首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
The reduction of immobile cations La3+ and Ce3+ in fluoride-conducting solid electrolytes (FSE) LaF3 (Eu2+ 0.8 mol %), LaF3 (Sr2+ 5 mol %), and CeF3 (Sr2+ 5 mol %) in contact with Ag, Bi, Si, La, Ce, and Sm working electrodes is studied by chronoamperometry and voltammetry with linear potential scan. Discovered is linear dependence of initial segments of potentiostatic transients of cathodic current on t 1/2 at FSE interfaces with Ag, Bi, La, Ce, and Sm. The dependence is due to diffusion-controlled instantaneous nucleation of Ln and Ce. The La3+ and Ce3+ reduction at the FSE/Ag interface is reversible in a narrow region. The reduction and oxidation of La3+ and Ce3+ (cations of the FSE rigid lattice) at the FSE/Me (Me = La, Ce and Sm, Bi, Si) interface is irreversible and involves a chemical reaction.__________Translated from Elektrokhimiya, Vol. 41, No. 5, 2005, pp. 662–672.Original Russian Text Copyright © 2005 by Turaeva, Kot, Urchukova, Murin.  相似文献   

2.
The kinetics of low-sized phase formation on polarization of the interface between LaF3:Eu2+ and Pb–Sn, Sn–Bi, and Sb–Bi alloys is studied by the potentiostatic and linear voltammetry methods. The analysis of anodic transients shows that the new phase formation involving fluoride ions from the solid electrolyte proceeds by the mechanism of instantaneous two-dimensional or three-dimensional nucleation. Comparison of calculated and experimental transients describing the instantaneous nucleation with either two-dimensional growth on the I/I m vs. t/t m coordinates or three-dimensional growth on the I 2/I m 2 vs. t/t m coordinates shows adequate agreement between the model and the initial regions of experimental curves. The properties of phases formed depend on the alloy composition and the polarization conditions as well as on the energy of interaction between components in the alloy and in the new phase.  相似文献   

3.
The electrochemical processes at the interface between solid fluorine-conducting electrolyte LaF3(Eu2+ 0.8 mol %) and silver or bismuth electrodes in the two-electrode cell with nonpolarizable reference electrode are studied using the galvanostatic method. The anodic galvanostatic transients of LaF3: Eu2+/Ag and LaF3: Eu2+/Bi interfaces are linearized on the log(η ? ηmax), vs. t coordinates, i.e. the rate of LaF3|MF n |M electrode formation is limited by slow surface diffusion of metal adions. The initial portions of cathodic galvanostatic transients in the range of solid-electrolyte lanthanum reduction are approximated by the linear dependence of η on log(1 ? √t/τ). The plots of logI vs. 1/η are linear both for the lanthanum reduction and for silver and bismuth oxidation involving mobile fluoride ion of solid electrolyte, which is typical for two-dimensional growth of new phase.  相似文献   

4.
The effect of the reference electrode (Ag, AgCl∣KF + KCl or Sn, SnF2) on the kinetics of new phase growth at interfaces formed by LaF3:Eu2+ or CeF3:Sr2+ single crystal solid electrolytes with metal electrodes of Ag and Bi is studied by chronoamperometry and linear scan voltammetry. It is shown that when a solid-phase reference electrode is used, the current transients reflect hindrances associated with instantaneous two- or three-dimensional nucleation as well as limitations for fluoride ion diffusion in the solid electrolyte.  相似文献   

5.
Complexation behavior of NpO2 + with ortho-silicic acid (o-SA) has been studied using solvent extraction at ionic strengths varying from 0.10 to 1.00M (NaClO4) at pcH 3.68±0.08 and 25 °C with bis-(2-ethylhexyl) phosphoric acid (HDEHP) as the extractant. The stability constant value (log β1) for the 1:1 complex, NpO2(OSi(OH)3), was found to decrease with increase in ionic strength of the aqueous phase [6.83±0.01 at I=0.10M to 6.51±0.02 at I = 1.00M]. These values have been fitted in the SIT model expression and compared with similar values of complexation of the metal ions Am3+, Eu3+, UO2 2+, PuO2 2+, Np4+, Ni2+ and Co2+. The speciation of NpO2 +-o-silicate/carbonate system has been calculated as a function of pcH under ground water conditions. On leave from Radiochemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai-400 085, India.  相似文献   

