Modeling of the reaction interdiffusion in the polycrystalline systems with limited component solubility

2019 ◽  
Vol 85 (9) ◽  
pp. 35-41
Author(s):  
N. N. Afonin ◽  
V. A. Logacheva

that may be accompanied by the processes of mutual diffusion and phase formation. Controlled technological process of forming coatings with the given properties entails the necessity of forecasting the evolution of the phase composition. This in turn requires the development of algorithms and quantitative models of the processes. Reactive mutual diffusion in polycrystalline metal (oxide film systems with limited component solubility) has not been simulated before. The simulation allows selecting the annealing conditions (time and temperature) necessary for the inclusion and uniform distribution of metal in the oxide lattice. A quantitative model of the interaction in a multi-layer system metal — polycrystalline oxide of the other metal under conditions of limited solubility is developed. The model is based on the concepts of mutual diffusion of the components and the bulk reactions of the formation of complex oxides. The developed model was applied to the analysis of the process of modifying thin films of titanium oxide with transition metals. The model allowed us to perform a numerical analysis of the experimental concentrations of the component distributions in polycrystalline Co - Ti02 and Fe - Ti02 thin-film systems. The individual diffusion coefficients of the studied metals and titanium under conditions of vacuum annealing were determined. The model provides a good description of the basic systematic features of the process: the appearance of titanium in the metal film and deep penetration of Fe and Co into the film of titanium oxide. It also explains the fact that complex oxides are formed not by layer-by-layer growth at the metal-oxide interface, but throughout the entire thickness of Ti02 film. The results of analysis of the processes of interracial interaction in layered systems accompanied by the reaction mutual diffusion can be used to predict the evolution of the phase composition, as well as to control the technological processes of obtaining materials with the desired properties.

CORROSION ◽  
10.5006/2807 ◽  
2018 ◽  
Vol 74 (9) ◽  
pp. 939-946 ◽  
Author(s):  
Xiao-xiang Yu ◽  
Ahmet Gulec ◽  
Christopher M. Andolina ◽  
Evan J. Zeitchick ◽  
Kateryna Gusieva ◽  
...  

Results of in situ transmission electron microscopy experiments on the early stage oxidation of Ni-Cr and Ni-Cr-Mo alloys are reported. An epitaxial rock-salt oxide with compositions outside the conventional solubility limits initiated at the surface of both alloys, progressing by a layer-by-layer mode. Kirkendall voids were found in Ni-Cr alloys near the metal/oxide interface, but were not seen in the Ni-Cr-Mo. The voids initiated in the oxide then diffused to the metal/oxide interface, driven by the misfit stresses in the oxide. A sequential oxide initiation was observed in NiCr alloys: rock-salt → spinel → corundum; however, for NiCrMo alloys, the metastable Ni2-xCrxO3 (corundum structure) phase formed shortly after the growth of the rock-salt phase. Chemical analysis shows that solute atoms were captured in the initial oxide before diffusing and transforming to more thermodynamically stable phases. The results indicate that Mo doping inhibits the formation of Kirkendall voids via an increase in the nucleation rate of corundum, which was verified by density functional theory calculations.


2003 ◽  
Vol 547 (1-2) ◽  
pp. L859-L864 ◽  
Author(s):  
R Lindsay ◽  
E Michelangeli ◽  
B.G Daniels ◽  
M Polcik ◽  
A Verdini ◽  
...  

2012 ◽  
Vol 59 ◽  
pp. 148-156 ◽  
Author(s):  
Jérôme Issartel ◽  
Sébastien Martoia ◽  
Frédéric Charlot ◽  
Valérie Parry ◽  
Guillaume Parry ◽  
...  

2000 ◽  
Vol 07 (01n02) ◽  
pp. 135-139 ◽  
Author(s):  
V. P. ZHDANOV ◽  
P. R. NORTON

A seminal model describing the kinetics of growth of thin oxide films on metal crystals was proposed by Cabrera and Mott (CM). The model is based on the assumption that the growth is limited by the field-facilitated activated jumps of metal ions located in steps on the metal–oxide interface. We generalize the CM model by (i) exploring the interplay of jumps of metal ions from the step and terrace sites at the metal–oxide interface, and (ii) scrutinizing the processes at the oxide–gas-phase interface. The former factor is found to change the physical meaning of the parameters in the CM growth law. The latter factor results in modification of the growth law. In particular, the oxidation kinetics becomes dependent on the O2 pressure. More specifically, the oxidation rate is predicted to increase with increasing pressure. This effect is, however, rather weak and becomes progressively weaker with increasing oxide film thickness.


2019 ◽  
Vol 742 ◽  
pp. 842-850 ◽  
Author(s):  
Aaron W. Colldeweih ◽  
Adrienn Baris ◽  
Philippe Spätig ◽  
Sousan Abolhassani

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