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dc.creatorRadojković, Aleksandar
dc.creatorLuković Golić, Danijela
dc.creatorJOVIĆ ORSINI, Nataša
dc.creatorĆirković, Jovana
dc.creatorBranković, Zorica
dc.creatorBranković, Goran
dc.date.accessioned2023-03-01T08:24:31Z
dc.date.available2023-03-01T08:24:31Z
dc.date.issued2022
dc.identifier.urihttp://rimsi.imsi.bg.ac.rs/handle/123456789/1738
dc.description.abstractBiFeO3 is one of the few multiferroic perovskites that exhibits magnetic and ferroelectric properties at room temperature. However, it is also distinguished by high leakage current, low remnant electric and magnetic polarization, and high electric coercive field. These features keep it away from any practical use in electronics. Therefore, many attempts have been made to improve the properties of BiFeO3 by Bi- or Fe-site doping or by both. Previous investigations suggest that doping with Nbat Fe-site can positively affect the magnetic behavior of BiFeO3 and decrease the leakage current. In this study, various cation substitutions at Bi-site (La3+, Eu3+) and Fe-site (Nb5+, Zr4+) were examined to investigate their possible synergism and benefit for the ferroelectric properties. The role of the cations with higher valence is to suppress the formation of structural defects during synthesis, such as oxygen and bismuth vacancies. These defects are responsible for high leakage currents and, consequently, low breakdown voltages characteristic of the pure BiFeO3. On the other hand, rare earth cations at the Bisite usually enable densification of the ceramics in a wider range of temperatures, preventing bismuth loss and forming defects and secondary phases during sintering. However, do pant concentrations above 10–15mol% may give rise to transition from polar, rhombohedral (R3c) to non-polar, orthorhombic (Pnma) symmetry. The carefully selected compositions of doped BiFeO3 were synthesized by a simple hydro-evaporation method. The ceramics samples were characterized using X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), and polarization techniques, including leakage current measurements. Although the introduction of Nb5+or Zr4+decreased the leakage current, they surprisingly deteriorated the ferroelectric properties even at concentrations as low as 1 mol%. This effect was more pronounced for the samples containing Nb. On the contrary, both La3+ and Eu3+ (incorporated at the Bi-site) improved the ferroelectric properties as their concentrations increased. The La-doped samples exhibited higher remnant electric polarizations at observed electric fields. The highest remnant electric polarization of31.9 μC/cm2at 150 kV/cm was measured for Bi0.85La0.15Fe0.998Zr0.002O3, indicating the synergetic effect of La3+ and Zr4+, which is limited to very low Zr4+concentrations.sr
dc.language.isoensr
dc.publisherLinkin Science Pvt. Ltdsr
dc.relationinfo:eu-repo/grantAgreement/MESTD/inst-2020/200053/RS//sr
dc.rightsopenAccesssr
dc.source5TH EDITION OF NANOTECHNOLOGY, NANOMEDICINE & OPTICS PHOTONICS HYBRID CONFERENCEsr
dc.subjectBiFeO3sr
dc.subjectferroelectric propertiessr
dc.subjectleakage currentsr
dc.titleFerroelectric properties of BiFeO3 ceramics with cation substitutions at Bi-site (La3+, Eu3+) and Fe-site (Nb5+, Zr4+)sr
dc.typeconferenceObjectsr
dc.rights.licenseARRsr
dc.citation.spage10
dc.identifier.fulltexthttp://rimsi.imsi.bg.ac.rs/bitstream/id/4411/bitstream_4411.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_rimsi_1738
dc.type.versionpublishedVersionsr


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