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91.
F-doped TiO2 (FTO) powders were synthesized by spray pyrolysis (SP) from an aqueous solution of H2TiF6. The resulting FTO powders possessed spherical particles with a rough surface morphology and a strong surface acidity. The fluorine concentrations in the FTO powders calculated from XPS spectra significantly depended on SP temperature and ranged from 2.76 to 9.40 at.%. The FTO powder prepared at SP temperature of 1173 K demonstrated the highest photocatalytic activity for the decomposition of gas-phase acetaldehyde under both ultraviolet (UV) and visible light (vis) irradiations, and it was higher than that of commercial P 25. This high photocatalytic activity was ascribed to several beneficial effects produced by F-doping: enhancement of surface acidity, creation of oxygen vacancies, and increase of active sites. It was interesting to point out that the vis photocatalytic activity of FTO powders was achieved by the creation of surface oxygen vacancies rather than the improvement of optical absorption property of bulk TiO2 in vis region.  相似文献   
92.
The present paper is focused on multilayer Er3+-doped silica-titania planar waveguides, co-doped with silver, which were prepared by spin-coating on silica glass, or buffered single crystal silicon substrates. The single layer thickness (0.4 m) and refractive index (1.60–1.63) were measured by spectroscopic ellipsometry at 715 nm. The thickness of the waveguides (measured by mechanical profilometry) was 1 m and their optical propagation losses were measured at different laser wavelengths (488 nm, 514 nm and 633 nm), exhibiting an approximately Rayleigh-like behavior. The thermal precipitation of silver nanocrystallites was achieved, both in air and under a controlled atmosphere (dry nitrogen) and these were characterized by visible absorption spectroscopy, which clearly showed the development of a plasmon absorption band near 415 nm, by X-ray diffraction (XRD) and Transmission Electron Microscopy (TEM). The Er3+ metastable level lifetimes for the emission at ca. 1.54 m were found to be ca. 4–6 ms, for Er3+ concentrations varying between 0.2–2.0 mol% (or (0.4–4.4) × 1020 ions/cm3), but no significant variation was observed with the Ag concentration added (up to 2.5 mol%).  相似文献   
93.
Extralithiated chromium-doped finely divided lithium-manganese spinels are synthesized as a result of a two-step solid-phase process with use made of the fusion-saturation method. The spinels are intended for application as cathodic materials in lithium-ion batteries. The phase composition and structural characteristics of samples of cathodic materials of the type Li x Mn2?y Cr y O4 are studied. The samples with x = 1.0?1.2 and y = 0?0.5 are characterized by phase purity and cubic syngony with parameter a = 0.817?0.823 nm and a disperseness equal to 1–2 nm. The maximum content of chromium and lithium in Li x Mn2?y Cr y O4 that does not lead to violation of cubic syngony is determined. Lithium excess in the cathodic material that does not exceed 0.2 formula units may be used for compensating the irreversible capacity. Replacing some manganese atoms by chromium may facilitate retention of the structures’s integrity in the course of cycling.  相似文献   
94.
EPR, UV/Vis and FTIR spectroscopy as well as thermal analysis (TA/MS) were applied to study the influence of sulfate species present in the anatase support on the specific nature of VOx species in supported VOx/TiO2 catalysts. Those sulfate species modify the local structure of the supported vanadyl species and lead to the formation of two types of VO2+ sites instead of only one type being formed on sulfate‐free anatase. EPR and FTIR spectroscopic measurements revealed that a part of the VO2+ species are directly bound to the surface sulfate species. By TA/MS it was found that SO2 is released at lower temperature from VOx/TiO2 in comparison to the vanadium‐free support. The direct bonding between sulfate and VOx species stabilizes the latter on the surface of VOx/TiO2 resulting in three effects: 1) a higher V site dispersion in comparison to sulfate‐free TiO2, 2) a better resistance of surface vanadyls against diffusion into the bulk of the support and 3) a much faster reoxidation of reduced V sites than observed on sulfate‐free TiO2.  相似文献   
95.
Complex dielectric permittivities of pure and KOH-doped (x = 1.8 x 10–4) tetrahydrofuran clathrate hydrates were measured in the temperature range 20–260 K and in the frequency range 20 Hz-1 MHz. The relaxation time of the water reorientational motion was found to decrease drastically as a result of the doping; e.g., the relaxation time of the doped sample was 10–9 times shorter than that of the pure sample at 70 K. The activation enthalpy of the motion was reduced to 7.4 kJ mol–1. On cooling the crystal, the value of decreased suddenly at the 62 K phase transition to the 2 value of the pure sample and at the same time disappeared. No dispersion effect due to the guest reorientation was observed below the transition. These data indicate that both the host and guest molecules become ordered or, at least, change their mobility drastically. In the pure sample, a relaxation phenomenon of 02 was found around the glass transition region. The relaxation times agreed well with those derived from the enthalpy of relaxation in a calorimetric study.Dedicated to Dr D. W. Davidson in honor of his great contributions to the sciences of inclusion phenomena.  相似文献   
96.