6.
Fine Eu3+-doped lutetium oxide (Lu2O3:Eu3+) nanophosphor were synthesized using a low-temperature solution-combustion method in a methyl-alcohol solution. The characteristics of the nanophosphors synthesized at various sintering temperatures with different Eu3+ concentrations were analyzed to determine the optimum synthesis conditions. Thermogravimetry/differential thermal analysis showed that Lu2O3:Eu3+ crystallizes completely when the dry powder is sintered at 500 °C. The Lu2O3:Eu3+ crystals had a cubic structure and monoclinic phase. The peak position of the luminescence spectrum did not differ with the concentration of Eu or the sintering temperature or atmosphere, whereas the luminescence intensity was strongly dependent on the concentration and sintering conditions.  相似文献   

7.
CaAl2O4:Eu2+, Nd3+@TiO2 composite powders were synthesized by a sol–gel method under mild conditions (i.e. low temperature and ambient pressure). The as-prepared powders were characterized by transmission electron microscopy (TEM) and analyzed by X-ray diffraction (XRD). The photocatalytic behavior of the TiO2-base surfaces was evaluated by the degradation of nitrogen monoxide gas. It suggested that CaAl2O4:Eu2+, Nd3+@TiO2 composite powders were composed of anatase titania and that CaAl2O4:Eu2+, Nd3+. TiO2 particles were deposited on the surface of CaAl2O4:Eu2+, Nd3+ to form uniform film. CaAl2O4:Eu2+, Nd3+@TiO2 composite powders exhibited higher photocatalytic activity compared with pure TiO2 under visible light. And the result also clearly indicated that the long afterglow phosphor absorbed and stored lights for the TiO2 to remain photocatalytic activity in the dark.  相似文献   

8.
In the Bi2O3-SiO2-V25++O5 system, single crystal solid solutions of the sillenite family of the general composition Bi24(Bi,Si,V)2O40 are obtained by a hydrothermal method and for the first time characterized by neutron and X-ray diffraction analysis. The tetrahedral position is found to contain vanadium ions with different formal charges (V4+ and V5+) responsible for green and orange colors, respectively, of the samples. For the first time, for some sillenites of this system dissymmetrization of the structure (a transition from the I23 space group into P23) is revealed, which is caused by the presence of several atoms in one crystallographic position and also by crystal growth conditions.  相似文献   

9.
The flower-like phosphors of Sr2MgSi2O7: Eu2+, Dy3+ with high brightness and long afterglow were obtained by sol–gel method. X-ray diffraction pattern (XRD) shows that single-phased Sr2MgSi2O7 phosphor is prepared by sol–gel method under 1250 °C. Scanning electron microscope (SEM) indicates that the phosphor consists of nano-sized whiskers which are detected for the first time in Eu2+ and Dy3+ co-doped long-lasting phosphorescence silicates. Furthermore, the investigation on the mechanism indicates that the internal structure and gas, liquid and solid phase effect play important roles in the formation of flower-like Sr2MgSi2O7: Eu2+, Dy3+ nanostructure. Finally, the optical properties of flower-like Sr2MgSi2O7 nanostructure have been characterized by photoluminescence (PL) spectra.  相似文献   

10.
Abstract  A EuIII cryptate complex constructed from a CuII cryptand with an L tBu ligand, [EuIIICu2II(L tBu)2(NO3)3(MeOH)], and the corresponding CaII and NaI cryptates, [CaIICu2II(L tBu)2(NO3)2(MeOH)2] and [NaICu2II(L tBu)2(Me2CO)](BPh4), have been synthesized and characterized in order to shed light on the essential role of CuII in the luminescence of a EuIII cryptate. The unprecedented role of a CuII cryptand makes it possible to produce lanthanide luminescence in a EuIII cryptate complex and is successfully elucidated by comparison with the corresponding CaII and NaI cryptates. Graphical abstract   Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

11.
Fluorescence and spectral hole burning properties of Eu3+ ions were studied in nanocrystals-precipitated SnO2-SiO2 glasses. The glasses were prepared to contain various amount of Eu2O3 using the sol-gel method, in which SnO2 nanocrystals were precipitated by heating in air. In the glasses containing Eu2O3 less than 1%, the Eu3+ ions were preferentially doped in the SnO2 nanocrystals and their fluorescence intensities were enhanced by the energy transfer due to the recombination of electrons and holes excited in SnO2 crystals. The SnO2 nanocrystals-precipitated glasses exhibited the persistent spectral holes with the depth of ∼25% of the total fluorescence intensities of the Eu3+ ions. With the increasing Eu2O3 concentration, the amount of SnO2 nanocrystals decreased and the Sn4+ ions formed the random glass structure together with the silica network. This structure change induced the fluorescence intensities and the hole depth to decrease.  相似文献   

