Iron oxide (Fe₂O₃) nanoclusters exhibit significant potential in the biomedical and pharmaceutical fields due to their strong magnetic properties, stability in solutions, and compatibility with living systems. They excel in magnetic separation processes, displaying high responsiveness to external magnetic fields. In contrast to conventional Fe₂O₃ nanoparticles that can aggregate in aqueous solutions due to their ferrimagnetic properties, these nanoclusters, composed of multiple nanoparticles, maintain their magnetic traits even when scaled to hundreds of nanometers. In this study, we develop a simple method using solvothermal synthesis to precisely control the size of nanoclusters. By adjusting precursor materials and reducing agents, we successfully control the particle sizes within the range of 90 to 420 nm. Our study not only enhances the understanding of nanocluster creation but also offers ways to improve their properties for applications such as magnetic separation. This is supported by our experimental results highlighting their size-dependent magnetic response in water. This study has the potential to advance both the knowledge and practical utilization of Fe₂O₃ nanoclusters in various applications.

In this study, we demonstrate the photoelectrochromic devices composed of TiO₂ and WO₃ nanostructures prepared by anodization method. The morphology and the crystal structure of anodized TiO₂ nanotubes and WO₃ nanoporous layers are investigated by SEM and XRD. To fabricate a transparent photoelectrode on FTO substrate, a TiO₂ nanotube membrane, which has been detached from Ti substrate, is transferred to FTO substrate and annealed at 450°C for 1 hr. The photoelectrode of TiO₂ nanotube and the counter electrode of WO₃ nanoporous layer are assembled and the inner space is filled with a liquid electrolyte containing 0.5 M LiI and 5 mM I₂ as a redox mediator. The properties of the photoelectrochromic devices is investigated and Pt-WO₃ electrode system shows better electrochromic performance compared toWO₃ electrode.

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