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Orbiting charge , mass q,
All substances show a magnetisation in opposition to the
radius , angular velocity
applied magnetic field — caused by perturbation of the
electron orbits.
Current
General idea can be seen from simple model
moment
Area (need QM to cope with electron spin (next year)).
radius , angular velocity
q
If , balance of forces
Quite general result, but elementary particles have
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DIAMAGNETISM — NON-EXAMINABLE
2
4
6
5
Expand to first order in
9
=
9
=
3
3
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6
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6
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BC
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Q. Why is ?
8
8
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e e
_
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A. Because is quantised, and doesn’t change when
Leading terms cancel
is applied.
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a
f
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c
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e Q. But isn’t e , so ?
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3
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2
4
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6
6
8
8
In fact is very small compared to (not A. No, it isn’t that angular momentum that is quantised.
obvious!) The correct momentum to use is the canonical momentum
H
k
k
@
i
g
h
c
j
L
b
J
>
6
6
K
q ( = vector potential).
<
D
L
e
k
6
@
D
K
Q. But what is ?
where L e is the Larmor frequency.
l
k
n
m
`
X
o
Z
q
b
p
2
A. will generate in the -direction, so for
l
j
r
c
t
r
Z
b
b
e
e
d
electron ( ) e .
applied field (Lenz’ law)
d
7
7
v
w
H
u
u
c
^
r
Z
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@
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b
b
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d
N
N
Q
M
M P
constant constant
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B
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L e
K
K
K
8
A
<
<
R
B
D
e
x
2
Average (factor of 2/3) over orientations of orbit:
field (next section).
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DIAMAGNETISM — INDUCTION EFFECTS PARAMAGNETISM
z
{
y
Suppose magnetic field is increasing at rate
Due to permanent magnetic dipoles in medium.
y
~
If dipoles have random orientation.
|
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If field tends to align dipoles.
y
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¢
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Dipole energy ,
charge so that
z
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Probability of alignment in
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µ
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But we have already show that solid angle Boltzmann factor
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Set and
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PARAMAGNETISM II
CURIE-WEISS THEORY
Ä
Average alignment along is
Ð
Ó
ÕÖ
ö
ø
ú
õ
û
Ç
Ï
ÏÔ
ù
È
÷
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Æ
Í
Æ
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Ì
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At low field strengths
ÉÊË
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Ï
Î
Î
È
È
Ñ
Ð
Ó
ÕÖ
ÏÔ
Ñ
ý
Ò
þ
þ
ÿ
ü
ù
û
(Curie’s Law)
þ
×
Ü
Ý
Ä
Ë
Ú
Ø
Denominator =
Ø
ô
×
×
Curie’s Law:
Ü
Ý
Ü
Ý
Û
Û
Ù
Ä
ÉÊË
Ë
Ø
Ú
Ø
Þ
ß
Numerator =
Ø
Ø
is the Curie constant.
á
ã
ô
ä
ç
Ç
â
Approximate theory of paramagnetism. We have so far
Ü
Ý
Ü
Ý
Û
é
à
è
ÉÊ
Ø
Ø
Î
Þ
Ç
Ø
È
ignored the effect of the dipoles on each other.
Ü
Ý
é
Cooperative effects: Microscopic moments tend to align
Ä
Ø
is the Langevin function
with each other.
ö
ø
Å
ê
Ä
High or low — Macroscopic fields satisfy but field
Ü
Ý
é
ë
Ø
saturates 1 local at the atom can can be very different from the
Ü
Ý
Ä
Ø
ì
Ø
macroscopic .
Low field strength
ô
Ø
Ø
ó
Ü
Ý
Ü
Ý
é
ñ
Ø
Ø
Î
Þ
í
ï ð
WEISS THEORY CURIE-WEISS THEORY
0
5
,
1
3 4
+
.
-
/
Weiss (1907) suggested model Weiss theory:
6
/
:
+
local
7 8
0
5
4
1
4
/
/
<
7
8
6
;
Expresses cooperative effect as increased contribution
?
4
1
from local .
+
>
-
Define , rearrange to get
J
?
7
=
:
local
6
.
;
6
.
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-
-
J
E
?
@
7
3
7
8
=
=
A
F
B
B
6
.
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8
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Curie-Weiss law:
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c
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(
&
J
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K
K
7
+
;
6
.
-
/
8
8
Changes weak field limit c is the critical, or Curie temperature: c .
8
8
L
M
Predicts spontaneous magnetisation below a critical Curie c paramagnetism, with Curie-Weiss law.
8
8
N
M
p
q
r
o
FERROMAGNETISM — EXAMPLE At constant , plot against .
o
Can make plots as follows:
S
S
O
P
U
U
Q
T
y
{
s
q
r
u
q
r
B, B
t
t
t
w
v
x
local
V
u
_`
a
Y
S
\]
^
^
U
R
R
T
Langevin Weiss Macroscopic
S
JT
P
B
e
b
_h
b
f
g
\]
^
^
c
e
[
O
d
T
Density of iron (7800 kg m ) m
O
U
P
d
R
Q
Q
p
p
p
p
|
}
_
j
i
l
k
\
]
O
U
P
d
R
Q
Q
T
Curie constant K.
o
m
\]
]
]
O
p
p
p
p
|
}
O
p
p
q
r
o
~
Very strong cooperative quantum interactions of spins, For the ( ) graph is multivalued
c
q
r
v
v
P
Q
at atom site.
o
MAGNETIC DOMAINS Can make permanent magnets using materials which
have high potential barriers to formation of domain walls.
Curie-Weiss Law Iron highly magnetised for c. Even non-permanent magnetic materials present some
potential barrier
But can easily get unmagnetised iron bars.
— hence hysteresis.
Measure resulting
field in small gap.
or
Some remains
when
Finite required
Called Coercivity c.
HYSTERESIS AND PERMANENT MAGNETS
WEISS THEORY AND MAGNETIC HYSTERESIS
Magnetic ring length
Saturate with current
What is the field in the gap?
No current
¡
£
¢
¤
¤
£
¢
If gap small g i
Scale of is approximately correct.
Scale of is much too large (by factor of about ) for
most ferromagnets.
¤
¢
§
(sloping up to left)
¨
i
©
Coercivity is very variable between different materials.
¤
¦
changes by movement of domain walls, rather than by i is small, opposing i.
¦
¦
rotation of dipoles.
g is a little less than r.
MAGNETISATION PROCESS IN IRON
COERCIVITY OF MAGNETIC MATERIALS
ª
¬
ª
The dipoles of the atoms are ‘flipped’, rather than being hysteresis.
continuously rotated.