Published April 2003
| Version v1
Journal article
Synthesis of cobalt ferrite nanocrystallites by the forced hydrolysis method and investigation of their magnetic properties
Creators
Description
Cobalt ferrite powder has been synthesized by the forced hydrolysis method in 1,2-propanediol. The particles, having a cubic spinel structure, are nanocrystallites with a mean diameter of 4 nm with almost equiaxial shapes and a narrow size distribution. These particles are superparamagnetic at room temperature and ferrimagnetic at temperatures below the blocking temperature of about 180 K. A remarkable shift of the blocking temperature with frequency was observed in the AC susceptibility measurements. The calculated value of anisotropy constant at 0 K, KA(0)=5.36x107 erg/cm3, is higher than that in the bulk material. The saturation magnetization and the coercivity measured at 5 K are 75 emu/g and 10.3 kOe, respectively
Additional details
Identifiers
- DOI
- 10.1016/S0921-4526(02)01750-7;
- arXiv
- arXiv:math/0411079v3;
- PII
- S0921452602017507;
Publishing Information
- Journal Title
- Physica. B, Condensed Matter
- Journal Volume
- 327
- Journal Issue
- 2-4
- Journal Page Range
- p. 382-384
- ISSN
- 0921-4526
- CODEN
- PHYBE3
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 36091958
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- ANISOTROPY; CHANNELING; COBALT COMPOUNDS; COERCIVE FORCE; CUBIC LATTICES; DISTRIBUTION; FERRITES; HYDROLYSIS; MAGNETIC SUSCEPTIBILITY; MAGNETIZATION; NANOSTRUCTURES; PARTICLES; POWDERS; SUPERPARAMAGNETISM; SYNTHESIS; TEMPERATURE DEPENDENCE
- Descriptors DEC
- CHEMICAL REACTIONS; CRYSTAL LATTICES; CRYSTAL STRUCTURE; DECOMPOSITION; FERRIMAGNETIC MATERIALS; IRON COMPOUNDS; LYSIS; MAGNETIC MATERIALS; MAGNETIC PROPERTIES; MAGNETISM; MATERIALS; OXYGEN COMPOUNDS; PHYSICAL PROPERTIES; SOLVOLYSIS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2002 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.