Graphitic Carbon‐Coated FeCo Nanoparticles for Enhanced Magnetic Hyperthermia Therapy
Superparamagnetic iron oxide nanoparticles are widely used for magnetic hyperthermia, yet their modest saturation magnetization limits heating efficiency. Here, a simple route to graphitic carbon–coated iron–cobalt (FeCo) nanocrystals that retain near‐bulk saturation magnetization and deliver competitive heating is reported. Single‐phase FeCo ingots are arc‐melted, crushed, mechanically milled with graphite for 5 h under argon and annealed at 400–800 °C in forming gas to form protective graphitic shells. X‐ray diffraction and transmission electron microscopy confirm body‐centered cubic FeCo cores encapsulated by a continuous carbon shell. After annealing at 400 °C, the sample achieves a saturation magnetization of 240 emu g −1 and a specific absorption rate (SAR, a measure of heating efficiency) of 191.5 W g −1 at 300 kHz and 325 Oe. Higher annealing temperatures increase graphitization and coarsening and reduce both saturation magnetization and SAR. Optimum performance at 400 °C is attributed to oxidation‐limiting shells of near‐optimal thickness. These results identify graphitic carbon–coated FeCo nanocrystals as a promising platform for magnetic hyperthermia. Although ethanol is nonphysiological, it was used to benchmark intrinsic heating capacity; biocompatibility and colloidal stability in aqueous media will be addressed in future work.
Authors
- Mehmet Burak Kaynar (ORCID: https://orcid.org/0000-0002-4854-8142)
- Cem Bayram (ORCID: https://orcid.org/0000-0001-8717-4668)
- Tuncay Şimşek (ORCID: https://orcid.org/0000-0002-4683-0152)
- Telem Şimşek (ORCID: https://orcid.org/0000-0003-4852-2230)
- Eser Uçar (ORCID: https://orcid.org/0000-0002-4812-4390)
- Şadan Özcan (ORCID: https://orcid.org/0000-0001-7966-1845)
- Mervenur Keleş
Institutions
- Antalya IVF (TR)
- Medical Technologies (Czechia) (CZ)
- Hacettepe University (TR)
Publication Details
- Journal
- physica status solidi (b)
- Published
- 2025-09-29
- DOI
- https://doi.org/10.1002/pssb.202500393
- Citations
- 1
- Primary Topic
- Nanoparticle-Based Drug Delivery
- Type
- article
- Field-Weighted Citation Impact
- 0.60