Synthesis and luminescence properties of bluish-green emitting K2MgSi3O8:Eu2+ phosphor

Eu2+-doped K2 Mg Si3O8 phosphors were synthesized by conventional solid-state reaction method. The phase formation of as-prepared samples was characterized by X-ray powder diffraction. The luminescence properties were investigated by the photoluminescence excitation and emission spectra, decay curve and CIE coordinates. The phosphor showed bluish-green emission centered at 460 nm under the excitation of UV and near UV light with the wavelength range of 250–430 nm. Two Eu2+ emission centers existed in the K2 Mg Si3O8:Eu2+ phosphor according to the luminescence spectra and the decay curves. The critical quenching concentration of Eu2+ doping was determined to be 3.0 mol.% and the concentration quenching mechanism was dipole-dipole interactions between Eu2+ ions. These results suggested that K2 Mg Si3O8:Eu2+ was a potential bluish-green phosphor candidate for white UV-LED.     

Synthesis and luminescence properties of a novel phosphor Ca2–x/2Si1–xPxO4:Eu2+for near UV-excited white-light-emitting diodes

A novel green-emitting phosphor,Eu2+-doped Ca2-x/2 Si1-x Px O4(0.25≤x≤0.30),was prepared through a conventional solidstate reaction.X-ray diffraction(XRD),photoluminescence(PL) and decay studies were employed to characterize the sample,which was assigned to P63mc space group in the hexagonal system.The effect of P-doping on the α-Ca2 SiO4 was studied and P2 O5 broken down by the raw material of(NH4)2 HPO4 played an important role in stabilizing α-Ca2 SiO4 which can only be stable at high temperature.The XRD patterns of the Ca2-x/2 Si1-x Px O4 host were found pure and optimized when the mole fraction of P2 O5 was 14.5%.The diffuse reflectance spectra of the Ca1.855 Si0.71 P0.29 O4 and Ca1.845 Si0.71 P0.29 O4 :0.01Eu2+covered the spectral region of 230-400 nm,implying that the phosphor was suitable for UV or near-UV LED excitation.The phosphor could be effectively excited in the near UV region with the maximum at 372 nm.The emission spectrum of the Ca1.845 Si0.71 P0.29 O4 :0.01Eu2+phosphor showed an asymmetrical single intensive band centered at 513 nm,which corresponded to the 4f65d1→4f7transition of Eu2+.Eu2+ions might occupy two types of Ca2+sites in the Ca1.855 Si0.71 P0.29 O4 lattice and form two corresponding emission centers,which led to the asymmetrical emission of Eu2+in Ca1.855 Si0.71 P0.29 O4.The effects of Eu2+-doped concentration in Ca1.855-x Si0.71 P0.29 O4 :xEu2+on the PL were also discussed,the optimum doping concentration of Eu2+was 1 mol.% and the critical distance of the energy transfer was also calculated by the concentration-quenching method.The non-radiative energy transfer between Eu2+seemed to be caused by the multipole-multipole interaction.The fluorescence lifetime of Eu2+was found to be 0.55711 μs.The results suggested that these phosphors might be promising candidates used for near UV light excited white LEDs.     

Luminescence properties of Eu2＋ -doped Ba3Si6O12N2 green phosphor： concentration quenching and thermal stability

The efficient Eu2+ -doped Ba3 Si6O12N2 green phosphors were prepared by a traditional solid state reaction method under N2 /H2 atmosphere at a temperature up to 1350 oC for 12h. Photoluminescence (PL) properties showed a broad emission band with a peak of 525 nm and the full width of half-emission maximums (FWHM) of 70 nm under 460 nm light irradiation. The X-ray diffraction patterns (XRD) and scanning electron microscope (SEM) images of the synthesized powder demonstrated its pure phase and excellent crystallization. Quenching concentration in this phosphor was found to be 0.3. The mechanisms of concentration quenching and redshift of emission peak with increasing concentration of Eu2+ were studied. The temperature dependence measurement of this green phosphor revealed excellent thermal quenching property compared to silicate green phosphor. It is believed that Ba3 Si6O12N2 :Eu2+ is an excellent green phosphor for UV or blue chip based white LEDs.     

