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In contrast to dia- and
paramagnetism, ferromagnetism is of
prime importance for electrical
engineering. It is, however, one of the most difficult material properties to
understand. |
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It is not unlike
"ferro"electricity, in
relying on strong interactions between neighbouring atoms having a permanent
magnetic moment m stemming from the spins of electrons. |
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But while the interaction between electric
dipoles can, at least in principle, be understood in classical and
semi-classical ways, the interaction between spins of
electrons is an exclusively quantum mechanical effect with no classical
analogon. Moreover, a theoretical treatment of the three-dimensional
case giving reliable results still eludes the theoretical physicists. |
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In the advanced section, a very
simplified view will be
presented, here we just accept the fact that only Fe, Co,
Ni (and some rare earth metals) show strong interactions between spins
and thus ferromagnetism in elemental crystals. |
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In compounds,
however, many more substances exist with spontaneous magnetization coming from
the coupling of spins. |
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There is, however, a relatively
simple theory of ferromagnetism, that gives
the proper relations, temperature dependences etc., - with one major drawback:
It starts with an unphysical
assumption. |
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This is the
mean field theory or
the Weiss
theory of ferromagnetism. It
is a phenomenological theory based on a central (wrong) assumption: |
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Substitute the elusive spin - spin
interaction between electrons
by the interaction of the spins with a very strong magnetic field. |
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In other words, pretend, that in addition to your external field
there is a built-in magnetic field which we
will call the Weiss field. The Weiss field
will tend to line up the magnetic moments - you are now treating ferromagnetism
as an extreme case of paramagnetism. The
scetch below illustrates this |
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Of course, if the material you are
looking at is a real ferromagnet, you don't
have to pretend that there is a built-in
magnetic field, because there is a large
magnetic field, indeed. But this looks like mixing up cause and effect! What
you want to result from a calculation is what you start the calculation with!
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This is called a self-consistent approach. You
may view it as a closed circle, where cause and effect loose their meaning to
some extent, and where a calculation produces some results that are fed back to
the beginning and repeated until some parameter doesn't change anymore. |
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Why are we doing this,
considering that this approach is rather questionable? Well - it works! It
gives the right relations, in particular the temperature dependence of the
magnetization. |
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The local magnetic field
Hloc for an external field
Hext then will be |
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Note that this has not much to do with the
local electrical field
in the Lorentz treatment. We call it "local" field, too, because
it is supposed to contain everything that acts locally, including the modifications we ought to
make to account for effects as in the case of electrical fields. But since our
fictitious "Weiss field" is so much larger than everything coming
from real fields, we simply can forget about that. |
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Since we treat this fictive field HWeiss as an
internal field, we write it as a superposition of the external field H
and a field stemming from the internal magnetic polarization J:
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With J =
magnetic
polarization and w = Weiss´s
factor; a constant that now contains the
physics of the problem. |
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This is the decisive step. We now
identify the Weiss field with the magnetic polarization that is caused by it.
And, yes, as stated above, we now do mix up cause and effect to some degree:
the fictitiuos Weiss field causes the alignments of the individual magnetic
moments which than produce a magnetic polarization that causes the local field
that we identify with the Weiss field and so on. |
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But that, after all, is what happens: the (magnetic moments of the) spins
interact causing a field that causes the interaction, that ....and so on . If
your mind boggles a bit, that is as it should be. The magnetic polarization
caused by spin-spin interactions and mediating spin-spin interaction just
is - asking for cause and effect is a
futile question. |
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The Weiss factor w now contains
all the local effects lumped together - in
analogy to the Lorentz
treatment of local fields, µ0, and the interaction
between the spins that leads to ferromagnetism as a result of some fictive
field. |
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But lets be very clear:
There is no internal magnetic field
HWeiss in the material before the spins become
aligned. This completely fictive field just leads - within limits - to the same
interactions you would get from a proper quantum mechanical treatment. Its big
advantage is that it makes calculations possible if you determine the parameter
w experimentally. |
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All we have to do now is to repeat
the calculations done for paramagnetism, substituting
Hloc wherever we had H. Lets see where
this gets us. |
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What we really want is the magnetic
polarization J as a function of the external field
H. Unfortunately we have a transcendental equation for J which
can not be written down directly without a "J" on the
right-hand side. |
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What we also like to have is the value of the
spontaneous magnetization J for no external field, i.e. for H
= 0. Again, there is no analytical solution for this case. |
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There is an easy graphical solution, however: We
actually have two equations for which must
hold at the same time: |
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The argument b
of the Langevin function is |
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| b |
