Investigation on luminescence of Na3Ca6(PO4)5:Eu2+ phosphor for LEDs

In this paper, a series of Na₃Ca_6(1−x)(PO₄)₅:xEu²⁺ (NCP:xEu²⁺, 0 ≤ x ≤ 4%) phosphors were prepared by conventional solid-state reaction method, and their photoluminescence properties were studied. Upon 365 nm excitation, the typical NCP:2%Eu²⁺ phosphor shows an asymmetric bluish green emission band with the dominant peak at 498 nm which could be attributed to the 4f⁶5d¹-4f⁷ transition of Eu²⁺. By measuring the time-resolved photoluminescence spectra, it reveals more than one Eu²⁺ emission center in the Eu²⁺-activated NCP phosphors. By monitoring 498 nm, the excitation spectrum of NCP:2%Eu²⁺ demonstrates a broad excitation band ranging from 240 to 450 nm, which can match well with the emission wavelength of the NUV LED chip. The SEM image shows that the average particle size of NCP:2%Eu²⁺ is about 19.4 µm. The above results imply that the NCP:Eu²⁺ phosphor could have potential application in LEDs.     

Effect of alkali metal ions co-doping on the structure and luminescent properties of phosphor Zn3(BO3)2:Eu3+

A series of the Zn₃(BO₃)₂:Eu³⁺ without or with alkali metal ions doping at a low sintering temperature were synthesized by the solid-state reaction method. The XRD pattern shows that all samples exhibit Zn₃(BO₃)₂ crystalline phase. The samples co-doped with alkali metal ions have better crystallinity compared with the un-compensated ones. The different charge compensation approaches have no influence on the shape and position of the emission and excitation spectra. However, the luminescent intensity of samples has been obviously enhanced with different alkali metal ions co-doping. The introduction of Li⁺ can increase the red emission of Eu³⁺ compared with the others. Thus, the volume compensation and the equilibrium of mole number can be taken into consideration by charge compensated (CC) approaches.     

Synthesis and photoluminescent properties of orange-emitting Sm3+-activated KPb4(PO4)3 phosphor for LEDs

A series of Sm³⁺-doped KPb₄(PO₄)₃ phosphors have been successfully synthesized by high-temperature solid-state reaction method, and the structure, morphology and luminescent properties were investigated. The SEM images suggest that the prepared phosphor has an irregular morphology with a diameter of about 10 ~ 20 μm. Under near-ultraviolet (NUV) light (404 nm) excitation, all prepared phosphors KPb_4-xSm_xP₃O₁₂ (x = 0, 0.02, 0.04, 0.06, 0.08, 0.1, 0.15, 0.2, 0.3, 0.4 and 0.5) show the characteristic f → f emission bands of the Sm³⁺ activator. And the emission intensities have an upward trend with increasing the Sm³⁺ concentration when x is lower than 0.1. By monitoring 598 nm emission, the excitation spectrum of KPb_3.9Sm_0.1(PO₄)₃ contains a series of sharp bands in the range of 250 ~ 500 nm, which matches well with the NUV LED chip. The CIE coordinates of KPb_3.9Sm_0.1(PO₄)₃ phosphor was evaluated to be (0.5714, 0.4253), corresponding to orange color with a high color purity of about 90%.     

Red emitting MTiO3 (M = Ca or Sr) phosphors doped with Eu3+ or Pr3+ with some cations as co-dopants

Ca (or Sr)TiO₃:Eu³⁺, M (Li⁺ or Na⁺ or K⁺) and CaTiO₃:Pr³⁺, M (Li⁺ or Na⁺ or Ag⁺ or K⁺ or Gd³⁺ or La³⁺) powders were prepared by combustion synthesis method and the samples were further heated to ～1000 °C to improve the crystallinity. The structure and morphology of materials were examined by X-ray diffraction (XRD) and a scanning electron microscopy (SEM). The morphologies of SrTiO₃:Eu³⁺, CaTiO₃:Eu³⁺ or CaTiO₃:Pr³⁺ powders co-doped with other metal ions were very similar. Small and coagulated particles of nearly cubical shapes with small size distribution having smooth and regular surface were formed. Photo-luminescence spectra of CaTiO₃:Pr³⁺ and co-doped either with Li⁺, Na⁺, K⁺, Ag⁺, La³⁺ or Gd³⁺ ions showed red emissions at 613 nm due to the ¹D₂ → ³H₄ transition of Pr³⁺. The variation of intensity of emission peak with different co-doping follows the order: K⁺ > Ag⁺ > Na⁺ > Li⁺ > La³⁺ > Gd³⁺. The characteristic emissions of CaTiO₃:Eu³⁺ lattices had strong emission at 614 and 620 nm for ⁵D₀ → ⁷F₂ with other weak transitions observed at 580, 592, 654, 705 nm for ⁵D₀ → ⁷F_n transitions where n = 0, 1, 3, 4 respectively in all host lattices. Photoluminescence intensity in SrTiO₃:Eu³⁺ is more than CaTiO₃:Eu³⁺ lattices. A remarkable increase of photoluminescence intensity (in ⁵D₀ → ⁷F₂ transition) was observed if co-doped with Li⁺ ions in CaTiO₃:Eu³⁺ and SrTiO3:Eu³⁺.     

