Shell-mediated control of surface chemistry of highly stoichiometric magnetite nanoparticles. Issue 25 (19th June 2020)

• Record Type: Journal Article
• Authors: Lavorato, Gabriel C.; Rubert, Aldo A.; Xing, Yutao; Das, Raja; Robles, Joshua; Litterst, F. Jochen; Baggio-Saitovitch, Elisa; Phan, Manh-Huong; Srikanth, Hariharan; Vericat, Carolina; Fonticelli, Mariano H.
• Is Part Of: Nanoscale. Volume 12:Issue 25(2020)
• Page Start: 13626
• Page End: 13636
• Publication Date: 2020-06-19
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/d0nr02069a
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : Magnetite nanostructures gradually oxidize under environmental conditions. Here we demonstrate that a Zn-ferrite epitaxial coating protects magnetite cores from oxidation and provides a core/shell system with enhanced magnetic properties. Abstract : Magnetite (Fe3 O4 ) nanoparticles are one of the most studied nanomaterials for different nanotechnological and biomedical applications. However, Fe3 O4 nanomaterials gradually oxidize to maghemite (γ-Fe2 O3 ) under conventional environmental conditions leading to changes in their functional properties that determine their performance in many applications. Here we propose a novel strategy to control the surface chemistry of monodisperse 12 nm magnetite nanoparticles by means of a 3 nm-thick Zn-ferrite epitaxial coating in core/shell nanostructures. We have carried out a combined Mössbauer spectroscopy, dc magnetometry, X-ray photoelectron spectroscopy and spatially resolved electron energy loss spectroscopy study on iron oxide and Fe3 O4 /Zn0.6 Fe2.4 O4 core/shell nanoparticles aged under ambient conditions for 6 months. Our results reveal that while the aged iron oxide nanoparticles consist of a mixture of γ-Fe2 O3 and Fe3 O4, the Zn-ferrite-coating preserves a highly stoichiometric Fe3 O4 core. Therefore, the aged core/shell nanoparticles present a sharp Verwey transition, an increased saturation magnetization and the possibility of tuning the effective anisotropy through exchange-coupling at the core/shell interface. The inhibition of the oxidation of the Fe3 O4 cores can be accounted for in terms of the chemical nature of the shell layer and an epitaxial crystal symmetry matching between the core and the shell.