= |
m · µ0 · (H + w · J)
kT |
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Rewritten for J, we get our first
equation: |
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| J |
= |
kT · b
w · m · µ0 |
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H
w |
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This is simply a straight line with a slope and
intercept value determined by the interesting variables H,
w, and T. |
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On the other hand we have the
equation for J, and this is our second independent equation
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| J |
= N · m ·
µ0 · L(b) = |
N · m · µ0 · L |
æ
è |
m · µ0 · (H + w
· J)
kT |
ö
ø |
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This is simply the Langevin function which we
know for any numerical value for b |
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All we have to do is to draw both functions in a J -
b diagram |
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We can do that by simply putting in some number
for b and calculating the results. The
intersection of the two curves gives the solutions of the equation for
J. |
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This looks like this |
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Without knowing anything about b, we can draw a definite conclusion: |
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For H = 0 we have two solutions (or none at all, if the straight line
is too steep): One for J = 0 and one for a rather large
J. |
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It can be shown that the solution for J
= 0 is unstable (it disappears for an arbitrarily small field
H) so we are left with a spontaneous
large magnetic polarization without an external magnetic field as
the first big result of the mean field theory. |
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We can do much more with the mean
field theory, however. |
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First, we
note that switching on an external magnetic
field does not have a large effect. J increases
somewhat, but for realistic values of H/w the change
remains small. |
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Second, we
can look at the temperature dependence of
J by looking at the straight lines. For T ® 0, the intersection point moves all the way out
to infinity. This means that all dipoles are now lined up in the field and
L(b) becomes 1. We obtain the saturation value Jsat |
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Third, we
look at the effect of increasing temperatures. Raising T increases the
slope of the straight line, and the two points of intersection move together.
When the slope is equal to the slope of the Langevin function (which, as
we know, is
1/3), the two points of solution merge at J = 0; if we
increase the slope for the straight line even more by increasing the
temperature by an incremental amount, solutions do no longer exist and the
spontaneous magnetization disappears. |
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This means, there is a critical
temperature above which ferromagnetism disappears. This is, of
course, the Curie temperature
TC. |
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At the Curie temperature
TC, the slope of the straight line and the slope of
the Langevin function for b = 0 must be
identical. In formulas we obtain: |
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dJ
db |
= |
kTC
w · m · µ0 |
= |
slope of the straight line |
dJ
db |
÷
÷
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b = 0 |
= |
N · m · µ0 · |
dL(b)
db |
= |
N · m · µ0
3 |
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We made use of our
old insight
that the slope of the Langevin function for b
® 0 is 1/3. |
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Equating both slopes
yields for TC |
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| TC |
= |
N · m 2 · µ02 ·
w
3k |
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This is pretty cool. We did not solve
an transcendental equation nor go into deep quantum physical calculations, but
still could produce rather simple equations for prime material parameters like
the Curie temerature. |
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If we only would know w, the Weiss
factor! Well, we do not know
w, but now we can turn the equation around: If we know
TC, we can calculate the Weiss factor w and thus
the fictive magnetic field that we need to
keep the spins in line. |
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In Fe, for example, we have
TC = 1043 K, m = 2,2 ·
mBohr. It follows that |
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| HWeiss |
= |
w · J = 1.7 · 109 A/m |
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This is a truly gigantic field strength telling us that quantum
mechanical spin interactions, if existent, are not to be laughed at. |
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If you do not have a feeling of what this number
means, consider the unit of H: A field of 1,7 ·
109 A/m is produced if a current of 1,7 · 109
A flows through a loop (= coil) with 1 m2 area. Even if
you make the loop to cover only 1 cm2, you still need 1,7
· 105 A. |
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We can go one step further and
approximate the
Langevin function again for temperatures >TC,
i.e. for b < 1 by |
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This yields |
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| J(T > TC) |
» |
N · m2 · µ02
3kT |
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(H + w · J) |
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From the equation for TC
we can extract w and insert it, arriving at |
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| J(T > TC) |
» |
N · m2 · µ02
3k(T TC) |
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H |
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Dividing by H gives the
susceptibility c for T >
TC and the final formula |
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| c |
= |
J
H |
= |
N · m2 · µ02
3k · (T TC) |
= |
const.
T TC |
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This is the famous
Curie law for the
paramagnetic regime at high temperatures which was a phenomenological thing so
far. Now we derived it with a theory and will therefore call it
Curie - Weiss law. |
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In summary, the mean field approach
ain´t that bad! It can be used for attacking many more problems of
ferromagnetism, but you have to keep in mind that it is only a description, and
not based on sound principles. |
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© H. Föll (Advanced Materials B, part 1 - script)