Controlled growth of epitaxial BiFeO3 films using self-assembled BiFeO3-CoFe2O4 multiferroic heterostructures as a template

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Epitaxial BiFeO3 multiferroic thin film heterostructures.

Enhancement of polarization and related properties in heteroepitaxially constrained thin films of the ferroelectromagnet, BiFeO3, is reported. Structure analysis indicates that the crystal structure of film is monoclinic in contrast to bulk, which is rhombohedral. The films display a room-temperature spontaneous polarization (50 to 60 microcoulombs per square centimeter) almost an order of magn...

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Comment on "Epitaxial BiFeO3 multiferroic thin film heterostructures".

Wang et al. (1) recently reported multiferroic behavior, with ferromagnetic and ferroelectric polarizations that are both large at room temperature, in thin strained films of BiFeO 3 (BFO). Although at room temperature, bulk BFO is ferroelectric (2) and antiferromagnetic (3–5), Wang et al. (1) reported that a 70-nm film shows both an enhanced ferroelectric polarization (90 mC cm) and a substant...

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Single-domain multiferroic BiFeO3 films

The strong coupling between antiferromagnetism and ferroelectricity at room temperature found in BiFeO3 generates high expectations for the design and development of technological devices with novel functionalities. However, the multi-domain nature of the material tends to nullify the properties of interest and complicates the thorough understanding of the mechanisms that are responsible for th...

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Directed self-assembly of epitaxial CoFe2O(4)-BiFeO3 multiferroic nanocomposites.

CoFe(2)O(4) (CFO)-BiFeO(3) (BFO) nanocomposites are an intriguing option for future memory and logic technologies due to the magnetoelectric properties of the system. However, these nanocomposites form with CFO pillars randomly located within a BFO matrix, making implementation in devices difficult. To overcome this, we present a technique to produce patterned nanocomposites through self-assemb...

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ژورنال

عنوان ژورنال: Applied Physics Letters

سال: 2012

ISSN: 0003-6951,1077-3118

DOI: 10.1063/1.4734508