The magnetic and structural properties of cobalt-implanted ZnO single crystals are reported. High-quality, (110)-oriented single-crystal Sn-doped ZnO substrates were implanted at ∼350 °C with Co to yield transition metal concentrations of 3–5 at. % in the near-surface (∼2000 Å) region. After implantation, the samples were subject to a 5 min rapid thermal annealing at 700 °C. Magnetization measurements indicate ferromagnetic behavior, with hysteresis observed in the M vs H behavior at T=5 K. Coercive fields were ⩽100 Oe at this measurement temperature. Temperature-dependent magnetization measurements showed evidence for ordering temperatures of >300 K, although hysteresis in the M vs H behavior was not observed at room temperature. Four-circle x-ray diffraction results indicate the presence of (110)-oriented hexagonal phase Co in the ZnO matrix. From the 2θ full width at half maximum (FWHM) of the Co (110) peak, the nanocrystal size is estimated to be ∼3.5 nm, which is below the superparamagnetic limit at room temperature. In-plane x-ray diffraction results show that the nanocrystals are epitaxial with respect to the ZnO host matrix. The magnetic properties are consistent with the presence of Co nanocrystals, but do not preclude the possibility that a component of the magnetism is due to Co substitution on the Zn site in the ZnO matrix.
6%Comparisons have been made in laboratory isothermal and cyclic oxidation tests of the degradation of oxide scales grown on single crystal superalloy substrates and bond coating alloys intended for use in thermal barrier coatings systems. The influence of desulphurisation of the superalloy and bond coating, of reactive element addition to the bond coating alloy, and of oxidation temperature on the spallation behavior of the alumina scales formed was assessed from oxidation kinetics and from SEM observations of the microstructure and composition of the oxide scalei. Desulphurisation of a nickel-base superalloy (in the absence of a Y addition) resulted in an increase in the lifetime of a state-of-the-art thermal bamier coating applied to it compared to aY,-free, non-desulphurised version of the alloy. The lifetime of the same ceramic coating applied without a bond coating to a non-desulphurised model alloy that formed an 'ideal' alumina scale was also found to be at least four times longer than on the Y-doped superalloy plus state-of-the-art bond coating combination. Some explanations are offered of the factors controlling the degradation of such coatings.
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