Large enhancement of upconversion luminescence in Er<Superscript>3+</Superscript>/In<Superscript>3+</Superscript>:Ba<Subscript>0.85</Subscript>Ca<Subscript>0.15</Subscript>TiO<Subscript>3</Subscript> lead-free piezoelectric ceramics

A series of In³⁺-doped Ba_0.85Ca_0.15TiO₃:0.75%Er³⁺/xIn³⁺ (BCT:Er/xIn) lead-free piezoelectric ceramics with excellent upconversion luminescence were synthesized by the solid state reaction method. The effects of In³⁺ content on the crystal structure, ferroelectric, dielectric, piezoelectric, and upconversion luminescence properties were systematically studied. Under 980 nm excitation, a giant enhancement of the green emission (550 nm) by 10 times is achieved upon 2.5% mol In³⁺ doping, which is rarely observed in rare-earth ions-doped perovskite ferroelectric materials. The ultraviolet-visible-near infrared absorption measurements show that the In³⁺ doping may improve the dissolution of Er³⁺ ions and modify the isolate-/clustered-Er³⁺ ratio for x?≤?2.5%, resulting in the enhancement of the absorption cross-section, thereby contributing to the enhancement of green luminescence. Unfortunately, the In³⁺ doping suppresses the ferroelectric and piezoelectric properties of the BCT:Er/xIn ceramics. This problem can be resolved by adding a small amount (1 mol%) of Yb³⁺ to the BCT:Er/xIn ceramics to restore their good ferroelectric and piezoelectric properties. Such In³⁺ and rare-earth ions co-doped ceramics with greatly enhanced upconversion luminescence and good ferroelectricity and piezoelectricity may have potential applications in electro-optical devices.     

Effects of Ge<Superscript>4+</Superscript> acceptor dopant on sintering and electrical properties of (K<Subscript>0.5</Subscript>Na<Subscript>0.5</Subscript>)NbO<Subscript>3</Subscript> lead-free piezoceramics

Lead-free (K_0.5Na_0.5)(Nb_1-xGe _x )O₃ (KNN-xGe, where x = 0-0.01) piezoelectric ceramics were prepared by conventional ceramic processing. The effects of Ge⁴⁺ cation doping on the phase compositions, microstructure and electrical properties of KNN ceramics were studied. SEM images show that Ge⁴⁺ cation doping improved the sintering and promoted the grain growth of the KNN ceramics. Dielectric and ferroelectric measurements proved that Ge⁴⁺ cations substituted Nb⁵⁺ ions as acceptors, and the Curie temperature (T_C) shows an almost linear decrease with increasing the Ge⁴⁺ content. Combining this result with microstructure observations and electrical measurements, it is concluded that the optimal sintering temperature for KNN-xGe ceramics was 1020°C. Ge⁴⁺ doping less than 0.4 mol.%can improve the compositional homogeneity and piezoelectric properties of KNN ceramics. The KNN-xGe ceramics with x = 0.2% exhibited the best piezoelectric properties: piezoelectric constant d₃₃ = 120 pC/N, planar electromechanical coupling coefficient k_p = 34.7%, mechanical quality factor Q_m = 130, and tanδ = 3.6%.     

Luminescence performance of Eu<Superscript>3+</Superscript>-doped lead-free zinc phosphate glasses for red emission

In this study, the luminescence performance of zinc phosphate glasses containing Eu³⁺ ion with the chemical compositions (60–x)NH₄H₂PO₄-20ZnO-10BaF₂-10NaF–x Eu₂O₃ (where x = 0.2, 0.5, 1.0 and 1.5 mol%) has been studied. These glasses were characterized by several spectroscopic techniques at room temperature. All the glasses showed relatively broad fluorescence excitation and luminescence spectra. Luminescence spectra of these glasses exhibit characteristic emission of Eu³⁺ ion with an intense and most prominent red emission (614 nm), which is attributed to ⁵D₀ → ⁷F₂ transition. Judd-Ofelt (Ω₂, Ω₄) parameters have been evaluated from the luminescence intensity ratios of ⁵D₀ → ⁷F_J (where J = 2 and 4) to ⁵D₀ → ⁷F₁ transition. Using J-O parameters and excitation spectra, the radiative parameters are calculated for different Eu³⁺-doped glasses. Effect of γ-irradiation at fixed dose has been studied for all the Eu³⁺-doped glass matrices. The lifetimes of the excited level, ⁵D₀, have been measured experimentally through decay profiles. The colour chromaticity coordinates are calculated and represented in the chromaticity diagram for Eu³⁺-doped zinc phosphate glasses for all concentrations.     

