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1.
The Er3+-Yb3+ codoped strontium molybdate (SrMoO4) phosphors have been synthesized via chemical co-precipitation method by adding ammonium hydroxide as a base reagent. The phase, crystal structure and formation of spindle-like particles present in the prepared phosphors have been recognized by using the X-ray powder diffraction (XRPD) and Field emission scanning electron microscopy (FE-SEM) techniques. The Fourier transform infrared (FTIR) spectroscopy of the developed phosphors has been analyzed to mark the different functional groups present in synthesized phosphors. The multicolour upconversion emissions observed upon excitation with 980 nm and 808 nm laser diode have been explained on the basis of dopants ions concentration, pump power dependence, energy level structure and decay curve analysis. The colour co-ordinate study confirmed that the codoped phosphor emits non-tunable green colour when excited with the 980 nm laser diode, whereas it shows the colour tunability from yellow to green region upon excitation with the 808 nm laser diode. The applicability of non-tunable green colour emission has been demonstrated in the security ink and latent finger print detection. This shows the utility of the developed phosphors in the photonic and forensic applications.  相似文献   

2.
An alkali metal-rare earth phosphate crystal of NaLa(PO3)4 has been synthesized by high temperature solid-state reactions and structurally characterized by single crystal X-ray diffraction analysis, for the first time. It crystallizes in the monoclinic P21/n space group with lattice parameters: a=7.2655(3), b=13.1952(5), , β=90.382°(1), , Z=4. It is composed of LaO8 polyhedra and [(PO3)4]4− chains sharing oxygen atoms to form a three-dimensional framework, delimiting intersecting tunnels in which the sodium ions are located. The IR spectrum, absorption spectrum, and emission spectrum of the compound have been investigated. The absorption edge is located at 340 nm (3.60 eV). The calculated total and partial densities of states indicate that the top of valence bands is mainly built upon O-2p states which interact with P-3p states via σ (P-O) interactions, and the low conduction bands mostly originates from unoccupied La-5d states. The P-O bond is mostly covalent in character, and the ionic character of the Na-O bond is larger than that in the La-O bond.  相似文献   

3.
An alkali-metal indium phosphate crystal, K3In3P4O16, has been synthesized by a high-temperature solution reaction and exhibits a new structure in the family of the alkali-metal indium phosphates system. Single-crystal X-ray diffraction analysis shows the structure to be monoclinic with space group P21/n, and the following cell parameters: a=9.7003(18), b=9.8065(18), c=15.855(3) Å, β=90.346(3)°, V=1508.2(5) Å3, Z=4, R=0.0254. It possesses three-dimensional anionic frameworks with tunnels occupied by K+ cations running along the a-axis. The emission and absorption spectra of the compound have been investigated. Additionally, the calculations of energy band structure, density of states, dielectric constants and refractive indexes have been performed with the density functional theory method. Also, the two-photon absorption spectrum is simulated by two-band model. The obtained results tend to support the experimental data.  相似文献   

4.
在本研究中,使用(iPrC6H4SAg)n作为合成银硫纳米簇合物的前驱体。当存在辅助的双膦配体1, 3-双(二苯基膦)丙烷(dppp)及可溶性银盐(CF3SO3Ag),在超声合成条件下,获得了一例二十五核银硫簇合物Ag25,并借助X射线单晶衍射技术确定相应的分子结构。该银硫簇合物具有夹心三明治的骨架结构:分别由两个结构相似的圆柱体共享一个七核纯银簇所构成的金属簇平面。固态紫外可见漫反射光谱测试表明该簇合物的能级带隙为2.5 eV,属于半导体材料的范畴。固态发光测试显示,该簇合物在室温下发射绿光。  相似文献   

5.
Eu3+-doped monophosphate CsBPO4 (B = Mg, Zn) was synthesized by conventional solid state reaction. The crystal phase formations and morphology of the phosphates were analyzed by X-ray powder diffraction (XRD) and scanning electron microscope (SEM) measurements, respectively. The luminescence properties, including the photoluminescence excitation and emission spectra, decay curve (lifetime), the color coordinates and the internal quantum efficiency were investigated. Two Eu3+-doped monophosphates display very distinct luminescence properties. CsMgPO4:Eu3+ presents the dominant reddish-orange emission from magnetic dipole transition 5D0 → 7F1 and a long luminescence lifetime. In contrast, CsZnPO4:Eu3+ has a pure red color with the dominant induced electric-dipole transition 5D0 → 7F2 and a fast decay. Different results on the luminescence features of CsBPO4 (B = Mg, Zn):Eu3+ were discussed on the base of crystal structure. Eu3+ has structure-dependent transitions due to the special microstructure occupied in a given host.  相似文献   

