Ferromagnetic cluster glass in Pr0.7 Sr0.3 Mn1- xCoxO3 (x= 0, 0.05, 0.10 and 0.15) system

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Feriel Zdiri
  • Taoufik Mnasri
  • Jose Maria Alonso
  • Patricia de la Presa
  • Irene Morales
  • Pilar Marin

Externe Organisationen

  • University of Gafsa
  • Complutense Universität Madrid (UCM)
  • Spanish National Research Council (CSIC)
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Aufsatznummer107517
Seitenumfang13
FachzeitschriftSolid state sciences
Jahrgang151
Frühes Online-Datum28 März 2024
PublikationsstatusVeröffentlicht - Mai 2024
Extern publiziertJa

Abstract

We have investigated the structural, morphological and magnetic properties of a series of ABO3-type perovskite compounds Pr0.7 Sr0.3Mn1-xCoxO3 (0 ≤ x ≤ 0.15) synthesized by conventional high temperature solid state reac- tion, which strongly depends on the doping level x. The room temperature powder X ray diffraction data shows the single-phase nature of the sample and confirms the orthorhombic crystal structure with Pnma space group. The SEM images show that the grains are dispersed in shape and size. Energy dispersive X-ray analysis (EDAX) confirms the expected stoichiometry of all samples. Upon Co doping on the Mn-site, the lattice parameters, the unit cell volume and the Mn O Mn bond angle are slightly reduced from x = 0.05 to x = 0.15. The M H curves shows saturation magnetizations almost independent of Co contain, confirming that Co3+ replaces Mn3+ in B sites and, in addition, Co3+ is in high spin configuration (teg4 eg2). All samples exhibit a single magnetic transition from ferromagnetic to paramagnetic phase, with a large distribution in Curie temperature TC (260, 220, 180 and 160 K for x = 0, 0.05, 0.10 and 0.15 respectively) and an increase in magnetization M at low temperature. The results are promising for magnetic refrigeration materials and spintronic devices and warrant further investigation.

ASJC Scopus Sachgebiete

Zitieren

Ferromagnetic cluster glass in Pr0.7 Sr0.3 Mn1- xCoxO3 (x= 0, 0.05, 0.10 and 0.15) system. / Zdiri, Feriel; Mnasri, Taoufik; Alonso, Jose Maria et al.
in: Solid state sciences, Jahrgang 151, 107517, 05.2024.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Zdiri F, Mnasri T, Alonso JM, de la Presa P, Morales I, Marin P. Ferromagnetic cluster glass in Pr0.7 Sr0.3 Mn1- xCoxO3 (x= 0, 0.05, 0.10 and 0.15) system. Solid state sciences. 2024 Mai;151:107517. Epub 2024 Mär 28. doi: 10.1016/j.solidstatesciences.2024.107517
Zdiri, Feriel ; Mnasri, Taoufik ; Alonso, Jose Maria et al. / Ferromagnetic cluster glass in Pr0.7 Sr0.3 Mn1- xCoxO3 (x= 0, 0.05, 0.10 and 0.15) system. in: Solid state sciences. 2024 ; Jahrgang 151.
Download
@article{f7b6796077b143198ecc993f0538b56d,
title = "Ferromagnetic cluster glass in Pr0.7 Sr0.3 Mn1- xCoxO3 (x= 0, 0.05, 0.10 and 0.15) system",
abstract = " We have investigated the structural, morphological and magnetic properties of a series of ABO3-type perovskite compounds Pr0.7 Sr0.3Mn1-xCoxO3 (0 ≤ x ≤ 0.15) synthesized by conventional high temperature solid state reac- tion, which strongly depends on the doping level x. The room temperature powder X ray diffraction data shows the single-phase nature of the sample and confirms the orthorhombic crystal structure with Pnma space group. The SEM images show that the grains are dispersed in shape and size. Energy dispersive X-ray analysis (EDAX) confirms the expected stoichiometry of all samples. Upon Co doping on the Mn-site, the lattice parameters, the unit cell volume and the Mn O Mn bond angle are slightly reduced from x = 0.05 to x = 0.15. The M H curves shows saturation magnetizations almost independent of Co contain, confirming that Co3+ replaces Mn3+ in B sites and, in addition, Co3+ is in high spin configuration (teg4 eg2). All samples exhibit a single magnetic transition from ferromagnetic to paramagnetic phase, with a large distribution in Curie temperature TC (260, 220, 180 and 160 K for x = 0, 0.05, 0.10 and 0.15 respectively) and an increase in magnetization M at low temperature. The results are promising for magnetic refrigeration materials and spintronic devices and warrant further investigation.",
keywords = "Magnetic properties, Manganite, Microstructure, Perovskite, Rietveld refinement",
author = "Feriel Zdiri and Taoufik Mnasri and Alonso, {Jose Maria} and {de la Presa}, Patricia and Irene Morales and Pilar Marin",
note = "Publisher Copyright: {\textcopyright} 2024 Elsevier Masson SAS",
year = "2024",
month = may,
doi = "10.1016/j.solidstatesciences.2024.107517",
language = "English",
volume = "151",
journal = "Solid state sciences",
issn = "1293-2558",
publisher = "Elsevier Masson SAS",