Effects of Nb doping on the microstructure,ferroelectric and piezoelectric properties of 0.7BiFeO<Subscript>3</Subscript>–0.3BaTiO<Subscript>3</Subscript> lead-free ceramics

Donor-doped lead-free Bi_0.7Ba_0.3(Fe_0.7Ti_0.3)_1?x Nb_0.66x O₃ + 1 mol% MnO₂ ceramics were prepared by a conventional oxide-mixed method and the effects of Nb-doping on microstructure, piezoelectric and ferroelectric properties of the ceramics were investigated. All the ceramics exhibit a pure perovskite structure with rhombohedral symmetry. The grain growth of the ceramics is inhibited after the addition of Nb doping. High electric insulation (R = 10⁹–10¹⁰ Ω?cm) and the poor piezoelectric performance and weak ferroelectricity are observed after the addition of Nb₂O₅ in the ceramics. Different from the donor effect of Pb-based perovskite ceramics, the introduction of Nb into 0.7BiFeO₃–0.3BaTiO₃ degrades the piezoelectricity and ferroelectricity of the ceramics. The Bi_0.7Ba_0.3(Fe_0.7Ti_0.3)_1?x Nb_0.66x O₃ + 1 mol% MnO₂ ceramic with x = 0 exhibits the optimum piezoelectric properties with d ₃₃ = 133 pN C^?1 and k _p = 0.29 and high Curie temperature (T_C = 603^°C).     

Luminescent properties of europium-activated yttrium gadolinium phosphates

Nanocrystalline Y_{1 ? x ? y} Gd _x Eu _y PO₄ phosphors have been prepared via precipitation from aqueous solutions. From their luminescence and excitation spectra, the intensity ratio I ₆₁₅/I ₅₉₄ of the Eu³⁺ luminescence bands corresponding to electric dipole and magnetic dipole transitions has been determined as a function of Gd³⁺ content. The critical concentration and effective energy transfer radius in Y_{1 ? x ? y} Gd _x Eu _y PO₄ have been evaluated. Excitation of Gd³⁺⁸ S _J ?⁶ D _J and ⁸ S _J ?⁶ J _J transitions to Eu³⁺ luminescence excitation levels in Y_{0.99 ? x} Gd _x Eu_0.01PO₄ involves efficient energy transfer. Under 250-nm excitation, the Eu³⁺ luminescence yield in Y_{0.99 ? x} Gd _x Eu_0.01PO₄ is a factor of 2.5–3 higher than that in Y_0.99Eu_0.01PO₄.     

Sintering behavior,phase structure and electric properties of KNNTS-BKNZ ceramics with excessive alkali metals

We investigated the effect of excessive alkali metals on sintering character, phase structure, dielectric, piezoelectric and ferroelectric properties in KNN-based ceramics thoroughly. The 0.96(K_0.48Na_0.52)_1+xNb_0.93Sb_0.02Ta_0.05O₃–0.04Bi_0.5(K_0.12Na_0.88)_0.5ZrO₃ [(KN) _x NTS-BKNZ] lead-free piezoelectric ceramics were prepared by conventional solid-state reaction method. The sintering temperature of (KN) _x NTS-BKNZ ceramics increases gradually while the sintering temperature zone becomes narrow with the increasing x value. For the composition of x?>?0.03, the grains could not grow in all sintering temperature. The coexistence system of rhombohedral and tetragonal phases has been found in (KN) _x NTS-BKNZ ceramics and the T_R?T, T_C, d₃₃, and ε_r show a upward tendency with the increasing x when 0?≤?x?≤?0.03. The maximal piezoelectric coefficient d₃₃ of 415 pC/N was obtained at x?=?0.03. In addition, these ceramics presented good temperature stability. This study exhibits that excessive alkali metals influence sintering character and electrical properties on KNN ceramics deeply. It was believed that this work would be helpful for further understanding the effect of excessive alkali metals on sintering behavior and electric properties in KNN-based ceramics.     