6.
A series of red-emitting phosphors Eu3+-doped M2Gd4(MoO4)7 (M=Li, Na) have been successfully synthesized at 850 °C by solid state reaction. The excitation spectra of the two phosphors reveal two strong excitation bands at 396 nm and 466 nm, respectively, which match well with the two popular emissions from near-UV and blue light-emitting diode chips. The intensity of the emission from 5D0 to 7F2 of M2(Gd1−xEux)4(MoO4)7 phosphors with the optimal compositions of x=0.85 for Li or x=0.70 for Na is about five times higher than that of Y2O3:Eu3+. The quantum efficiencies of the entitled phosphors excited under 396 nm and 466 nm are also investigated and compared with commercial phosphors Sr2Si5N8:Eu2+ and Y3A5O12:Ce3+. The experimental results indicate that the Eu3+-doped M2Gd4(MoO4)7 (M=Li, Na) phosphors are promising red-emitting phosphors pumped by near-UV and blue light.  相似文献   

7.
8.
Nd3+:NaLa(WO4)2 crystals with a dimension up to 7 mm were grown from a high temperature solution using a double-crucible method. Scanning electron microscopy observations of the crystals showed that there were no small cracks on the surface of the crystals although they underwent two phase transitions when cooling down from high temperatures. X-ray diffraction studies indicated that the as-obtained product is pure low- temperature tetragonal Nd3+:NaLa(WO4)2. The absorption and fluorescence spectra for Nd3+:NaLa(WO4)2 were measured at room temperature. The absorption band at 804 nm has a wide full-width half maximum of 23 nm whose origin is discussed. The absorption and emission cross sections were calculated to be 7.24*10-20 cm2 at 804 nm and 6.54*10-20 cm2 at 1057 nm, respectively.  相似文献   

9.
ZnS nanosheets were prepared via egg albumin and microwave-assisted method. The phases, crystalline lattice structures, morphologies, chemical and optical properties were characterized by X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM), field-emission scanning electron microscope(FE-SEM), selected area electron diffraction (SAED), Fourier transform infrared (FTIR) spectroscopy, ultraviolet–visible (UV–Vis) spectroscopy and fluorescence(FL) spectrometer and growth mechanism of ZnS nanosheets was investigated. The results showed that all samples were pure cubic zinc blende with polycrystalline structure. The width of ZnS nanosheets with a rectangular nanostructure was in the range of 450–750 nm. The chemical interaction existed between egg albumin molecules and ZnS nanoparticles via the amide/carboxylate group. The band gap value calculated was 3.72 eV. The band at around 440 nm was attributed to the sulfur vacancies of the ZnS nanosheets. With increasing volumes of egg albumin, the photoluminescence (PL) intensity of ZnS samples firstly increased and then decreased, attributed to concentration quenching.  相似文献   

10.
We report the absorption, luminescence and decay analysis of Eu3+-doped lead telluroborate (PTBEu) glasses for different Eu3+ concentrations ranging from 0.1 to 2.0 mol%. Judd-Ofelt intensity parameters obtained from 5D07FJ=0-6 emission transitions of Eu3+ were used to calculate the radiative transition probabilities, luminescence branching ratios and radiative decay times. The luminescence spectra and decay times were measured at 464 nm excitation. The optical band gap energies are also determined. The luminescence intensity ratio, color purity and emission cross-section values support that the PTBEu20 glass is a suitable candidate for red laser source applications.  相似文献   

11.
Mn4+-activated double perovskite phosphors with composition diversity have presented excellent luminescent performances. However, the charge imbalance between Mn4+ and matrix cations would increase non-radiative recombination and reduce the structural stability. Here, novel high-efficiency stable Li+/Mn4+ co-incorporated Sr2YSbO6 red phosphors are successfully synthesized via a solid-state reaction method for warm w-LEDs, where the Li+ ions have the effect of charge balance for Sr2YSbO6:Mn4+ and reduce the non-radiative energy transfer among Mn4+ ions. It is demonstrated that the substitution of Li+–Mn4+ pairs for Sb5+ can enhance the bonding with low-shifted diffraction peaks and high emission intensity, and prolong the decay lifetime, compared with those of Mn4+ single-doped ones. Impressively, the thermal stability is enhanced to 89.72% from 84.61% at the original value of 303 K. Finally, a w-LED device based on the optimal phosphor Sr2YSbO6:0.01Mn4+/0.01Li+ red component exhibits a correlated color temperature of 4487 K and color rendering index of 80.2. Therefore, the incorporated Li+ ions serve as both charge compensator and co-activator in Mn4+-activated double perovskite phosphors with the aim of high luminescent performance and thermal stability.  相似文献   

