Enhanced afterglow performance of CaAl_2O_4:Eu~(2+),Nd~(3+) phosphors by co-doping Gd~(3+)

In order to effectively improve the afterglow properties of CaAl_2 O_4:Eu~(2+),Nd~(3+) phosphors,a series of Ca_(0.982-x)Al_2 O_4:0.012 Eu~(2+),0.006 Nd~(3+),xGd~(3+)(x=0,0.012,0.024,0.036,0.048,0.060 mol) phosphors were prepared by a high-temperature solid-phase approach.Crystalline composition and microstructure were characterized by XRD,TEM,HRTEM,and XPS,luminescence properties were systematically analyzed by fluorescence spectra,afterglow decay curves and TL glow curve.Results show that all of Ca_(0.982-x)Al_2 O_4:0.012 Eu~(2+),0.006 Nd~(3+),xGd~(3+)phosphors belong to monoclinic CaAl_2 O_4,without other cystalline phase.The blue emission at 442 nm is observed,which is assigned to the 4 f~65 d→4 f~7 transition of Eu~(2+) ions.Doping with appropriate amount of Gd~(3+) ions(x=0.036 mol) significantly improves the afterglow properties of phosphors,but the excessive doping of Gd~(3+) induces the fluorescent quenching.The doping of moderate Gd3+changes the traps states,the trap depth varies from 0.598 to 0.644 eV and the trap concentration is also greatly improved,thus significantly improving afterglow performance.     

Blue-emitting Sr_(1-x)Ca_xLu_2O_4:Ce~(3+) phosphors for high CRI white LEDs

A broadband blue-emitting Sr_(1-x)Ca_xLu_2 O_4:Ce~(3+)(x=0-0.2) phospho rs were synthesized,which can be used for near-UV pumped white light-emitting diodes(w-LEDs).The crystal structures,photoluminescence pro perties,external quantum efficiency,the rmal stability and application perfo rmance of Sr_(1-x)Ca_xLu_2 O_4:Ce~(3+),by partially substituting Sr~(2+) with Ca~(2+)(x=0-0.2),were studied by various analytical techniques.When the Ca/Sr ratio of Sr_(1-x)Ca_xLu_2 O_4:Ce~(3+) gradually increases,the emission peak of Sr_(1-x)Ca_xLu_2 O_4:Ce~(3+) red-shiftes from 459 to 465 nm,corrected external quantum efficiency increases from 31.8% to 42.9%,and the thermal stability is also improved.The mechanism of the changes of the photoluminescence emission and excitation spectra,external quantum efficiency and thermal stability properties was also investigated in detail.In addition,a w-LED was fabricated by using SrLu_2 O_4:Ce~(3+)(blue),β-sialon:Eu~(2+)(green) and(Sr,Ca)AlSiN_3:Eu~(2+)(red) phosphors combined with a 405 nm near-UV LED chip,and its color rendering index(CRI) reaches 96.0.When Sr_(0.8)Ca_(0.2)Lu_2 O_4:Ce~(3+)is applied as blue phosphor to substitute SrLu_2 O_4:Ce~(3+),the obtained w-LED devices have high luminous efficiency,and CRI greater than 95.0.These re sults show that the Sr_(1-x)Ca_xLu_2 O_4:Ce~(3+) can be potential blue phosphors for n-UV pumped high CRI w-LEDs application.     

