Rare earth magnets are the strongest type of permanent magnets and are integral to the high tech industry, particularly in clean energies, such as electric vehicle motors and wind turbine generators. However, the cost of rare earth materials and the imbalance in supply and demand still remain big problems to solve for permanent magnet related industries. Thus, a magnet with abundant elements and moderate magnetic performance is required to replace rare-earth magnets. Recently, a”-Fe₁₆N₂ has attracted considerable attention as a promising candidate for next-generation non-rare-earth permanent magnets due to its gigantic magnetization (3.23 T). Also, metastable a”-Fe₁₆N₂ exhibits high tetragonality (c/a = 1.1) by interstitial introduction of N atoms, leading to a high magnetocrystalline anisotropy constant (K₁ = 1.0MJ/m³). In addition, Fe has a large amount of reserves on the Earth compared to other magnetic materials, leading to low cost of raw materials and manufacturing for industrial production. In this paper, we review the synthetic methods of metastable a”-Fe₁₆N₂ with film, powder and bulk form and discuss the approaches to enhance magnetocrystalline anisotropy of a”-Fe₁₆N₂. Future research prospects are also offered with patent trends observed thus far.

Citations

Citations to this article as recorded by  

• Failure Cases according to Photocuring-Based Alumina 3D Printing
  So-Young Ko, Shin-Il Go, Kyoung-Jun Jang, Sang-Jin Lee
  Korean Journal of Materials Research.2024; 34(10): 457.     CrossRef

We report a facile method for preparing KIT-1 mesoporous silicates with two different macroporous structures by dual templating. As a template for macropores, polystyrene (PS) beads are assembled into uniform three dimensional arrays by ice templating, i.e., by growing ice crystals during the freezing process of the particle suspension. Then, the polymeric templates are directly introduced into the precursor-gel solution with cationic surfactants for templating the mesopores, which is followed by hydrothermal crystallization and calcination. Later, by burning out the PS beads and the surfactants, KIT-1 mesoporous silicates with macropores are produced in a powder form. The macroporous structures of the silicates can be controlled by changing the amount of EDTANa4 salt under the same templating conditions using the PS beads and inverse-opal or hollow structures can be obtained. This strategy to prepare mesoporous powders with controllable macrostructures is potentially useful for various applications especially those dealing with bulky molecules such as, catalysis, separation, drug carriers and environmental adsorbents.

In this study, we synthesize silica-core gold-satellite nanoparticles (SGNPs) for the surface-enhanced Raman scattering (SERS) based sensing applications. They consist of gold satellite nanoparticles (AuNPs) fixed on the silica core nanoparticles, which sizes of AuNPs can be tunned by varying the amount of reactants (growth solution and reducing agent). Their surface plasmon resonance (SPR) properties were characterized by using UV-vis spectroscopy, showing that the growth of AuNPs on silica cores leads to the light absorption in the longer wavelength region. Furthermore, the size increase of AuNPs exhibited the dramatic change in SERS activity due to the formation of hot spots. The optimized SGNPs showing enhancement factor~3.8×10⁶ exhibited a detection limit of rhodamine 6G (R6G) as low as 10⁻⁸ M. These findings suggest the importance of size control of SGNPs and their SPR properties to develop highly efficient SERS sensors.

In this study, we prepare polymer solar cells incorporating organic ligand-modified Ag nanoparticles (OAgNPs) highly dispersed in the P3HT:PCBM layer. Ag nanoparticles decorated with water-dispersible ligands (WAgNPs) were also utilized as a control sample. The existence of the ligands on the Ag surface was confirmed by FTIR spectra. Metal nanoparticles with different surface chemistries exhibited different dispersion tendencies. O-AgNPs were highly dispersed even at high concentrations, whereas W-AgNPs exhibited significant aggregation in the polymer layer. Both dispersion and blending concentration of the Ag nanoparticles in P3HT:PCBM matrix had critical effects on the device performance as well as light absorption. The significant changes in short-circuit current density (J_SC) of the solar cells seemed to be related to the change in the polymer morphology according to the concentration of AgNPs introduced. These findings suggested the importance of uniform dispersion of plasmonic metal nanoparticles and their blending concentration conditions in order to boost the solar cell performance.

Citations

Citations to this article as recorded by  

• Reactive ceramic pellets incorporated iron for removing As(III), As(V), and Cr(VI) from aqueous solutions
  Sunwon Rha, Yun Sik Gong, Ho Young Jo
  Desalination and Water Treatment.2019; 158: 174.     CrossRef
• Application of Physical and Chemical Enhanced Backwashing to Reduce Membrane Fouling in the Water Treatment Process Using Ceramic Membranes
  Seogyeong Park, Joon-Seok Kang, Jeong Jun Lee, Thi-Kim-Quyen Vo, Han-Seung Kim
  Membranes.2018; 8(4): 110.     CrossRef
• Effects of particle size and forming pressure on pore properties of Fe-Cr-Al porous metal by pressureless sintering
  Bon-Uk Koo, Yujeong Yi, Minjeong Lee, Byoung-Kee Kim
  Metals and Materials International.2017; 23(2): 336.     CrossRef
• Characterization and Microstructure of an Extruded Flat-Tubular-Type Alumina Filter
  Byung-Seo Bae, Jang-Hoon Ha, In-Hyuck Song
  Journal of the Korean Ceramic Society.2014; 51(5): 406.     CrossRef