Published July 2009 | Version v1
Journal article

Magnetic and dielectric properties of YbFe2-xMnxO4 (0≤x≤1)

  • 1. Japan Atomic Energy Agency, Sayo, Hyogo 679-5148 (Japan)
  • 2. Department of Physics, Okayama University, Okayama 700-8530 (Japan)
  • 3. Department of Physics, Osaka Prefecture University, Osaka 599-8531 (Japan)
  • 4. Department of Physics and Astronomy, Rutgers, The State University of New Jersey, New Brunswick, NJ 08854-8019 (United States)
  • 5. Department of Materials Science, Osaka Prefecture University, Osaka 599-8531 (Japan)

Description

We have investigated the magnetic and dielectric properties of YbFe2-xMnxO4 (0≤x≤1), which is an Fe-site-substituted system of new multiferroic oxides RFe2O4 (R=Y, Ho-Lu). X-ray diffraction measurements show that a solid solution is formed between YbFe2O4 (x=0) and YbFeMnO4 (x=1) for 0≤x≤1, whereas only compounds with x=1 (i.e., RM1M2O4; M1 and M2=trivalent and divalent cations, respectively) have been known for the Fe-site substitution in RFe2O4. The valence of the Mn ion is determined to be ∼2+, consistently with the suppression of low-temperature magnetization by the Mn substitution. The magnetic transition temperature (TN) and the dielectric constant (ε') decrease monotonically with increasing x. This result plausibly confirms that the magnetic and dielectric properties in oxides isostructural with RFe2O4 are governed by the electron transfer between Fe-site ions, unlike ordinary ferroelectrics and dielectrics, in which the ionic displacement plays a key role. The possibility for application is briefly discussed as well. - Graphical abstract: Dielectric constant (ε') and magnetic transition temperature (TN) of YbFe2-xMnxO4 (0≤x≤1), which is a solid-solution system of new multiferroic oxides RFe2O4 (R=Y, Ho-Lu).

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jssc.2009.04.008

Additional details

Identifiers

DOI
10.1016/j.jssc.2009.04.008;
PII
S0022-4596(09)00172-8;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
182
Journal Issue
7
Journal Page Range
p. 1611-1618
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.