}

Download

TY - JOUR

T1 - Ferromagnetic cluster glass in Pr0.7 Sr0.3 Mn1- xCoxO3 (x= 0, 0.05, 0.10 and 0.15) system

AU - Zdiri, Feriel

AU - Mnasri, Taoufik

AU - Alonso, Jose Maria

AU - de la Presa, Patricia

AU - Morales, Irene

AU - Marin, Pilar

N1 - Publisher Copyright: © 2024 Elsevier Masson SAS

PY - 2024/5

Y1 - 2024/5

N2 - We have investigated the structural, morphological and magnetic properties of a series of ABO3-type perovskite compounds Pr0.7 Sr0.3Mn1-xCoxO3 (0 ≤ x ≤ 0.15) synthesized by conventional high temperature solid state reac- tion, which strongly depends on the doping level x. The room temperature powder X ray diffraction data shows the single-phase nature of the sample and confirms the orthorhombic crystal structure with Pnma space group. The SEM images show that the grains are dispersed in shape and size. Energy dispersive X-ray analysis (EDAX) confirms the expected stoichiometry of all samples. Upon Co doping on the Mn-site, the lattice parameters, the unit cell volume and the Mn O Mn bond angle are slightly reduced from x = 0.05 to x = 0.15. The M H curves shows saturation magnetizations almost independent of Co contain, confirming that Co3+ replaces Mn3+ in B sites and, in addition, Co3+ is in high spin configuration (teg4 eg2). All samples exhibit a single magnetic transition from ferromagnetic to paramagnetic phase, with a large distribution in Curie temperature TC (260, 220, 180 and 160 K for x = 0, 0.05, 0.10 and 0.15 respectively) and an increase in magnetization M at low temperature. The results are promising for magnetic refrigeration materials and spintronic devices and warrant further investigation.

AB - We have investigated the structural, morphological and magnetic properties of a series of ABO3-type perovskite compounds Pr0.7 Sr0.3Mn1-xCoxO3 (0 ≤ x ≤ 0.15) synthesized by conventional high temperature solid state reac- tion, which strongly depends on the doping level x. The room temperature powder X ray diffraction data shows the single-phase nature of the sample and confirms the orthorhombic crystal structure with Pnma space group. The SEM images show that the grains are dispersed in shape and size. Energy dispersive X-ray analysis (EDAX) confirms the expected stoichiometry of all samples. Upon Co doping on the Mn-site, the lattice parameters, the unit cell volume and the Mn O Mn bond angle are slightly reduced from x = 0.05 to x = 0.15. The M H curves shows saturation magnetizations almost independent of Co contain, confirming that Co3+ replaces Mn3+ in B sites and, in addition, Co3+ is in high spin configuration (teg4 eg2). All samples exhibit a single magnetic transition from ferromagnetic to paramagnetic phase, with a large distribution in Curie temperature TC (260, 220, 180 and 160 K for x = 0, 0.05, 0.10 and 0.15 respectively) and an increase in magnetization M at low temperature. The results are promising for magnetic refrigeration materials and spintronic devices and warrant further investigation.

KW - Magnetic properties

KW - Manganite

KW - Microstructure

KW - Perovskite

KW - Rietveld refinement

UR - http://www.scopus.com/inward/record.url?scp=85189751498&partnerID=8YFLogxK

U2 - 10.1016/j.solidstatesciences.2024.107517

DO - 10.1016/j.solidstatesciences.2024.107517

M3 - Article

VL - 151

JO - Solid state sciences

JF - Solid state sciences

SN - 1293-2558

M1 - 107517

ER -

Von denselben Autoren