Strong up-conversion luminescence and electrical properties of SrBi<Subscript>4</Subscript>Ti<Subscript>4</Subscript>O<Subscript>15</Subscript> multifunctional ceramics by Er<Superscript>3+</Superscript> doping

Novel green-emitting piezoelectric ceramics of SrBi_4?x Er _x Ti₄O₁₅ (SBT-xEr) were prepared. Strong up-conversion with bright green (524 and 548 nm) and a relatively weak red (660 nm) emission bands were obtained under 980 nm excitation at room temperature, which is attributed to the intra 4f–4f electronic transition of (²H_11/2, ⁴S_3/2)–⁴I_15/2 and the transition from ⁴F_9/2 to ⁴I_15/2 of Er³⁺ ions, respectively. Simultaneously, Er³⁺ doping promotes the electrical properties. At 0.8 mol%Er, the optimal electric properties with high Curie temperature of T _c?~527?°C, large remanent polarization of 2P _r?~14.92 μC/cm² and piezoelectric constant of d ₃₃?~17 pC/N was achieved. As a multifunctional material, Er³⁺ doped SBT showed a great potential to be used in 3D-display, bio-imaging, solid state laser and optical temperature sensor.     

Influence of the Preparation Conditions and Percolation Threshold on the Properties of Lead Zirconate Titanate/Cobalt Nickel Ferrite Magnetoelectric Composites

We have prepared magnetoelectric (ME) composite ceramics, free of foreign phases, in the lead zirconate titanate–cobalt nickel ferrite two-phase system: xPZT-36 + (100–x)Ni_0.9Co_0.1Fe₂O₄. The sol–gel derived ferrite powder used in our preparations seems to be doped with titanium cations from the PZT-36. The ceramics have a percolation threshold at x = 50–70 wt %, which is due to the increased electrical conductivity of Ni_0.9Co_0.1Fe₂O₄. As a consequence, the piezoelectric parameters of the ME ceramics drop sharply at x < 50–70 wt %: the piezoelectric moduli |d_ij| and piezoelectric voltage coefficients |g_ij| decrease by a factor of 3–5 in this composite range. The piezoelectric parameters |d_ij| and |g_ij| of the composites produced using the fine ferrite powder exceed those of the materials prepared using macrocrystalline Ni_0.9Co_0.1Fe₂O₄ powder by more than a factor of 2. The piezoelectric voltage coefficient g33 correlates with the ME coefficient ΔE/ΔH. The highest ME conversion efficiency (up to 45 mV/(cm Oe)) is offered by the 80 wt % PZT-36 + 20 wt % Ni_0.9Co_0.1Fe₂O₄ composites, whose composition lies in a subpercolation region. Even though the composites produced using the fine ferrite powder possess improved piezoelectric properties, they have smaller ΔE/ΔH coefficients (no greater than 25 mV/(cm Oe)), which can be tentatively attributed to the degradation of the properties of the ferrite as a consequence of doping with Ti⁴⁺ cations during the sintering of the composite ceramics.     

Structure and Magnetic Properties of Ce-Substituted Yttrium Iron Garnet Prepared by Conventional Sintering Techniques

Y_3?xCe _x Fe₅ O ₁₂ (CeYIG) ceramics, with x = 0, 0.15, 0.25, 0.35, 0.45, and 0.5, were fabricated by a conventional ceramic sintering technique. We studied the structures and magnetic fields of a series of CeYIG ceramics using X-ray powder diffraction, a scanning electron microscope, and a superconducting quantum interference device magnetometer. Findings showed that the substitution limit of the concentration of Ce³⁺ ions in the yttrium iron garnet structure was approximately x = 0.25. An extra CeO₂ phase was detected in the ceramic when the addition of CeO₂ content overtook the limit. The lattice constants and relative densities increased by increasing the Ce³⁺ contents in the ceramics. First, the saturation magnetization increased gradually with increases in the substitute concentration of Ce³⁺ ions and then decreased gradually when x = 0.35, 0.45, and 0.5. Overall, this study showed that the Y_3?xCe _x Fe₅ O ₁₂ material with x ≤ 0.15 exhibited excellent magnetic properties. Hence, the material show promise for magneto-optical and microwave communication applications.     

Structure and electrical properties of MnO doped (Ba<Subscript>0.96</Subscript>Ca<Subscript>0.04</Subscript>)(Ti<Subscript>0.92</Subscript>Sn<Subscript>0.08</Subscript>)O<Subscript>3</Subscript> lead free ceramics

