Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-08T01:57:53.725Z Has data issue: false hasContentIssue false

A Study on The Phase Transformation and Exchange-Coupling of (Nd0 95La0 05)9 5FebalCo5Nb2B10.5 Nanocomposites

Published online by Cambridge University Press:  21 February 2011

Q. Chen
Affiliation:
Rhodia Inc., Rare Earths and Gallium, CN 7500, Cranbury, New Jersey 08512
B. M. Ma
Affiliation:
Rhodia Inc., Rare Earths and Gallium, CN 7500, Cranbury, New Jersey 08512
B. Lu
Affiliation:
Department of Materials Science and Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213
M. Q. Huang
Affiliation:
Department of Materials Science and Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213
D. E. Laughlin
Affiliation:
Department of Materials Science and Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213
Get access

Abstract

The phase transformation and the exchange coupling in (Ndo095Lao005)9.5FebaICOsNb 2BI05 have been investigated. Nanocomposites were obtained by treating amorphous precursors at temperatures ranging from 650TC to 9500C for 10 minutes. The magnetic properties were characterized via the vibrating sample magnetometer (VSM). X-ray diffraction (XRD), thermomagnetic analysis (TMA), and transmission electron microscopy (TEM) were used to perform phase identification, measure grain size, and analyze phase distribution. The strength of the exchange coupling between the magnetically hard and soft phases in the corresponding nanocomposite was analyzed via the AM-versus-H plot. It was found that the remanence (Br), coercivity (Hci), and maximum energy product (BHmax) obtained were affected by the magnetic phases present as well as the grain size of constituent phases and their distribution. The optimal magnetic performance, BHm, occurred between 700°C to 750°C, where the crystallization has completed without excessive grain growth. TMA and TEM indicated that the system was composed of three phases at this point, Nd2(Fe Co) 14B, ca-Fe, and Fe3B. The exchange coupling interaction among these phases was consistently described via the AM-versus-H plot up to 750°C. The Br, Hci, and BHmax degraded severely when the thermal treatment temperature increased from 750°C. This degradation may be attributed to the grain growth of the main phases, from 45 to 68nm, and the development of precipitates, which grew from 5nm at 750°C to 12nm at 850°C. Moreover, the amount of the precipitates was found to increase with the thermal treatment temperatures. The precipitates, presumably borides, may cause a decrease in the amount of the a-Fe and Fe 3B and result in a redistribution of the Co in the nanocomposites. The increase of the Co content in the Nd 2(Fe Co) 14B may explain the increase of its Curie temperature with the thermal treatment temperatures. In this paper, we examine the impacts of these factors on the magnetic properties of (Ndo 95Lao 05)9 5FebaICosNb2B10.5 nanocomposite.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

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

REFERENCES

[1] Lu, B., Huang, M.Q., Chen, Q., Ma, B.M., and Laughlin, D.E., Proc. Of 43rd Annual Conference on Magnetism and Magnetic Materials, Miami, Florida (1998), in press.Google Scholar
[2] Kneller, E. F. and Hawig, R., IEEE Trans. Mag. 27, p.3588 (1991).Google Scholar
[3] Skomski, R. and Coey, J. M. D., Phys. Rev. B 48, p.1581 (1993).Google Scholar
[4] Schrefl, T., Fidler, J.. and Kronmuller, H., Phys. Rev. B, 49, p.6100 (1994).Google Scholar
[5] Fischer, R., Schrefl, T., Kronmuller, H., and Fidler, J., J. Magn. Magn. Mater. 153, p.35 (1996).Google Scholar
[6] Ormerod, J., Constantinides, S., J. Appl. Phys. 81, p.4816 (1997).Google Scholar
[7] Wohlfarth, E. P., J. Appl. Phys. 29, p.595 (1958).Google Scholar
[8] Kelly, P. E., Grady, K. O., Mayo, P. I., and Chantrell, R. W., IEEE Trans. Mag. 25, p. 3881 (1989).Google Scholar
[9] Fearon, M., Chantrell, R. W., Wohlfarth, E.P., J. Magn. Magn. Mater. 86, p.197 (1990).Google Scholar
[10] Chang, W. C., Wu, S. H., Ma, B. M., Bounds, C. O., Yao, S. Y., J. Appl. Phys. 83, p.2147 (1998).Google Scholar
[11] Manaf. Buckley, R. A.. and Davies, H. A., J. Magn. Magn. Mater. 128, p. 302 (1993).Google Scholar
[12] Withanawasam, L., Murphy, A.S., Hadjipanayis, G. C., Lawles, K. R., Krause, R. F., J. Magn. Magn. Mater. 140–145, p.1057 (1995).Google Scholar