Magnetic transition and defect characteristics of multiferroic CuFe1-xGaxO2 studied by positron annihilation spectra

[Display omitted] •A systematic investigation of the effect of Ga doping on the structural and magnetic properties of CuFeO2.•Crystal defects are determined by positron annihilation spectroscopy.•There is a good correlation between antiferromagnetic stability and lattice distortion.•Crystal defects...

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Veröffentlicht in:Materials research bulletin 2018-12, Vol.108, p.1-4
Hauptverfasser: Zhang, L., Xiong, D.K., Goodman, B.A., Chen, Z.P., Deng, W., Huang, Y.Y.
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container_title Materials research bulletin
container_volume 108
creator Zhang, L.
Xiong, D.K.
Goodman, B.A.
Chen, Z.P.
Deng, W.
Huang, Y.Y.
description [Display omitted] •A systematic investigation of the effect of Ga doping on the structural and magnetic properties of CuFeO2.•Crystal defects are determined by positron annihilation spectroscopy.•There is a good correlation between antiferromagnetic stability and lattice distortion.•Crystal defects and interlayer ions in polycrystalline samples influence the magnetic properties. The structure, crystal defects and magnetic properties of multiferroic CuFe1-xGaxO2 (CFGO; x = 0–0.07) ceramics are studied systemically. Substitution of Ga3+ for Fe3+ shrinks the CFO lattice, decreases the particle size, and causes small liquid phase formation. Positron annihilation spectroscopy demonstrates that all samples contain a considerable number of vacancy defects. The overall defect environment is virtually unaffected by Ga3+ doping, but the open-volume of the defects is redistributed. Magnetic susceptibility measurements show that Ga doping enhances the strength of the antiferromagnetic interaction between high-spin Fe3+ ions as a result of reduced magnetic correlation length, but decrease the stability of the antiferromagnetic phase. The antiferromagnetic transition temperature, TN2, decreases from 11 K for x = 0 to 8 K for x = 0.07, and this destabilization of the antiferromagnetic phase is closely related to the crystal structure and defects, which are discussed in detail in this work.
doi_str_mv 10.1016/j.materresbull.2018.08.030
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The structure, crystal defects and magnetic properties of multiferroic CuFe1-xGaxO2 (CFGO; x = 0–0.07) ceramics are studied systemically. Substitution of Ga3+ for Fe3+ shrinks the CFO lattice, decreases the particle size, and causes small liquid phase formation. Positron annihilation spectroscopy demonstrates that all samples contain a considerable number of vacancy defects. The overall defect environment is virtually unaffected by Ga3+ doping, but the open-volume of the defects is redistributed. Magnetic susceptibility measurements show that Ga doping enhances the strength of the antiferromagnetic interaction between high-spin Fe3+ ions as a result of reduced magnetic correlation length, but decrease the stability of the antiferromagnetic phase. The antiferromagnetic transition temperature, TN2, decreases from 11 K for x = 0 to 8 K for x = 0.07, and this destabilization of the antiferromagnetic phase is closely related to the crystal structure and defects, which are discussed in detail in this work.</description><subject>A. Ceramics</subject><subject>ANNIHILATION</subject><subject>ANTIFERROMAGNETISM</subject><subject>B. Magnetic properties</subject><subject>B. Microstructure</subject><subject>C. 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The structure, crystal defects and magnetic properties of multiferroic CuFe1-xGaxO2 (CFGO; x = 0–0.07) ceramics are studied systemically. Substitution of Ga3+ for Fe3+ shrinks the CFO lattice, decreases the particle size, and causes small liquid phase formation. Positron annihilation spectroscopy demonstrates that all samples contain a considerable number of vacancy defects. The overall defect environment is virtually unaffected by Ga3+ doping, but the open-volume of the defects is redistributed. Magnetic susceptibility measurements show that Ga doping enhances the strength of the antiferromagnetic interaction between high-spin Fe3+ ions as a result of reduced magnetic correlation length, but decrease the stability of the antiferromagnetic phase. The antiferromagnetic transition temperature, TN2, decreases from 11 K for x = 0 to 8 K for x = 0.07, and this destabilization of the antiferromagnetic phase is closely related to the crystal structure and defects, which are discussed in detail in this work.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.materresbull.2018.08.030</doi><tpages>4</tpages></addata></record>
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subjects A. Ceramics
ANNIHILATION
ANTIFERROMAGNETISM
B. Magnetic properties
B. Microstructure
C. Positron annihilation spectroscopy
CERAMICS
CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY
DEFECTS
GALLIUM IONS
IRON IONS
MAGNETIC SUSCEPTIBILITY
MICROSTRUCTURE
PARTICLE SIZE
POLYCRYSTALS
POSITRON ANNIHILATION SPECTROSCOPY
POSITRONS
SPECTRA
SPIN
TRANSITION TEMPERATURE
VACANCIES
title Magnetic transition and defect characteristics of multiferroic CuFe1-xGaxO2 studied by positron annihilation spectra
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