Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0jm04026f
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dc.titleMultiferroic and fatigue behavior of silicon-based bismuth ferrite sandwiched structure
dc.contributor.authorWu, J.
dc.contributor.authorWang, J.
dc.contributor.authorXiao, D.
dc.contributor.authorZhu, J.
dc.date.accessioned2014-10-07T09:52:15Z
dc.date.available2014-10-07T09:52:15Z
dc.date.issued2011-05-28
dc.identifier.citationWu, J., Wang, J., Xiao, D., Zhu, J. (2011-05-28). Multiferroic and fatigue behavior of silicon-based bismuth ferrite sandwiched structure. Journal of Materials Chemistry 21 (20) : 7308-7313. ScholarBank@NUS Repository. https://doi.org/10.1039/c0jm04026f
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86571
dc.description.abstractSandwich structured (Bi0.92La0.08)(Fe 0.87Zn0.13)O3/(Bi0.92La 0.08)(Fe0.93Zn0.07)O3/(Bi 0.92La0.08)(Fe0.87Zn0.13)O 3 thin films were prepared on Pt/TiO2/SiO 2/Si(100) substrates by radio frequency sputtering. High (110) orientation is induced in these sandwiched structures due to the introduction of the bottom (Bi0.92La0.08)(Fe0.87Zn 0.13)O3 layer with a (110) orientation. The space-charge-limited current mechanism is identified to dominate the leakage behavior of these sandwiched structures, and the lowest leakage current density is well established in such a sandwiched structure with a thickness ratio of 1:1:1 owing to its denser microstructure. All sandwiched structures demonstrate good fatigue behavior at a switching cycle of ∼2.96 × 109 and similar saturated M-H loops with 2M ∼ 15.5 emu cm-3 due to the interface coupling among these constituent layers. The sandwiched structure with a thickness ratio of 1:1:1 possesses a better P-E loop with a high remanent polarization of 2Pr ∼ 142.6 μC cm-2 and a low coercive field of 2Ec ∼ 695.0 kV cm-1. As a result, the sandwiched structure is an effective way to improve the multiferroic and fatigue behavior of bismuth ferrite materials. © 2011 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0jm04026f
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1039/c0jm04026f
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume21
dc.description.issue20
dc.description.page7308-7313
dc.description.codenJMACE
dc.identifier.isiut000290167200038
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