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논문 기본 정보

자료유형
학술저널
저자정보
Trinh Nguyen Thi (Chungnam National University) Phuoc Cao Van (Chungnam National University) Kirakosyan Artavazd (Chungnam National University) Chanyong Hwang (Korea Research Institute of Standards and Science) Jihoon Choi (Chungnam National University) Hyojin Kim (Chungnam National University) Jong-Ryul Jeong (Chungnam National University)
저널정보
한국자기학회 Journal of Magnetics Journal of Magnetics Vol.28 No.3
발행연도
2023.9
수록면
239 - 244 (6page)
DOI
10.4283/JMAG.2023.28.3.239

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초록· 키워드

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ε-Fe<SUB>2</SUB>O<SUB>3</SUB> has received attention with particular interest because of its large coercive field at room temperature, high-frequency millimeter-wave absorption, and the coupling of its magnetic and dielectric properties. This work investigated the effect of heat treatment on the formation of ε-Fe<SUB>2</SUB>O<SUB>3</SUB>/SiO<SUB>2</SUB> composites fabricated using reverse-micelle and sol-gel methods. The heating process was performed at various temperatures to figure out the optimal conditions for acquisition of the ε-Fe<SUB>2</SUB>O<SUB>3</SUB> phase, which exhibits the largest coercive field among the Fe oxides. The sample treated at 1,075 °C had the highest percentage of ε-Fe<SUB>2</SUB>O<SUB>3</SUB> phase, with a coercivity (HC) of 21.57 kOe measured at room temperature that reached a maximum of 23.7 kOe at 230 K. The measurement of the magnetization-temperature (M-T) curve for this sample also reveals the characteristic magnetic transition associated with ε-Fe<SUB>2</SUB>O<SUB>3</SUB> within the temperature range of 40-150 K. The crystal structure of ε-Fe<SUB>2</SUB>O<SUB>3</SUB> was confirmed using X-ray powder diffraction. Transmission electron micrographs revealed a broad size distribution of iron oxide nanoparticles ranging from 12 to 22 nm. The findings indicate that ε-Fe<SUB>2</SUB>O<SUB>3</SUB> is a promising candidate with high electromagnetic-wave absorption capacity that is appropriate for high-speed wireless communication applications.

목차

1. Introduction
2. Experimental
3. Results and Discussion
4. Conclusion
References

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