First principle study of electronic,mechanical, optical and thermoelectric properties of CsMO3 (M = Ta,Nb) compounds for optoelectronic devices

The electronic, mechanical, optical and thermoelectric properties of Cesium based perovskites CsMO₃ (M = Nb, Ta) in the cubic phase has been performed through PBEsol-mBJ scheme in the framework of DFT. The electronic band structures and density of states show the studied materials having a direct band gap in the visible range. The mechanical stability and ductile behavior have been analyzed from elastic constants. Moreover, the optical behavior of the studied materials has been analyzed in terms of dielectric functions, refractive index, extinction coefficient, absorption coefficient, optical conductivity, reflectivity and energy loss factor. Finally, the material response with temperature has been elaborated by electrical conductivity, thermal conductivity, Seebeck coefficient, power factor, heat capacity, Hall coefficient, susceptibility and electron density by using BoltzTraP code. This first principle calculation of optical and thermoelectric properties of the novel compounds provides a new route to the experimentalist for the potential application in energy renewable devices.     

Predictions on the solubility and equiscale line of water content for the quaternary system (Li+Na+Cl+SO4+H2O) at 298.15 K

Pitzer ion-interaction theory is widely used to calculate the solubilities of salt–water systems. In the paper, the solubilities and equiscale lines of water contents of the reciprocal quaternary system (Li+Na+Cl+SO₄+H₂O) at 298.15 K were calculated using Pitzer theory and Harvie, Møller, Weare solubility modeling approach (HMW model). In this predictive calculation, the quasi-Newton and dichotomy methods were used to solve the system of simultaneous equations of the equilibrium expressions among solid and liquid phases, and to obtain the ionic molalities, Jänecke indices of phase diagram and the Jänecke indices of the equiscale lines of water contents in the reciprocal quaternary system. Based on the Jänecke indices, the dry-salt phase diagram and the equiscale lines of water-phase diagram were plotted. The predictive phase diagram via the theoretical calculation agrees well with the experimental phase diagram except for the phase region of double salt 2 (Li₂SO₄·Na₂SO₄, Db2). Distributions of equiscale lines of water-phase diagram on the dry-salt diagram of the reciprocal quaternary system reflect that phase areas of double salts of Db1 and Db2 bear maximal water contents. The predictive phase diagram and equiscale lines of water-phase diagram are often necessary in the technological design of chemical engineering for the utilization of inorganic salts in salt lake brines.     

A potential red-emitting phosphors scheelite-like triple molybdates LiKGd_2(MoO_4)_4:Eu~(3+) for white light emitting diode applications

A series of novel red-emitting phosphors scheelite-like triple molybdates LiKGd2-xEux(MoO4)4(0.1 ≤ x ≤ 1.9) were synthesized by solid state reaction method and their photoluminescence properties were investigated. The photoluminescence results show that all samples can be excited efficiently by UV (396 nm) light and blue (466 nm) light and emit red (615 nm) light with line spectra,which are coupled well with the characteristic emission from UV-LED and blue LED,respectively. The experimental results and thei...     

Fusion of Region and Boundary/Surface-Based Computer Vision and Pattern Recognition Techniques for 2-D and 3-D MR Cerebral Cortical Segmentation (Part-II): A State-of-the-Art Review

Extensive growth in functional brain imaging, perfusion-weighted imaging, diffusion-weighted imaging, brain mapping and brain scanning techniques has led tremendously to the importance of cerebral cortical segmentation both in 2-D and 3-D from volumetric brain magnetic resonance imaging data sets. Besides that, recent growth in deformable brain segmentation techniques in 2-D and 3-D has brought the engineering community, such as the areas of computer vision, image processing, pattern recognition and graphics, closer to the medical community, such as to neuro-surgeons, psychiatrists, oncologists, neuro-radiologists and internists. In Part I of this research (see Suri et al [1]), an attempt was made to review the state-of-the-art in 2-D and 3-D cerebral cortical segmentation techniques from brain magnetic resonance imaging based on two main classes: region- and boundary/surface-based. More than 18 different techniques for segmenting the cerebral cortex from brain slices acquired in orthogonal directions were shown using region-based techniques. We also showed more than ten different techniques to segment the cerebral cortex from magnetic resonance brain volumes using boundary/surface-based techniques. This paper (Part II) focuses on presenting state-of-the-art systems based on the fusion of boundary/surface-based with region-based techniques, also called regional-geometric deformation models, which takes the paradigm of partial differential equations in the level set framework. We also discuss the pros and cons of these various techniques, besides giving the mathematical foundations for each sub-class in the cortical taxonomy. Special emphasis is placed on discussing the advantages, validation, challenges and neuro-science/clinical applications of cortical segmentation. Received: 25 August 2000, Received in revised form: 28 March 2001, Accepted: 28 March 2001