2015
DOI: 10.1016/j.jmmm.2015.05.066
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Synthesis and characterization of Bismuth ferrite (BiFeO3) nanoparticles by solution evaporation method

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Cited by 53 publications
(37 citation statements)
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“…From the above studies it was concluded that upon increasing calcination temperature, pure form of the BFO-T nanoparticles was obtained [18,19], i.e. pure perovskite form of BFO-T nanoparticles was obtained [1]. This result was also in concord as discussed earlier in FT-IR analysis.…”
Section: 1 Structural and Morphology Analysissupporting
confidence: 71%
See 1 more Smart Citation
“…From the above studies it was concluded that upon increasing calcination temperature, pure form of the BFO-T nanoparticles was obtained [18,19], i.e. pure perovskite form of BFO-T nanoparticles was obtained [1]. This result was also in concord as discussed earlier in FT-IR analysis.…”
Section: 1 Structural and Morphology Analysissupporting
confidence: 71%
“…Multiferroic materials are a class of materials that got immense interest owing to the coexistence of electrical and magnetic properties. In addition, multiferroic materials have potential applications in field of spin valves, information storage devices, microelectronic devices spintronic devices, and sensors [1]. Among various multiferroic materials, magneto electric multiferroic are one of the most commonly studied materials in which magnetization can be affected by electric field and vice-versa.…”
Section: Introductionmentioning
confidence: 99%
“…6. BiFeO 3 is an antiferromagnetic system but it shows ferromagnetic properties at room temperature [31]. The result confirmed that the BiFeO 3 nanoparticles exhibited ferromagnetic ordering, as evidenced by the magnified view of the M − H curves at lower applied field [29] which showed that hysteresis appeared with a residual magnetic moment of 8.83× 10 −2 emu/g and coercive field of 79.95 Oe when applied with a magnetic field of 20 kOe.…”
Section: Magnetic Propertiessupporting
confidence: 62%
“…The increase in degradation with increasing dose of catalyst was due to the increase in catalytic active sites which were present on the surface of the catalyst. These catalytic active sites were further responsible for an increase in the production of hydroxyl and superoxide radicals which were necessary for the photocatalytic reaction . But when we further increased the catalyst amount, i.e.…”
Section: Resultsmentioning
confidence: 99%