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Solid State Physics The important quantity for many purposes is the energy density of

the magnet.

MAGNETISM I
Lecture 27

A.H. Harker
Physics and Astronomy
UCL

10 Magnetic Materials 10.1 Magnetic properties - reminder

Magnet technology has made enormous advances in recent years – There are two fields to consider, the magnetic field H which is gener-
without the reductions in size that have come with these advances ated by currents according to Ampère’s law, and the magnetic induc-
many modern devices would be impracticable. tion, or magnetic flux density, B, which gives the torque experienced
by a dipole moment m as G = m × B. H is measured in A m−1 (Oer-
steds in old units), B in Wb m−2 or T (Gauss in old units). In free
space, B = µ0H. In a material
B = µ0(H + M)
= µ0 µr H
= µ0(1 + χ)H,
where µr is the relative permeability, χ is the magnetic susceptibility,
which is a dimensionless quantity.

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Note, though, that χ is sometimes tabulated as the molar susceptibility 10.2 Measuring magnetic properties
χm = Vmχ, 10.2.1 Force method
where Vm is the volume occupied by one mole, or as the mass suscep- Uses energy of induced dipole
tibility
χ 1 1
χg = , E = − mB = − µ0χV H2,
ρ 2 2
where ρ is the density. M, the magnetisation, is the dipole moment so in an inhomogeneous field
per unit volume. dE 1 dH2 dH
M = χH. F =− = µ0 V χ = µ0V χH .
dx 2 dx dx
In general, µr (and hence χ) will depend on position and will be ten- Practically:
sors (so that B is not necessarily parallel to H). Even worse, some
materials are non-linear, so that µr and χ are field-dependent. • set up large uniform H;
• superpose linear gradient with additional coils
• vary second field sinusoidally and use lock-in amplifier to measure
varying force

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10.2.2 Vibrating Sample magnetometer

• oscillate sample up and down


• measure emf induced in coils A and B
• compare with emf in C and D from known magnetic moment
The effects are highly exaggerated in these diagrams. • hence measured sample magnetic moment
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10.3 Experimental data If we assume the charge keeps moving in a circle of the same radius (a
vague nod towards quantum mechanics?) it will have a new angular
velocity ω 0,
meω 02a = F − ∆F
so
meω 02a = meω 2a − eωaB,
or
eωB
ω 02 − ω 2 = − .
me
If the change in frequency is small we have
ω 02 − ω 2 ≈ 2ω∆ω,
where ∆ω = ω 0 − ω. Thus
eB
∆ω = − ,
2me
the Larmor frequency. Substituting back into
In the first 60 elements in the periodic table, the majority have nega- µ = IA = eωa2/2.
tive susceptibility – they are diamagnetic.
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10.4 Diamagnetism we find a change in magnetic moment


Classically, we have Lenz’s law, which states that the action of a mag- e2a2
µ=− B.
netic field on the orbital motion of an electron causes a back-emf 4me
which opposes the magnetic field which causes it. Frankly, this is Recall that a was the radius of a ring of current perpendicular to the
an unsatisfactory explanation, but we cannot do better until we have field: if we average over a spherical atom
studied the inclusion of magnetic fields into quantum mechanics us- 2h 2 i 2
ing magnetic vector potentials. Imagine an electron in an atom as a = hx i + hy i = hx i + hy i + hz i = hr2i,
2 2 2 2 2
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a charge e moving clockwise in the x-y plane in a circle of radius a, so
area A, with angular velocity ω. This is equivalent to a current e2hr2i
µ= B,
I = charge/time = eω/(2π), 6me
and finally, if we have n atoms per volume, each with p electrons in
so there is a magnetic moment
the outer shells, the magnetisation will be
µ = IA = eωa2/2.
M = npµ,
The electron is kept in this orbit by a central force
F = meω 2a. and
M M µ npe2hr2i
Now if a flux density B is applied in the z direction there will be a χ= = µ0 =− 0 .
H B 6me
Lorentz force giving an additional force along a radius
∆F = evB = eωaB
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Values of atomic radius are easily calculated: we can confirm the Diamagnetic susceptibility:
phr2i dependence. • Negative
• Typically −10−6 to −10−5
• Independent of temperature
• Always present, even when there are no permanent dipole mo-
ments on the atoms.

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10.5 Paramagnetism
Paramagnetism occurs when the material contains permanent mag-
netic moments. If the magnetic moments do not interact with each
other, they will be randomly arranged in the absence of a magnetic
field. When a field is applied, there is a balance between the internal
energy trying to arrange the moments parallel to the field and en-
tropy trying to randomise them. The magnetic moments arise from
electrons, but if we they are localised at atomic sites we can regard
them as distinguishable, and use Boltzmann statistics.

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10.5.1 Paramagnetism of spin- 12 ions Clearly, though, for low T or large B the magnetic moment per atom
saturates – as it must, as the largest magnetisation possible saturation
The spin is either up or down relative to the field, and so the magnetic magnetisation has all the spins aligned fully,
moment is either +µB or −µB, where
e~ Ms = nµB.
µB = = 9.274 × 10−24 Am2.
2me
The corresponding energies in a flux density B are −µBB and µBB,
so the average magnetic moment per atom is
µBeµBB/kBT − µBe−µBB/kBT
hµi =
eµBB/k T −µ B/k T
B +e B B
µB B
= µB tanh .
kB T
For small z, tanh z ≈ z, so for small fields or high temperature
µ2 B
hµi ≈ B .
kB T
If there are n atoms per volume, then,
nµ0µ2B
χ= .
kB T
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