Tracer diffusion of selected cations in single crystal MgO
Abstract
The diffusion of various cations in single crystal magnesium
oxide has been measured over a wide temperature range using radioactive
tracers and a sectioning technique. Self-diffusion studies may be
interpreted in such a manner as to suggest that the enthalpy of formation
of a Schottky defect in this oxide is (3.8 ± 0.3) eV, while the
enthalpy of motion of a cation vacancy is (1.56 ± 0.08) eV.
Intrinsic diffusion occurs above 1900 °C, with a 'knee' temperature,
for the material used here, of 1800 °C. Impurityprecipitation-controlled
diffusion has been observed below 1500 °C.
Atmosphere, apparently, has no effect on diffusion rates. The radius
of a diffusing ion seems to have no detectable influence on its
enthalpy of motion in MgO, whereas electronic properties (polarisability
and charge) are evidently important in this respect. Most impurities
diffuse by a vacancy mechanism, but beryllium diffusion may possibly
proceed via interstitial sites.
Short-circuit enhancement of diffusion in MgO involves two
(or more) mechanisms, one being dependent on the presence of impurity
precipitates at dislocations, while the other is independent of this
phenomenon and operates for ions which are large compared with the host
cation. Such enhancement is believed to have obscured precipitationcontrolled
lattice diffusion in many studies and also accounts for the
variation in activation energies reported by different authors for the
diffusion of a given impurity.
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