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A New Strategy for the Synthesis of Size-controlled L1<sub>0</sub> FePt Nanoparticles on Nanotube Substrate
Author(s) -
Reza Moradi,
S. A. Sebt,
Hadi Arabi,
Arsalan Beigzadeh
Publication year - 2014
Publication title -
current nanoscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.285
H-Index - 44
eISSN - 1875-6786
pISSN - 1573-4137
DOI - 10.2174/15734137113096660104
Subject(s) - materials science , superparamagnetism , carbon nanotube , coercivity , nanoparticle , transmission electron microscopy , chemical engineering , ferromagnetism , nanotechnology , scanning electron microscope , annealing (glass) , fourier transform infrared spectroscopy , substrate (aquarium) , analytical chemistry (journal) , magnetization , composite material , magnetic field , condensed matter physics , chemistry , organic chemistry , oceanography , physics , quantum mechanics , geology , engineering
In this paper, a CVD method is used for the synthesis of multi-wall carbon nanotubes (MWCNT) which have been purified and functionalized. The approach consists of thermal oxidation and subsequent chemical oxidation. Accord- ing to TEM images, the CNTs have a diameter about 20-30 nm. We synthesized the FePt nanoparticles on the surface of the functionalized carbon nanotubes through a polyol process. The synthesized FePt nanoparticles have the chemically- disordered face-centered cubic (fcc) structure with superparamagnetic behavior and with a size of about 2.5 nm. To achieve phase transition from fcc to ordered structure (fct-L10 phase), high-temperature annealing under a reducing at- mosphere (90% Ar + 10% H2) is required. The CNTs as a substrate prevent the aggregation of particles during thermal treatment. The FePt nanoparticles after phase transition have ferromagnetic behavior. Furthermore, they have finite size with an average about 5.6 nm and their coercivity reaches to 5.1 KOe at 700°C. We characterized the structure, composi- tion and magnetic properties of FePt/CNT by X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscope (FE-SEM), Fourier transform infrared spectroscopy (FT-IR) and vibrating sample magnetometer (VSM).

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