Search results for "medium"
showing 10 items of 3746 documents
Metal film growth on regular and defective MgO(001) surface: A comparative ab initio simulation and thermodynamic study
2006
Abstract In order to understand the difference in metallic film growth modes on perfect and defective oxide substrates, we have combined ab initio B3LYP periodic calculations on the slab models of the corresponding Me/MgO(0 0 1) interfaces (Me = Ag, Cu) with thermodynamic theory of solid solutions. For a defectless magnesia surface, we confirm the experimentally observed submonolayer growth of 3D metallic islands (Ag possesses a higher trend than Cu). Formation of Fs centers (neutral O vacancies) on the substrate markedly enhances metal atom adsorption as compared to physisorption over regular sites on a defect-free substrate. For the first time, we predict that the presence of these surfac…
Quantitative phase analysis and thickness measurement of surface-oxide layers in metal and alloy powders by the chemical-granular method
1998
The principles of the chemical-granular analysis of metal and alloy powders are reviewed and the results are compared with those provided by the spectroscopic analytical techniques XPS, AES and SIMS, including ion etching in their depth-profiling mode, when they are applied to the same materials. Several examples are analysed and it is shown that the chemical-granular method alone can provide the very same information as depth profiling. However, it is averaged over a macroscopic powder sample in contrast to one or a few single particles. Nevertheless, it is the combination of the chemical-granular and depth-profiling analyses that really provides an unparalleled description in quantitative…
Electrochromic absorbance changes in the chlorophyll-c-containing alga Pleurochloris meiringensis (Xanthophyceae)
1994
Flash-induced absorbance changes were measured in the Chl-c-containing alga Pleurochloris meiringensis (Xanthophyceae) between 430 and 570 nm. In addition to the bands originating from redox changes of cytochromes, three major positive and tow negative transient bands were observed both 0.7 and 20 ms after the exciting flash. These transient bands peaking at 520, 480 and 451 nm and 497 and 465 nm, respectively, could be assigned to an almost homogeneous shift of the absorbance bands with maxima at 506, 473 and 444 nm, respectively. The shape of the absorbance transients elicited from PS I or PS II was identical, and the two photosystems contributed nearly equally to the absorbance changes. …
Analysis of Mn2+EPR spectral shapes for studies of the oxyfluoride glass ceramics
2011
We investigated the EPR superhyperfine structure of the Mn 2+ ion in the disordered BaF2 crystalline media which tends to crystallize in the oxyfluoride glass-ceramics material. Obtained EPR spectra reveal explicit shf structure due to Mn 2+ ion building into the BaF2 lattice showing its usefulness as a probe in orientationally disordered and amorphous structures. Two types with explicit shf structure of Mn 2+ ion characteristic EPR spectra were obtained in BaF2 powder samples characteristic with broad (type 1) and narrow (type 2) hyperfine structure lines. Spectra of the ZnF2-BaF2 oxyfluoride glass-ceramics samples revealed explicit fine structure lines.
Phase composition of Fe-containing Langmuir-Blodgett layers after thermal treatment in a reactive atmosphere
1993
By the Langmuir-Blodgett technique, mono- and multilayers of ferric stearate were drawn onto silicon wafers. They were thermodesorbed in air at 250–300°C, and the layers formed in this way were found to consist of γ-FeOOH with defective stoichiometry. By heating in H2, the layers can be reduced to Fe2− and even to α-Fe. The latter is magnetically ordered and highly corrosion resistant. Chloride ions, however, induce fast corrosion. FeCl2, formed by this corrosion, is rather unstable and transforms to an Fe3+ phase. The high corrosion resistance of the metallic Fe layer is assumed to be due to its excellent homogeneity. The experiments were performed using XPS, AES, CEMS, and SEM.
MoO (x≤2) ultrathin film growth from reactions between metallic molybdenum and TiO2 surfaces
2001
Abstract Exposures to oxygen at room temperature and annealings under vacuum were carried out on deposits obtained from molybdenum interacting with (1 1 0) TiO 2 surfaces in order to obtain molybdenum oxide ultra thin films. Exposures to oxygen at room temperature show that the interfacial molybdenum oxide layers resulting from the TiO 2 /Mo interactions are inactive towards oxygen whereas the metallic molybdenum clusters, which grew on top of the interfacial layers, oxidise into MoO 3 . Besides, during annealings under vacuum, substrate oxygen anions can diffuse into the deposit. Thus, between 400 and 500°C, molybdenum oxide layers are progressively oxidised into MoO 2 . Moreover, from the…
Reactivity between molybdenum and TiO2(110) surfaces: evidence of a sub-monolayer mode and a multilayer mode
2005
Small amounts of molybdenum (from 0.03 to 1.3 eqML) were deposited on non-stoichiometric TiO 2 (1 1 0) surface. The deposits were investigated by means of LEED and X-ray/UV photoemission using synchrotron radiation. For the smallest coverage (<0.2 eqML), deposition leads to oxidation of molybdenum into species close to Mo 4+ .In such a case, states appearing in TiO 2 band gap are mainly due to reduced titanium. For higher coverages, metallic behaviour of molybdenum is observed. This phenomenon was explained, thanks to first principle calculations, as a decrease of the Mo-O interactions for the benefit of the Mo-Mo interactions as the surface molybdenum atom density increases.
Thermo‐optical investigations of NaNbO 3 thin films by spectral ellipsometry
2009
In this work a spectroscopic ellipsometry was applied to the thermo-optical investigations of sodium niobate NaNbO3 (NN) thin films at the wide temperature range of 5–820 K. The temperature dependence of complex refractive index dispersions and optical bang energy of the direct allowed electron transitions were evaluated. Additionally dynamic scans of the main ellipsometric angles at the several fixed wave lengths of 300, 400, 500 and 635 nm were performed to acquire more detailed temperature dependences of the refractive index and extinction coefficient. Pronounced minima/maxima and substantial jumps in the temperature dependence of complex refractive index and band gap energy were found a…
The Reduction Pathway of End-on Coordinated Dinitrogen. I. Vibrational Spectra of Mo/W−N2, −NNH, and −NNH2 Complexes and Quantum Chemistry Assisted N…
1999
Infrared and Raman spectra of [M(N(2))(2)(dppe)(2)] (M = W, Mo) and the two protonated derivatives [WF(NNH)(dppe)(2)] and [WF(NNH(2))(dppe)(2)](+) (dppe = 1,2-bis(diphenylphosphino)ethane) are presented. Using isotope substituted compounds ((15)N and D) the vibrations of the Y-M-N(2)H(x)() (x = 0, 1, 2; Y = N(2), F) central unit are identified, in particular the M-N and N-N stretching modes. In case of the monoprotonated systems, an equilibrium between metal- and nitrogen-protonated species exists that is clearly detectable in the IR spectra. Making use of theoretical force fields, a quantum chemistry assisted normal coordinate analysis (QCA-NCA) is performed for all three tungsten systems …
High activity of brookite TiO2 nanoparticles in the photocatalytic abatement of ammonia in water
2015
Abstract The effects of the TiO 2 crystal structure and its surface modification with Pt nanoparticles on the photocatalytic oxidation of NH 3 in the aqueous phase were studied with home-made TiO 2 photocatalyst powders synthesized by a thermo-hydrolysis approach that allowed a fine control of the crystallographic phase composition. Ammonia conversion and the selectivity toward mildly oxidized N 2 and highly oxidized nitrite and nitrate anions were monitored during the runs. Pure brookite powders modified by Pt nanoparticles, deposited either from a colloidal suspension or by deposition–precipitation, were found to be the most efficient photocatalysts in NH 3 degradation, with a desired goo…