Samarium doped apatite-type orange-red emitting phosphor Ca_5(PO_4)_2SiO_4 with satisfactory thermal properties for n-UV w-LEDs

A novel single-phase Sm~(3+) activated Ca_5(PO_4)_2SiO_4 phosphor was successfully fabricated via a conventional solid-state method, which can be e fficie ntly excited by near ultraviolet(n-UV) light-emitting chips.The crystal structure and luminescence properties were characterized and analyzed systematically by using relevant instruments. The Ca_5(PO_4)_2SiO_4:Sm~(3+) phosphor shows an orange-red emission peaking at600 nm under the excitation of 403 nm and the optimal doping concentration of Sm~(3+) is determined to be 0.08, The critical distance of Ca_5(PO_4)_2SiO_4:0.08 Sm~(3+) is calculated to be 1.849 nm and concentration quenching mechanism of the Sm~(3+) in Ca_5(PO_4)_2SiO_4 host is ascribed to energy transfer between nearestneighbor activators. The decay time of Ca_5(PO_4)_2 SiO_4: 0,08 Sm~(3+) is determined to be 1.1957 ms. In addition, the effect of temperature on the emission intensity was also studied, 72.4% of the initial intensity is still preserved at 250 ℃, better thermal stability compared to commercial phosphor YAG:Ce~(3+) indicates that Ca_5(PO_4)_2SiO_4:0.08 Sm3+ has excellent thermal stability and active energy is deduced to be 0.130 eV.All the results demonstrate that orange-red emitting Ca_5(PO_4)_2SiO_4:0.08 Sm~(3+) phosphor exhibits good luminescent properties. Owing to the excellent thermal quenching luminescence property,Ca_5(PO4)_2SiO_4:0.08 Sm~(3+) phosphor can be applied in n-UV white light emitting diodes and serve as the warm part of white light.     

Luminescent properties of red phosphors K2Ba（MoO4）2：Eu3＋ for white light emitting diodes

K2Ba(MoO4)2:Eu3+ phosphors were synthesized by solid-state reaction. The emission and excitation spectra of K2 Ba(MoO4)2:Eu3+ phosphors exhibited that the phosphors could be effectively excited by near ultraviolet (394 nm) and blue (465 nm) light, and emitted red light at 616 nm. The influence of Eu3+concentration, sintering temperature and charge compensators (K+, Na+ or Li+ ) on the emission intensity were investigated. The results indicated that concentration quenching of Eu3+ was not observed within 30mol.% Eu 3+, 600 oC was a suitable sintering temperature for preparation of K2 Ba(MoO4)2:Eu3+phosphors, and K+ ions gave the best improvement to enhance the emission intensity. The CIE chromaticity coordinates of K2 Ba(MoO4)2:0.05Eu3+phosphor were calculated to be (0.68, 0.32), and color purity was 97.4%.     

Luminescent Properties of SrGa2S4 :Eu and Its Application in Green-LEDs

Phosphor SrGa2S4Eu2 was synthesized with a high temperature solid state reaction.Its absorption spectrum, photoluminescence spectra, and fluorescence lifetime were studied in details.The excitation spectrum extended from UV to visible light region, and matched the emission of GaN chip.(Sr1-xEux)Ga2S4 emits strong green light and the concentration quenching did not occur; while the thermal quenching was evident.The emission peak shifted to long wavelength with increasing Eu2 concentration because of the changing of the crystal field strength.The lifetime of Eu2 ion was in the order of microsecond, which was reasonable for d→f transition.The electroluminescence spectrum of as-fabricated PC-LED at IF=20 mA was measured and most of the blue light of blue-LED chip at 460 nm was absorbed by the phosphor and simultaneously down-converted into an intensive green light at 540 nm.The color coordinate was (0.32, 0.63).SrGa2S4Eu2 was a promising phosphor for GaN-based green LEDs.     

Effect of gadolinium incorporation on optical characteristics of YNbO_4：Eu~（3＋） phosphors for lamp applications

Eu3+-doped (Y,Gd)NbO4 phosphor was synthesized by solid-state reaction for possible application in cold cathode fluorescent lamps. A broad absorption band with peak maximum at 272 nm was observed which was due to the charge transfer between Eu3+ ions and neighboring oxygen anions. A deep red emission at the peak wavelength of 612 nm was observed which could be attributed to the 5D0→7F2 transition in Eu3+ ions. The highest luminance for Y1-x-yGdyNbO4:Eux3+ under 254 nm excitation was achieved at Eu3+ concentration of 18 mol.% (x=0.18) and Gd3+ concentration of 8.2 mol.% (y=0.082). The luminance of Y0.738Gd0.082NbO4:Eu3+0.18 was higher than that of a typical commercial phosphor Y2O3:Eu3+ and the CIE chromaticity coordinate was (0.6490, 0.3506), which was deeper than that of Y2O3:Eu3+. The particle size of the synthesized phosphors was controlled by the NaCl flux and particle size as high as 8 μm with uniform size distribution of particles was obtained.     