In this work, (Ba_0.96Ca_0.04)(Ti_0.92Sn_0.08)O₃–xmol MnO (BCTS–xMn) lead-free piezoelectric ceramics were fabricated by the conventional solid-state technique. The composition dependence (0 ≤ x ≤ 3.0 %) of the microstructure, phase structure, and electrical properties was systematically investigated. An O–T phase structure was obtained in all ceramics, and the sintering behavior of the BCTS ceramics was gradually improved by doping MnO content. In addition, the relationship between poling temperature and piezoelectric activity was discussed. The ceramics with x = 1.5 % sintering at temperature of 1330 °C demonstrated an optimum electrical behavior: d ₃₃ ~ 475 pC/N, k _p ~ 50 %, ε _r ~ 4060, tanδ ~ 0.4 %, P _r ~ 10.3 μC/cm², E _c ~ 1.35 kV/mm, T _C ~ 82 °C, strain ~0.114 % and \(d_{33}^{*}\) ~ 525 pm/V. As a result, we achieved a preferable electric performance in BaTiO₃-based ceramics with lower sintering temperature, suggesting that the BCTS–xMn material system is a promising candidate for lead-free piezoelectric ceramics.     

Stability region of Eu<Subscript>2−<Emphasis Type="Italic">x</Emphasis></Subscript>Mn<Subscript>x</Subscript>O<Subscript>3+δ</Subscript> solid solutions in air

The homogeneity range of EuMnO₃ has been determined using x-ray diffraction analysis of single-and mixed-phase Eu_2?x Mn_xO_3+δ samples (0.90≤x≤1.20, Δx = 0.02) prepared from oxide mixtures by solid-state reactions in air between 900 and 1400°C. The results have been used to construct a partial phase diagram of the Eu-Mn-O system in air. The dependences of unit-cell parameters on x and synthesis temperature are presented for the samples synthesized at 1100 and 1400°C and for EuMnO₃, respectively. The solubility of europium oxide in EuMnO₃ is tentatively attributed to structural defects, and that of managanese oxides is interpreted in terms of structural defects, oxygen nonstoichiometry of europium manganite, the disproportionation reaction 2Mn³⁺ = Mn²⁺ + Mn⁴⁺, and partial substitution of the resulting Mn²⁺ for Eu³⁺ on the cuboctahedral site of the perovskite-like structure. To check these assumptions, systematic studies of the oxygen nonstoichiometry and structure of Eu_2?x Mn_xO_3+δ solid solutions synthesized at different temperatures are needed.     

Tunable luminescence properties and energy transfer of single-phase Ca<Subscript>4</Subscript>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript>O: Dy<Superscript>3+</Superscript>, Eu<Superscript>2+</Superscript> multi-color phosphors for warm white light

The novel Ca_4?x(PO₄)₂O: xDy³⁺ and Ca_4?x?y(PO₄)₂O: xDy³⁺, yEu²⁺ multi-color phosphors were synthesized by traditional solid-state reaction. The crystal structure, particle morphology, photoluminescence properties and energy transfer process were investigated in detail. The X-ray diffraction (XRD) results demonstrate that the products showed pure monoclinic phase of Ca₄(PO₄)₂O when x < 0.1. The scanning electron microscopy (SEM) indicated that the phosphors were grain-like morphologies with diameters of ~ 3.7–7.0 μm. Under excitation of 345 nm, Dy³⁺-doped Ca₄(PO₄)₂O phosphors showed multi-color emission bands at 410, 481 and 580 nm originated from oxygen vacancies and Dy³⁺. Interestingly, Ca₄(PO₄)₂O: Dy³⁺, Eu²⁺ phosphors exhibited blue emission band at 481 nm and broad emission band from 530 to 670 nm covering green to red regions. The energy transfer process from Dy³⁺ to Eu²⁺ was observed for the co-doped samples, and the energy transfer efficiency reached to 60% when Eu²⁺ molar concentration was 8%. In particular, warm/cool/day white light with adjustable CCT (2800–6700 K) and high CRI (R_a > 85) can be obtained by changing the Eu²⁺ co-doping contents in Ca₄(PO₄)₂O: Dy³⁺, Eu²⁺ phosphors. The optimized Ca_3.952(PO₄)₂O: 0.04Dy³⁺, 0.008Eu²⁺ phosphor can achieve the typical white light with CCT of 4735 K and CRI of 87.     

New NaSrPO<Subscript>4</Subscript>:Sm<Superscript>3+</Superscript> phosphor as orange-red emitting material

Sm³⁺-activated NaSrPO₄ phosphors could be efficiently excited at 403 nm, and exhibited a bright red emission mainly including four wavelength peaks of 565, 600, 646 and 710 nm. The highest emission intensity was found for NaSr _1?x PO₄: xSm³⁺ with a composition of x = 0.007. Concentration quenching was observed as the composition of x exceeds 0.007. The decay time values of NaSr_1?x PO ₄ : xSm³⁺ phosphors range from around 2.55 to 3.49 ms. NaSr_1?x PO₄: xSm³⁺ phosphor shows a higher thermally stable luminescence and its thermal quenching temperature T ₅₀ was found to be 350°C, which is higher than that of commercial YAG:Ce³⁺ phosphor and ZnS:(Al, Ag) phosphor. Because NaSr_1?x PO₄: xSm³⁺ phosphor features a high colour-rendering index and chemical stability, it is potentially useful as a new scintillation material for white light-emitting diodes.     