It is shown, for the first time, that single-component continuous networks of a low molecular weight electron acceptor additive can be grown in a polymer matrix. Such networks can be doped using, e.g., iodine vapor and converted into conductive CT complexes without losing continuity, thereby making the polymer film conductive. Polyethylene films with tetrathiotetracene networks are obtained, and their doping with iodine vapor in air is investigated by means of conductivity and spectrophotometry in the visible range. It is concluded that doping of the surface layer of the microcrystallites is sufficient to observe a significant increase in the film conductivity, which makes possible the use of such systems as sensors.  相似文献   
97.
A series of titanocene(III) alkoxides L2Ti(III)OR where L = Cp, R = Et(1b), tBu(1a), 2,6-Me2C6H3(1c), 2,6-tBu2-4-Me-C6H2(1d), or L = Cp*, R = Me(2e), tBu(2a), Ph(2f) was synthesized and subjected to reaction with [CpM(CO)3]2 [M = Mo, W], [CpRu(CO)2]2, and Co2(CO)8. The Ti(III) precursors 1a, 1c, 2a, 2e, and 2f reacted with [CpM(CO)3]2 [M = Mo, W] to form heterobimetallic complexes L2Ti(OR)(μ-OC)(CO)2MCp [M = Mo, W], of which Ti and M are linked by an isocarbonyl bridge. Reactions of these Ti(III) complexes with Co2(CO)8 resulted in formation of Ti-Co1 heterobimetallic complexes, from 2a, 2e, or 2f, or Ti-Co3 tetrametallic complexes, Cp2Ti(OtBu)(μ-OC)Co3(CO)9 from 1a, 1b, or 1c. The products were characterized by NMR, IR, and X-ray crystallography. Reaction mechanisms were proposed from these results, in particular, from steric/electronic effects of titanium alkoxides.  相似文献   
98.
It has been found that thin polyaniline films doped with several zinc salts in solutions at pH 5.5 become electroconductive and electroactive in neutral aqueous electrolytes. The shape of the voltammetric characteristics depends on the initial state of the film. The effect of secondary doping withm-cresol is observed for polyaniline complexes with zinc salt of camphorsulfonic acid.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1450–1452, June, 1996.  相似文献   
99.
锂离子电池具有比能量高、功率大、使用寿命长、无记忆效应、性能价格比高等优点,从而成为可充式电源的主要选择对象.锰由于资源丰富、价廉、环境友好等优点,使锰酸锂(LiMn2O4)成为最有希望取代钴酸锂的正极材料.但锰酸锂的放电容量相对较低,结构欠稳定,容量衰减严重,作为正极材料还无法与钴酸锂相比,近年来做了大量的研究工作以改善它的电化学性能[1~6].最近Youngjoon Shin等研究发现[7]用少量的Li与Ni共同替代LiMn2O4中的Mn得到的LiMn2-2yLiyNiyO4的电化学性能要优于单元素替代的LiMn2-xMxO4(M=Li,Cr,Fe,Co,Ni)的电化学性能.  相似文献   
100.
We have studied the generation mechanisms of H(II) paramagnetic centers in Ge-doped silica by investigating up to 104 mol ppm sol-gel Ge-doped silica materials. We have considered materials with the same concentrations of Ge but that are produced by two different densification routes that give rise to different concentrations of Ge-related oxygen deficient centers (GeODC(II)). These centers are characterized by an optical absorption band at ∼5.2 eV (B2β band) and two related emissions at ∼3.2 eV and ∼4.3 eV. The GeODC(II) content was estimated by absorption and emission measurements. The H(II) centers were induced by room temperature γ-ray irradiation and their concentration was determined by electron paramagnetic resonance measurements. The comparison between the two kinds of materials, obtained by different preparations, shows that the GeODC(II) concentration increases with the Ge content and is enhanced by vacuum densification. The comparison of irradiated samples shows that beyond the already known process of conversion of preexisting GeODC(II) into H(II) centers, another generation process of H(II) centers is effective that involves irradiation induced GeODC(II).  相似文献   
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