4.5 Article

Differences between the multiferroic properties of hexagonal and orthorhombic ion-doped YFeO3 nanoparticles

Journal

INTERNATIONAL JOURNAL OF MODERN PHYSICS B
Volume 37, Issue 21, Pages -

Publisher

WORLD SCIENTIFIC PUBL CO PTE LTD
DOI: 10.1142/S0217979223502016

Keywords

h- and o-YFeO3 nanoparticles; ion doping; magnetization; bandgap; polarization; dielectric constant; microscopic model

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The multifunctional properties of ion-doped YFeO3 nanoparticles in hexagonal and orthorhombic structures were investigated theoretically. It was found that the magnetization of h-YFO nanoparticles increases with decreasing size, while for o-YFO nanoparticles it decreases. Both types of YFO nanoparticles exhibit a peak in the dielectric constant around T-C1 at approximately 450 K, with an additional anomaly appearing only in h-YFO at T-C2 around 300 K, potentially related to a phase transition. The polarization in doped o-YFO nanoparticles increases with a magnetic field, and doping with Ti4+ ions results in a shift in the magnetization curve. The transformation between the hexagonal and orthorhombic phases can be achieved by doping ions on Y or Fe sites in YFO.
The multiferroic properties of ion-doped hexagonal and orthorhombic YFeO3 (YFO) nanoparticles (NPs) are studied theoretically. The magnetization M-s in h-YFO NPs increases, whereas for o-YFO NPs it decreases with decreasing NP size. In the dielectric constant (DC) both h- and o-YFO have a peak around T-C1 similar to 450 and 460 K, respectively, but only in h-YFO an anomaly appears at T-C2 similar to 300 K in the DC and the polarization which could be connected with a possible P6(3)mc-P63cm phase transition. The polarization in pure and Bi-doped o-YFO NPs increases with increasing magnetic field. M-s(x) is studied by doping of a o-YFO NP with Ti4+ ions at the octahedral Fe3+ sites. M-s(T) in undoped YFO shows a small kink at TC1 similar to 450 K, whereas in the doped YFO it shows at similar to 480 K. By different ion doping on the Y or Fe sites in YFO there is a transformation from the h- to the o-phase or vice versa. In M-n-doped o-YFO a spin-reorientation transition appears. The bandgap of h-YFO is smaller compared to that of o-YFO.

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