Nanoscale Physical and Chemical Structure of Iron Oxide Nanoparticles for Magnetic Particle Imaging

Abstract

In this work, the role of the nanoscale chemical and magnetic structure on relaxation dynamics of iron oxide nanoparticles in the context of magnetic particle imaging (MPI) is investigated with Mössbauer spectroscopy (MS) and electron energy loss spectroscopy (EELS). Two samples of 27 nm monodisperse iron oxide nanoparticles are compared, with and without an additional oxidation optimization step, with corresponding differences in structure and properties. Iron oxide nanoparticles synthesized in the presence of sufficient oxygen form single crystalline, inverse‐spinel magnetite (Fe3O4) and display magnetic properties suitable for MPI. A secondary wüstite (FeO) phase is observed in the diffraction pattern of unoptimized nanoparticles, which is antiferromagnetic and therefore unsuitable for MPI. Mössbauer spectra confirm the composition of the optimized nanoparticles to be ≈70% magnetite, with the remaining 30% oxidized to maghemite; in contrast, the as‐synthesized particles (without the oxidation step) contained about 40% wüstite and 60% magnetite. The authors use scanning transmission electron microscopy (STEM) with electron energy loss spectroscopy (EELS) to probe iron 2p‐3d electronic transitions and correlate their intensities with the oxidation state with sub‐nanometer spatial resolution. The optimally oxidized nanoparticles are uniform in crystallography and phase, while the mixed phase nanoparticles are core‐shell wüstite/magnetite. Further confirming the core‐shell structure of the mixed phase nanoparticles, considerable spin canting in the in‐field Mössbauer spectrum, likely caused by interface coupling, is observed.