Gas phase synthesis of large directly ordered L10 FePt nanoparticles was studied. Simultaneous control of the chemical ordering and the size of the FePt nanoparticle was successfully achieved. It was found that the chemical ordering of the FePt nanoparticles was mainly influenced by the energy conditions (thermal environments at nucleation and growth regions), which could be adjusted by varying the process parameters including the sputtering current density, the Ar gas pressure, etc. The sizes of ordered FePt nanoparticles were more related to the Fe and Pt atoms’ density at the initial stage (close to target surface). Multiply twinned structures were observed in L10 FePt nanoparticles with 12 and 17 nm mean sizes, but were absent in L10 FePt nanoparticles with 6 nm mean size, which caused the relatively low coercivity of large L10 FePt nanoparticles.Gas phase synthesis of large directly ordered L10 FePt nanoparticles was studied. Simultaneous control of the chemical ordering and the size of the FePt nanoparticle was successfully achieved. It was found that the chemical ordering of the FePt nanoparticles was mainly influenced by the energy conditions (thermal environments at nucleation and growth regions), which could be adjusted by varying the process parameters including the sputtering current density, the Ar gas pressure, etc. The sizes of ordered FePt nanoparticles were more related to the Fe and Pt atoms’ density at the initial stage (close to target surface). Multiply twinned structures were observed in L10 FePt nanoparticles with 12 and 17 nm mean sizes, but were absent in L10 FePt nanoparticles with 6 nm mean size, which caused the relatively low coercivity of large L10 FePt nanoparticles.
[1]
J. Qiu,et al.
Tuning the Crystal Structure and Magnetic Properties of FePt Nanomagnets
,
2007
.
[2]
M. Farle,et al.
Layer resolved structural relaxation at the surface of magnetic FePt icosahedral nanoparticles.
,
2008,
Physical review letters.
[3]
J. Staunton,et al.
Long-range chemical order effects upon the magnetic anisotropy of FePt alloys from an ab initio electronic structure theory
,
2004
.
[4]
C. Ross.
Patterned Magnetic Recording Media
,
2001
.
[5]
T. Miyazaki,et al.
Chemical-order-dependent magnetic anisotropy and exchange stiffness constant of FePt (001) epitaxial films
,
2002
.
[6]
Zhong Lin Wang,et al.
Phase Transformation, Coalescence, and Twinning of Monodisperse FePt Nanocrystals
,
2001
.
[7]
Paolo Milani,et al.
Cluster beam deposition: a tool for nanoscale science and technology
,
2006
.
[8]
Sun,et al.
Monodisperse FePt nanoparticles and ferromagnetic FePt nanocrystal superlattices
,
2000,
Science.
[9]
M. Farle,et al.
Multiply twinned morphologies of FePt and CoPt nanoparticles.
,
2008,
Physical review letters.
[10]
Jianping Wang,et al.
In situ magnetic field alignment of directly ordered L10 FePt nanoparticles
,
2006
.
[11]
D. Peng,et al.
Formation and magnetic properties of Fe-Pt alloy clusters by plasma-gas condensation
,
2003
.
[12]
Margaret Evans Best,et al.
High K/sub u/ materials approach to 100 Gbits/in/sup 2/
,
2000
.
[13]
K. Albe,et al.
Structural stability of multiply twinned FePt nanoparticles
,
2007
.