Supercapacitors have been recognized as one of the more promising energy storage devices, with great potential use in portable electronics and hybrid vehicles. In this study, a composite made of clusters of iron oxide (Fe3O4-γFe2O3) nanoparticles and reduced graphene oxide (rGO) has been developed through a simple one-step solvothermal synthesis method for a high-performance supercapacitor electrode. Electrochemical assessment via cyclic voltammetry, galvanostatic charge–discharge experiments, and electrochemical impedance spectroscopy (EIS) revealed that the Fe3O4-γFe2O3/rGO nanocomposite showed much higher specific capacitance than either rGO or bare clusters of Fe3O4-γFe2O3 nanoparticles. In particular, specific capacitance values of 100 F g−1, 250 F g−1, and 528 F g−1 were obtained for the clusters of iron oxide nanoparticles, rGO, and the hybrid nanostructure, respectively. The enhancement of the electrochemical performance of the composite material may be attributed to the synergistic interaction between the layers of graphene oxide and the clusters of iron oxide nanoparticles. The intimate contact between the two phases eliminates the interface, thus enabling facile electron transport, which is key to attaining high specific capacitance and, consequently, enhanced charge–discharge time. Performance evaluation in consecutive cycles has demonstrated that the composite material retains 110% of its initial capacitance after 3000 cycles, making it a promising candidate for supercapacitors.

In this study, nanocrystals of antiferromagnetic Cr2O3 are shown via Raman spectroscopy to display peculiar lattice dynamics in terms of phonon softening and the occurrence of an exceptionally strong spin‐phonon coupling. This effect, which is observed to persist well above the onset of the antiferromagnetic ordering temperature, is ascribed to locally correlated spin fluctuations due to the modulation of the magnetic exchange interactions as the chromium atoms oscillate about their equilibrium position. It is found that the spin‐phonon coupling strength is governed by the competing antiferromagnetic and ferromagnetic interactions, where changes in the surface spin configuration can also play a crucial role. Overall, this work proves the size dependence of the interplay between the crystalline and magnetic structures in 3D antiferromagnets varying the surface‐to‐volume ratio and helps establish the fundamentals for a spin‐phonon coupling engineering at the nanoscale via a simple route in a very stable and easy to synthesize material. More importantly, it demonstrates the possibility of coupling phononic excitations with the magnetization dynamics at room temperature, offering a highly prospective nanomaterial for the design of novel magnonic devices.