Self-Stabilized Carbon-L1(0) FePt Nanoparticles for Heated Dot Recording Media
- Authors
- Medwal, Rohit; Gautam, Sanjeev; Gupta, Surbhi; Chae, Keun Hwa; Asokan, Kandasami; Deen, Gulam Roshan; Rawat, Rajdeep Singh; Katiyar, Ram Singh; Annapoorni, Subramanian
- Issue Date
- 2018-05
- Publisher
- IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
- Citation
- IEEE MAGNETICS LETTERS, v.9
- Abstract
- Heated dot magnetic recording (HDMR) technology promises to achieve ultrahigh storage density well above 4 Tb/in(2) by making use of L1(0) FePt bimetallic islands HDMR media require the development of thermally stable, noninteracting magnetic patterns to circumvent the signal noise and writability challenges We prepared self-stabilized carbon-L1(0) FePt nanoparticles (NPs) with average diameter of about 7.2 nm for the HDMR media FePt NPs synthesized by chemical reduction using oleic acid and oleylamine transform to the carbon-L1(0) FePt phase with optimized heat treatment at 873 K. The high-temperature annealing not only helps to achieve the desired L1(0) phase but also helps in the formation of a carbon coating on the FePt NPs due to degradation of the organic cap We investigated the effect of carbon coating on the electronic states of Fe using X-ray absorption measurements and corroborated with high-resolution transmission electron microscopy and Fourier-transform infrared spectroscopy X-ray magnetic circular dichroism reveals the presence of magnetocrystalline anisotropy in the carbon-L1(0) FePt NPs, which is also supported by the structural and magnetic measurements A magnetization-field loop at 300 K shows high coercivity of approximate to 1.6 T. The synthesized carbon-L1(0) FePt NPs can be used as FePt islands and should be suitable for high-density HDMR media.
- Keywords
- BIT-PATTERNED MEDIA; BIT-PATTERNED MEDIA; Hard magnetic materials; heated dot magnetic recording; FePt
- ISSN
- 1949-307X
- URI
- https://pubs.kist.re.kr/handle/201004/121401
- DOI
- 10.1109/LMAG.2018.2840990
- Appears in Collections:
- KIST Article > 2018
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