Synthesis and luminescence characteristics of Li2Y4-xEux（WO4）7-y（MoO4）y red-emitting phosphor for white LED

Li2Y4-xEux（WO4）7-y（MoO4）y red-emitting phosphors were synthesized by solid state reaction and characterized by powder X-ray diffraction （XRD） and photoluminescence （PL） spectrum. The excitation spectra showed that the phosphors could be efficiently excited by near-UV light of 395 nm. When the relative molar ratio of Mo/W was 7：0, and the optimum doped concentration of Eu3＋was 2.8 mol, the phosphor showed strong red emission lines at 615 nm corresponding to the forced electric dipole 5D0→7F2 transition of Eu3＋. Compared with Na2Y2Eu2（MoO4）7 and K2Y2Eu2（MoO4）7, the fluorescence intensity of Li2Y1.2Eu2.8（MoO4）7 phosphor was the strongest. The CIE chromaticity coordinates of Li2Y1.2Eu2.8（MoO4）7 phosphor was calculated to be （0.66, 0.34）.     

Hydrothermal preparation and photoluminescent property of LiY(MoO4)2:Pr3+red phosphors for white light-emitting diodes

Praseodymium doped lithium yttrium molybdate Li Y1-8x Pr x(Mo O4)2(x=0.005–0.025) phosphors were successfully prepared by the hydrothermal method. The phase, morphology, and luminescent property of the prepared phosphors were investigated by X-ray diffraction and scanning electron microscopy. The results indicated that doping of Pr3+ ions did not change the main phase of the phosphors. The samples emitted red luminescence upon excitation at 453 nm and the strongest emission peak corresponding to the characteristic transition of the Pr3+ ion: 3P0→3F2 was observed at 657 nm. Li Y(Mo O4)2:Pr3+ red phosphors could be effectively excited by blue light emitting-diodes to emit red light; thus, acting as potential candidates for compensating the red light deficiency of cerium doped yttrium aluminum garnet yellow phosphor.     

Combustion synthesis and luminescence properties of blue NaBaPO4:Eu2+ phosphor

The blue-emitting phosphor NaBaPO4:Eu2+ was prepared by the combustion method. The phase structure and microstructure of the as-prepared samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. Under the excita-tion wavelength of 360 nm, the emission spectrum exhibited only one blue band centering at 435 nm, which was ascribed to the 4f65d1→4f7 transition on Eu2+ ions. Compared with the phosphor obtained by solid-state reaction method, the relative emission intensity of sample ob-tained by combustion method increased slightly. The decay times and the temperature dependence luminescence intensities (25-300 oC) were discussed in order to further investigate the potential applications. Furthermore, Eu2+-doped NaBaPO4 phosphor showed higher thermally sta-ble luminescence comparable to commercially available Y3Al5O12:Ce3+ (YAG:Ce3+) phosphor. All the investigated suggestions that Na-BaPO4:Eu2+ is a good phosphor candidate applied in white light emitting diode.     

Preparation and luminescence properties of orange-red Ba3Y4O9:Sm3+ phosphors

A novel orange-red emitting Ba₃Y₄O₉:Sm³⁺ phosphors were prepared by a high temperature solid-state reaction in air. X-ray diffraction (XRD), photoluminescence spectra, fluorescence decay and temperature-dependent emission spectra were utilized to characterize the structure and luminescence properties. The results show that the excitation spectrum includes a series of linear peaks at 350, 367, 382, 410, 424, 445, 470 and 495 nm, respectively. Under 410 nm excitation, the emission peaks were located at 574 nm (⁴G_5/2—⁶H_5/2), 608 nm (⁴G_5/2—⁶H_7/2), 659 nm (⁴G_5/2—⁶H_9/2) and 722 nm (⁴G_5/2—⁶H_11/2), respectively. The concentration quenching occurs when x equals 0.08 for Ba₃Y_4–xO₉:xSm³⁺ phosphor and its mechanism is ascribed to the dipole–dipole interaction. The chromaticity coordinates of Ba₃Y_3.92O₉:0.08Sm³⁺ phosphor are in the orange-red region. The temperature-dependent study shows that this phosphor has excellent luminescence thermal-stability. And the luminescence intensity of Ba₃Y_3.92O₉:0.08Sm³⁺ phosphor at 473 K only declines by about 25.75% of its initial intensity. The experimental data indicate that Ba₃Y₄O₉:Sm³⁺ phosphor may be promising as an orange-red emitting phosphor for white light emitting diodes.     

