# Ferrimagnetic structures with rare-earth induced spin-reorientation in the Mn self-doped perovskite (Er0.7Mn0.3)MnO3

https://mdr.nims.go.jp/datasets/2a2613da-8d30-4385-8c8a-c71bb26b7695

## File

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## Id

2a2613da-8d30-4385-8c8a-c71bb26b7695

## Local identifier



## Visibility

open_to_public

## State

published

## Created at

2024-10-02T00:49:34.166030Z

## Updated at

2024-10-02T01:15:50.576832Z

## Published at

2026-08-11T23:30:01.218580Z

## Doi

https://doi.org/10.48505/nims.4788

## First published url

https://doi.org/10.1016/j.ceramint.2024.08.191

## Date published

2024-08-12

## Recorded date published

2024-11

## Resource type

journal_article

## Manuscript type

accepted_manuscript

## Collection



## Title

- title: Ferrimagnetic structures with rare-earth induced spin-reorientation in the
    Mn self-doped perovskite (Er0.7Mn0.3)MnO3
  title_type: original
  lang: en

## Description

- description: The search for spin-reorientation (SR) phase transitions, a spontaneous
    rotation of ordered magnetic moments, in ferrimagnetic (FiM) materials, which
    carry a net magnetization, is of fundamental and practical interest for applications
    in the field of spintronics. In this work, we have investigated Mn self-doped
    (Er0.7Mn0.3)MnO3 solid solution with GdFeO3-type Pnma perovskite structure by
    combining specific heat, magnetic susceptibility and neutron powder diffraction
    measurements. We provide experimental evidence for FiM order below TC = 104 K,
    and a spontaneous SR transition at TSR = 11 K. A FiM structure appears in all
    (R1-xMnx)MnO3 compounds with R = Dy-Lu for x >= 0.2. But in this structural family,
    R = Er is the only material with a SR transition. FiM order in (Er0.7Mn0.3)MnO3
    appears with ferromagnetic (FM) ordering of Mn3+ and Mn4+ cations at the B site
    along the a-direction, which are antiferromagnetically (AFM) coupled with Er3+
    and Mn2+ cations at the A site. At TSR, ordered Er3+ change direction from the
    magnetically harder a-axis to the magnetically easy b-axis and induce a change
    of the whole FiM structure, including the direction of all Mn spins from the irreducible
    representation mGM3+ to mGM4+. We calculated the crystal-field (CF) anisotropy
    for Ho3+ in (Ho0.8Mn0.2)MnO3 and Er3+ in (Er0.7Mn0.3)MnO3, based on the point
    charge model, and showed large magnetic anisotropies. For the FiM structure of
    (Ho0.8Mn0.2)MnO3, the magnetically easy a-axis of Ho3+ keeps the high-temperature
    magnetic directions along the a-axis and gives rise to a pronounced magnetization
    reversal effect at low temperature because of a significant rise of Ho3+ ordered
    moments. On the other hand, for the FiM structure of (Er0.7Mn0.3)MnO3, the magnetically
    easy b-axis of Er3+ gives rise to a SR phase transition at TSR, which does not
    lead to magnetization reversal even though Er3+ ordered moments rise significantly
    at low temperatures.
  description_type: abstract
  lang: und

## Creator

- name: Andreas Dönni
  role: author
  orcid: https://orcid.org/0000-0002-7300-9175
  organization: National Institute for Materials Science
  ror: https://ror.org/026v1ze26
- name: Vladimir Y. Pomjakushin
  role: author
- name: Martin Rotter
  role: author
- name: Lei Zhang
  role: author
  orcid: https://orcid.org/0000-0003-1173-4328
  organization: National Institute for Materials Science
- name: Kazunari Yamaura
  role: author
  orcid: https://orcid.org/0000-0003-0390-8244
  organization: National Institute for Materials Science
  ror: https://ror.org/026v1ze26
- name: Alexei A. Belik
  role: author
  orcid: https://orcid.org/0000-0001-9031-2355
  organization: National Institute for Materials Science
  ror: https://ror.org/026v1ze26

## Contact agent



## Publisher

organization: Elsevier BV

## Managing organization



## Keyword

- subject: Perovskites
  schema: not_defined
- subject: Crystal structure
  schema: not_defined
- subject: magnetic structure
  schema: not_defined
- subject: spin-reorientation
  schema: not_defined
- subject: ferrimagnets
  schema: not_defined

## Rights

- identifier: http://rightsstatements.org/vocab/InC/1.0/

## Other identifier(s)



## Data origin

- data_origin_type: other

## Embargo

start_date: 2024-08-12
end_date: 2026-08-12

## Journal

- title: Ceramics International
  issn: '02728842'
  volume: '50'
  issue: '21'
  start_page: 43414
  end_page: 43423

## Conference



## Related item



## Funding

- funder_name: World Cancer Research Fund International
- identifier: JP22H04601
  funder_name: Japan Society for the Promotion of Science
- identifier: 2022-11
  funder_name: The Kazuchika Okura Memorial Foundation

## Instrument



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## Specimen



## Chemical composition



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## Fileset

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  filename: Ceramics International-V50-43414-ErMnO3-Mn_Accepted_Version.pdf
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  size: 1609849
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- id: cf1847c2-97e5-41df-a3ca-4688bcad6a55
  filename: Ceramics International-V50-43414_Supplement.pdf
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## Thumbnail

fileset_id: cf1847c2-97e5-41df-a3ca-4688bcad6a55
filename: Ceramics International-V50-43414_Supplement.pdf