Monodisperse micro-spherical Sr2–zMg1+yYzAl22–xO36:xMn4+ red phosphors

With narrow red photoluminescence (PL) bands, tetravalent Mn⁴⁺ doped phosphors show promising prospect in commercial application to effectively expand color gamut of phosphor converted LED displays. Here, we report a type of Sr_2–zMg_1+yY_zAl_22–xO₃₆:xMn⁴⁺ phosphors with regular cage-like micro-spherical morphologies. The micron size spherical precursors were synthesized with a propylene oxide (PO) driven fast sol–gel method. The cage -like spherical morphology is beneficial to efficiently trapping much incident light to enhance the PL of the phosphors. Being calcined at 1300 ^°C, Sr₂MgAl_21.978O₃₆:0.022Mn⁴⁺ only exhibits the internal quantum efficiency (IQE) of 24.91%. With the Mg²⁺-Mn⁴⁺ codoping and Y³⁺/Sr²⁺ substituting strategies, to fulfill charge balance and produce John-Teller distortion, IQE of Sr_2–zMg_1+yY_zAl_22–xO₃₆:xMn⁴⁺ can be further improved up to 36.45%. The CIE color coordinates of Sr_2–zMg_1+yY_zAl_22–xO₃₆:xMn⁴⁺ under near ultraviolet excitation can be stably fixed to (0.723, 0.227) at deep red region. It thus finds a potential application as pc-LED display with much broader color gamut than that of the NTSC standard. Therefore, Sr_2–zMg_1+yY_zAl_22–xO₃₆:xMn⁴⁺ micron size spheres can be employed as promising red phosphors for high performance LED displays.     

Emission tunable of Mg_(0.695)Si_(0.695)Al_(1.39)O_(3.65)N_(0.35):Eu~(2+),Mn~(2+) oxynitride phosphors via energy transfer for WLEDs

A series of Eu~(2+)doped and Eu~(2+)/Mn~(2+) co-doped Mg_(0.695)Si_(0.695)Al_(1.39)O_(3.65)N_(0.35)(MSAON) phosphors were synthesized by solid-state reaction at a lower temperature of 1500℃.The crystal morphology and structure of MSAON host were characterized by SEM,TEM and XRD.The quantum yield(QY) for Eu~(2+)doped MSAON phosphors was measured as high as 62%,indicating the excellent luminous efficiency.For the Eu~(2+)/Mn~(2+)co-doped MSAON phosphor,the photoluminescence spectrum and delay curves reveal the efficient energy transfer(ET) process from Eu2+to Mn~(2+)ions.Meanwhile,the corresponding energy transfer efficiency,critical distance and mechanism are discussed in detail.Temperature-dependent emission spectrum shows the thermal and color stabilities.The emission color of MSAON:Eu~(2+),Mn~(2+)phosphors could be tuned from blue through white to red via varying the concentration of Mn~(2+) ions.White-light-emitting diodes(WLEDs) were successfully fabricated by encapsulating the phosphors in nUV LED(365 nm) devices obtaining white light with color rendering index(CRI) as high as 87.7.The results reveal that the MSAON:Eu~(2+),Mn~(2+)phosphors could have potential application in the field of n-UV WLEDs.     

Photoluminescence properties of Ca-doped BaMg Al10O17）：Eu2＋,Mn2＋ blue phosphor using BaF2 and CaF2 as co-flux

Ca-doped Ba Mg Al10O17：Eu2＋,Mn2＋（BAM） blue phosphors were synthesized by flux assisted solid-state reaction method using Ca F2 and Ba F2 as co-flux.Good dispersity and particle size homogenization of hexagonal pure phase BAM were obtained by sintering at 1400 ℃.The effects of the Ca2＋ ions content on the structure, morphology and photoluminescence properties of the phosphors were studied.The results indicated that the incorporation of Ca could decrease the lattice constant, improve the homogeneity and dispersity and enhance the photoluminescence（PL） intensity of the phosphor effectively.The optimum Ba0.86Ca0.04Mg0.97Al10O17：0.1Eu2＋,0.03Mn2＋ PL intensity was enhanced for about 30% and relative brightness was improved about 4%.Furthermore, the synthesized BAM and commercial BAM phosphors were annealed for 30 min at 600 oC in air.The Ca-doped phosphors had stronger emission intensity, higher brightness and better chromaticity stability than that of the commercial phosphor.These results indicated that Ca-doped blue phosphors had good potential applications in the commercial tricolor fluorescent lamps as well as in other display and lamps.     

