Part II. Chromatography using ultra-stable metal oxide-based stationary phases for HPLC

In this part of the review authors discuss methods used for modification of metal oxide surfaces. On the basis of literature data it is shown, that silanization of the surfaces do not form stable supports for chromatography. On the other hand, the success of polymer modified surfaces such as polybutadiene (PBD) and polystyrene (PS) is emphasized. Permanent modification of metal oxide surfaces with Lewis bases is also widely discussed. Chromatographic properties of polymer modified surfaces of zirconia are discussed in details. The perspectives of carbon-coated metal oxide surfaces in HPLC and high temperature separations are described.     

Electrochemical study of the Nd1.95NiO4 + δ/oxide electrolyte interface

Nickelate-based oxides are potential cathodes in Solid Oxide Fuel Cells operating at intermediate temperatures. The chemical compatibility between apatite electrolyte, i.e., La₉Sr₁Si₆O_26.5, and Nd-deficient nickelate, i.e., Nd_1.95NiO_4 + δ, has been characterized. The equilibrium between the nickelate material and the gas phase has been studied as functions of temperature and oxygen partial pressure, using potentiometric measurements with microelectrodes, i.e., metallic or ceramic point electrodes. Two solid electrolytes were used, i.e., apatite and yttria-stabilized zirconia. The response of the nickelate is discussed in terms of oxygen stoichiometry.     

Microstructure and electrical properties of YSZ–NiO composites

The microstructure and electrical properties of YSZ (ionic)–NiO (electronic) composites were investigated. The electrical properties of the composites were examined using impedance spectroscopy between 160 and 630°C. The effects of grains and grain boundaries on the electrical conductivity of the composites vary with composition and temperature. With increasing temperature, the contribution of grain boundary to the total resistivity decreases for YSZ-rich compositions (NiO≤30 mol%). For NiO-rich compositions (NiO>50 mol%), the contribution of grain boundary resistance is variable with temperature, showing maxima near 530°C. Above 630°C, the grain boundary resistance is small for all compositions. With varying composition, grain boundary resistance is greater when the number of YSZ/NiO contacts is greater than the number of YSZ/YSZ or NiO/NiO contacts below 500°C. The temperature- and composition-dependence of grain and grain boundary conductivity is explained by the microstructure and thus by the distribution of the two phases together with variations in activation energy according to the composition.     

Stress driven phase transformation in ZrO2 film

Zirconia thin layers (250 nm) were deposited on stainless steel substrates using organo-metallic injection chemical vapour deposition (MOCVD) process with zirconium beta-diketonate as precursor at low oxygen pressure and 900 °C. Low roughness zirconia films were made up of a mixture of tetragonal and monoclinic phases depending on the process conditions. As the zirconia tetragonal phase is known to be stabilized by small grain size and/or internal compressive stresses, tensile and/or compressive external stress fields were applied at room temperature using a bending test device. Then, XRD measurements were used to determine tetragonal/monoclinic phase ratio and also residual stresses in the films before and after the tests. The film surface was observed at the various stages of the experiments by field electron gun-scanning electron microscopy (FEG-SEM).Under these stress fields, phase transformation occurs in the film, from tetragonal structure to a monoclinic one. Some preferential tetragonal planes give rise to monoclinic ones. The external stress field is also likely to redistribute the internal stresses within the films.     

Thermal spreading of WO3 onto zirconia support

This study focused on preparation of tungsten oxide supported on zirconia by thermal spreading. The prepared samples were characterized by infrared spectroscopy, UV-vis diffuse reflection spectroscopy, X-ray diffraction, and also by methanol dehydration reaction. It was observed that isolated octahedral tungsten dispersed species and dispersed polytungstate were formed on zirconia surface, although some WO₃ that remained after the thermal treatment could also be detected. The presence of these species led to an increase of the number of Lewis sites and the generation of Brönsted acid sites. High calcination temperatures promoted the creation of Brönsted sites as a consequence of polytungstate species formation. The activity on methanol dehydration was also determined by the concentration of these species, whereas the isolated WO_x species were found poorly active. The correlation observed between the catalytic performance and the tungsten dispersed species, as revealed by spectroscopic techniques, evidenced the occurrence of thermal spreading of WO₃ on ZrO₂. The results presented in this work show that WO₃ thermal spreading on ZrO₂ may be effectively accomplished as predicted by thermodynamics.     

