Magnetothermal Energy Conversion of Polydopamine-Coated Iron Oxide Ferrogels Under High-Frequency Rotating Magnetic Fields
This study provides a comparison between magnetic-to-thermal energy conversion efficiency in liquid and gel phases under high-frequency magnetic fields. Magnetite cores (11 ± 2 nm) were tested as water-based ferrofluids and as 5 wt% agar ferrogels, both with and without a biocompatible polydopamine (PDA) shell. A custom two-phase coil switched between rotating (RMF) and alternating (AMF) modes, enabling phase- and coating-dependent effects to be measured at identical field strengths and frequencies (100–300 kHz, 1–4 kA/m). Across all conditions, RMF generated 1.7–2.1 times more specific loss power (SLP) than AMF, and moving from the liquid to the gel phase reduced SLP by 5–8%, indicating that heating is controlled by Néel relaxation with negligible Brownian contribution. SLP rose with magnetic-field amplitude according to a power law, while hysteretic losses remained minimal. PDA improved colloidal stability and biocompatibility without harming the heating performance, lowering SLP by <17%. Within Brezovich limits, the system still exceeded therapeutic hyperthermia thresholds. Thus, in this iron-oxide/PDA system, neither medium viscosity nor the PDA shell’s non-magnetic mass significantly affects thermal energy output, an important finding for translating laboratory calorimetry data into reliable, application-oriented modelling for magnetic hyperthermia.
Authors
- Artur Jędrzak (ORCID: https://orcid.org/0000-0002-0875-9826)
- Rafał Bielas (ORCID: https://orcid.org/0000-0001-6260-6444)
- Andrzej Skumiel (ORCID: https://orcid.org/0000-0002-2501-4965)
- Jakub Musiał (ORCID: https://orcid.org/0000-0002-8886-9434)
Institutions
- Poznań University of Technology (PL)
- Adam Mickiewicz University in Poznań (PL)
Publication Details
- Journal
- Energies
- Published
- 2025-08-12
- DOI
- https://doi.org/10.3390/en18164291
- Primary Topic
- Characterization and Applications of Magnetic Nanoparticles
- Type
- article
- Field-Weighted Citation Impact
- 0.00