Green and red phosphor for LED backlight in wide color gamut LCD

Wide color gamut(WCG) backlight for liquid crystal display(LCD) utilizing white light-emitting diodes(LED) has attracted considerable attention for their high efficiency and color reduction.In this review,recent developments in crystal structure,luminescence and applications of phosphors for wide color gamut LED backlight are introduced.As novel red phosphors,Mn~(4+)activate fluoride and aluminate phosphors are advanced in quantum efficiency,thermal quenching and color saturation for their characteristic spectrum with broad excitation band and linear emission.The crystal structure and fluorescence properties of Mn~(4+)doped fluosilicate,fluorogermanate,fluotitanate,as well as Sr_4 Al_(14)O_(25),CaAl_(12)O_(19) and BaMgAl_(10)O_(17) phosphors are discussed in detail.A serial of narrow-band red-emitting Eu~(2+),Eu~(3+)and Pr~(3+)-doped nitride silicates and molybdate phosphors are also introduced.Rare-earth-doped oxynitride and silicate green-emitting phosphors have attracted more and more attention because of the wide excitation,narrow emission,high quenching temperature,high quantum efficiency,such as β-sialon:Eu~(2+),Ba_3Si_6O_(12)N_2:Eu~(2+),MSi_2O_2N_2:Eu~(2+)(M=Ca,Sr,Ba),y-AlON:Mn~(2+)and Ca_3Sc_2Si_3O_(12):Ce~(3+).All above phosphors demonstrate their adaptability in wide color gamut LCD display.Especially for Mn~(4+)doped fluosilicate red phosphor and β-sialon:Eu~(2+)green phosphor.To achieve an ultra-high color gamut in white LED backlight and against the OLED,innovative narrow-band-emission red and green phosphor materials with independent intellectual property rights are continuously pursed.     

Tunable emission properties of tri-doped Ca_9LiY_(2/3)(PO_4)_7:Ce~(3+),Tb~(3+),Mn~(2+) phosphors with warm white emitting based on energy transfer

Tri-doped Ca_9 LiY_(2/3)(PO_4)_7:Ce~(3+),Tb~(3+),Mn~(2+)phosphors were prepared by a high-temperature solid state method.Under UV light excitation,Ca_9 LiY_(2/3)(PO_4)_7:Ce~(3+)samples exhibit a broad band ranging from 320 to 500 nm.At 77 K,the emission spectra of Ca_9 LiY_(2/3)(PO_4)7:Ce~(3+)samples present two obvious emission peaks,indicating that Ce~(3+)ions occupy two different kinds of lattice sites(Ca(1/2) and Ca(3)),As a good sensitizer for Tb~(3+),Ce~(3+)ions in Ca_9 LiY_(2/3)(PO_4)_7 lattice can effectively transfer part of energy to Tb~(3+),and the energy trans fer mechanism is determined to be dipole-dipole interaction.Consequently,the emitting color for Ce~(3+) and Tb~(3+) co-doped Ca_9 LiY_(2/3)(PO_4)_7 samples can be tuned from bluish violet to green.In order to further enlarge the emission gamut,Mn~(2+)ions as red emission components were added,forming tri-doped single-phase Ca_9 LiY_(2/3)(PO_4)_7:Ce~(3+),Tb~(3+),Mn~(2+)phosphors.The Ca_9 LiY_(2/3)(PO_4)_7:Ce~(3+),Tb~(3+),Mn~(2+)phosphors exhibit tunable emission properties through controlling the relative doping concentration of Ce~(3+),Tb~(3+)and Mn~(2+).Especially,Ca_9 LiY_(2/3)(PO_4)_7:0.09 Ce~(3+),0.12 Tb~(3+),0.30 Mn~(2+)can emit warm white light.The sample shows good thermal stability.At 150℃,the emission intensity for Ce~(3+)(360 nm),Tb~(3+)(545 nm) and Mn~(2+)(655 nm) decreases to 63%,69%,and 72% of its initial intensity,respectively.Moreover,the sample obtains good stability after 10 cycles between room temperature and150℃.     

