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and
I ( r ) e −i q · r d r .
I ( q )= 1
V
(1 . 4 . 17)
Summing over the lattice sites, counting each interaction once only, we
find that the indirect-exchange interaction takes the familiar isotropic
Heisenberg form:
χ ( q ) I ( q ) I (
(2 π ) 3
ij
1
2
V
N 2 µ 2 B
V
q ) e i q · ( R i R j ) S i · S j d q
H ff =
2 N
q
ij J S ( q ) e i q · ( R i R j ) S i · S j
1
=
2
1
=
ij J S ( ij ) S i · S j ,
(1 . 4 . 18)
where
N
J S ( ij )= 1
q J S ( q ) e i q · ( R i R j )
(1 . 4 . 19)
and
V
2 B |
2 χ ( q ) .
J S ( q )=
I ( q )
|
(1 . 4 . 20)
In the presence of an orbital moment, it is convenient to express
(1.4.18) in terms of J rather than S , which we may do within the ground-
state multiplet by using (1.2.29) to project S on to J , obtaining
2
1
H ff =
ij J
( ij ) J i · J j ,
(1 . 4 . 21)
with
1) 2
q J S ( q ) ,
N
1
J
( q )=( g
J S ( q )
(1 . 4 . 22)
where we have also subtracted the interaction of the i th moment with
itself, as this term only leads to the constant contribution to the Hamil-
tonian;
1
1) 2 N
J S ( ii ) J ( J + 1). The origin of the indirect ex-
change in the polarization of the conduction-electron gas by the spin
on one ion, and the influence of this polarization on the spin of a
second ion, is apparent in the expression (1.4.20) for
2 ( g
J S ( q ).
As we
shall see, it is the Fourier transform [
( 0 )] which may be di-
rectly deduced from measurements of the dispersion relations for the
magnetic excitations, and its experimentally determined variation with
q in the c -direction for the heavy rare earths is shown in Fig. 1.17.
J
( q )
−J
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