Ferromagnetic-to-antiferromagnetic transition in (Hf1-xTix)Fe2 intermetallic compounds induced by geometrical frustration of the Fe(2a) sites
- 1. Institute of Nuclear Physics, Moscow State University, 119991 Moscow (Russian Federation)
Description
The ferromagnetic-to-antiferromagnetic transition in the hexagonal (Hf1-xTix)Fe2 (0≤x≤1) intermetallic compounds has been investigated by 57Fe Moessbauer spectroscopy. At 10 K, the transition occurs within rather narrow concentration limits, around x=0.55-0.65. We found that the key factor governing the unexpected quick change of the magnetic structure is the magnetic frustration of the Fe(2a) sites. The magnetic frustration is caused by the noncollinearity of the Fe(6h) magnetic sublattice. The noncollinearity arises from the rotation of the magnetic moments due to the competition between the ferromagnetic exchange interactions and the antiferromagnetic Fe(6h)-Ti-Fe(6h) interaction. In the compounds with x=0.4-0.6, the temperature transitions to the antiferromagnetic state are observed. As an example, the Hf0.4Ti0.6Fe2 compound is completely antiferromagnetic above 200 K
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jmmm.2008.02.149Additional details
Identifiers
- DOI
- 10.1016/j.jmmm.2008.02.149;
- PII
- S0304-8853(08)00243-6;
Publishing Information
- Journal Title
- Journal of Magnetism and Magnetic Materials
- Journal Volume
- 320
- Journal Issue
- 12
- Journal Page Range
- p. 1853-1857
- ISSN
- 0304-8853
- CODEN
- JMMMDC
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 40005464
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ANTIFERROMAGNETISM; EXCHANGE INTERACTIONS; FERROMAGNETISM; HAFNIUM ALLOYS; INTERMETALLIC COMPOUNDS; IRON ALLOYS; MAGNETIC MOMENTS; MOESSBAUER EFFECT; TITANIUM ALLOYS; TRANSITION TEMPERATURE
- Descriptors DEC
- ALLOYS; INTERACTIONS; MAGNETISM; PHYSICAL PROPERTIES; THERMODYNAMIC PROPERTIES; TRANSITION ELEMENT ALLOYS
Optional Information
- Copyright
- Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.