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Submitted on 1 Jan 1988
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FINITE-SIZE EFFECTS IN ULTRATHIN MAGNETIC
LAYERS
U. Gummich, G. Cabrera, C. E. T. da Silva
To cite this version:
JOURNAL DE PHYSIQUE
Colloque C8, Suppl6ment au no 12, Tome 49, d6cembre 1988
FINITE-SIZE EFFECTS IN ULTRATHIN MAGNETIC LAYERS
U. Gummich, G. G. Cabrera and C. E. T. Gon~alves da SilvaInstituto de Fisica "Gleb Wataghin" , Universidade Estadual de Campinas, Caixa Postal 61 65, 13.081 Campinas, S6o Paulo, Brazil
Abstract.
-
We study thin ferro and antiferromagnetic films for the Heisenberg model using a modified version of the Onsager reaction field approximation adapted for finite-size layered systems. No phase transition is obtained for the finite system, but spin-spin correlations are enhanced when the number of layers increases.Introduction
Molecular beam epitaxy techniques have become a sophisticated tool to produce ultrathin magnetic films approaching the monolayer limit. In particular the MnSeIZnSe superlattice in the zinc-blende structure has been recently studied with special interest on the magnetic properties of MnSe ultrathin layers [I]. Al- though bulk MnSe is known to be antiferromagnetic, the ultrathin layer behaves as paramagnetic. It has been suggested that this result can be explained in terms of a dimensionality crossover when the layer thickness is reduced to a few monolayers [I], with no phase transition for the two dimensional system. This fact agrees with some general theorems which preclude the presence of long-range orde in two dimensions [2].
Stimulated by the above experiments, we engaged ourselves in the theoretical study of the size effects in a layered Heisenberg system as a function of the layer thickness, using a modified version of the Onsager re- action field approximation (RFA) [3] adapted to treat a multilayer thin film. Preliminary results for the ferro- magnetic system have been published elsewhere [4]. In
Full two-dimensional periodicity in the yz directions is maintained and we use two dimensional lattice vectors {Rj) for sites and an index n to lab el the different layers. In the antiferromagnetic case Rj is a lattice vector in a Bravais latticee with a basis of two spins to describe possible antiferromagnetic ordering.
Partial Fourier transform in two dimensions is done using Q vectors in a two dimensional Brillouin zone,
Q
= ( Q Y , Q Z )where the subscript v labels the spin components, v =
x,
y, z ; No is the number of spins per layer (and per sublattice in the case of antiferromagnetism), and the spin has been chosen as S = 5 / 2 which is the case of Mn.The Heisenberg Hamiltonian with nearest neighbors interactions
the present contribution we want to report additional
is treated through a mean field approach where the results which include both, the ferro and antiferromag-
local effective field is given by netic cases. Our analytical results point to the absence
of a phase transition in a film of finite thickness, in
contrast to approaches using different approximations H% (Q, n) = J (Q
I
nm)(s'
(Q, m ) ) - ~(9,
n)-
The model
We model our layered system through layer depen- dent quantities: magnetization parameters for each layer (two sublattices for antiferromagnetic coupling) which measure the long-range order if present; RF pa- rameters which play the role of local short-range order parameters and are normalized t o the number of near- est neighbors for a given layer.
The presence of an external magnetic field paral- lel to the film surface is allowed, in order to avoid demagnetizing effects. The direction of spin quanti- zation (ziaxis) is then chosen along the direction of the field (and corresponding to one of the cube axis).
H ~ E (Q, n) = J (Q
I
nm) (SP (Q, m ) ) - H (Q, n) -where a and
p
stand for the two different sublat- tices in the case of antiferromagnetism (for the fer- romagnetic system both expressions in (3) are iden- tical), J (QI
nm) is the partial Fourier transform of the exchange interaction, and the angle brackets stand for statistical averages. The standard mean field ap- proximation is obtained without the last term in the right hand side of formulae (3), being X u (n) the RF parameter for the wth layer and the cr sublattice (cr = a,p)
.
