad excitation band at approximately 365?nm was observed in the excitation spectra of CeO₂:Sm³⁺ phosphors owing to the charge transfer transition from O 2p to Ce 4f orbitals. The Sm³⁺ doped CeO₂ phosphors emitted sharp luminescence with a main peak at 615?nm under excitation at 360?nm. The spectral analysis revealed that the CeO₂:Sm³⁺ phosphors exhibited strong orange-red emission. Concentration quenching was observed in the CeO₂:Sm³⁺ phosphors with 0.5?mol% of critical concentration of Sm³⁺ ions due to dipole dipole interaction of two nearest Sm³⁺ ions. The quantum efficiency was observed as high as 58%. The thermal stability of the present materials was estimated with the evaluation of activation energy as 0.31?eV. The broad excitation band and sharp orange–red emission indicated the potential use of CeO₂:Sm³⁺ phosphors for white light-emitting diodes.     

Red-emitting enhancement of Bi4Si3O12:Sm3+ phosphor by Pr3+ co-doping for White LEDs application

In this account, Bi₄Si₃O₁₂:Sm³⁺ and (Bi₄Si₃O₁₂:Sm³⁺, Pr³⁺) red phosphors were prepared by solution combustion method fueled by citric acid at 900 °C for 1 h. The effects of co-doping Pr³⁺ ions on red emission properties of Bi₄Si₃O₁₂:Sm³⁺ phosphors, as well as the mechanism of interaction between Sm³⁺ and Pr³⁺ ions were investigated by various methods. X-ray diffraction (XRD) and Scanning electron microscopy (SEM) revealed that smaller amounts of doped rare earth ions did not change the crystal structure and particle morphology of the phosphors. The photoluminescence spectroscopy (PL) indicated that shape and position of the emission peaks of (Bi₄Si₃O₁₂:Sm³⁺, Pr³⁺) phosphors excited at λ_ex=403 nm were similar to those of Bi₄Si₃O₁₂:Sm³⁺ phosphors. The strongest emission peak was recorded at 607 nm, which was attributed to the ⁴G_5/2→⁶H_7/2 transition of the Sm³⁺ ion. The photoluminescence intensities of Bi₄Si₃O₁₂:Sm³⁺ phosphors were significantly improved by co-doping with Pr³⁺ ions and were maximized at Sm³⁺ and Pr³⁺ ions doping concentrations of 4 mol% and 0.1 mol%, respectively. The characteristic peaks of Sm³⁺ ions were displayed in the emission spectra of (Bi₄Si₃O₁₂:Sm³⁺, Pr³⁺) phosphors excited at respectively λ_ex=443 nm and λ_ex=481 nm (Pr:³H₄→³P₂, ³H₄→³P₀). This indicated the existence of Pr³⁺→Sm³⁺ energy transfer in (Bi₄Si₃O₁₂:Sm³⁺, Pr³⁺) phosphors.     

Synthesis and luminescence properties of novel Y2Si4N6C:Sm3+ carbonitride phosphor

Novel Y₂Si₄N₆C:Sm³⁺ phosphors for white light-emitting diodes (w-LEDs) were prepared by a carbothermal reduction and nitridation method. X-ray diffraction (XRD) and photoluminescence spectra were utilized to characterize the structure and luminescence properties of the as-synthesized phosphors. The emission spectrum obtained by excitation into 291 nm contains exclusively the characteristic emission of Sm³⁺ at 568, 607 and 654 nm which correspond to the transitions from ⁴G_5/2 to ⁶H_5/2, ⁶H_7/2, and ⁶H_9/2 of Sm³⁺, respectively. The strongest one is located at 607 nm due to ⁴G_5/2–⁶H_7/2 transition of Sm³⁺. It was found that concentration quenching occurred as a result of dipole–dipole interaction according to Dexter's theory. The temperature dependence of photoluminescence properties was investigated from 25 to 300 °C and the prepared Y₂Si₄N₆C:Sm³⁺ phosphors showed superior thermal quenching properties.     

