Abstract

SmCo-based permanent magnets possessing high Curie temperature and outstanding magnetocrystalline anisotropy are of great scientific and technological value on high temperature applications. It is widely accepted the coercivity mechanism as well as its temperature dependence is closely related to the microstructure and microchemistry. However, direct domain wall pinning observation with Lorentz microscopy is extremely difficult to explore the strength of domain wall pinning under high temperature and strong magnetic field. The quantitatively understanding of coercivity mechanism such as micromagnetic simulations cannot be carried out without the intrinsic magnetism of 1:5H and 2:17R inside the cellular microstructure of SmCo sintered magnets. Up to nowadays, there are no methods to directly measure the intrinsic magnetism of nanometer scale 1:5H and 2:17R, which retards the exploring of coercivity mechanism especially at high temperature. Herein, we prepared Sm(CoCuFeZr)z high-temperature permanent magnets with the ratio z values ranging from 7.0 to 7.8 and measured the microchemistry of 1:5H and 2:17R phases with transmission electron microscopy. Then single-phase solid solution samples with the same composition as 1:5H and 2:17R phases were prepared and the high temperature magnetic properties are measured directly. The coercivity mechanism can be well explained based on the difference of domain wall energy density qualitatively, including the abnormal temperature dependence of coercivity. More importantly, the quantitatively calculated coercivity according to the pinning-hardened coercivity theory with the obtained intrinsic parameters were found to agree well with the experiment results. Our work on the intrinsic magnetism of 1:5H and 2:17R phases at varying temperatures may offer important guidance for compositions design of the magnets with higher performance.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call