2004 Eq 7 Fit
2004 Eq 7 Fit
Ernst Schlömann
A review of high magnetic moment thin films for microscale and nanotechnology
applications
Applied Physics Reviews 3, 011301 (2016); https://doi.org/10.1063/1.4941311
A general theory concerning the properties of magnetic ~aterials h~vin~ a nonuniform saturation
magne t·Izat'IOn IS
. de loped
v In ethl's theory
. , the local saturatIOn magnetizatIOn . and the h local exchange
d h
interaction are assumed to vary in an arbitrary. manner througho~t the sample. It}S furt. er assume t ~t a
dc magnetic field is applied which is sufficiently large to magnetIz~ thesample ~ubstantIa~ly to saturatIOn.
The general theo;y is then specialized for a calculation of the static magnetlza~lOn? assummg.that ~he host
material contains inclusions of a material with a different satur~~ion magnetizatIOn. If. all mclus~ons are
. Iy Iarge, the effect of the exchange interaction becomes.neghglble
fair . h and a result
. .prevIOusly
f . denved
t f by
Nee! is obtained. The inclusion of exchange reduces the deViation of t. e magnehzatI~n rOI? I~S sa ura IOn
I 'cularly at low values'· of the internal field. If exchange IS neglected, this deViatIOn becomes
va ue, partl .• . h d . . . . fi't Th
infinitely large at zero internal fie!d. If exchange is mc~uded, how~ver, t e eVlatlOn remams ill e. e
theory is, therefore (for suitable materials), still approximately vahd at remanence.
to approximate the square roots in Eq. (1) by unity. The dipolar energy is, therefore,
The Fourier transforms of the magnetization are thus JCdip=27rV L k-2[k·M( -k) ][k·M(k)]. (14)
given by k
M+(k) = (2'YIi(M o)/V) 1/2L: 1f(k-k')a+( -k'), We now use Eq. (8) to express the energy in terms of
k' the operators a(k) and a+(k). It is apparent that
M_(k) = (2'YIi(Mo)/V) 1/2 L: 1fCk-k')aCk'), terms of zero, first and second order in these operators
k' occur, in addition to higher order terms which may be
Mz(k)=Mo(k)-C'/'h/V) La+(-k+k')a(k'), (8) neglected in the present context. Detailed expressions
k' for the first- and second-order terms are given below.
where Mo(k) is the kth Fourier component of the local The exchange energy in an inhomogeneous (but iso-
saturation magnetization Mo(r). tropic) material can generally be expressed as l3
In the following the spatial average of M.(r) is of
particular interest. According to the third line of JCex = f d3rC(r) [(VMx)2+ CVMy) 2+ (VMz)2], (15)
Eq. (8),
where C(r) is a local exchange constant, which is
(M z )= V-If d rMzCr)
3 proportional to the local exchange integral. Expressed
in terms of the operators a and a+ the exchange energy
=M.(k=O) contains terms of zeto and second order, in addition
to the higher order terms, which are here neglected.
= (Mo)- ('YIi/V) L a+(k)a(k). (9) The zero-order term of the Hamiltonian is of no
k
interest in the present context. The relevant terms of
Consider now the various contributions to the energy. the total Hamiltonian (sum of Zeeman, dipolar, and
If the applied dc magnetic field is Ho, the Zeeman exchange energy) can be expressed as
energy is
JC= L[fka+(k) +H.c.]
k
JCZ eeman = - !M.Hod3r= - V (M.)Ho
+ L{Akk,a+(k)a(k') +tCBkk'a+(k)a+( -k') +H.c.]l
kk'
=[ - V(Mo)+'Y1i L a+(k)a(k)]Ho. (10)
(16)
The dipolar energy is where H.c. represents the Hermitian conjugate of the
~ fM.HdiPd3r,
expression preceding it. The first-order contribution
JCdip= - (11) to the Hamiltonian arises from the dipolar energy. The
coefficientjk are according to Eqs. (14) and (8)
where the dipolar field H dip is the field generated by
the magnetization. In the quasistatic approximation jk= 27r (2')'1i (MoW) 1/2 L 1f(k- k') MoCk') k/k_' /k'2,
k'
Hdip(r) satisfies
(17)
V XHdip=O, where
V·Hdip = -47rv·M. (12) (18)
Thus, its Fourier transform Hdip(k) is given by The second-order term of the Hamiltonian contains
contributions from all three types of energy here con-
H diP (k)=-(47r/k2)k[k·M(k)]. (13) sidered. The coefficients A kk , and Bkk' are given by
These expressions contain indeterminate contributions (zero over zero) which arise from the uniform com-
ponent (zeroth Fourier component) of the dipolar field. Since this field is identical with the macroscopic de-
magnetizing field, we can combine it with the applied field and define the sum as the internal magnetic field. This
applies both to the de and the rf fields. In the following, we adopt this convention. The internal (demagnetized)
dc magnetic field is denoted by H, the externally applied magnetic field by Ho. We similarly distinguish between
the internal rf field h and the externally applied rf field h o. If all formulas are expressed in terms of the internal
fields, the indeterminate contributions to Akk' and B kk , must be set equal to zero for consistency.
