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Core-shell nanoparticles of MnO|Mn3O4 with average particle sizes of 5-60 nm, composed of an antiferromagnetic (AFM) core and a ferrimagnetic (FiM) shell, have been synthesized and their magnetic properties investigated. The core-shell structure has been generated by the passivation of the MnO cores, yielding an inverted AFM-core|FiM-shell system, as opposed to the typical FM-core|AFM-shell. The exchange-coupling between AFM and FiM gives rise to an enhanced coercivity of approximately 8 kOe and a loop shift of approximately 2 kOe at 10 K, i.e., exchange bias. The coercivity and loop shift show a non-monotonic variation with the core diameter. The large coercivity and the loop shift are ascribed to the highly anisotropic Mn3O4 and size effects of the AFM (i.e., uncompensated spins, AFM domains, and size-dependent transition temperature).

The magnetization reversal in exchange-biased ferromagnetic-antiferromagnetic (FM-AFM) bilayers is investigated. Different reversal pathways on each branch of the hysteresis loop, i.e., asymmetry, are obtained both experimentally and theoretically when the magnetic field is applied at certain angles from the anisotropy direction. The range of angles and the magnitude of this asymmetry are determined by the ratio between the FM anisotropy and the interfacial FM-AFM exchange anisotropy. The occurrence of asymmetry is linked with the appearance of irreversibility, i.e., finite coercivity, as well as with the maximum of exchange bias, increasing for larger anisotropy ratios. Our results indicate that asymmetric hysteresis loops are intrinsic to exchange-biased systems and the competition between anisotropies determines the asymmetric behavior of the magnetization reversal.

The crystal and magnetic structures of orthorhombic ε-Fe2O3 have been studied by simultaneous Rietveld refinement of X-ray and neutron powder-diffraction data in combination with Mössbauer spectroscopy, as well as magnetization and heat-capacity measurements. It has been found that above 150 K, the ε-Fe2O3 polymorph is a collinear ferrimagnet with magnetic moments directed along the a axis, whereas the magnetic ordering below 80 K is characterized by a square-wave incommensurate structure. The transformation between these two states is a second-order phase transition and involves subtle structural changes mostly affecting the coordination of the tetrahedral and one of the octahedral Fe sites. The temperature dependence of the ε-Fe2O3 magnetic properties is discussed in light of these results.

The magnetic properties of ferromagnetic-antiferromagnetic Co-CoO core-shell nanoparticles are investigated as a function of the in-plane coverage density from 3.5% to 15%. The superparamagnetic blocking temperature, the coercivity, and the bias field radically increase with increasing coverage. This behavior cannot be attributed to the overall interactions between cores. Rather, it can be semiquantitatively understood by assuming that the shells of isolated core-shell nanoparticles have strongly degraded magnetic properties, which are rapidly recovered as nanoparticles come into contact.

Electric-field-controlled magnetism can boost energy efficiency in widespread applications. However, technologically, this effect is facing important challenges: mechanical failure in strain-mediated piezoelectric/magnetostrictive devices, dearth of room-temperature multiferroics, or stringent thickness limitations in electrically charged metallic films. Voltage-driven ionic motion (magneto-ionics) circumvents most of these drawbacks while exhibiting interesting magnetoelectric phenomena. Nevertheless, magneto-ionics typically requires heat treatments and multicomponent heterostructures. Here we report on the electrolytegated and defect-mediated O and Co transport in a Co 3 O 4 single layer which allows for room-temperature voltage-controlled ON−OFF ferromagnetism (magnetic switch) via internal reduction/oxidation processes. Negative voltages partially reduce Co 3 O 4 to Co (ferromagnetism: ON), resulting in graded films including Co-and O-rich areas. Positive bias oxidizes Co back to Co 3 O 4 (paramagnetism: OFF). This electric-field-induced atomic-scale reconfiguration process is compositionally, structurally, and magnetically reversible and self-sustained, since no oxygen source other than the Co 3 O 4 itself is required. This process could lead to electric-field-controlled device concepts for spintronics.

Conventional photocatalytic micromotors are limited to the use of specific wavelengths of light due to their narrow light absorption spectrum, which limits their effectiveness for applications in biomedicine and environmental remediation. We present a multiwavelength light-responsive Janus micromotor consisting of a black TiO microsphere asymmetrically coated with a thin Au layer. The black TiO microspheres exhibit absorption ranges between 300 and 800 nm. The Janus micromotors are propelled by light, both in HO solutions and in pure HO over a broad range of wavelengths including UV, blue, cyan, green, and red light. An analysis of the particles' motion shows that the motor speed decreases with increasing wavelength, which has not been previously realized. A significant increase in motor speed is observed when exploiting the entire visible light spectrum (>400 nm), suggesting a potential use of solar energy, which contains a great portion of visible light. Finally, stop-go motion is also demonstrated by controlling the visible light illumination, a necessary feature for the steerability of micro- and nanomachines.

A large coercive field, HC=20kOe, is obtained at room temperature in ε-Fe2O3 nanoparticles embedded in a silica matrix, produced by sol-gel chemistry. The combination of a relatively high magnetic anisotropy together with the small saturation magnetization are responsible for this large HC. Upon cooling, a strong reduction of HC is observed at T∼100K, which is accompanied by a drastic reduction of the squareness ratio MR∕MS. Neutron-diffraction measurements reveal the existence of a low-temperature magnetic transition to which the softening of this material can be ascribed.