“…Recently, iron/iron oxide core/shell nanoparticle systems have been exploited for such applications because the combination of the high magnetization of the core (Fe) and the chemical stability and biocompatibility of the shell (Fe 3 O 4 or γ-Fe 2 O 3 ) lead to more suitable overall properties than either material alone [24,25,26]. These systems also provide excellent models for probing the roles played by interface and surface spins and their impacts on EB in exchange-coupled nanostructures, inspiring a large body of work on core/shell Fe/γ-Fe 2 O 3 [27,28,29], Fe/Fe 3 O 4 [30,31], FeO/Fe 3 O 4 [32,33,34], Fe 3 O 4 /γ-Fe 2 O 3 [35], γ-Fe 2 O 3 /CoO [36], and Au/Fe 3 O 4 particles [37,38,39]. Oxidization-driven migration of metal atoms from the core to the shell of iron/iron oxide nanoparticle systems has been shown to occur via the Kirkendall effect, leading to a morphological transformation into hollow nanoparticles, where the additional (inner) surface area strongly affects magnetic properties including EB [40,41,42,43,44].…”