Title
Growth dominant co-precipitation process to achieve high coercivity at room temperature in CoFe<inf>2</inf>O<inf>4</inf> nanoparticles
Date Issued
01 January 2002
Access level
metadata only access
Resource Type
journal article
Author(s)
Publisher(s)
Institute of Electrical and Electronics Engineers Inc.
Abstract
Applications of CoFe2O4 are limited due to the lack of synthesis technique to produce monodispersed, single domain and high coercivity (Hc) nanoparticles. Here, we describe the growth dominant co-precipitation process to achieve high Hc with moderate magnetization at room temperature (RT) in CoFe2O4 nanoparticles. It is well known that the particle size is closely related to the relative interdependence between the nucleation and growth steps, which in turn can strongly be affected by the solution chemistry and precipitation conditions. Based on this premise, the effect of 1) reaction temperature, 2) NaOH concentration, and 3) feeding rate of metal ions into the alkali solution were evaluated. The maximum Hc of 2.29 kOe (RT) was observed for the CoFe2O4 prepared at 98 °C, 1.13-mol NaOH, and the metal ion feeding rate of 0.00103 M/min. To improve the coercivity, single domain CoFe2O4 nanoparticles were produced by in situ growth of the CoFe2O4 seeds followed by size separation method. A coercivity of 4.3 kOe was achieved at RT for 40-nm single domain CoFe2O4 nanoparticles, which is close to the theoretical value of 5.3 kOe.
Start page
2640
End page
2642
Volume
38
Issue
5 I
Language
English
OCDE Knowledge area
Nano-materiales
Subjects
Scopus EID
2-s2.0-0036762090
Source
IEEE Transactions on Magnetics
ISSN of the container
00189464
Sponsor(s)
Manuscript received February 9, 2002; revised May 12, 2002. This work was supported by CREST of the Japan Science and Technology Program and by the Japan Society for Promotion of Science. C. N. Chinnasamy, B. Jeyadevan, K. Shinoda and K. Tohji are with Department of Geoscience and Technology, Tohoku University, Sendai 980-8579, Japan (e-mail: chins@cir.tohoku.ac.jp) O. Peralez-Perez is with the School of Metallurgy, Universidad Naciaonal de Ingenieria, Lima 25, Peru. A. Kasuya is with the Center for Interdisciplinary Research, Tohoku University, Sendai 980-8578, Japan. Digital Object Identifier 10.1109/TMAG.2002.801972.
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