Thermoluminescence Characteristics of SrB6O10 ： Tb

SrB6010：Tb phosphor was synthesized by high-temperature solid state reaction. The influences of Ce or Li as a co-dopant, Tb concentration and irradiation dose exposure on TL of SrB6010 ： Tb were investigated. Results show that Ce or Li as a co-dopant can not improve the sensitivity of SrB6010：Tb phosphor. TL response depends on Tb concentration and 0.02 is the optimum in the concentration range from 0.01 to 0.10. Using the optimum Tb concentration, we calculated the kinetic parameters of SrB6010：Tb employing the peak shape method, and suggested the phosphor obeying the second order kinetics. TL emission intensity is linearly dependent on the irradiation dose within the dose range of 50 - 200 Gy. The characteristic Tb^3＋ ion emission was observed in TL emission spectrum.     

Luminescence properties of near-UV excitable yellow-orange light emitting warm CaSrAl2SiO7:Sm3+ phosphors

Single-phase CaSrAl_2 SiO_7:Sm~(3+) phosphors were synthesized by traditional high temperature solid state reaction method. Formation of samples and phase analysis were confirmed by X-ray diffraction technique. Morphology was done by field emission scanning electron microscopy and elemental compositions were confirmed by energy dispersive X-ray analysis. Present phosphors have tetragonal crystallography with space group P42_1 m. Average crystallite size was calculated by using Scherrer and Williamson-Hall method. Photoluminescence study of CaSrAl_2 SiO_7:Sm~(3+) phosphor was investigated.Under different excitation wavelengths, PL spectra consist of four emission bands at 564, 570, 601 and650 nm. The emission bands located at 564 and 570 nm are associated with the transition ~4 G_(5/2)→~6 H_(5/2)while emission bands at 601 and 650 nm are due to ~4 G_(5/2)→~6 H_(7/2) and ~4 G_(5/2)→~6 H_(9/2),respectively.Intense emission was obtained when phosphor was excited under 404 nm wavelength. Non-radiative energy transfer process involved in concentration quenching, was also discussed. CIE coordinate is found in yellow-orange region, hence CaSrAl_2SiO_7:Sm~(3+) phosphors emit yellow-orange light when efficiently excited by near UV(～400 nm) LED chip. Color purity and CCT of the phosphor were determined; CCT suggests that present phosphor is a good candidate as a warm yellow-orange color emitting phosphor. Effect of different heating rates and different UV exposure time on the TL glow curve of the phosphor was investigated. Activation energies and kinetic parameters for different traps were calculated by using peak shape method. TL emission spectrum was also recorded. Present article explains all the possible mechanisms associated with luminescence process in CaSrAl_2 SiO_7:Sm~(3+) phosphors.     

Preparation,structure, luminescence properties of europium doped zinc spinel structure green-emitting phosphor ZnAl2O4:Eu2+

The Zn_(1-x)Al_2 O_4:xEu~(2+) phosphor powders were synthesized by the solid-state reaction method.The synthesis temperature for ZnAl_2 O_4 was optimized,whereas the phase structure,TEM images,photoluminescence(PL) properties,the concentration quenching mechanism,the fluorescence decay curves,as well as the CIE chromaticity coordinates of the samples were investigated in details.Under the excitation at 379 nm,the phosphor exhibits an asymmetric broad-band green emission with a peak at 532 nm,which is ascribed to the 5 d-4 f transition of Eu2+.When the doping concentration of Eu2+ ions is 0.01,the luminescence intensity of the sample reaches the maximum value.It is further proved that the exchange interaction results in the concentration quenching of Eu2+ in the Zn_(1-x)Al_2 O_4:xEu~(2+) phosphor powders.The thermal quenching property of ZnAl_2 O_4:Eu~(2+)phosphor was investigated and the quantum efficiency(QE) values of the selected Zn_(0.99)Al_2 O_4:0.01 Eu~(2+) phosphor was measured and determined as 54.85%.The lifetime of the optimized sample Zn_(0.99)Al_2 O_4:0.01 Eu~(2+) is 3.0852 μs and the CIE coordinate of the sample was calculated as(0.3323,0.5538) with high-color-purity green emission.All properties indicate that the green-emitting ZnAl_2 O_4:Eu~(2+) phosphor powder has potential application in white LEDs.     