12.
Nd(3+) doped unconventional sodium leadbismuthate glass is prepared through the melt quenching method. The amorphous nature of the glass is confirmed through the X-ray diffraction study. The differential thermal study was performed to identify the glass transition and approximate glass thermal stability measurements. To identify the local structure of the glass, Fourier transform infrared spectral analysis was also carried out. By performing the Judd-Ofelt theory, the theoretical and experimental oscillator strengths were calculated.  相似文献   

13.
A sodium gadolinium phosphate crystal, Na3GdP2O8, has been synthesized by a high-temperature solution reaction, and it exhibits a new structural family of the alkali-metal-rare-earth phosphate system. Although many compounds with formula M3LnP2O8 have been reported, but they were shown to be orthorhombic [R. Salmon, C. Parent, M. Vlasse, G. LeFlem, Mater. Res. Bull. 13 (1978) 439] rather than monoclinic as shown in this paper. Single-crystal X-ray diffraction analysis shows the structure to be monoclinic with space group C2/c and the cell parameters: a=27.55 (25), b=5.312 (4), c=13.935(11) Å, β=91.30(1)°, and V=2038.80 Å3, Z=4. Its structure features a three-dimensional GdP2O83− anionic framework with two different types of interesting tunnels at where Na atoms are located by different manners. The framework is constructed by Gd polyhedra and isolated PO4 tetrahedra. It is different from the structure of K3NdP2O8 [R. Salmon, C. Parent, M. Vlasse, G. LeFlem, Mater. Res. Bull. 13 (1978) 439] with space group P21/m that shows only one type of tunnel. The emission spectrum and the absorption spectrum of the compound have been investigated. Additionally, the calculations of band structure, density of states, dielectric constants, and refractive indexes have been also performed with the density functional theory method. The obtained results tend to support the experimental data.  相似文献   

14.
Some copper(I) complexes of the formula [Cu(L)(PPh3)2]X (1-4) [where L = 2-phenyl-3-(benzylamino)-1,2-dihydroquinazolin-4(3H)-one; PPh3 = triphenylphosphine; X = Cl, NO3, ClO4 and BF4] have been prepared and characterized on the basis of elemental analysis, IR, UV-Vis and 1H NMR spectral studies. The representative complex of the series 4 has been characterized by single crystal X-ray diffraction which reveal that in the complex the central copper(I) ion assumes the irregular distorted-tetrahedral geometry. Cyclic voltammetry of the complexes indicate a quasireversible redox behavior corresponding to Cu(II)/Cu(I) couple. All the complexes exhibit intraligand (π → π) fluorescence with high quantum yield in dichloromethane solution.  相似文献   

15.
The title complexes, (C12H8N2) ? [La(C7H3NO5)(C7H4NO5) ? 3H2O] ? 1.75H2O (1), (C12H8N2) ? [Pr(C7H3NO5)(C7H4NO5) ? 3H2O] ? 2H2O (2), (C12H8N2)[Nd(C7H3NO5)(C7H4NO5) ? 3H2O] ? 2.25H2O (3), and (C12H8N2) ? [Fe(C7H3NO5)(C7H4NO5)] ? 2H2O (4), were synthesized and characterized by single-crystal X-ray diffraction. The crystal structures of 13 reveal that they are isomorphous, among which the metal atoms are all nine-coordinate with distorted tricapped trigonal prismatic coordination geometries. The Fe is six-coordinate with a distorted octahedron by two chelidamic acid ligands in 4. Complexes 14 are formed into 3-D networks by H-bonds and π–π stacking interactions. The fluorescence spectra of 13 were investigated and all exhibit strong luminescence.  相似文献   

16.
Ytterbium-sensitized erbium-doped oxide-halide tellurite and germanate-niobic-lead glasses have been synthesized by conventional melting method. Intense green and red emissions centered at 525, 546 and 657 nm, corresponding to the transitions 2H11/2-->4I15/2, 4S3/2-->4I15/2 and 4F9/2-->4I15/2, respectively, were simultaneously observed at room temperature in these glasses. The quadratic dependence of the 525, 546 and 657 nm emissions on excitation power indicates that a two-photon absorption process occurs. Tellurite glass showed a weaker up-conversion emission than germanate-niobic-lead glass, which is inconsistent with the prediction from the difference of maximum phonon energy between tellurite and germanate-niobic-lead glasses. In this paper, Raman spectroscopy was employed to investigate the origin of the difference in up-conversion luminescence in the two glasses. Compared with phonon side-band spectroscopy, Raman spectroscopy extracts more information including both phonon energy and phonon density. Our results reveal that the phonon density and the maximum phonon energy of host glasses are both important factors in determining the up-conversion efficiency.  相似文献   

