The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Synthesis and Magnetic Properties of Silica-Coated FePt Nanocrystals
Abstract
Colloidal FePt nanocrystals, 6 nm in diameter, were synthesized and then coated with silica (SiO2) shells. The silica shell thickness could be varied from 10 to 25 nm. As-made FePt@SiO2 nanocrystals have low magnetocrystalline anisotropy due to a compositionally disordered FePt core. When films of FePt@SiO2 particles are annealed under hydrogen at 650 degrees C or above, the FePt core transforms to the compositionally ordered L1(0) phase, and superparamagnetic blocking temperatures exceeding room temperature are obtained. The SiO2 shell prevents FePt coalescence at annealing temperatures up to approximately 850 degrees C. Annealing under air or nitrogen does not induce the FePt phase transition. The silica shell limits magnetic dipole coupling between the FePt nanocrystals; however, low temperature (5 K) and room temperature magnetization scans show slightly constricted hysteresis loops with coercivities that decrease systematically with decreased shell thickness, possibly resulting from differences in magnetic dipole coupling between particles.
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Cites
Monodisperse FePt Nanoparticles and Ferromagnetic FePt Nanocrystal Superlattices
Sun, S., Murray, C. B., Weller, D., Folks, L., & Moser, A. (2000) · Science · doi:10.1126/science.287.5460.1989 · Cited by 6,137
One-Step Synthesis of FePt Nanoparticles with Tunable Size
Chen, M., Liu, J. P., & Sun, S. (2004) · Journal of the American Chemical Society · doi:10.1021/ja047648m · Cited by 368
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Metadata
- Authors
- Lee, D. C., Mikulec, F. V., Pelaez, J. M., Koo, B., & Korgel, B. A.
- Venue
- The Journal of Physical Chemistry B
- Publisher
- American Chemical Society (ACS)
- Published
- 2006-05-18
- Volume
- 110
- Issue
- 23
- Pages
- 11160-11166
- ISSN
- 1520-5207 (ISSN-L)
- 1520-6106
- OpenAlex
- W2007244995
- Cited by
- 218
- References
- 2
- FWCI
- 8.94
- Type
- journal article
- Language
- en
- Open access
- closed
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