Influence of Nd doping on microwave dielectric properties of SrTiO<Subscript>3</Subscript> ceramics

Sr_1?x Nd _x TiO₃ (x?=?0.08–0.14) ceramics were prepared by conventional solid-state methods. The analysis of crystal structure suggested Sr_1?x Nd _x TiO₃ ceramics appeared to form tetragonal perovskite structure. The relationship between charge compensation mechanism, microstructure feature and microwave dielectric properties were investigated. Trivalent Nd³⁺ substituting Sr²⁺ could effectively decrease oxygen vacancies. This reduction and relative density were critical to improve Q?×?f values of Sr_1?x Nd _x TiO₃ ceramics. For ε _r values, incorporation of Nd could restrain the rattling of Ti⁴⁺ cations and led to the reduction of dielectric constant. The τ _f values were strongly influenced by tilting of oxygen octahedral. The τ _f values decreased from 883 to 650 ppm/°C with x increasing from 0.08 to 0.14. A better microwave dielectric property was achieved for composition Sr_0.92Nd_0.08TiO₃ at 1460 °C: ε _r ?=?160, Q?×?f?=?6602 GHz, τ _f ?=?883 ppm/°C.     

Improved electrical properties of Co-doped 0.92NBT–0.04KBT–0.04BT lead-free ceramics

The (1???2x)NBT–xKBT–xBT ternary piezoelectric system has been extensively studied in recent years. However, its electrical performance is far inferior to lead-based counterparts, and could not meet the requirements for practical applications. In this contribution, the 0.92NBT–0.04KBT–0.04BT (abbreviated as NKBT4) ceramics were prepared by traditional solid-state method. The effects of doped cobalt content on the structure and electrical performance of NKBT4 ceramics were studied systematically. The content of Co₂O₃ affects the average grain size, maximum dielectric constant, piezoelectric properties and the ferroelectric responses of the ceramics. It was found that the introduction of cobalt did not affect the phase structure of the ceramics, but is beneficial for the improvement of the dielectric and piezoelectric properties. When x?=?0.2, the piezoelectric coefficient (d₃₃) is around 130 pC/N, which is greatly improved compared to pure NKBT4 ceramics. Besides, a relatively high dielectric constant (ε_r?=?1150) was obtained at the same composition. This work paves a new way for the further development of high performance lead-free piezoelectric ceramics.     

Effects of Cr<Subscript>2</Subscript>O<Subscript>3</Subscript> doping on the microstructure and electrical properties of (Ba,Ca)(Zr,Ti)O<Subscript>3</Subscript> lead-free ceramics

Lead-free ceramics (Ba_0.85Ca_0.15)(Zr_0.1Ti_0.9)O₃?x wt.%Cr₂O₃ (BCZT-xCr) were prepared via the conventional solid-state reaction method. The microstructure and electrical properties of BCZT-xCr samples were systematically studied. XRD and Raman results showed that all samples possessed a single phased perovskite structure and were close to the morphotropic phase boundary (MPB). With the increase of the Cr content, the rhombohedral-tetragonal phase transition temperature (T _R-T) increases slightly, and the Curie temperature (T _C) shifts towards the low temperature side. XPS analysis reveals that Cr³⁺ and Cr^{5 +} ions co-existed in Cr-doped BCZT ceramics, indicating the different impact on the electrical properties from Cr ions as “acceptor” or “donor”. For the x = 0.1 sample, relative high piezoelectric constants d ₃₃ (～316 pC/N) as well as high Q _m (～554) and low tanδ (～0.8%) were obtained. In addition, the AC conductivity was also investigated. Hopping charge was considered as the main conduction mechanism at low temperature. As the temperature increases, small polarons and oxygen vacancies conduction played important roles.     