Effects of Sr2+ on structure and luminescent properties of BaAl12O19:Eu phosphors

Ba_0.9-ySr_yAl₁₂O₁₉:Eu_0.1 phosphors were prepared by sol-gel technique, the crystalline structures of samples characterized by XRD, and the luminescence properties were investigated. The influence of crystallographic positions on the luminescent properties of Sr²⁺-doped BaAl₁₂O₁₉:Eu was investigated in detail. The results indicated that the crystal lattice of BaAl₁₂O₁₉:Eu was not influenced by the Sr²⁺ and doping Sr²⁺ in BaAl₁₂O₁₉:Eu enhanced the luminescent properties of the phosphors at the proper concentration of Sr²⁺. With the increasing of concentration of Sr²⁺ doped in BaAl₁₂O₁₉:Eu, the relative luminescent intensity of Ba_0.9-ySr_yAl₁₂O₁₉:Eu_0.1 strengthened and blue-shifted.     

Luminescence thermal quenching of M_2SiO_4:Eu~(2+)(M=Sr,Ba) phosphors

In this paper,luminescence thermal quenching of M_2SiO_4:Eu~(2+)(M=Sr,Ba) orthosilicate phosphors and mechanisms for thermal quenching proposed by different authors are briefly reviewed.Depending on preparation conditions and/or Eu~(2+)-doping concentrations,the quenching temperature(T_(1/2)) and activation energy for thermal quenching of the same orthosilicate phosphor reported by different authors are inconsistent.The common conclusion is that T_(1/2) of the intermediate compound(Ba_(1-x)Sr_x)_2 SiO_4:Eu~(2+)(x≈0.5) is higher than that of either Sr_2So_4;Eu~(2+)or Ba_2SiO_4;Eu~(2+)end-member.Moreover,T_(1/2) of the best-performing SrBaSiO_4:Eu~(2+)is evidently lower than that of YAG:Ce~(3+)and some Eu~(2+)-doped nitride phosphors.Rega rding the quenching mechanism,most of the investigators attributed thermal quenching to a thermally assisted 4f-5d cross-over in the configuration coordinate diagram.Only a few authors ascribed thermal quenching to a thermally assisted photoionization of 5 d electron to conduction band of the host.Nonetheless,a close inspection of T_(1/2) and Stokes shift derived from the vibrational spectra of the intermediate compound and end-member phosphors indicates that the 5d electron photo ionization model instead of the 4f-5d crossing decay model should be the genuine mechanism for the thermal quenching of M_2 SiO_4:Eu~(2+)(M=Sr,Ba) phosphors.Since the relationship between T_(1/2) and Stokes shift of the phosphors does not support the 4 f-5 d crossing decay model.The ionization probability of the 5 d electron depends on the energy gap(E_(dC)) between 5 d_1 level of the Eu~(2+)and conduction band minimum(CBM) of the host at higher temperatures.Lattice thermal expansion would result in an elevating 5 d_1 level of the Eu~(2+)along with a diminishing CBM of the host and as a consequence a reduction in E_(dC) and an enhanced photo ionization probability at elevated temperatures.A less rigid lattice and hence a larger coefficient of thermal expansion of M_2SiO_4 hosts should be the physical origin of poorer thermal quenching properties of the orthosilicate phosphors.     

Structure and luminescence properties of color-tunable phosphor Sr2La3(SiO4)3F:Tb3+,Sm3+

A series of single-phase and color-tunable phosphors Sr₂La₃(SiO₄)₃F:0.15Tb³⁺,xSm³⁺(SLSOF:0.15Tb³⁺,xSm³⁺) was prepared using solid-state route.The X-ray diffraction(XRD) was used to characterize the phase of the as-prepared samples.The synthesized phosphors have apatite-type structure without other impurities.Sm³⁺ and Tb³⁺ ions substitute La³⁺ into the lattice and form a single...     