A building-block strategy for dynamic anti-counterfeiting by using (Ba,Sr)Ga2O4:Sm3+ new red persistent luminescent phosphor as an important component

Long persistent luminescence materials developed to commercial standards are primarily concentrated in the blue and green regions, with only a few in the red region. Red, as one of the three basic colors, can be mixed in various proportions with blue and green to yield various colors. The development of red persistent phosphors has a broader application potential but remains a challenge. A solid-state reaction method was used to synthesize new red persistent luminescent materials of Ba_1-xSr_xGa₂O₄:Sm³⁺ (x = 0–0.09). In BaGa₂O₄, both Sr²⁺ and Sm³⁺ preferentially occupy the Ba²⁺ site rather than the Ga³⁺ site. When exposed to UV light at 254 nm, the phosphors emit the characteristic red emission of Sm³⁺ at wavelengths ranging from 500 nm to 750 nm. After removing the UV light source, an intense red afterglow that lasted more than 1400 s was observed. The red afterglow signal reappears after a heating process. Doping Sr²⁺ reduces the trap depth and improves the red persistent luminescence significantly. Because the escaped electrons from traps compensate for the emission loss of Sm³⁺ during the heating process, the red phosphors have unimaginably luminescent thermal stability. Thus, the emission intensity at 200 ^°C is 1.6 times that at room temperature. The prepared red persistent phosphors show multimode luminescence, with the output signal being time and temperature sensitive, indicating that they are potential luminescent materials for anti-counterfeiting applications. Finally, a building-block strategy for advanced anti-counterfeiting applications of dynamic display information is proposed, with red persistent phosphors serving as an important component combined with upconversion phosphors of NaYF₄:Yb³⁺, Tm³⁺, and green persistent phosphors of SrAl₂O₄:Eu²⁺, Dy³⁺.     

Dazzling cool white light emission from Ce3+/Sm3+ activated LBZ glasses for W-LED applications

We synthesized a batch of co-doped (Ce³⁺+Sm³⁺): LBZ glass specimens by melt quenching process and their structural and radiation properties were studied by employing XRD, FE-SEM, optical absorption, photoluminescence and lifetime measurements. UV–Vis–NIR absorption studies of the co-doped (Ce³⁺+Sm³⁺): LBZ glassy matrix displays pertinent bands of both Ce³⁺ and Sm³⁺ ions. Individually doped Sm³⁺: LBZ glass exhibit bright orange emission at 603?nm (⁴G_5/2 → ⁶H_7/2) under the excitation of 403?nm. Nevertheless, the luminescence intensities pertaining to Sm³⁺ were extraordinarily increased by co-doping with Ce³⁺ ions to Sm³⁺: LBZ glassy matrices because of energy transfer from Ce³⁺ to Sm³⁺. The fluorescence spectra of co-doped (Ce³⁺+Sm³⁺): LBZ exhibits characteristic emission bands of Ce³⁺ (441?nm, blue) and Sm³⁺ (603?nm, reddish orange) under the excitation of 362?nm. Decay curves of Ce³⁺ and Sm³⁺ ions in co-doped glass has been fitted to double exponential nature. The decreasing lifetime of donor ion and rising lifetime of acceptor ion in double doped glass could support the energy transfer from Ce³⁺ to Sm³⁺ ions in the host matrix. The CIE coordinates and CCT values were calculated for all the obtained co-doped glassy samples from their luminescence spectra. By adding Ce³⁺ ions to individually doped Sm³⁺: LBZ glass matrix, the emitting color changes from reddish orange to white light which resembles the energy transfer from Ce³⁺ to Sm³⁺ ions. These studies, perhaps implied that attained co-doped (Ce³⁺+Sm³⁺): LBZ glassy samples are potential materials for white lighting appliances.     

Photoluminescence of Sr2P2O7:Sm3+ Phosphor as Reddish Orange Emission for White Light‐Emitting Diodes

A reddish orange emission Sr₂P₂O₇:Sm³⁺ phosphor is prepared by the solid‐state reaction method in air, and the crystal structure and luminescence properties of phosphors are investigated. Sr₂P₂O₇:Sm³⁺ phosphor shows Commission International de I'Eclairage (CIE) chromaticity coordinates (x = 0.5753, y = 0.4147). White light‐emitting diodes (W‐LEDs) fabricated using Sr₂P₂O₇:Sm³⁺ phosphor etc. show CIE chromaticity coordinates (x = 0.3471, y = 0.3124). These results indicate that Sr₂P₂O₇:Sm³⁺ phosphor could be a potential suitable reddish orange emitting phosphor candidate for W‐LEDs with excitation of a ~400 nm n‐UV LED chip.     

