Advanced permanent magnets based on rare-earth-free MnBi intermetallic alloys are considered energy-critical materials due to their applications in high temperature power electronics and green energy-related generators and motors, owing to their positive temperature coefficient of magnetic anisotropy. However, a direct method to achieve high saturation magnetization, without the significant loss of coercivity, is critical for attaining high performance MnBi magnets. Here, we demonstrate the synthesis and processing of magnetic nanocomposites, consisting of metal-redox MnBi nanoparticles and electro-spun FeCo nanowires. The composition ratio, processing dependent magnetism, and increased coercivity with increasing temperature, were studied in MnBi-FeCo nanocomposites. The magnetic performance of nanocomposites was dictated by interfacial coupling between magnetically hard MnBi and semi-hard FeCo nanowires, as well as the composition ratio and processing conditions. Solution processed MnBi-FeCo nanocomposites allow the potential for the development of high temperature and high performance rare-earth-free permanent magnets.

Ternary FeCoNi metallic nanostructures have attracted significant attention due to their high saturation magnetization, unique mechanical properties, and large corrosion resistance. In this study, we report a controlled synthesis of ternary FeCoNi nanocrystals using solution-based epitaxial core–shell nanotechnology. The thickness and stoichiometry of the FeCoNi nanocrystals affect their magnetic characteristics, which can be controlled by a phase transformation-induced tetragonal distortion. Furthermore, surface oxidation of the stoichiometry-controlled FeCoNi nanostructures can drastically enhance their magnetic coercivity (up to 8, 881.6 Oe for AuCu–FeCo), and optimize the AuCu–FeCo_0.8Ni_0.2 performance corresponding to the saturated magnetization of 134.4 emu·g^-1 and coercivity of 4, 036.7 Oe, which opens the possibility of developing rare-earth free high energy nanomagnets.

Multiferroic charge-transfer crystals have drawn significant interest due to their simultaneous dipolar and spin ordering. Numerous theoretical and experimental studies have shown that the molecular stacking between donor and acceptor complexes plays an important role in tuning charge-transfer enabled multifunctionality. Herein, we show that the charge-transfer interactions can be controlled by the segregated stack, consisting of polythiophene donor- and fullerene acceptor-based all-conjugated block copolymers. Room temperature magnetic field effects, ferroelectricity, and anisotropic magnetism are observed in charge-transfer crystals, which can be further controlled by photoexcitation and charge doping. Furthermore, the charge-transfer segregated stack crystals demonstrate external stimuli controlled polarization and magnetization, which opens up their multifunctional applications for all-organic multiferroics.