2016
DOI: 10.1016/j.jmmm.2016.05.023
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The influence of oxidation process on exchange bias in egg-shaped FeO/Fe3O4 core/shell nanoparticles

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Cited by 30 publications
(31 citation statements)
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“…As pointed out by Chen et al 20 , the Wüstite phase is formed as consequence of reactions involving some commonly used hydrocarbon solvents and its formation contributes to significant cationic disorder. The later formation of the bimagnetic core-shell system due to the surface oxidation of Wüstite results in very distinct magnetic properties with respect to the monophasic nanoparticles [21][22][23][24][25][26] . Therefore, it is very important determine the factors that govern the core/shell nanoparticles formation to establish the reproducibility of this synthesis method and the magnetic response of the system.…”
Section: Introductionmentioning
confidence: 99%
“…As pointed out by Chen et al 20 , the Wüstite phase is formed as consequence of reactions involving some commonly used hydrocarbon solvents and its formation contributes to significant cationic disorder. The later formation of the bimagnetic core-shell system due to the surface oxidation of Wüstite results in very distinct magnetic properties with respect to the monophasic nanoparticles [21][22][23][24][25][26] . Therefore, it is very important determine the factors that govern the core/shell nanoparticles formation to establish the reproducibility of this synthesis method and the magnetic response of the system.…”
Section: Introductionmentioning
confidence: 99%
“…The interfacial structure of the branch was investigated by HR-TEM analysis. As shown in Figure 2f, the spacing lattice fringe of 0.252, 0.245, and 0.492 nm were implied the presence of (110)Fe 2 O 3 planes, 30 (111) FeO(OH) planes, 31 and (111) magnetite planes, 32 respectively. Moreover, it has been found that the dendrimerlike structure was significantly affected by the Fe/biomass ratios.…”
Section: ■ Experimental Sectionmentioning
confidence: 93%
“…The metal oleate complex was prepared according to the procedure described by Leszczyński et al [36], mixing 30 mL of deionized water, 40 mL of ethanol 96%, 70 mL of hexane 96%, 3.25 g of anhydrous iron(III) chloride, and 18.25 g of sodium oleate. The resulting solution was heated to 60 • C and kept at that temperature for 5 h. The dark hydrophobic phase was separated in a separator funnel, washed with deionized water, and heated to 40 • C to evaporate hexane.…”
Section: Synthesis Of Iron(iii) Oleate Complexmentioning
confidence: 99%