Published June 2013 | Version v1
Journal article

Interfacial reaction of Co–Fe films with SiO2 substrates

  • 1. Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899 (United States)
  • 2. Institute of Metal Physics, Urals Branch of the Academy of Sciences, Ekaterinburg 620219 (Russian Federation)
  • 3. Department of Material Science and Engineering, University of Maryland, College Park, MD 20742 (United States)

Description

The interdiffusion reaction between Co1−xFex deposited films of various compositions (x = 0.27, 0.32 and 0.50) and an amorphous SiO2 substrate during annealing in vacuum at 800 °C was identified by analytical transmission electron microscopy. The reaction results in the formation of Fe2SiO4 mixed silicate of olivine structure as an interfacial phase. The following microstructural changes occurring during this reaction are inferred: (a) recrystallization of as-deposited films during the 800 °C annealing results in large grains of the body centered cubic Co–Fe solid solution; (b) metals diffuse into the SiO2 substrate and nucleate grains of the Fe2SiO4 silicate along the film/SiO2 interface; (c) silicon and oxygen partially released during the reaction, in turn, diffuse into an unreacted metallic film and form precipitates of the (Co,Fe)3O4 spinel phase and solid solution of Si in Co–Fe. To our best knowledge, the formation of silicates with olivine-type structure (known as fayalite for Fe) as products of the metal/SiO2 reaction has never been reported before. Thermodynamic evaluation of the reaction employing the semi-empirical CALPHAD (Calculation of Phase Diagrams) method supports the experimental findings, although the reaction requires an excess of oxygen

Availability note (English)

Available from http://dx.doi.org/10.1016/j.actamat.2013.03.044

Additional details

Identifiers

DOI
10.1016/j.actamat.2013.03.044;
PII
S1359-6454(13)00254-1;

Publishing Information

Journal Title
Acta Materialia
Journal Volume
61
Journal Issue
11
Journal Page Range
p. 4180-4190
ISSN
1359-6454
CODEN
ACMAFD

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.