George C. Hadjipanayis

The tetragonal R_1−xZr_x(FeCo)₁₁Ti alloys, where R is a rare earth and Ti a transition metal, are promising candidates for permanent magnets. Sm_1−xZr_x(Fe_0.8Co_0.2)_12−yTi_y (x = 0 and 0.25; y = 1 and 0.7) master alloys were prepared by arc melting under argon atmosphere. Some of the samples were almost single-phase compounds at 1:12, with a very small amount of a-Fe(Co). Partially replacing Sm with Zr produced alloys with small amounts of Sm(FeCo)₂ Laves-type phases. The as-cast ingots were milled using high-energy ball milling (HEBM) for different times in an argon atmosphere and then annealed at 973 K–1173 K at different interval times (15–90 min). After annealing, the sample milled for 4 h contained a large variation of grain size from 2–4 μm to 20 μm or larger, while, after annealing, the other sampled milled for 8 h exhibited grains size in the range of 2–6 μm; therefore, their coercivity was higher, reaching a maximum value of 5.5 kOe for SmFe₉Co₂Ti annealed at 1123 K for 60 min. Coercivity was strongly affected by the annealing temperature and time. The microstructure evolution with emphasis on the particles size during annealing and their correlation with coercivity are herein discussed.

Bimetallic colloidal CoPt nanoalloys with low platinum content were successfully synthesized following a modified polyol approach. Powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), and transmission electron microscopy (TEM) studies were performed to estimate the crystal structure, morphology, and surface functionalization of the colloids, respectively, while the room-temperature magnetic properties were measured using a vibrating sample magnetometer (VSM). The particles exhibit excellent uniformity, with a narrow size distribution, and display strong room-temperature hysteretic ferromagnetic behavior even in the as-made form. Upon annealing at elevated temperatures, progressive formation and co-existence of exchange coupled, of both chemically ordered and disordered phases significantly enhanced the room-temperature coercivity.

Bimetallic colloidal CoPt nanoalloys, with a very low platinum content, were successfully synthesized following a modified polyol approach. Powder X-ray diffraction, IR spectroscopy, thermogravimetric analysis, and Transmission Electron Microscopy studies were performed to estimate the crystal structure, morphology and surface functionalization of the colloids respectively, while the room temperature magnetic properties were measured using Vibrating Sample Magnetometer. The particles exhibit excellent uniformity, with a narrow size distribution, and display strong room temperature hysteretic ferromagnetic behavior even in the as-made form. Upon annealing at elevated temperatures, progressive formation and co-existence of exchange coupled both chemically ordered and disordered phases, significantly enhance the room temperature coercivity.

Sm-Fe-Ti and Sm-Fe 0.8 Co 0.2 -Ti alloys were prepared via arc-melting and directionally solidified on a water-cooled copper hearth. The alloys featured cells of the Sm(Fe,Co,Ti) 12 - Ti(Fe,Co) 2 -(αFe) lamellar eutectic, with the lamellae of Sm(Fe,Co,Ti) 12 phase (crystal structure of the ThMn 12 type) less than 0.2 μm thick and with their [001] directions oriented along the temperature gradient of the solidification. Although this eutectic microstructure also led to an increased coercivity, the latter reached only a modest value of 0.07 T (0.7 kOe), which is believed to be insufficient for utilization of the directionally solidified alloys as anisotropic permanent magnets.

Fe₃O₄ nanoparticles “decorated” by LAPONITE® nanodisks have been materialized utilizing the Schikorr reaction and tested as mediators of heat for localized magnetic hyperthermia (MH) and as magnetic resonance imaging (MRI) agents.

