Photoluminescence Spectra of CaS:Er and CaS:Tb Powder Phosphors

This paper reports the method of preparation and the emission level assignments for the light emitting powder phosphors of CaS:Er³⁺ and CaS:Tb³⁺. The recorded photoluminescence spectra of these powder phosphors have shown that the light emission would be better at lower dopant concentrations.     

Sensitization in CaS:Bi:Tm phosphors

The emission spectra of calcium sulphide phosphors activated with bismuth, thulium, and both together are studied in the spectral range of 4000 Å to 8000 Å. The results indicate resonance transfer of excitation energy from Bi to Tm. Sensitizer to sensitizer transfer also appears to be appreciable. A plausible energy level diagram is proposed to explain the sensitization mechanism.     

Relaxation kinetics of Sm: Ce-doped CaS phosphors

Different samples of calcium sulphide (CaS):CaS(Sm) and CaS(Sm,Ce) phosphors have been prepared. To study the phosphorescence decay systematically, the samples were excited to a saturation using 259 nm line of xenon lamp and phosphorescence emission was monitored for a wavelength 569 nm of samarium. The trap depth has been evaluated by analyzing the decay curves. The observed decay could be explained satisfactorily by assuming a superposition scheme. The thermoluminescence properties of the doped CaS phosphors are also investigated in detail by computerized deconvolution technique of the glow curves obtained by UV irradiation.     

Photoluminescence of SrS: Cu phosphors

Results of the investigation on the spectral characteristics of PL of SrS:Cu phosphors are presented. Probable emitters for the three observed bands, viz. 4710 Å, 5200 Å and 5480 Å, have been suggested.     

Thermally stimulated luminescence of CaS : Bi : Pd phosphors

CaS phosphors co-activated with Bi⁺³ and Pd⁺² impurities in varying concentrations have been prepared and their thermoluminescence has been systematically studied. The general features of the curves are discussed and the activation energies have been estimated in three different ways. The escape frequency factor is determined using the theoretical model of Randall and Wilkins. Conclusions are drawn regarding the type of kinetics involved in the thermoluminescence process.     

Photoluminescence of ion-implanted phosphors

Ion-implanted phosphors were prepared by implanting Sb in CaS at 25 keV with concentration ranging from 0.05 to 0.2% by weight. Samples of similar concentration were also prepared using the conventional technique. The spectral response under UV excitation of both types of samples is compared.     

Emission and thermoluminescence characteristics of CaS:Bi:Fe phosphors

The emission and thermoluminescence characteristics of CaS:Bi,Fe phosphors were studied. It is observed that addition of Fe quenches the luminescence of CaS:Bi, which may be attributed to non-radiative transitions to deep Fe levels. The trap depth (0.6 eV) obtained from glow curve maxima is attributed to the CaS host lattice.     

ac anddc electroluminescence in CaS:Cu,Sm phosphors

Theac anddc electroluminescence in CaS:Cu, Sm have been investigated. The luminescence spectra show three peaks in the visible region. The brightness-voltage dependence satisfies the relationB=B ₀ exp (−b/V ^1/2) with two modes of variation. The nature of this dependence indc andac at different frequencies is discussed. The electroluminescence brightness also depends on the temperature of the phosphors and shows a peak around 80.0;C. The electroluminescence efficiency increases with applied voltage up to 2200 V and this dependence on V is explained on the basis of a transport process of the Schottky emission type.     

Thermally stimulated luminescence and infrared studies of CaS : Bi,Tm phosphors

Calcium sulphide phosphors doped with bismuth and thulium are prepared from Indian minerals. The glow curves are recorded in the temperature range of 96–320 °K. The activation energies are determined by analyzing the glow peaks after thermal cleaning, using different methods. The results show that, in these phosphors, the electron traps responsible for thermoluminescence are present prior to irradiation. The infrared absorption spectra are recorded in the range of 4000-250 cm^-1. It is concluded that the traps are due to host lattice defects which may arise from S^-2 ion vacancies, created during phosphor preparation.     

Kinetics of luminescence as revealed from photo-, thermo- and electro-luminescence studies on CaS : Ag phosphors

Phosphorescence decay, thermoluminescence and electroluminescence of CaS : Ag phosphors prepared with a varying amount of silver as activator have been studied at room temperature, 301 K. The observations have been analysed to obtain the information about the type of kinetics involved in the luminescence process. In addition to this, the effect of the addition of an activator on the luminescence behaviour of the phosphors and on the distribution of trapping levels is discussed.     

