Room-temperature ferrimagnetism of anti-site-disordered Ca2MnOsO6

Hai L. Feng (冯海), Madhav Prasad Ghimire, Zhiwei Hu, Sheng-Chieh Liao, Stefano Agrestini, Jie Chen, Yahua Yuan, Yoshitaka Matsushita, Yoshihiro Tsujimoto, Yoshio Katsuya, Masahiko Tanaka, Hong-Ji Lin, Chien-Te Chen, Shih-Chang Weng, Manuel Valvidares, Kai Chen, Francois Baudelet, Arata Tanaka, Martha Greenblatt, Liu Hao Tjeng, and Kazunari Yamaura
Phys. Rev. Materials 3, 124404 – Published 16 December 2019
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Abstract

Room-temperature ferrimagnetism was discovered for the anti-site-disordered perovskite Ca2MnOsO6 with Tc=305K. Ca2MnOsO6 crystallizes into an orthorhombic structure with a space group of Pnma, in which Mn and Os share the oxygen-coordinated-octahedral site at an equal ratio without a noticeable ordered arrangement. The material is electrically semiconducting with variable-range-hopping behavior. X-ray absorption spectroscopy confirmed the trivalent state of the Mn and the pentavalent state of the Os. X-ray magnetic circular dichroism spectroscopy reveals that the Mn and Os magnetic moments are aligned antiferromagnetically, thereby classifying the material as a ferrimagnet which is in accordance with band structure calculations. It is intriguing that the magnetic signal of the Os is very weak, and that the observed total magnetic moment is primarily due to the Mn. The Tc=305K is the second highest in the material category of so-called disordered ferromagnets such as CaRu1xMnxO3, SrRu1xCrxO3, and CaIr1xMnxO3, and hence, may support the development of spintronic oxides with relaxed requirements concerning the anti-site disorder of the magnetic ions.

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  • Received 7 August 2019

DOI:https://doi.org/10.1103/PhysRevMaterials.3.124404

©2019 American Physical Society

Physics Subject Headings (PhySH)

Condensed Matter, Materials & Applied Physics

Authors & Affiliations

Hai L. Feng (冯海)1,2,3,*,†, Madhav Prasad Ghimire4,5,6, Zhiwei Hu2, Sheng-Chieh Liao2, Stefano Agrestini2,7, Jie Chen1,8, Yahua Yuan1,9, Yoshitaka Matsushita10, Yoshihiro Tsujimoto1,8, Yoshio Katsuya11, Masahiko Tanaka11, Hong-Ji Lin12, Chien-Te Chen12, Shih-Chang Weng12, Manuel Valvidares7, Kai Chen13, Francois Baudelet13, Arata Tanaka14, Martha Greenblatt3, Liu Hao Tjeng2, and Kazunari Yamaura1,8,*

  • 1Research Center for Functional Material, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan
  • 2Max Planck Institute for Chemical Physics of Solids, Nöthnitzer Str. 40, 01187 Dresden, Germany
  • 3Department of Chemistry and Chemical Biology, Rutgers, the State University of New Jersey, 610 Taylor Road, Piscataway, New Jersey 08854, USA
  • 4Central Department of Physics, Tribhuvan University, Kirtipur, 44613 Kathmandu, Nepal
  • 5Leibniz Institute for Solid State and Materials Research, IFW Dresden, P.O. Box 270116, D-01171 Dresden, Germany
  • 6Condensed Matter Physics Research Center, Butwal-11, Rupandehi, Nepal
  • 7ALBA Synchrotron Light Source, E-08290 Cerdanyola del Vallès, Barcelona, Spain
  • 8Graduate School of Chemical Sciences and Engineering, Hokkaido University, North 10 West 8, Kita-ku, Sapporo, Hokkaido 060–0810, Japan
  • 9School of Physics and Electronics, Central South University, Changsha 410083, China
  • 10Materials Analysis Station, National Institute for Materials Science, 1-2-1 Sengen, Tsukuba, Ibaraki 305-0047, Japan
  • 11Synchrotron x-ray Station at SPring-8, National Institute for Materials Science, Kouto 1-1-1, Sayo-cho, Hyogo 679–5148, Japan
  • 12National Synchrotron Radiation Research Center, 101 Hsin-Ann Road, Hsinchu 30076, Taiwan, ROC
  • 13Synchrotron SOLEIL, L’Orme des Merisiers, Saint-Aubin, 91192 Gif-sur-Yvette Cedex, France
  • 14Department of Quantum Matter, ADSM, Hiroshima University, Higashi-Hiroshima 739–8526, Japan

  • *Corresponding authors hai.feng@iphy.ac.cn, hai.feng_nims@ hotmail.com; yamaura.kazunari@nims.go.jp
  • Present address: The Institute of Physics, Chinese Academy of Sciences, P.O. Box 603, Beijing 100190, China.

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Issue

Vol. 3, Iss. 12 — December 2019

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