scholarly journals Absence of stable collinear configurations in Ni(001) ultrathin films: Canted domain structure as ground state

2002 ◽  
Vol 65 (21) ◽  
Author(s):  
G. Gubbiotti ◽  
G. Carlotti ◽  
M. G. Pini ◽  
P. Politi ◽  
A. Rettori ◽  
...  
1996 ◽  
Vol 156 (1-3) ◽  
pp. 1-6 ◽  
Author(s):  
E. Bauer ◽  
T. Duden ◽  
H. Pinkvos ◽  
H. Poppa ◽  
K. Wurm

2010 ◽  
Vol 168-169 ◽  
pp. 269-272 ◽  
Author(s):  
A.A. Ivanov ◽  
V.A. Orlov ◽  
N.N. Podolsky

The ground state magnetization of nanowires built of ferromagnetic crystallites is considered taking into account the magnetostatic interaction. The criterion of formation of domains is found. The thickness of a domain wall is calculated analytically and the results are compared with the numerical simulations. We show that when the exchange coupling between crystallites is absent its role is played by magnetostatics that ensures the existence of stable domain structure. The direction of the induced anisotropy axis is shown to be determined by the shape of crystallites.


1990 ◽  
Vol 42 (3) ◽  
pp. 1668-1673 ◽  
Author(s):  
J. Z. Wu ◽  
S. B. Trickey ◽  
J. C. Boettger

1991 ◽  
Vol 232 ◽  
Author(s):  
G. Lugert ◽  
G. Bayreuther ◽  
S. Lehner ◽  
G. Gruber ◽  
P. Bruno

ABSTRACTUltrathin epitaxial films grown in UHV – Fe(110) on Au(111) and Ag(111), Co(0001) on Au(111) – , sputtered Fe films between Ag and sputtered Fe/Au multilayers were studied by SQUID magnetometry and Mössbauer spectroscopy (CEMS). It could be shown that the magnetic anisotropy relative to the film normal, the, ground state magnetic moment per Fe atom and thermal spin excitations are affected by the structure of the films. In particular, a more 3-dimensional growth mode in the early state of film formation which is observed except in a certain temperature range around 300 K reduces the apparent magnetic interface anisotropy and the ferromagnetic ground state moment, and it enhances the thermal spin fluctuations and the tendency for superparamagnetic relaxation in the thinnest films.


Sign in / Sign up

Export Citation Format

Share Document