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Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub> Core/Shell Nanoparticles: The Silica Coating Regulations with a Single Core for Different Core Sizes and Shell Thicknesses
548
Citations
58
References
2012
Year
NanoparticlesMagnetic PropertiesEngineeringMetal NanoparticlesFe3o4 NpsChemistrySol-gel SynthesisChemical EngineeringShell ThicknessesNanoscale ChemistryCoating RegulationsNanostructure SynthesisSingle CoreMaterials ScienceNanotechnologyFe3o4 NanoparticlesSilica Coating RegulationsNanocrystalline MaterialPowder SynthesisNanomaterialsNanocompositesNanostructuresMaterial Preparation
The authors develop coating regulations for Fe₃O₄ nanoparticles using a reverse microemulsion method to produce Fe₃O₄@SiO₂ core/shell particles. They employ a reverse microemulsion approach that adjusts TEOS and ammonia concentrations to control shell thickness, prevent core‑free silica, and observe ligand exchange during coating. The results demonstrate that optimal silica coating depends on core size and aqueous domain volume, enabling uniform Fe₃O₄@SiO₂ nanoparticles with tunable shell thickness and a generalizable strategy for other core–shell systems.
In this work, we present the coating regulations of Fe3O4 nanoparticles (NPs) by the reverse microemulsion method to obtain the Fe3O4@SiO2 core/shell NPs. The regulation produces the core/shell NPs with a single core and with different shell thicknesses, and it especially can be applied to different sizes Fe3O4 NPs and avoid the formation of core-free silica particles. Our results reveal that the silica coating parameters suitable for Fe3O4 NPs with certain size are not definitely applicable to that with other sizes, and the match of the number of Fe3O4 NPs with aqueous domain is essential. We found that the small aqueous domain is suitable to coat ultrathin silica shell, while the large aqueous domain is indispensable for coating thicker shells. To avoid the formation of core-free silica particles, the thick silica shell can be achieved by increasing the content of either TEOS through the equivalently fractionated drops or ammonia with a decreased one-off TEOS. The ligand exchange between the intermediate processes of the silica coating is evidenced. Our results provide not only a strategy for synthesizing uniform Fe3O4@SiO2 core/shell NPs with controlled shell thickness, but also a regulation that can be applied to preparation other core–shell NPs.
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