2018年第79回応用物理学会秋季学術講演会

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10 スピントロニクス・マグネティクス » 10 スピントロニクス・マグネティクス(ポスター)

[18p-PB1-1~73] 10 スピントロニクス・マグネティクス(ポスター)

2018年9月18日(火) 13:30 〜 15:30 PB (白鳥ホール)

13:30 〜 15:30

[18p-PB1-52] Ir substitution site analysis of Corundum-type oxide films by extended X-ray absorption fine structure

Tomohiro Nozaki1、Satya Prakash Pati1、Yohei Shiokawa1、Motohiro Suzuki2、Toshiaki Ina2、Muftah Al-Mahdawi1、Sujun Ye1、Masashi Sahashi1,3 (1.Tohoku Univ.、2.JASRI、3.ImPACT)

キーワード:antiferromagnet, X-ray absorption fine structure, Corundum

Cr2O3 and α-Fe2O3 are Corundum-type oxide antiferromagnets. Cr2O3 is a well-known magnetoelectric material and attract much attentions as an electrically controllable antiferromagnet. α-Fe2O3 is a high Néel temperature antiferromagnet (TN ~ 950 K), which has a spin reorientation transition called Morin transition. We’ve been reported the enhancement of Morin transition temperature (thus enhancement of perpendicular magnetic anisotropy (PMA)) for α-Fe2O3 by tiny amount of Ir-doping. In contrast, we didn’t observe a distinguish change in PMA for Cr2O3 by Ir-doping. To investigate the difference, in this study, we tried to identify the Ir-substitution site in both Cr2O3 and α-Fe2O3 from extended X-ray absorption fine structure (EXAFS) analysis.
Ir-doped Cr2O3 and α-Fe2O3 films were fabricated on Al2O3 (0001) substrate by a reactive sputtering method. We simulated radial distribution function |χ(R)| of Ir L3 edge with three different substitution site; 1) cation (Cr or Fe) site, 2) O-site, and 3) interstitial-site. Then we fitted experimentally obtained |χ(R)| by the three simulation results. The fitting results indicate that Ir most likely substitute cation site of both Cr2O3 and α-Fe2O3, rather than interstitial-site and O-site.