Synthesis, structure, microstructure and mechanical characteristics of MOCVD deposited zirconia films

Zirconia (ZrO₂) thin films were deposited by metal organic chemical vapor deposition (MOCVD) on (1 0 0) Si over temperature and pressure ranges from 700 to 900 °C and 100 to 2000 Pa, respectively. The oxide films were characterized by field emission microscopy and X-ray diffraction so that microstructure and ratios of monoclinic and tetragonal phases could be estimated according to the process conditions. The mechanical behaviour of the substrate-film systems was investigated using Vickers micro-indentation and Berkovitch nano-indentation tests. The characteristics of silicon are not modified by the presence of a thin film of silicon oxide (10 nm), formed in the reactor during heating. Young's modulus and the hardness of tetragonal zirconia phase, 220 and 15 GPa, respectively, are greater than values obtained for monoclinic phase, 160 and 7 GPa, respectively. The zirconia films are well adherent and the toughness of tetragonal zirconia phase is greater than that of monoclinic phase.     

Polydimethylsiloxane at the interfaces of fumed silica and zirconia/fumed silica

Polydimethylsiloxane (PDMS)/fumed silica A-300 and PDMS/ZrO₂/A-300 were studied using adsorption, thermogravimetry, temperature-programmed desorption (TPD) mass-spectrometry, infrared spectroscopy, XRD, and broadband dielectric relaxation spectroscopy. ZrO₂ was synthesized on fumed silica with zirconium acetylacetonate in CCl₄ at 350 K for 1 h and calcinated at 773 K for 1 h (1-4 reaction cycles). PDMS (5-40 wt.%) was adsorbed onto silica and zirconia/silica from hexane solution and then dried. Grafted zirconia changes the chemistry of the surface (because of its catalytic capability) and the topology of secondary particles (because of occupation of voids in aggregates of primary silica particles by zirconia nanoparticles) responsible for the textural porosity of the powders. Therefore, many properties (such as structural characteristics of the composites, reactions on heating in air and vacuum, interfacial relaxation phenomena, hydrophobicity as a function of treatment temperature, etc.) of PDMS/zirconia/silica strongly differ from those of PDMS/A-300. Broadening of the α-relaxation of PDMS at the interfaces of disperse oxides suggests both weakening of the PDMS-PDMS interaction and strengthening of the PDMS-oxide interaction.     

Magnetic properties of ZrO2-diluted magnetic semiconductors

Monoclinic zirconia (ZrO₂) as a potential host for diluted magnetic semiconductors (DMS) was investigated using density functional theory (DFT). Our calculations assessed the feasibility of long-range magnetic order at room temperature for transition metal ions substituting Zr. The defect-related d states split into e_g and t_2g bands. The exchange mechanism was shown to have strong nearest-neighbour coupling for several dopants reaching up to 150 meV for Fe. However, there was little to no long-range coupling extending beyond nearest-neighbour coordination, resulting in a non-physically high-defect concentration necessary for room temperature ferromagnetism.     

Effect of uniaxial stress on ionic conductivity of 14 mol%-yttria-stabilized zirconia single crystal

In the present study, the ionic conductivity of the 14 mol%-yttria stabilized zirconia single crystal subjected to the tensile or compressive stress was examined at various temperatures. The conductivity was increased by the tensile stress and the improvement in the conductivity was higher at the lower temperature and also for the specimen with the <100> orientation. On the other hand, the conductivity was decreased by the compressive stress. The change by the compressive stress was higher at the lower temperature, but it was generally smaller than that in the tensile test. The maximum improvement achieved by applying the tensile stress was about 18% at 850 K in the present study. The present experimental results qualitatively agreed with the molecular dynamics simulations on the oxygen diffusion. The oxygen displacement in the fluorite lattice caused by the applied stress could be attributed to the change in the conductivity.     

Influence of oxygen partial pressure on the properties of pulsed laser deposited nanocrystalline zirconia thin films

ZrO₂ thin films were deposited at various oxygen partial pressures (2.0 × 10⁻⁵-3.5 × 10⁻¹ mbar) at 973 K on (1 0 0) silicon and quartz substrates by pulsed laser deposition. The influence of oxygen partial pressure on structure, surface morphology and optical properties of the films were investigated. X-ray diffraction results indicated that the films are polycrystalline containing both monoclinic and tetragonal phases. The films prepared in the oxygen partial pressures range 2.0 × 10⁻⁵-3.5 × 10⁻¹ mbar contain nanocrystals of sizes in the range 54-31 nm for tetragonal phase. The peak intensity of the tetragonal phase decreases with the increase of oxygen partial pressures. Surface morphology of the films examined by AFM shows the formation of nanostructures. The RMS surface roughness of the film prepared at 2.0 × 10⁻⁵ mbar is 1.3 nm while it is 3.2 nm at 3.5 × 10⁻¹ mbar. The optical properties of the films were investigated using UV-visible spectroscopy technique in the wavelength range of 200-800 nm. The refractive index is found to decrease from 2.26 to 1.87 as the oxygen partial pressure increases from 2.0 × 10⁻⁵ to 3.5 × 10⁻¹ mbar. The optical studies show two different absorption edges corresponding to monoclinic and tetragonal phases.