Vacuum ultraviolet excited photoluminescence properties of Gd2O2CO3：Eu^3＋ phosphor

The Gd2O2CO3：Eu^3＋ with type-Ⅱ structure phosphor was successfully synthesized via flux method at 400 ℃ and their photoluminescence properties in vacuum ultraviolet （VUV） region were examined. The broad and strong excitation bands in the range of 153-205 nm owing to the CO3^2- host absorption and charge transfer （CT） of Gd^3＋-O2^- were observed for Gd2O2CO3：Eu^3＋. Under 172 nm excitation, Gd2O2CO3：Eu^3＋ exhibited strong red emission with good color purity, indicating Eu^3＋ ions located at low symmetry sites and the chromaticity coordination of luminescence for Gd2O2CO3：Eu^3＋ was （x=0.652, y=0.345）. The photoluminescence quenching concentration of Eu^3＋ excited by 172 nm for Gd2O2CO3：Eu^3＋ was about 5%. Gd2O2CO3：Eu^3＋ would be a potential VUV-excited red phosphor applied in mercury-free fluorescent lamps.     

Luminescence properties of phosphate phosphors Ba3Gd1−x(PO4)3:xSm3+

A series of reddish orange phosphors Ba_3Gd_(1-x)(PO_4)_3:xSm~(3+)(x = 0.02.0.04,...,0.12) were prepared by the high-temperature solid-state reaction. X-ray powder diffraction(XRD) and diffuse reflectance and photoluminescence spectra were utilized to characterize the structure and spectral properties of the phosphors. The phosphors have strong absorption in the near-UV region. CIE chromaticity coordinates of the phosphors are located in the reddish orange region since the strongest emission band is around 598 nm and related to the ~4 G_(5/2)→~6 H_(7/2) transition of Sm~(3+). Optimal concentration of Sm~(3+) in the phosphors is about 6.0 at%. The quantum yield of the Ba_3Gd_(0.94)(PO_4)_3:0,06 Sm~(3+) under excitation at 403 nm is about 52.07%. Temperature dependent photoluminescence spectra of the Ba_3Gd_(0.94)(PO_4)_3:0.06 Sm~(3+) were measured and the phosphor exhibits high thermal stability of emission. All the results show that the Ba_3Gd(PO_4)_3:Sm~(3+) phosphor may be a potential red phosphor for near-UV based white LEDs.     

Luminescent properties of amorphous phosphor 1.4YeO3·2.5Al2O3·0.1Tb2O3 prepared by sol-gel method

Amorphous phosphor 1.4YeO3·2.5Al2O3·0.1Tb2O3 （the same composition as Y2.8Tb0.2Al5O12） was prepared via a sol-gel method at relatively low temperature （i.e., below 650℃）, which is much lower than that for the preparation of polycrystalline Y3Al5O12：Tb^3＋ （above 1400℃）. The amorphous phosphor prepared in the optimized conditions showed a bright green-yellowish luminescence, the intensity of which was comparable with that of polycrystalline sample and the emissions of which were assigned to 5D4 → 7Fj transitions of Tb^3＋. Besides the emissions of Tb^3＋, the amorphous samples prepared at temperatures below 500 ℃ presented a weak blue emission band around 420 nm.     

Synthesis and photoluminescent properties of Sm~(3+)-activated La_3Si_6N_(11) as an orange-red emitting phosphor

A series of Sm³⁺-doped La₃Si₆N₁₁phosphor materials we re synthesized by a high temperature solid-state reaction method.The crystal structure,micro structure,photoluminescence properties,decay curves as well as thermal quenching properties of the as-prepared phosphors were investigated systematically.The excitation spectra contain a wide asymmetric band below 350 nm originating from the host absorption,several sharp excitation peaks in the range of 300-550 nm corresponding to f-f transition of Sm³⁺.Under the excitation of 369 and 414 nm light,the phosphors exhibit strong narrow-band orangered emission peaked at 605 nm.The average decay time of La_2.99Si₆N₁₁:0.01 Sm³⁺sample is fitted to be0.38 ms and the CIE coordinates were calculated to be(0.6105,0.3833).For water resistance,La₃Si₆N₁₁:Sm³⁺is better than K₂SiF₆:Mn⁴⁺phosphor.After soaking in deionized water for 300 min,the La₃Si₆N₁₁:Sm³⁺sample retains approximately 80%of its initial relative emission intensity.When the temperature rises to 423 K(150℃),the emission intensity of La_2.99Si₆N₁₁:0.01 Sm³⁺sample remains 85%in co mparison to that of room tempe rature.The activation energy was calculated to be 0.63253 eV,which is higher than those of Sm³⁺-activated oxide phosphors,indicating that the phosphor has relatively good thermal stability.