13 See, e.g., C. Herring and C. Kittel, Phys. Rev. 81,.869 (1951).
5030 ERNST SCHLOMAC-;I'\
The diagonal components of the matrices Akk' and B kk , are of particular interest. They are given by
Ad'Yn==Akkhn=H+27r(Mo) L 11f(k-kz) 121 k2+ 12/kl+2(Mo) L1f(k-kz)C(k2-k3)1f(ka-k)k2'ka, (21)
k2 k2k,
B k hh==Bkkhh=27r(M o) L 11f(k-k
k2
2) 12 kZ_2/k22. (22)
For convenience, we introduce two significant approximations at this stage. The first of these is to assume the
exchange interaction C(r) to be uniform. With this approximation, the double sums in Eqs. (19) and (21) reduce
to single sums. The result of the calculation shows that the exchange energy is of secondary importance in the
present context. Thus, a more elaborate consideration of nonuniform exchange appears unwarranted.
We further assume that the inhomogeneity of the local saturation magnetization Mo(r) is "weak". This implies
that
(23)
k";O
Consistent with these approximations, Eqs. (17), (19), and (22) become
jk= 27r(2'YhMo V) J 12Mo(k) kzL/k2, (17a)
Akk'hh=+27r(Mo)1f(k-k') II k+ \z/k2 +1 k/ \2/k'2_4[(k z -k/)z/(k-k')2]1
+1¥(k-k') (4k· k'-kZ -k'2) krfk', (19a)
Bkk'hh= 27r(Mo)1f( k- k') (k_2/k2+k_'2/k'2) krfk', (20a)
Akhh=H+27r(Mo)(1 k+ 12/k ) +Dk2, 2 (21a)
Bkhh=27r(Mo)L2/k2, (22a)
actually depend only upon the magnitude of knot where the function <I>(k) depends only upon the magni-
upon its direction. The summation in Eq. (32) can, tude, not upon the direction of k, and is normalized
therefore, be carried out by first taking an average such that
over the angular factors and then summing the terms
dependent upon 1 k 1= k.
The problem simplifies considerably if the local
saturation magnetization varies relatively "slowly" From Eqs. (32), (33), and (39), we now obtain
with position. This is the case treated by Neel,1·2
In this case Mo(k) is significantly large only for small k. (Mz)=(Mo)[1-tuF(u)], (41)
In the present context, the variation of Mo(r) is where
called "slow", if the exchange contribution to Ak is
negligible (i.e., Dk2«H) for all k with a significantly F(u) = (V/27r2) ["k 2dk<I>(k)f(U+Dk 2/47r(Mo»)
o
large Mo(k). We show later that this applies for
instance in the case of spherical inclusions, if the
radius of the inclusions is sufficiently large. (42)
For convenience, we introduce the abbreviation
Here,f(u) is given by Eq. (38),
u= 2: 1Mo(k) 12/Mo(0) 2. (33)
kr'O ~=Dk2/47r(Mo), (43)
Here the sum is equal to the mean square deviation and
of the local saturation magnetization from its average wW = (V~1/2/ 47r2) (47r(Mo)/ D) 3/2<I>[ (~47r(Mo)/ D)1/2]
value
(44)
2: 1Mo(k) 12= 2: 1Mo(k) 12_Mo(0)2
kr'O all k is a weight function which is normalized to unity:
= (M02)- (MO)2
(45)
= «~MO)2), . (34)
where the angular brackets denote a spatial average. In the Appendix, the Fourier spectrum <I>(k) and the
The parameter associated weight function w(~) are calculated in detail
(35) for the case of spherical inclusions. If all inclusions are
assumed to have the same saturation magnetization
is a measure of the degree of inhomogeneity. and the same radius Ti, the result is
We also introduce a reduced, dimensionless variable
u proportional to the internal field wW =tt"lJ3/2 2 [(Uc)1/2], (46)
where
u=H/47r(Mo). (36) C = D/T147r(Mo) ( 47)
With this convention from Eq. (32), and J3/2 is the Bessel function of order t.
