Published April 30, 2004
| Version v1
Journal article
High magnetic field study of HoBaCo2O5.5 and GdBaCo2O5.5 layered cobaltites: the effect of rare-earth size
Description
By means of high-pulsed magnetic field up to μ0H=32 T we have studied HoBaCo2O5+δ (δ=0.52(1)). The high-field M(H) integrated curves evidence a magnetic field-induced phase transition visible from about T=75 to 275 K. The obtained results are compared with the field-induced transition found for GdBaCo2O5+δ (with δ=0.54(2)). The jump of the magnetization at the field-induced transition is independent of the rare earth at this level of oxygen content. In contrast, we have observed larger values of the critical field, and that the transition persists up to higher temperature, when reducing the rare-earth size. This indicates that the low-temperature antiferromagnetic phase becomes more stable when the size of the rare earth is reduced
Additional details
Identifiers
- DOI
- 10.1016/j.physb.2004.01.059;
- PII
- S0921452604000742;
Publishing Information
- Journal Title
- Physica. B, Condensed Matter
- Journal Volume
- 346-347
- Journal Issue
- 1-4
- Journal Page Range
- p. 246-249
- ISSN
- 0921-4526
- CODEN
- PHYBE3
Conference
- Title
- 7. international symposium on research in high magnetic fields
- Dates
- 20-23 Jul 2003
- Place
- Toulouse (France)
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 37001007
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ANTIFERROMAGNETISM; BARIUM COMPOUNDS; COBALT OXIDES; CRITICAL FIELD; GADOLINIUM COMPOUNDS; HOLMIUM COMPOUNDS; MAGNETIZATION; OXYGEN; PHASE TRANSFORMATIONS; TEMPERATURE DEPENDENCE
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; CHALCOGENIDES; COBALT COMPOUNDS; ELEMENTS; MAGNETIC FIELDS; MAGNETISM; NONMETALS; OXIDES; OXYGEN COMPOUNDS; RARE EARTH COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.