Synthesis and luminescence properties of Sr3-z（AlxSi1-x）O5-xFx：zCe^3＋phosphors

Sr3-z(Alx,Si1-x)O -5-xFx:zCe3+ phosphors were synthesized by high-temperature solid-state reaction.The structure and luminescence properties of phosphors with various Al/Si ratios and Ce3+ concentrations were characterized using various methods such as X-ray diffraction,photoluminescence excitation and photoluminescence spectra.XRD result displayed that a complete solid solution between Sr3AlO4F and Sr3SiO5 was formed.With the increasing of x value,a broader excitation band and stronger absorption appeared in the blue light region.Moreover,the emission band shifted to a shorter wavelength and the emission intensity reached a maximum at x=0.6.By adjusting the concentration of Ce3+,a widely tunable range of emission wavelength under the excitation of 460 nm was obtained from the green to yellow regions.In addition,the concentration and thermal quenching were also discussed.     

High thermal stability and blue-violet emitting phosphor CaYAlO4:Ti4+ with enhanced emission by Ca2+ vacancies

Blue-violet light can not only enhance the total content of biomass and glucoside but also enrich the taste of the fruit. Thus, it is meaningful to study the blue-violet luminescent materials for plant cultivation. In this study, titanium (IV) -activated CaYAlO₄ (CYAO) phosphors were synthesized by conventional high-temperature solid–state reaction. X-ray powder diffraction was employed to analyze the crystal-structure of CYAO. It is found that the doped Ti⁴⁺ ions do not change obviously the crystal structure of phosphors. Upon 246 nm excitation, CaYAl_1-xO₄:xTi⁴⁺ phosphors exhibit broad blue-violet emission band peaking at 395 nm, which can be attributed to the charge transfer of Ti⁴⁺–O^2–. Moreover, this phosphor exhibits strong thermal stability. The luminescence emission intensity at 150 °C maintained about 91 mol% of its initial value at room temperature. Additionally, the electron transition process and concentration quenching mechanism of CaYAl_1–xO₄:xTi⁴⁺ are discussed in detail. The excellent luminescent properties indicate that CaYAl_1-xO₄:xTi⁴⁺ phosphor may have promising application in indoor plant cultivation.     

A novel long lasting phosphor Sr5 （PO4）3FxCll_x：Eu2＋,Gd3＋ prepared in air condition

A series of blue long afterglow mixed halide-phosphate phosphors Sr5 （PO4）3 FxCll-x：Eu2＋,Gd3＋ were synthesized in air by traditional solid-state reaction routte. The crystal structures, photoluminescence, thermolurninescenee properties and afterglow proper- ties of the phosphors were characterized systematically using X-ray diffraction （XRD）, luminescence spectrophotometer, microcom- puter thermoluminescence dosimeter and single photon counter, respectively. Under 280 nm excitation, the broadband emissions of Eu2＋ ions were observed at 445 nm （blue） due to the 4f7→4f65d transition. It was demonstrated that there existed the self-reduction of the Eu3＋ to Eu2＋ ions in this special halide-phosphate matrix in air condition. The addition of Gd3＋ ions obviously enhanced the after- glow properties of the single doped Eu2＋ ions in the halide-phosphate phosphors. And the content of the fluoride anions also had sig- nificant influence on the afterglow properties. All results indicated that Srs （PO4）3 FxCI1-x：Eu2＋,Gd3＋ might be potential phosphors for long lasting phosphorescence （LLP） materials.     

Influence of dysprosium concentration on sensitivity of luminescent thermometers of phosphors Ca_9Tb(PO_4)_5(SiO_4)F_2

Tb~(3+),Dy~(3+)-co-doped Ca_9 Tb_xDy_(1-x)(PO_4)_5(SiO_4)F_2 phosphors were prepared via high-temperature solidphase reaction method and the potential application in optical temperature measurements due to their color-tunable property was investigated in detail.The photoluminescence emission(PL) and photoluminescence excitation(PLE) spectra results show that the as-prepared phosphors exhibit both Tb~(3+) and Dy~(3+) emissions at 546 nm(~5 D_4-~7 F_5 transition of Tb~(3+)) and 587 nm(~4 F_(9/2)-~6 H_(13/2) transition of Dy~(3+)) upon376 nm excitation,respectively.In addition,the fluorescence decay analysis shows that the lifetime of the Tb3+emission rapidly decreases,which confirms the energy transfer existence between Dy~(3+) and Tb~(3+).Under 376 nm excitation,the temperature dependence of the fluorescence intensity ratios for the dualmission bands peaked at 546 and 587 nm was studied in the temperature range from 303 to 573 K.The results show that with the increase of Dy~(3+) concentration,the relative sensitivity first increases and then decreases,what's more,the maximum relative sensitivity is 3.142×10~(-3)%/K for Ca_9 Tb_xDy_(1-x)(PO_4)_5(SiO_4)-F_2(x=0.4).As a consequence,this preliminary study provides a novel method for exploring the novel thermo meters.     