12.
The Ca2MgSi2O7:Eu2+ and Ca2MgSi2O7:Eu2+, Dy3+ long afterglow phosphors were synthesized under a weak reducing atmosphere by the traditional high temperature solid state reaction method. The synthesized phosphors were characterized by powder X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDX) techniques. The luminescence properties were investigated using thermoluminescence (TL), photoluminescence (PL), long afterglow, mechanoluminescence (ML), and ML spectra techniques. The crystal structure of sintered phosphors was an akermanite type structure, which belongs to the tetragonal crystallography. TL properties of these phosphors were investigated, and the results were also compared. Under the ultraviolet excitation, the emission spectra of both prepared phosphors were composed of a broad band peaking at 535 nm, belonging to the broad emission band. When the Ca2MgSi2O7:Eu2+ phosphor is co-doped with Dy3+, the PL, afterglow and ML intensity is strongly enhanced. The decay graph indicates that both the sintered phosphors contain fast decay and slow decay process. The ML intensities of Ca2MgSi2O7:Eu2+ and Ca2MgSi2O7:Eu2+, Dy3+ phosphors were proportionally increased with the increase of impact velocity, which suggests that this phosphor can be used as sensors to detect the stress of an object.  相似文献   

13.
The photoluminescence properties of xZnO–(100−x)SiO2 (x = 0, 5, 10, 20) containing 1% Eu2O3 prepared by a sol–gel method were systematically investigated. The results indicated that the relative proportion of f–f transitions to charge transfer (CT) absorption decreased with the increase of ZnO concentration. The intensity of 5D07FJ transitions of Eu3+ ions was enhanced with the increase of ZnO content due to local structure changes and decreased quantities of Eu3+ ions clusters. The results of fluorescence line narrow (FLN) spectra indicated that Eu3+ ions occupied one site in SiO2 glass and two sites in ZnO–SiO2 glasses. The second-order crystal field parameters were calculated. B20 and B22 for site 1 increased with excitation energy, while ones hardly changed for site 2.  相似文献   

14.
The details of the mechanism of persistent luminescence were probed by investigating the trap level structure of Sr2MgSi2O7:Eu2+,R3+ materials (R: Y, La-Lu, excluding Pm and Eu) with thermoluminescence (TL) measurements and Density Functional Theory (DFT) calculations. The TL results indicated that the shallowest traps for each Sr2MgSi2O7:Eu2+,R3+ material above room temperature were always ca. 0.7 eV corresponding to a strong TL maximum at ca. 90 °C. This main trap energy was only slightly modified by the different co-dopants, which, in contrast, had a significant effect on the depths of the deeper traps. The combined results of the trap level energies obtained from the experimental data and DFT calculations suggest that the main trap responsible for the persistent luminescence of the Sr2MgSi2O7:Eu2+,R3+ materials is created by charge compensation lattice defects, identified tentatively as oxygen vacancies, induced by the R3+ co-dopants.  相似文献   

15.
Eu2+/Dy3+-codoped BaAl2O4 phosphors were prepared by conventional solid-state reaction with boric acid flux. The effects of boric acid on structural and luminescent properties of BaAl2O4:(Eu2+, Dy3+) were investigated. The crystallinity of BaAl2O4 improved with increasing amount of H3BO3. Incorporation of Eu2+ and Dy3+ ions into effective lattice sites was promoted by H3BO3 addition. As a result, Eu2+ emission in BaAl2O4 was greatly enhanced by H3BO3, and the duration of persistent luminescence increased with the amount of H3BO3. However, the decay lifetime of persistent luminescence was not strongly influenced by the amount of H3BO3.  相似文献   

16.
Results of measurements of the yield of Nd3+ radioluminescence photons in inorganic laser liquids POCl3-MCln-235UO 2 2+ -Nd3+ (M = Ti, Zr, Sn, or Sb) during homogeneous excitation by uranium α-particles are presented. It was found that the intensity of radioluminescence corresponding to the 4 F 3/24 I 11/2 transition in neodymium ions depends on the solvent composition. Data on the radiation-chemical yield, G, of excited neodymium ions in the POCl3-MCln-235UO 2 2+ -Nd3+ (M = Ti, Zr, Sn, or Sb) system were obtained. At a neodymium concentration of 0.25 mol/l, the values of G for the excited ions were 0.60 ± 0.10, 0.84 ± 0.10, 1.20 ± 0.10, and 1.64 ± 0.16 ion/100 eV in solutions with TiCl4, ZrCl4, SnCl4, and SbCl5, respectively. The maximum yields of excited ions estimated at G = 1.68 ± 0.10 and 2.20 ± 0.24 ion/100 eV were obtained for the solutions with SnCl4 and SbCl5, respectively, at neodymium ion concentrations above 0.4 mol/l.  相似文献   

