Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-27T02:22:57.236Z Has data issue: false hasContentIssue false

Determination of the Chemical Potentials of Highly Supersaturated Cu-Co Alloys

Published online by Cambridge University Press:  15 February 2011

F. Gärtner
Affiliation:
Institut für Metallphysik, Hospitalstrasse 3-7, D-37073 Göttingen, F.R. Germany
R. Busch
Affiliation:
Institut für Metallphysik, Hospitalstrasse 3-7, D-37073 Göttingen, F.R. Germany
P. Haasen
Affiliation:
Institut für Metallphysik, Hospitalstrasse 3-7, D-37073 Göttingen, F.R. Germany
R. Bormann
Affiliation:
GKSS Research Centre, Institute for Materials Research, Max-Planck-Strasse, D-21502 Geesthacht, F.R. Germany
Get access

Abstract

With the CALPHAD approach based on the regular solution model, the thermodynamic functions of the Cu-Co system can be extrapolated to compositions where the homogeneous fee solid solution is thermodynamically unstable. Up to now it has been unclear how reliable such extrapolations are in view of the driving forces for decomposition and whether the Gibbs energy is well described by the model in the unstable region. Therefore, electromotive force measurements were performed to determine directly the chemical potentials of highly supersaturated Cu-Co alloys. Under the prerequisite that time scales of the electrochemical exchange reaction are fast compared with the kinetics of decomposition, the thermodynamics of the alloys can be investigated quasi statically. Within the experimental accuracy the results for both a metastable and an unstable alloy agree well with the calculated chemical potentials. In addition, the experiments demonstrate that the electrochemical cell reaction is reversible upon small external concentration fluctuations of the investigated alloys. Possible reasons for this unexpected stability are discussed taking the kinetics of the decomposition into account.

Type
Research Article
Copyright
Copyright © Materials Research Society 1996

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. LeGoues, F.K. and Aaronson, H.I., Acta Metall. 32, 1855 (1984).Google Scholar
2. Hattenhauer, R. and Haasen, P., Phil. Mag. A68,1195 (1993).Google Scholar
3. Wendt, H. and Haasen, P., Scripta Metall. 19, 1053 (1985).Google Scholar
4. Al-Kassab, T., Ph.D. Thesis, Georg-August-Universität, Göttingen, Germany, (1992).Google Scholar
5. Jiang, X, Wagner, W. and Wollenberger, H, Z. Metallk. 82, 192 (1991).Google Scholar
6. Wecker, J., Helmholdt, R, v., Schultz, L. and Samwer, K., Appl. Phys. Lett. 62, 1985 (1993).Google Scholar
7. Howson, M.A., Musa, S.O., Walker, M.J., Hickey, B.J., Cochrane, R., and Stevens, R., J. Appl. Phys. 75, 6546 (1994).Google Scholar
8. Berkowitz, A.E., Mitchell, J.R., Carey, M.J., Young, A.P., Zhang, S., Spada, F.E., Parker, F.T., Hütten, A. and Thomas, G., Phsy. Rev. Lett. 68, 3745 (1992).Google Scholar
9. Gente, C., Oehring, M. and Bormann, R., Phys. Rev. B 48, 13244 (1993).Google Scholar
10. Busch, R, Gärtner, F., Borchers, C., Haasen, P. and Bormann, R., Acta Metall. et Mater., 43, 3467 (1995).Google Scholar
11. Busch, R, Gärtner, F., Borchers, C., Haasen, P. and Bormann, R., Acta Met.all et Mater., in press.Google Scholar
12. Busch, R., Gärtner, F., Borchers, C., Haasen, P and Bormann, R., these proceedings.Google Scholar
13. Gärtner, F., Ph.D. Thesis, Georg-August-Universität, Göttingen, Germany, (1992).Google Scholar