Magnetization of 2-17 type Sm-Co transition metal sintered permanent magnets

1986 ◽  
Vol 22 (5) ◽  
pp. 769-771 ◽  
Author(s):  
H. Mildrum
1988 ◽  
Vol 49 (C8) ◽  
pp. C8-573-C8-574
Author(s):  
G. F. Zhou ◽  
X. K. Sun ◽  
Y. C. Chuang ◽  
L. Gao ◽  
Z. Yu ◽  
...  

1990 ◽  
Author(s):  
R. Grossinger ◽  
X.C. Kou ◽  
R. Krewenka ◽  
H.R. Kirchmayr ◽  
M. Tokunaga

2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Yong-Jin Kim ◽  
Chan-Ho Yang

AbstractTransition metal oxides (TMOs) are an important class of materials that show a wide range of functionalities involving spin, charge, and lattice degrees of freedom. The strong correlation between electrons in d-orbitals and the multivalence nature give rise to a variety of exotic electronic states ranging from insulator to superconductor and cause intriguing phase competition phenomena. Despite a burst of research on the multifarious functionalities in TMOs, little attention has been paid to the formation and integration of an electret—a type of quasi-permanent electric field generator useful for nanoscale functional devices as an electric counterpart to permanent magnets. Here, we find that an electret can be created in LaMnO3 thin films by tip-induced electric fields, with a considerable surface height change, via solid-state electrochemical amorphization. The surface charge density of the formed electret area reaches ~400 nC cm−2 and persists without significant charge reduction for more than a year. The temporal evolution of the surface height, charge density, and electric potential are systematically examined by scanning probe microscopy. The underlying mechanism is theoretically analyzed based on a drift-diffusion-reaction model, suggesting that positively charged particles, which are likely protons produced by the dissociation of water, play crucial roles as trapped charges and a catalysis to trigger amorphization. Our finding opens a new horizon for multifunctional TMOs.


1987 ◽  
Vol 18 (7-8) ◽  
pp. 93-96 ◽  
Author(s):  
D. Givord

2010 ◽  
Vol 123-125 ◽  
pp. 727-730 ◽  
Author(s):  
Abdulaziz A. Bagabas ◽  
Khalil A. Ziq ◽  
Ahmad F. Salem ◽  
Emad S. Addurihem

Nanoscale particle size of metal oxides and hydroxides showed enhanced various physical properties and performance. We established a simple, cost-effective, room-temperature (RT) precipitation method for the preparation of the magnetic, first-raw transition metal (TM) hydrated oxide and hydroxide nanoparticles. This method is based on the use of the TM nitrate, as the metal source, and cyclohexylamine (CHA), as a precipitating agent, either in the water (H2O) or ethanol (EtOH) medium. We found that the precipitation medium and the identity of precipitated TM strongly affect the morphology, particle size, and magnetism of the product. The morphology varies from spherical, to rectangular, to rod shape; while the size varies in the range of 5-30 nm. All samples showed paramagnetic behavior with Curie temperatures span over a wide range (20-150K). Huge hysteresis looses has been observed for manganese (Mn) sample, prepared in H2O. The coercively (Hc) at 4.2K for this sample is about 1.5T, which is comparable to the strongest permanent magnets (Nd-based magnets) available at room temperature. The energy product (Hc*MR) is about 4.5*105 (emu/g)Oe.


Sign in / Sign up

Export Citation Format

Share Document