Effect of Ho-doping on structural,electrical and magnetic properties of La<Subscript>0.7</Subscript>Sr<Subscript>0.3</Subscript>MnO<Subscript>3</Subscript> ceramics prepared by Plasma-Activated Sintering

Different components of La_0.7?x Ho _x Sr_0.3MnO₃ (LHSMO, x = 0, 0.1, 0.2, 0.3) ceramics were fabricated by Plasma-Activated Sintering (PAS), so as to study the correlation between the contents of Ho³⁺ and the structural, electrical, magnetic properties. XRD and SEM confirmed that LHSMO ceramics prepared by PAS exhibited high-purity phase and dense microstructure. The measurement of electrical resistivity showed that the resistivity of LHSMO ceramics increased, and the metal–insulator transition temperature decreased with the increasing Ho-doping content. The resistivity data were then fitted using various empirical equations, and the conduction mechanism of LHSMO ceramics was found to be in accord with the electron–magnon scattering process in the low-temperature region and the small polaron hopping model in the high-temperature region. Lastly, we calculated the values of magnetoresistance of the LHSMO ceramics, which increased with increasing Ho-doping content, from 3.5% for x = 0 to 14.6% for x = 0.3. Therefore, the doping of Ho³⁺ into La_0.7Sr_0.3MnO₃ can effectively enhance the low-field magnetoresistance effect.     

Optical and transport properties of Fe-doped Cd<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Hg<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Se (<Emphasis Type="Italic">x</Emphasis> = 0.35)

The optical and transport properties of Fe²⁺-doped Cd _x Hg_1?x Se crystals with a midgap Fe²⁺ level have been studied. The results demonstrate that Fe²⁺ ions influence both the optical and transport properties of Cd _x Hg_1?x Se〈Fe²⁺〉. The observed optical absorption bands are due to a donor Fe²⁺ level in the band gap, with a depth E _Fe = 0.21 eV, and to band-band transitions. Thermal anneals in Hg and Se vapors have different effects on the carrier concentration and mobility in the crystals. The effect of annealing on the transport properties of the Fe²⁺-doped crystals differs from that for undoped crystals and is governed by the state of point defects.     

Growth of LiF/LiBaF<Subscript>3</Subscript> eutectic scintillator crystals and their optical properties

Li-containing materials can be applied as neutron scintillators, and LiBaF₃ can discriminate neutron and gamma rays. Moreover, LIF/LiBaF₃ can have higher cross section of thermal-neutron capture compared with LiBaF₃. In this study, LiF (82.5 mol%) and (Ba_1?x RE _x )F₂ (17.5 mol%, RE = Ce and Eu, x = 0.002) eutectic crystals, LiF/RE:LiBaF₃, were grown by the micropulling down method with different pulling rates (growth rate) in order to observe the eutectic structure. Lamellar microstructure was formed for each pulling rate. LiF/Ce:LiBaF₃ excited by 5.5-MeV alpha rays had a broad peak at ~350 nm corresponding to 5d–4f transition of Ce³⁺. On the other hand, LiF/Eu:LiBaF₃ had two scintillation processes; a sharp emission was originated from ⁶P_7/2 → ⁸S_7/2 transitions in the 4f electronic configuration of Eu²⁺ at 360 nm, and a broad one was attributed to Eu²⁺ trapped exciton recombination at 400–450 nm. Since scintillation light was observed for these materials, these scintillators are sensitive to neutrons.     

Tunable luminescence of Sr<Subscript>5(1−x)</Subscript>Ba<Subscript>5x</Subscript>(PO<Subscript>4</Subscript>)<Subscript>3</Subscript>Cl:Eu<Superscript>2+</Superscript> (0 ≤ x ≤ 100%) phosphors from different Eu<Superscript>2+</Superscript> centers

In this paper, a series of Eu²⁺ activated Sr_5(1?x)Ba_5x(PO₄)₃Cl (0?≤?x?≤?100%) phosphors were prepared by solid-state reaction method, and their luminescence properties under near-ultraviolet excitation were investigated. For Eu²⁺-activated Sr₅(PO₄)₃Cl, a strong emission band located at 445 nm is observed upon 365 nm excitation, which could be attributed to the 4f ⁶5d ¹–4f ⁷ transition of different Eu²⁺ centers. When the Ba²⁺ is introduced into the Sr₅(PO₄)₃Cl:Eu²⁺, the emission band of Eu²⁺ is broadened largely. The fluorescence lifetimes for different Eu²⁺ centers were determined by the decay curves and time-resolved spectra. The excitation spectra of the as-prepared samples cover a wide wavelength range from 240 to 420 nm, which can well match the emission wavelength of the near ultraviolet LED chip. The investigation of the thermal luminescence stability reveals that the introduction of Ba²⁺ could improve the thermal quenching properties.