Size Control of Highly Monodisperse Citrate-Stabilized Magnetite Nanoparticles in Aqueous Media: The Role of Cerium Cations
Year: 2025
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Controlling the nucleation and growth of magnetite nanoparticles (NPs) via aqueous coprecipitation at room temperature is inherently challenging due to kinetic and thermodynamic constraints. Rapid pH increases trigger a burst nucleation event that depletes precursors before significant growth occurs, while NP surfaces are quickly passivated by water and hydroxyl ions, forming a dewetting barrier that impedes further growth. To address these challenges, we developed an innovative synthesis approach that incorporates lanthanide (Ln) cations, mainly Ce 3+, together with sodium citrate into the coprecipitation process. These additives act synergistically to lower surface energy and stabilize both precursors and reaction intermediates, thereby facilitating controlled crystal growth. We systematically investigated the impact of Ln cations by fine-tuning the Ce 3+ concentration, which enabled precise control over NP size, yielding diameters from 13 to 46 nm. Notably, at higher Ce 3+ concentrations, multidomain nanowires are formed, with diameters reaching up to 90 nm and lengths on the micron scale. Moreover, the synthesized NPs exhibit enhanced performance in magnetic hyperthermia (MH) and peroxidase-like activity compared with those produced without Ce 3+ . The improved catalytic activity is attributed to accelerated Fe 2+ regeneration in the reaction, mediated by the presence of the Ce 4+ /Ce 3+ redox couple, which boosts • OH radical production. Importantly, this strategy is versatile and can be extended to other Ln cations (Eu 3+, Gd 3+, Er 3+, Yb 3+, and Lu 3+ ), yielding single-crystal magnetite NPs of comparable sizes. Collectively, Ln-assisted synthesis addresses longstanding challenges in magnetite NP coprecipitation, providing a scalable route to high-performance magnetic NPs with tunable size and morphology. This approach not only improves control over NP growth but also broadens their potential applications in MH and catalysis.
Source: Chemistry of Materials
Institutions: Universitat Autònoma de Barcelona, Institut Català de Nanociència i Nanotecnologia, Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine, Institut de Ciència de Materials de Barcelona, University of Catania, Institute for Microelectronics and Microsystems, Institució Catalana de Recerca i Estudis Avançats, Vall d'Hebron Institut de Recerca
Language: English
Subfield: Materials Chemistry
Field: Materials Science
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W4414798238
