2014
DOI: 10.1016/j.jpcs.2014.03.001
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Enhanced multiferroic properties in La and Ce co-doped BiFeO3 nanoparticles

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Cited by 57 publications
(12 citation statements)
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“…Similar improvement of magnetic properties had been reported earlier for doped BFO system. 12,[28][29][30] The magnetization at the highest field applied 3T (H ¼ 3T) increase from 0.12 emu/g for the undoped system to 0.37 emu/g and 0.56 emu/g for the BBFT-900 and the BBLFT-900, respectively. The remnant magnetization r is similar and around 0.09 emu/g for doped samples, while the coercive field iHc decrease with dopant incorporation from 2270 Oe for BBFT-900 to 850 Oe for BBLFT-900.…”
Section: Resultsmentioning
confidence: 99%
“…Similar improvement of magnetic properties had been reported earlier for doped BFO system. 12,[28][29][30] The magnetization at the highest field applied 3T (H ¼ 3T) increase from 0.12 emu/g for the undoped system to 0.37 emu/g and 0.56 emu/g for the BBFT-900 and the BBLFT-900, respectively. The remnant magnetization r is similar and around 0.09 emu/g for doped samples, while the coercive field iHc decrease with dopant incorporation from 2270 Oe for BBFT-900 to 850 Oe for BBLFT-900.…”
Section: Resultsmentioning
confidence: 99%
“…Although a relatively large number of multiferroic materials have been discovered and studied in recent years 3,4,5 , there remains a number of open questions concerning the origin of the magnetoelectric coupling, particularly in systems exhibiting a magnetically-induced ferroelectric polarization. In order to elucidate the microscopic origins of the magnetoelectric coupling in these systems, there have been a number of investigations on the response of various multiferroic materials under different types of perturbations 6,7,8,9 . Within this broad field of study, chemical doping has been used effectively as a tool to study how the structural, magnetic, and electrical properties of multiferroics are affected by small changes in composition 10,11,12 .…”
mentioning
confidence: 99%
“…It is observed that it is difficult to assign exact phonon modes for pure BFO and substituted BFO [27,51,52]. The observed spectra and the phonon modes of polycrystalline BFO and substituted BFO were different [51,[53][54][55][56][57], because of the angular dispersion, which causes complexity behaviour in the polycrystalline samples because of the random orientation of grains.…”
Section: Ftir and Raman Studymentioning
confidence: 99%