Single-phase white-emitting and tunable color phosphor Na3Sc2(PO4)3:Eu2+,Dy3+: Synthesis,luminescence and energy transfer

A series of Eu²⁺/Dy³⁺ single doped and co-doped Na₃Sc₂(PO₄)₃ phosphors were synthesized by the high-temperature solid-state method, and their phase, morphology, and luminescence properties were characterized. Under the excitation of 370 nm, the Na₃Sc₂(PO₄)₃:Eu²⁺,Dy³⁺ phosphor can emit white light whose spectrum is composed of a broad emission band centered at 460 nm and the other three peaks at 483, 577, and 672 nm, respectively. There is energy transfer from Eu²⁺ to Dy³⁺ ion in Na₃Sc₂(PO₄)₃:Eu²⁺,Dy³⁺ phosphor due to the good overlap between the emission spectrum of Na₃Sc₂(PO₄)₃:Eu²⁺ and the excitation spectrum of Na₃Sc₂(PO₄)₃:Dy³⁺, which is further confirmed by the fluorescence lifetime decrease of Eu²⁺ ion with the increase of Dy³⁺ concentration. The process of energy transfer is via dipole–quadruple interaction which is confirmed by applying Dexter's theory. By increasing the Dy³⁺ concentration, the color coordinates of the Na₃Sc₂(PO₄)₃:0.01Eu²⁺,xDy³⁺ phosphors can be adjusted from blue to white, and then to yellow. The optimized concentration of Dy³⁺ ions is 4.0 mol%, beyond which the concentration quenching will take place. The Na₃Sc₂(PO₄)₃:Eu²⁺,Dy³⁺ phosphor shows fairly good resistance to thermal quenching behavior, of which the emission intensity at 423 K can maintain 90.3% of the initial value (298 K). These results suggest that the Na₃Sc₂(PO₄)₃:0.01Eu²⁺,xDy³⁺ phosphors have potential applications as the color-tunable or a single-phase white emitting phosphor in white LEDs.     

Spectral change and far-red emission of Mn2+ions co-doped NaSrB5O9:Dy3+luminescence material for plant growth LEDs

Due to the characteristic emission of phosphors,phosphor-converted LEDs have been employed to provide the requisite light sources for indoor plant growth in the optical agricultural industry.Herein,we prepared a series of Mn²⁺co-doped NaSrB5 O9:Dy³⁺phosphors via a solid-state reaction method.These phosphors have significant three-band emissions at 467 nm(blue region),606 nm(orange region),and765 nm(far-red region),ascribed to the⁴F_9/2-⁶H_15/2and 4 F9/2-6 H13/2 transitions of the Dy³⁺ions and the⁴T_1g(G)-⁶A_1g(S)spin-forbidden transition of the Mn²⁺ions,respectively,when excited by light of 376 nm(near-UV region).The co-dopant in the host material facilitates tunable photoluminescence(PL)due to energy transfer from the Dy³⁺ions to the Mn²⁺ions.The three emission peaks from the prepared phosphors well match with the absorption spectra of the photosynthesis pigments of plants,chlorophyll and phytochrome,which can absorb blue(400-500 nm),orange-red(550-700 nm),and infrared(IR)radiation,indicating that these phosphors have potential applications in the fabrication of plant-growth LEDs.Prior to the PL studies,the structure of the phosphors was determined by X-ray diffraction,refined by Rietveld method and chemically quantified by X-ray photoelectron spectroscopy.     