17.
The absorption and upconversion fluorescence spectra of a series of Er3+/Yb3+-codoped xBi(2)O(3)-(90-x)GeO2-10Na(2)O (BGN x, x=31, 36, 41, 46 and 51 mol%) glasses have been studied. Intense green and red emission bands at around 533, 548 and 659 nm, corresponding to the 2H(11/2)-->4I(15/2), 4S(3/2)-->4I(15/2) and 4F(9/2)-->4I(15/2) transitions of Er3+, respectively, were simultaneously observed at room temperature. The dependence of intensities of upconversion emission on excitation power and possible upconversion mechanisms were evaluated and analyzed. The important role of Bi(2)O(3) in upconversion intensity is observed and its influence on the green (533 and 548 nm) and red (659 nm) emissions is compared and discussed. The influence of Bi(2)O(3) on the upconversion emissions has been investigated based on the IR spectra.  相似文献   

18.
A novel compound Ba2ZnV2O8 has been synthesized in high temperature solution reaction and its crystal structure has been characterized by means of single crystal X-ray diffraction analysis. It crystallizes in monoclinic system and belongs to space group P21/c with a=7.9050(16), b=16.149(3), , β=90.49(3). It builds up from 1-D branchy chains of [ZnV2O84−], and the Ba2+ cations are located in the space among these chains. The IR spectrum, ultraviolet-visible diffuse reflection integral spectrum and fluorescent spectra of this compound have been investigated. The calculated results of energy band structure by the density functional theory method show that the solid-state compound of Ba2ZnV2O8 is an insulator with direct band gap of 3.48 eV. The calculated total and partial density of states indicate that the top valence bands are contributions from the mixings of O-2p, V-3d, and Zn-3d states and low conduction bands mostly originate from unoccupied antibonding states between the V-3d and O-2p states. The V-O bonds are mostly covalence characters and Zn-O bonds are mostly ionic interactions, and the ionic interaction strength is stronger between the Ba-O than between the Zn-O. The refractive index of nx, ny, and nz is estimated to be 1.7453, 1.7469, and 1.7126, respectively, at wavelength of 1060 nm for Ba2ZnV2O8 crystal.  相似文献   

19.
Currently, highly luminescent colloidal upconversion nanoparticles (UCNPs) have expanded an increasing interest of researchers because of their facilitating lability in the biomedical/clinical field. In this study, NaYF4:Yb,Er UCNPs are prepared by eco-friendly metal complexation-based thermal decomposition method at a lower temperature in aqueous media. The phase structure, crystallinity, phase purity, morphology, colloidal dispersibility, surface structure, surface charge, and optical and luminescent properties were evaluated carefully by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), energy dispersive x-ray analysis (EDX), Thermogravimetric analysis (TGA), zeta potential, Fourier transform infrared (FTIR), UV/visible and photoluminescent spectroscopic techniques. XRD pattern shows a pure single-phase cubic structure with an average grain size of 30–35 nm. TEM and SEM micrographs exhibited irregularly shaped spherical morphologies, porous surface structures highly aggregated UCNPs with the narrow-size distribution. Positive zeta potential has shown value signifying high absorption in the visible region which indicates particle's good colloidal stability in aqueous media. Under NIR-laser light excitation, the UCNPs emit strong UC emission transitions in the visible region. A broad infrared absorption peak of hydroxyl groups (–OH) in FTIR spectrum and mass loss at a lower temperature in TGA verified the surface functionality of UCNPs, with high colloidal stability, and excellent biocompatibility in aqueous media. In terms of their surface characteristics and high luminescent properties, the NaYF4:Yb,Er UCNPs could be interestingly applied in tagging of biomolecules, drug delivery, proteins labeling, and therapeutic and thermostats applications.  相似文献   

20.
Two new cationic octahedral rhenium cluster complexes [{Re6Q8}(4-NH2-py)6]2+ (Q=S, Se; 4-NH2-py = 4-aminopyridine) were synthesized by reactions of cesium salts of cluster anions [{Re6Q8}Br6]4?/3? with molten 4-aminopyridine. Both complexes were separated as salts with Br? as counterions and the structure of [{Re6S8}(4-NH2-py)6]Br2·6DMF was revealed by X-ray single-crystal diffraction analysis. The compounds were characterized by elemental analysis, energy dispersive X-ray, IR, NMR, and luminescence spectroscopies.  相似文献   

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