2020
DOI: 10.1007/s10854-020-03795-9
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Phase analysis and cation distribution correlated with magnetic properties of spinel Ba1−xSrxFe2O4 ferrites prepared at different annealing temperatures

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Cited by 13 publications
(7 citation statements)
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“…54 Particularly, spinel ferrites (SF) and their nanocomposites have captured the attention of researchers by virtue of their outstanding physical and chemical features, especially chemical stability with strong anisotropy, variety of oxidation states with higher operation voltage (À1.2-0.65 volts), good permeability and coercivity, excellent magnetic properties yet being cost-effective and eco-friendly. [55][56][57] A spinel ferrite is an intriguing oxide crystal structure with a face-centered cubic core with the chemical notation of MFe 2 O 4 generated by the combination of a triplet cation (Fe 3+ ) with another divalent metal cation, particularly a transition or posttransition metallic cation (M 2+ = Ba 2+ , Co 2+ , Cu 2+ , Mg 2+ , Mn 2+ , Sr 2+ , Zn 2+ , etc.). These cations may be settled in two distinct crystallographic locations (tetrahedral sites and octahedral sites) positioned among the cations and the adjoining oxygen ions due to changes in chemical composition, charge location, and consolidation energy.…”
Section: Introductionmentioning
confidence: 99%
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“…54 Particularly, spinel ferrites (SF) and their nanocomposites have captured the attention of researchers by virtue of their outstanding physical and chemical features, especially chemical stability with strong anisotropy, variety of oxidation states with higher operation voltage (À1.2-0.65 volts), good permeability and coercivity, excellent magnetic properties yet being cost-effective and eco-friendly. [55][56][57] A spinel ferrite is an intriguing oxide crystal structure with a face-centered cubic core with the chemical notation of MFe 2 O 4 generated by the combination of a triplet cation (Fe 3+ ) with another divalent metal cation, particularly a transition or posttransition metallic cation (M 2+ = Ba 2+ , Co 2+ , Cu 2+ , Mg 2+ , Mn 2+ , Sr 2+ , Zn 2+ , etc.). These cations may be settled in two distinct crystallographic locations (tetrahedral sites and octahedral sites) positioned among the cations and the adjoining oxygen ions due to changes in chemical composition, charge location, and consolidation energy.…”
Section: Introductionmentioning
confidence: 99%
“…Recent studies have also shown that the chemical structure of SF mechanisms, notably divalent cations rather than Fe 3+ cations, has a significant impact on their distinctive properties. 54,56,[58][59][60] Within SFs, CoFe @multi-walled carbon nanotube (MWCNTs) composite and reported the highest Sc as 390 F g À1 at a current density of 1 mA cm À2 in 2 M KOH electrolyte. Additionally, the fabricated ASC device resulted in a high ED of 26.7 W h kg À1 at a PD of 319 W kg À1 .…”
Section: Introductionmentioning
confidence: 99%
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“…However, few studies have been conducted on alkali and alkaline divalent cations. Based on the crystallographic structures, the ferrite NPs can be categorized as orthorhombic, hexagonal, and cubic [16][17][18]. The cubic MeFe 2 O 4 (Me = Ni 2+ , Fe 3+ , Co 2+ , Mg 2+ ) and orthorhombic MeFe 2 O 4 (Me = Ba 2+ or Ca 2+ ) magnetic materials are promising for various applications [19][20][21][22][23].…”
Section: Introductionmentioning
confidence: 99%
“…Here, Ba 2+ as A sites are tetrahedral and Fe 3+ as B sites are octahedral coordinated by oxygen atoms [4]. They can be effectively adjusted by using divalent ions such as Co, Ni, Mn, Zn, Ti and Sr [5][6][7]. The cobalt, nickel, manganese and barium ferrites come under low-cost materials that have good magnetic and dielectric properties.…”
Section: Introductionmentioning
confidence: 99%