17.
The Er3+-Li+ codoped TiO2 powders have been prepared by the non-aqueous sol–gel method. The green and red upconversion emissions centered at about 526, 550 and 663 nm were observed by the 2H11/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions of Er3+, respectively. Li+ codoping has opposite effect on the upconversion emissions intensities for Er3+-doped TiO2 at sintering temperatures of 1,073 and 1,273 K. At 1,073 K, the Er3+-doped TiO2 phase transition from anatase to rutile was accelerated with increasing Li+ codoping concentration, leading to the increase of crystal field symmetry of Er3+, thus the upconversion emissions intensities decreased. At 1,273 K, Li+ codoping had no effect on the phase structure of Er3+-doped TiO2 and only increased the Er–O bond length, it indicated that the upconversion emissions intensities greatly enhanced because of the decrease of crystal field symmetry of Er3+.  相似文献   

18.
Eu, Dy co-doped strontium aluminate nanophosphors were prepared by the combustion synthesis method. Their structure and morphology were investigated by X-ray diffraction (XRD), scanning electron microscopy, transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy. According to the XRD and the TEM analysis, the average crystallite size was found to be in the nanometer range. The phase structure of the prepared nanophosphor is consistent with a standard monoclinic phase with a space group P21. The prepared SrAl2O4:Eu2+, Dy3+ nanophosphor emitted green light with a peak at 510 nm showing blue shift, which is due to the reduction in the particle size. Two distinct peaks were observed in the ML intensity versus time curve. The two peaks in ML indicate the presence of charge transfer in an ML process.  相似文献   

19.
Eu3+ ion-doped LaPO4 nanowires or nanorods have been successfully synthesized by a simple hydrothermal method. The influence of varying the hydrothermal and subsequent sintering conditions on the morphology and structure of the LaPO4 host has been investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD). For comparison, the Eu3+ ions were also doped into monoclinic monazite LaPO4 nanoparticles and perovskite LaAlO3 nanoparticles. The relative intensities of the emission lines of the LaPO4:Eu3+ nanosystems were essentially independent of their shape. The optimal doping concentrations in the monoclinic LaPO4 and perovskite LaAlO3 nanosystems were determined to be about 5.0 and 3.5 mol%, respectively. Under appropriate UV-radiation, the red light emitted from LaAlO3:Eu3+ (3.5 mol%) was brighter than that from LaPO4:Eu3+ (5.0 mol%) nanomaterial, resulting from differences in their spin-orbit couplings and covalence, which indicates that the nanoscale LaAlO3 is a promising host material for rare earth ions. Electronic Supplementary Material  Supplementary material is available for this article at and is accessible for authorized users. Supported by the National Natural Science Foundation of China (Grant Nos. 20873039 & 90606001), Hunan Provincial Natural Science Foundation (No. 07jj4002), and the Students Innovation Training Fund of Hunan University  相似文献   

20.
Er3+-doped Al2O3 nanopowders have been prepared by the non-aqueous sol-gel method using the aluminum isopropoxide as precursor, acetylacetone as a chelating agent, nitric acid as a catalyzer, and hydrated erbium nitrate as a dopant under isopropanol environment. The different phase structure, including three crystalline types of (Al, Er)2O3 phases, α, γ, θ, and an Er–Al–O stoichiometric compound phase, Al10Er6O24, was observed for the 0.01–0.5 mol% Er3+-doped Al2O3 nanopowders at the sintering temperature of 1,000 °C. The green and red up-conversion emissions centered at about 523, 545 and 660 nm, corresponding respectively to the 2H11/2, 4S3/24I15/2 and 4F9/24I15/2 transitions of Er3+, were detected by a 978 nm semiconductor laser diodes excitation. With increasing Er3+ doping concentration from 0.01 to 0.1 mol%, the intensity of the green and red emissions increased with a decrease of the intensity ratio of the green to red emission. When the Er3+ doping concentration rose to 5 mol%, the intensity of the green and red emissions decreased with an increase of their intensity ratio. The maximum intensity of both the green and red emissions with the minimum of intensity ratio was obtained, respectively, for the 0.1 mol% Er3+-doped Al2O3 nanopowders composed of a single α-(Al,Er)2O3 phase. The intensity ratio of the green emission at 523 and 545 nm increased monotonously for all Er3+ doping concentrations. The two-photon absorption up-conversion process was involved in the green and red up-conversion emissions of the Er3+-doped Al2O3 nanopowders.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号