AI Article Synopsis

  • Understanding the microstructure of heterostructured nanoparticles is essential for utilizing their unique properties, but traditional microscopy is limited to analyzing only a few particles.
  • A new bulk approach combining synchrotron X-ray powder diffraction with modeling techniques has been developed, allowing for the study of the microstructural changes in FeO/Fe O core/shell nanocubes over time.
  • The findings reveal that a simple two-phase model is inadequate; instead, additional interface phases are necessary to accurately reflect the particle structure, indicating a stable yet evolving interface as oxygen content in the core changes.

Article Abstract

Understanding the microstructure in heterostructured nanoparticles is crucial to harnessing their properties. Although microscopy is ideal for this purpose, it allows for the analysis of only a few nanoparticles. Thus, there is a need for structural methods that take the whole sample into account. Here, a novel bulk-approach based on the combined analysis of synchrotron X-ray powder diffraction with whole powder pattern modeling, Rietveld and pair distribution function is presented. The microstructural temporal evolution of FeO/Fe O core/shell nanocubes is studied at different time intervals. The results indicate that a two-phase approach (FeO and Fe O ) is not sufficient to successfully fit the data and two additional interface phases (FeO and Fe O ) are needed to obtain satisfactory fits, i.e., an onion-type structure. The analysis shows that the Fe O phases grow to some extent (≈1 nm) at the expense of the FeO core. Moreover, the FeO core progressively changes its stoichiometry to accommodate more oxygen. The temporal evolution of the parameters indicates that the structure of the FeO/Fe O nanocubes is rather stable, although the exact interface structure slightly evolves with time. This approach paves the way for average studies of interfaces in different kinds of heterostructured nanoparticles, particularly in cases where spectroscopic methods have some limitations.

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http://dx.doi.org/10.1002/smll.201800804DOI Listing

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