Cobalt nanowires have been synthesized by electrochemical deposition using track-etched anodized aluminum oxide (AAO) templates. Nanowires with varying spacing-to-diameter ratios were prepared, and their magnetic properties were investigated. It is found that the nanowires’ easy magnetization direction switches from parallel to perpendicular to the nanowire growth direction when the nanowire’s spacing-to-diameter ratio is reduced below 0.7, or when the nanowires’ packing density is increased above 5%. Upon further reduction in the spacing-to-diameter ratio, nanowires’ magnetic properties exhibit an isotropic behavior. Apart from shape anisotropy, strong dipolar interactions among nanowires facilitate additional uniaxial anisotropy, favoring an easy magnetization direction perpendicular to their growth direction. The magnetic interactions among the nanowires were studied using the standard method of remanence curves. The demagnetization curves and Delta m (Δm) plots showed that the nanowires interact via dipolar interactions that act as an additional uniaxial anisotropy favoring an easy magnetization direction perpendicular to the nanowire growth direction. The broadening of the dipolar component of Δm plots indicate an increase in the switching field distribution with the increase in the nanowires’ diameter. Our findings provide an important insight into the magnetic behavior of cobalt nanowires, meaning that it is crucial to design them according to the specific requirements for the application purposes.

Today, magnetic hyperthermia constitutes a complementary way to cancer treatment. This article reports a promising aspect of magnetic hyperthermia addressing superparamagnetic and highly Fe/Au core-shell nanoparticles. Those nanoparticles were prepared using a wet chemical approach at room temperature. We found that the as-synthesized core shells assembled with spherical morphology, including face-centered-cubic Fe cores coated and Au shells. The high-resolution transmission microscope images (HRTEM) revealed the formation of Fe/Au core/shell nanoparticles. The magnetic properties of the samples showed hysteresis loops with coercivity (HC) close to zero, revealing superparamagnetic-like behavior at room temperature. The saturation magnetization (MS) has the value of 165 emu/g for the as-synthesized sample with a Fe:Au ratio of 2:1. We also studied the feasibility of those core-shell particles for magnetic hyperthermia using different frequencies and different applied alternating magnetic fields. The Fe/Au core-shell nanoparticles achieved a specific absorption rate of 50 W/g under applied alternating magnetic field with amplitude 400 Oe and 304 kHz frequency. Based on our findings, the samples can be used as a promising candidate for magnetic hyperthermia for cancer therapy.

In this work, the mechanochemical synthesis method was used for the first time to produce powders of the nanocrystalline Nd_1.1Fe₁₀CoTi compound from Nd₂O₃, Fe₂O₃, Co and TiO₂. High-energy-milled powders were heat treated at 1000 °C for 10 min to obtain the ThMn₁₂-type structure. Volume fraction of the 1:12 phase was found to be as high as 95.7% with 4.3% of a bcc phase also present. The nitrogenation process of the sample was carried out at 350 °C during 3, 6, 9 and 12 h using a static pressure of 80 kPa of N₂. The magnetic properties M_r, µ₀H_c, and (BH)_max were enhanced after nitrogenation, despite finding some residual nitrogen-free 1:12 phase. The magnetic values of a nitrogenated sample after 3 h were M_r = 75 Am² kg^–1, µ₀H_c = 0.500 T and (BH)_max = 58 kJ·m^–3. Samples were aligned under an applied field of 2 T after washing and were measured in a direction parallel to the applied field. The best value of (BH)_max ~ 114 kJ·m^–3 was obtained for 3 h and the highest µ₀H_c = 0.518 T for 6 h nitrogenation. SEM characterization revealed that the particles have a mean particle size around 360 nm and a rounded shape.

Fe-based colloids with a core/shell structure consisting of metallic iron and iron oxide were synthesized by a facile hot injection reaction of iron pentacarbonyl in a multi-surfactant mixture. The size of the colloidal particles was affected by the reaction temperature and the results demonstrated that their stability against complete oxidation related to their size. The crystal structure and the morphology were identified by powder X-ray diffraction and transmission electron microscopy, while the magnetic properties were studied at room temperature with a vibrating sample magnetometer. The injection temperature plays a very crucial role and higher temperatures enhance the stability and the resistance against oxidation. For the case of injection at 315 °C, the nanoparticles had around a 10 nm mean diameter and revealed 132 emu/g. Remarkably, a stable dispersion was created due to the colloids’ surface functionalization in a nonpolar solvent.