In Fig. 2, the function cw(~) is plotted vs Uc. For
(Mz)= (Mo)[1-tuf(u)], (37)
Uc»1, the weight function behaves as
where
2 2 w(~)"-'(3hr)cl/2t"3/2 cos2[(Uc)1/2]. (48)
fe u) -/'oldx (u+1-X
x (1-x
2)2
)
If the quasiperiodic variation is disregarded (i.e., the
cos2 term replaced by t) the weight function can for
3 3u+2 . ~»c be approximated by
=- -
2
+ 2(u+1)1/2 smh- (U- 1/2 )
l (38)
wW = (3/27r)Cl/2~-3/2. (49)
and x=cosO. This agrees with Neel's result,1·2
Consider now the effect of the exchange interaction This function is shown in Fig. 2 as a broken line.
upon the static magnetization. It is obvious that this For spherical inclusions of equal radius the weight
interaction tends to keep the local magnetization vectors function w(O depends only upon a single parameter
in adjacent regions of the sample more nearly aligned. (namely c). We shall denote the function F(u) cal-
In order to carry out the calculation the Fourier spec- culated using this particular weight function as F(u, c).
trum 1Mo(k) 12 of the local saturation magnetization In Fig. 3, the function F(u, c) is plotted vs u with
must be determined. As long as the magnetization is c as parameter. The curves were obtained by nu-
isotropically distributed the Fourier spectrum can, in merically integrating Eq. (42) using the actual weight
general, be expressed as function wW defined by Eq. (46) for O<Uc< 100
and the smoothed out, approximate function w(~) de-
fined by Eq. (49) for 100 < Uc< 00. It should be noted
5032 ERNST SCHL()MANN
appraximatian,
o.
(M.)= (Mo)(l-a/H) , (SO)
where in the limit c---c>O
ewl(lo t i'[l t Iyt 1]2
yo (Ie 1
J
(51)
The caefficient a is frequently referred to as the mag-
004 netic hardness caefficient.
0.03
IV. DISCUSSION
002
where In is l/V times the integral of exp( -ik.r) small the transition from Eg. (A7) to Eg. (AS) in-
taken over the nth inclusion. volves a finite error, because the inclusions cannot inde-
pendently assume all possible locations in the periodicity
f
In= (l/V) cPr exp( -ik·r) volume.
In order to estimate the magnitude of this error,
consider the special case in which all Mn are equal to Mi.
According to Eq. (34) L.kfo II Mo(k) 12 must generally
equal «IJ.MO)2)=(Mo2)_(Mo)2. It will be shown that
this is only approximately true for Eg. (AS). The dis-
x i:1d (cosO) exp( -ikp cosO) crepancy is a measure of the error involved in the
transition from Eq. (A7) to (AS).
=exp( -ik·Rn) (vn/V) g(kan). (A2) For the case under consideration
Here (Mo2)=M/(1-p) +Mlp (A9)
(A3) and hence
is the volume of the nth inclusion, and (A1O)
g(y) =3y-3 (siny-y cosy) Using well-known integral relations between Bessel
functions,17 the integration over the k dependent factors
= 3 (!1l') J 12y- 3/2J 3/ 2(y) , (A4) in Eg. (AS) can be carried out
where J a/2 is the Bessel function of order l
It should be noticed that g(O) = 1 and hence, assum-
ing that all Mn are equal to M i ( = saturation magnetiza-
tion of the inclusion), Thus, from Eqs. (AS), (A6) , and (All)
Mo(O) =M.(l-p)+MiP, (AS) L.I Mo(k) IAV2 = (M.-MYp. (AI2)
k
where
p= L. Vn/V (A6) Comparison of Eqs. (AlO) and (A12) shows that for
n
p«l the two results agree very closely, so that Eg.
is the ratio of the total volume of the inclusions to the (AS) appears well justified.
sample volume. We now define a normalized spectral function <I>(k)
Consider now I Mo(k) 12 for k~O. According to according to Eqs. (39) and (AS).
Eqs. (AI) and (A2)
<I>(k) = V-I L. vr,zg2(kan )/'E Vn • (AB)
I Mork) 12 = V-2 L. (M.-Mn) (M.-M n,) n n
nn' It can readily be shown that <I>(k) satisfies the normal-
X exp[ik· (Rn-Rn,)]vnvn'g(kan)g(kan')' (A7) ization condition (40) exactly. Thus, the slight error
made in the transition from Eq. (A7) to Eq. (A8) is
Since the location of the inclusions is not actually
largely compensated if we use this convention.
known, it is reasonable to take an average of I MoCk) 12
If all inclusions are equal in size (in addition to being
over all possible locations of the inclusions and to
spherical), the spectral function becomes
assume that this average value is representative of the
actual sample under consideration. If the total volume <I>(k) = (41l'rN3V)g2(kri)
of the inclusions is small each inclusion can be located
with equal probability at any point within the perio- = (61l'2/Vk3)[Ja/2(kri)]2, (A14)
dicity volume. Under these conditions the average of
where r i is the radius of each inclusion. The corre-
exp[ik· (Rn-R n,)] vanishes unless n=n'. Equation
sponding weight function wW as defined by Eg. (44)
(A7) thus becomes is given by Eg. (46).
I MoCk) IA,2= V-2 L.(M.-Mn)2Vn2g2 (ka n). (AS)
n
17 See, e.g., Handbook of Mathematical Functions, U.S. Dept.
If the volume of the inclusions is not infinitesimally of Commerce, Nat!. Bur. Std. Appl. Math. Ser. 55, Eq. (11.4.6)