In our approach the mean field is corrected by the reaction field in order to take into accountC8
-
1702 JOURNAL DE PHYSIQUE spin-spin correlations. The inclusion of this effect s u ppresses the phase transition in two dimensions. Since the
Xu
(n) parameters are essentially spin-spin corre- lations, they are directly linked to the susceptibility through the fluctuation-dissipation theorem. A self- consistent equation is obtained if one notes that the susceptibility can also be obtained from the magneti- zation as a derivative in relation to the external field [41.Summation over the two dimensional Brillouin zone has been done using the special point scheme devel- oped by Cunningham [6]. The particular cases N = 1
(two dimensions) and N --, co (three dimensions) can be studied analytically. In the limit N --, co one re- covers the three dimensional behavior (71 with a phase transition at a critical temperature given by
for the simple cubic structure, for both ferro (Jij
<
0) and antiferromagnetism (Jij>
0) .Tc, is the standardCurie-Weiss (mean field) transition temperature. Numerical results and discussions
For the ferromagnetic case, we have obtained nu- merical results up to 10 layer thicknesses for differ- ent values of temperature and magnetic field. All the cases display the same qualitative behavior with the absence of a phase transition. Surface effects for free end boundary conditions fall off very quickly when go- ing to the interior of the film: for all practical purpose, the N = 3 case illustrates the general situation. When an external magnetic field is applied the magnetization parameters saturate a t low temperature to the value S = 512, with a typical paramagnetic behavior. The
e
Fig. 1. - Magnetization parameters for the three layer sys- tem as a function of temperature. The magnetic field is
H = 2 I J I , where J is the exchange constant, and 6 is the reduced temperature (1 J] 0 = k B T )
.
Magnetization for the inner layer is M ( 2 ) , and the superscripts F and AF label the ferro and antiferromagnetic cases. For the surfaces we get M (1) = M (3) a s required by symmetry. The continu- ous line depicts the Brillouin function for S = 512 (spin of Mn), as a reference.Fig. 2. - RF parameters as functions of temperature for the three layer system. Notation is the same as in figure I, and the external magnetic field is also H = 2
1
JI.
Displayed quantities for t h e antiferromagnetic case are negative.same occurs for the RF parameters, where normaliza- tion at T = 0 is given by the coordination number. In figures 1 and 2 we are displaying their variation as a function of temperature for the three layer system, and for a particular value of the magnetic field.
Concerning the antiferromagnetic case (Jij
>
0),
the RE' parameters are mainly negative indicating the presence of distinctive antiferromagnetic correlations of short range. Long-range order does not develop in the system, as can be seen in figure 1 for the magnetiza, tion parameters. Since we are always in the paramag- netic region, both sublattice magnetizations are equal. The small values shown in figure 1 can be understood based on physical grounds: the spins are frustrated as a result of the competition between the antiferromag- netic coupling and the tendency of alignment along the applied field.Is is still not clear, within the approximation de- veloped here, if the inclusion of anisotropic effects will induce a phase transition in finite-width systems. This point is currently under study.
[I] Nurmikko, A. V., Lee, D;, Hefetz, Y., Kolodziejski, L. A. and Gunshor, R. L., Proc. 18th Intern. Conf. on Physics of Semiconductors, Ed. 0. Engstrom (World Scientific, Singapore) 1987, p. 775.
[2] Mermin, N. M. and Wagner, H., Phys. Rev. Lett. 17 (1966) 1133.
[3] Brout, R. and Thomas, H., Physics 3 (1967) 317. [4] Gummich, Ute, Cabrera, G. G. and Gon~alves da
Silva, C. E. T., Surf. Sci. 196 (1988) 643. [5] Diep-The-Hung, Levy, J. C. S. and Nagai, O.,
Phys. Status Solidi B 93 (1979) 351.
[6] Cunningham, S. L., Phys. Rev. B 12 (1974) 4988. [7] Scherer, C. and Aveline, I., Phys. Status Solidi B