Effect of SiO2 introduction on luminescence properties of LuAG:Mn2+ phosphors

Mn²⁺doped LuAG phosphors with different contents of Si⁴⁺ions were synthesized via the solid-state reaction method and the effects of Si⁴⁺doping on the crystal structure and luminescence properties of phosphors were studied.XRD patterns of all phosphors exhibit a pure phase but with different extents of deviations.Owing to the 4 T1→6 A1 transition of Mn²⁺,the LuAG:Mn²⁺,Si⁴⁺phosphors exhibit a broad emission band with an emission peak at 582 nm.Moreover,the introduction of Si⁴⁺not only improves the emission intensity but also induces a red-shift with the emission peak from 582 to 612 nm and the spectra broadening with the full width at half maximum value from 64 to 74 nm,which results from the decrease of bond length between O2-anions and Mn²⁺cations and the re-absorption of Mn²⁺-Mn²⁺pairs.Suitable content of Si⁴⁺replacement can weaken thermal quenching of Mn²⁺.Thus,via regulating the content of Si,the Mn²⁺,Si⁴⁺co-doped LuAG phosphor with low correlated color temperature is a candidate for warm wLEDs.     

Synthesis,structure and optical properties of novel thermally robust Dy~(3+)-doped Ca_9Sc(PO_4)_7 phosphors for NUV-excited white LEDs

The powder samples of Ca₉Sc(PO₄)₇:xDy^{^(3+})white emitting phosphors were prepared via a solid state reaction technique.The Ca₉Sc(PO₄)₇:Dy³⁺samples were researched by using the GSAS Rietveld refinement and X-ray diffraction(XRD) methods,and SEM images and elemental maps were recorded.Under 350 nm excitatio n,the emission spectra of Ca₉Sc(PO₄)₇:xDy³⁺samples have two obvious peaks and one weak peak at 484,572 and660 nm,corresponding to the characteristic electron transitions of(⁴F_9/2→ ⁶H_15/2,blue),(⁴F_9/2→ ⁶H_13/2,yellow) and(⁴F_9/2→ 6 H11/2,red),respectively.The concentration quenching effect,decay lifetime and thermal quenching of the as-synthesized Ca₉Sc(PO₄)₇:Dy³⁺samples were researched systematically.The Ca₉Sc(PO₄)₇:0.02 Dy³⁺phosphor possesses a good thermal stability,of which the emission intensity at 423 K can maintain 79% of the initial value(273 K).In addition,through the study of the chro maticity coordinates of the Ca₉Sc(PO₄)₇:0.02 Dy³⁺phosphor,it is found that it is located in the white region,and the Commission Internationalede L’Eclairage(CIE) chromaticity coordinates are(0.339,0.389),The above results show that Ca₉Sc(PO₄)₇:xDy³⁺phosphors can be excellent candidate material for applications in NUV-excited white LEDs.     

Wastewater treatment using Fe-doped perovskite manganites by photocatalytic degradation of methyl orange,crystal violet and indigo carmine dyes in tungsten bulb/sunlight

We documented(ⅰ) the decolorization of wastewater in visible light,which contains methyl orange,crystal violet and indigo carmine dyes,using La_0.7Sr_0.3Mn_1-xFe_xO₃(x=0.0,0.05,0.1 and 0.5) manganites and(ⅱ) efficient separation of photocatalysts from water using magnetic field.These ceramic photocatalysts were sintered at 1050℃ for 12 h.Ceramics were characterized by X-ray diffraction(XRD),soft X-ray absorption spectroscopy(SXAS),Fourier transf...     

Effective regulation of electronic structures and luminescence properties of LiGd9(SiO4)6-x(GeO4)xO2:Dy3+ phosphors by tetrahedral substitution

A series of Dy³⁺-activated phosphors with the general formula LiGd₉(SiO₄)_6-x(GeO₄)_xO₂:Dy₃₊(0 ≤ x≤ 3)characterized by an apatite-type structure were successfully synthesized via a simple solid-state technique involving a partial substitution of [SiO₄]^4-with [GeO₄]^4- species.The effects of homovalent[GeO₄]^4--[SiO₄]^4- substit...