Tuning the Color Emission of Sr2P2O7: Tb3+, Eu3+ Phosphors Based on Energy Transfer

A series of color tunable Tb³⁺‐ and Eu³⁺‐activated Sr₂P₂O₇ phosphors were synthesized by a traditional solid‐state reaction method in air atmosphere. The crystal structure, photoluminescence (PL) properties, energy transfer, thermal stability, and luminous efficiency were investigated. A series of characteristic emission of Tb³⁺ and Eu³⁺ were observed in the PL spectra and the variation in the emission intensities of the three emission peaks at around 416 nm (blue), 545 nm (green), and 593 nm (orange‐red) induced the multicolor emission evolution by tuning the Tb³⁺/Eu³⁺ content ratio. The energy‐transfer mechanism from Tb³⁺ to Eu³⁺ ion was determined to be dipole–dipole interaction, and the energy‐transfer efficiency was about 90%. The novel phosphors have excellent thermal stability in the temperature range of 77–473 K and the Commission International De L'Eclairage 1931 chromaticity coordinates of Sr₂P₂O₇: Tb³⁺, Eu³⁺ (λ_ex = 378 nm) move toward the ideal white light coordinates.     

Photoluminescence properties of a double perovskite tungstate based red-emitting phosphor NaLaMgWO6:Sm3+

In this work, the conventional solid-state method was applied to synthesize a series of red-emitting NaLaMgWO₆:Sm³⁺ phosphors. The crystal structure, phase purity, morphology, particle size distribution as well as elemental composition of the as-prepared phosphors were investigated carefully with the aid of XRD, SEM, EDS, FT-IR analyses, indicating the high-purity and micron-sized NaLaMgWO₆:Sm³⁺ phosphors with monoclinic structure were prepared successfully. The spectroscopic properties of Sm³⁺ in NaLaMgWO₆ host including UV–vis diffuse reflection spectrum, photoluminescence excitation and emission spectra, decay curves, chromaticity coordinates and internal quantum efficiency were investigated in detail. Upon excitation with UV (290 nm) and n-UV (406 nm), NaLaMgWO₆:Sm³⁺ phosphor presented red emission corresponding to the ⁴G_5/2→⁶H_J (J = 5/2, 7/2, 9/2, and 11/2) transitions of Sm³⁺, in which the hypersensitive electronic dipole transition ⁴G_5/2→⁶H_9/2 (645 nm) was with the strongest emission intensity because Sm³⁺ ions were located at a lattice site with anti-inversion symmetry. The optimal concentration of Sm³⁺ was different for the given excitation wavelength such as 290 nm and 406 nm, which was interpreted by the extra effect of the energy transfer from W⁶⁺-O^2- group to Sm³⁺. The decay lifetime for ⁴G_5/2→⁶H_9/2 transition of Sm³⁺ was very short (< 1 ms) and decreased with the increasing Sm³⁺ concentration. The present investigation indicates that NaLaMgWO₆:Sm³⁺ phosphor could be a potential red component for application in w-LEDs.     

Citrate-based sol–gel synthesis and luminescent properties of Y6WO12:Eu3+, Dy3+ phosphors for solid-state lighting applications

The rare-earth ions (Eu³⁺, Dy³⁺) doped Y₆WO₁₂ phosphors were prepared by a citrate-based sol–gel method. The morphologies and structural properties of the as-prepared and doped samples were analyzed by scanning electron microscope images and X-ray diffraction patterns. The luminescent properties were studied by examining the excitation and emission spectra of the samples. The Eu³⁺ and Dy³⁺ ions doped samples exhibited their characteristic emission bands in the visible region under ultraviolet light excitation. The temperature-dependent photoluminescence (PL) properties of the samples were also investigated. The PL spectra of the synthesized samples by the sol–gel method were compared with those of the bulk sample prepared by a solid-state reaction. Similarly, the Commission International de I’Eclairage chromaticity coordinates and the decay times of Y₆WO₁₂:Eu³⁺ (3 mol%) and Y₆WO₁₂:Dy³⁺ (2 mol%) phosphors were studied.