Electron beam induced green luminescence and degradation study of CaS:Ce nanocrystalline phosphors for FED applications

Green luminescence and degradation of Ce³⁺ doped CaS nanocrystalline phosphors were studied with a 2 keV, 10 μA electron beam in an O₂ environment. The nanophosphors were synthesized by the co-precipitation method. The samples were characterized using X-ray diffraction, Transmission electron microscopy, Scanning electron microscopy/electron dispersive X-ray spectroscopy and Photoluminescence (PL) spectroscopy. Cubic CaS with an average particle size of 42 ± 2 nm was obtained. PL emission was observed at 507 nm and a shoulder at 560 nm with an excitation wavelength of 460 nm. Auger electron spectroscopy and Cathodoluminescence (CL) were used to monitor the changes in the surface composition of the CaS:Ce³⁺ nanocrystalline phosphors during electron bombardment in an O₂ environment. The effect of different oxygen pressures ranging from 1 × 10⁻⁸ to 1 × 10⁻⁶ Torr on the CL intensity was also investigated. A CaSO₄ layer was observed on the surface after the electron beam degradation. The CL intensity was found to decrease up to 30% of its original intensity at 1 × 10⁻⁶ Torr oxygen pressure after an electron dose of 50 C/cm². The formation of oxygen defects during electron bombardment may also be responsible for the decrease in CL intensity.     

Photoluminescence of concentration series of CaF2: Mn phosphors excited by VUV radiation

Fluorescent characteristics of a series of powder CaF₂: Mn phosphors (from 0.01 to 2.47 wt. % of Mn in the mixture) excited by VUV radiation with quantum energies up to 14 eV at 293 K and up to 12 eV at 85 K are measured. Narrow excitation bands of Mn²⁺ centers found at 7.9 and 8.6 eV (at 293 K) are assigned to partially forbidden transitions of electrons from the ground state ⁶ S split by the crystalline field (10 Dq=0.71 eV from the literature) in two sublevels to the excited level corresponding to the ⁶ D term of a free Mn²⁺ ion (3d ⁵ → 3d ⁴4s transitions). A wide nonelementary excitation band in the region of 9.1–10.3 eV is interpreted as photogeneration of near-activator D-excitations: allowed transitions of electrons from levels that are split from the top of the valence band under the influence of an impurity ion to the free 4s-orbital of a Mn²⁺ ion. Channels of energy transport in the CaF₂: Mn system are briefly analyzed.     

Photoluminescence enhancement in manganese-doped magnesium stannate phosphors synthesized by millimeter-wave irradiation

We have investigated photoluminescence (PL) of Mg₂SnO₄:Mn phosphors synthesized by the irradiation with millimeter-wave of 24 GHz. The PL spectrum at room temperature is dominated by a green band peaking at 500 nm, suggesting the existence of tetrahedral Mn²⁺ sites. When the phosphors are grown by the millimeter-wave heating, the 500 nm band is so much intense compared to those by the electric furnace heating. To clarify the origin of the PL enhancement, we have carried out the measurements of scanning electron microscope (SEM) and electron spin resonance (ESR). The SEM image exhibits the growth of small round particles with an average size of 1.6 μm. Such well-grown micron-sized particles were not observed under the electric furnace heating. The ESR spectra exhibit six prominent lines, the intensity of which becomes greater for the phosphors obtained by the millimeter-wave heating. From this observation, it is supposed that the PL enhancement is mainly due to the increase in the number of tetrahedral Mn²⁺ sites. Therefore, the millimeter-wave heating has an important advantage over the electric furnace heating in the synthesis of Mg₂SnO₄:Mn phosphors.     

CaS2：Eu的直流电致发光

制备了CaS,Se:Eu红色DCEL屏.在CaS:Eu中掺入少量Se可以改进DCEL性能.研究了Pb对CaS:Eu的影响.通过发射、激发光谱及衰减的测量,认为Pb2+敏化了Eu2+.与常规的CaS:Eu相比,CaS:Eu,Pb的DCEL效率和寿命都明显提高了.     

Photoluminescence properties of color-tunable SrMgAl10O17:Eu2+,Mn2+ phosphors for UV LEDs

Aluminate phosphors SrMgAl₁₀O₁₇ codoped with Eu²⁺ and Mn²⁺ ions were prepared by solid-state reaction. The phase structure and photoluminescence properties of the as-prepared phosphors were characterized by powder X-ray diffraction, photoluminescence excitation and emission spectra. Upon excitation of UV light, two broad emission bands centered at 470 and 515 nm were observed, and they were assigned to Eu²⁺ and Mn²⁺ emissions, respectively. The emission color of the phosphors can be tuned from blue to cyan and finally to green by adjusting the concentration ratios of Eu²⁺ and Mn²⁺. Effective energy transfer occurs from Eu²⁺ to Mn²⁺ in the host due to the spectral overlap between the emission band of Eu²⁺ and the excitation bands of Mn²⁺. The energy transfer mechanism was demonstrated to be electric dipole–quadrupole interaction. The energy transfer efficiency and critical distance were also calculated. The phosphors exhibit strong absorption in near UV spectral region and therefore they are potentially useful as UV-convertible phosphors for white LEDs.     

Effect of magnetic field on luminescence of MgS,CaS and CaO phosphors activated with Bi3+ ions

The magnetic field dependence of the intensity I(A₀) of the zero-phonon line of the ³A_1u → ¹A_1g emission band is measured at 4.2 K for MgS, CaS and CaO phosphors activated with Bi³⁺ ions. The increase in I(A₀) is proportional to the square of the external magnetic field. The results are compared with those for Pb²⁺-activated phosphors.