Magnesium impurity diffusion in Co1− x O single crystals
Identifieur interne : 000490 ( France/Analysis ); précédent : 000489; suivant : 000491Magnesium impurity diffusion in Co1− x O single crystals
Auteurs : H. Boussetta ; C. Monty [France]Source :
- Journal of Physics and Chemistry of Solids [ 0022-3697 ] ; 1988.
Descripteurs français
- Pascal (Inist)
- Autodiffusion, Cobalt Oxyde, Coefficient diffusion, Composition non stoechiométrique, Composé minéral, Défaut ponctuel, Energie activation, Etude expérimentale, Haute température, Hétérodiffusion, Impureté, Lacune, Magnésium, Monocristal, Métal transition Composé, Oxygène, Pression partielle, Profil diffusion, Température.
- Wicri :
- topic : Composé minéral, Magnésium, Oxygène.
English descriptors
- KwdEn :
- Activation energy, Cobalt Oxides, Diffusion coefficient, Diffusion profile, Experimental study, High temperature, Impurity, Impurity diffusion, Magnesium, Non stoichiometric composition, Oxygen, Partial pressure, Point defect, Self diffusion, Single crystal, Temperature, Transition metal Compounds, Vacancy.
Abstract
The diffusion coefficients for magnesium were measured in Co1−xO single crystals as a function of temperature and oxygen partial pressures in the ranges 1000–1600°C and 10−8−0.21 atm. The results are well represented by the relations Dmg∗(cm2S−1=(1.4±0.5)10−2fxp− 1.95±0.03(eV) kTpO2=0.21atm and T=1000−1600°cDmg∗(cm2S−L)=(4.0±0.4)10−3exp− 2.07±0.03(ev) kTp2=10−5atm and T=1060−1455°Clog D mg∗(cm2S−1)=3.5 10−3(logPO2)2+0.22log pO2−8.4T=1200°C and pO2=10−8−0.21 atm These results show that the influence of the oxygen partial pressure is smaller on Mg impurity diffusion than on Co self-diffusion. This effect has been interpreted as the evidence of a preferential attractive interaction between VCo and Mg impurities.
Url:
DOI: 10.1016/0022-3697(88)90094-7
Affiliations:
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<term>Diffusion coefficient</term>
<term>Diffusion profile</term>
<term>Experimental study</term>
<term>High temperature</term>
<term>Impurity</term>
<term>Impurity diffusion</term>
<term>Magnesium</term>
<term>Non stoichiometric composition</term>
<term>Oxygen</term>
<term>Partial pressure</term>
<term>Point defect</term>
<term>Self diffusion</term>
<term>Single crystal</term>
<term>Temperature</term>
<term>Transition metal Compounds</term>
<term>Vacancy</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Autodiffusion</term>
<term>Cobalt Oxyde</term>
<term>Coefficient diffusion</term>
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<term>Composé minéral</term>
<term>Défaut ponctuel</term>
<term>Energie activation</term>
<term>Etude expérimentale</term>
<term>Haute température</term>
<term>Hétérodiffusion</term>
<term>Impureté</term>
<term>Lacune</term>
<term>Magnésium</term>
<term>Monocristal</term>
<term>Métal transition Composé</term>
<term>Oxygène</term>
<term>Pression partielle</term>
<term>Profil diffusion</term>
<term>Température</term>
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<front><div type="abstract" xml:lang="en">The diffusion coefficients for magnesium were measured in Co1−xO single crystals as a function of temperature and oxygen partial pressures in the ranges 1000–1600°C and 10−8−0.21 atm. The results are well represented by the relations Dmg∗(cm2S−1=(1.4±0.5)10−2fxp− 1.95±0.03(eV) kTpO2=0.21atm and T=1000−1600°cDmg∗(cm2S−L)=(4.0±0.4)10−3exp− 2.07±0.03(ev) kTp2=10−5atm and T=1060−1455°Clog D mg∗(cm2S−1)=3.5 10−3(logPO2)2+0.22log pO2−8.4T=1200°C and pO2=10−8−0.21 atm These results show that the influence of the oxygen partial pressure is smaller on Mg impurity diffusion than on Co self-diffusion. This effect has been interpreted as the evidence of a preferential attractive interaction between VCo and Mg impurities.</div>
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