Electron Thepry of Metals
Electron Thepry of Metals
Electron Thepry of Metals
2.1 CONDUCTIVITY
2.1.1 Introduction
In an ionic solid, the atom forming a cation gives up its valence electron that is captured by the atom forming an anion. Here the electrons are strictly localized. However in metals, the core electrons are localized at the atoms but the valence electrons are delocalized and belong to the entire solid. The behaviour and energy states of these delocalized electrons determine many properties of these solids. We shall try to understand the behavious of these electrons and see how they influence the property of the solid. The simplest approach is the classical free electron model that was successful in explaining some of the properties of metals. This was succeded by the more sophisticated band theory of solids. The general characteristics of electrical conductors are: (i) The current density in the steady state is proportional to the electric field strength (Ohms law). (ii) For pure specimens, the electrical conductivity () and the thermal conductivity (k) vary with temperature as follows: T1 and k = constant (for T > D) so that T is a constant independent of temperature (WiedemannFranz law); KT T5 and K T2 (for T < D) where D is the characteristic Debye temperature. The relation T5 is known as Bloch Gruneisen T5 law. (iii) For metals that exhibit the phenomenon of superconductivity, their resistivity disappears at temperature above 0 K and below the critical temperature (Tc) for the superconducting phase transition (Tc = 4.15 k) for mercury.
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(iv) For metals containing small amounts of impurities, the electrical resistivity () may be written as = 0 = p (T) where 0 is a constant that increases with increasing unpurity content and (T) is the temperature dependent part of the resistivity. This is known as Matthiessens rule. (v) For most metals the electrical resistivity decreases with increase of pressure. (vi) The resistivity of alloys that exhibit order-disorder transitions shows pronounced minimum corresponding to the ordered phase. Table 2.1: Electrical conductivity and concentration of electrons in some selected metals
Metal Number of valence electrons (Z) 1 4 2 1 3 2 2 Concentration of electrons in 1028/m3 8.47 13.2 13.2 5.90 18.1 9.27 17.0 Electrical conductivity at 100 K in W1 m1 2.9 1.5 6.2 1.6 2.1 4.3 8.0 108 108 108 108 108 108 108 Electrical conductivity at T = 300K 6.5 5.2 1.8 5.0 4.0 1.5 1.1 107 106 107 107 107 107 107
1 . The flow of current in a conductor is an indication that the electrons in it, under the action of the applied field, move in a specific direction. As a result the distribution function of the electrons in the conductor undergoes a change. This directional motion of the electrons is called a drift. The average velocity of this drift motion is called drift velocity.
the conductor. Its unit is ohm1 m1. The resistivity, = The force F acting on an electron in an electric field E is F = eE where e is the electronic charge. The minus sign introduced because the charge on the electron is negative. The electron drift is in a direction opposite to that of the applied field. Acted on by the applied field the electron will have to accelerate continuously. But in its accelerated motion, the electron collides with the defects in the lattice. As a result of the consequent scattering the electron loses the velocity it gains from the field. The effect of the lattice may be reduced formally to the action of a retarding force. This force is proportional to the velocity v and mass m of the electron. Thus the retarding force may be taken to be Kmv where K is a constant. We can then write the equation of motion of the electron as
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dv = eE Kmv ...(2.1.1) dt After the field is applied the velocity of the electron rises till the retarding force which is proportional to the velocity equals the force due to applied field. When these forces become equal the acceleration ceases. Thereafter the electron moves with the drift velocity. If this drift velocity is vd, then m
0 = eE K mvd i.e., vd =
eE Km
...(2.1.2)
The ratio of the drift velocity to the applied field intensity is called carrier mobility. Thus Carrier mobility, m =
e Km
...(2.1.3)
Suppose that as soon as the velocity of the directional motion of the electrons attains its steady value, the field is cut off. Because of the collisions of the electrons with the lattice defects the velocity starts decreasing. After some time the electron gas resumes its equilibrium condition. Such a process which leads to the establishment of equilibrium in a system from which it was previously disturbed is called a relaxation process. When the applied filed is cut off the equation of motion of the electron becomes:
dv = Kmv dt dv = Kv dt
...(2.1.4)
dv = Kdt v
Integrating log v = Kt + C Let us now find the value of integration constant C using the known conditions. When t = 0, v = vd and hence C = |log vd |C = log vd. Now Eqn. 2.1.4a becomes log v = Kt + log vd or v = vd exp ( Kt) The time taken by an electron to reach a directional velocity which is is called the relaxation time denoted by . vd = vd exp ( K) e ...(2.1.4a)
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eE m
V A
Let n be the density of electrons. The charge flowing per unit area per unit time is the current density. i.e., j = nevd [Referring Eqn. 2.1.2] or j =
ne 2 E m
...(2.1.6)
Defining the current density for unit electrial field as electrical conductivity, we get
j = or E
ne2 m
...(2.1.7)
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If we take the experimental value of s for copper as 6 107 (-m)1 and n = 8.5 10 /m3, we find t = 2 10-14 see. In discussing electrical conductivity it is convenient to introduce the mobility of charge carriers. The mobility m is the magnitude of the ratio of the drift velocity to the applied electric field. Thus (Refer Eqn. 2.1.5).
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= The unit of is
vd e = = m ne E
...(2.1.7a)
mm = m2 V1 s1 sec volt m 1 = ne 2
1 3 mc 2 = kT ...(2.1.8) 2 2 where k is the Boltzmann constant. Suppose an electric field E is applied. Under the influence of this eE where eE m is the force acting on the electron and m is the mass of the electron. The drift velocity is much smaller compared to random velocity . Further the drift velocity is not retained after a collision c with an atom because of the relatively large mass. Hence just after a collision the drift velocity is zero. If the mean free path is then the time that elapses before the next collision takes place is
field the electron acquires a drift velocity. The resulting acceleration of the electron is
. Hence the drift velocity acquired just before the next collision takes place is c
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u = acceleration time =
LM eE OP NmQ c
u eE = 2 2m c If the number of electrons per unit volume is n, then the number of electrons crossing unit area for unit time is nothing but current density, j.
vd = Thus i.e., j = nevd j = nevd = ne
R eE U S 2mc V T W
with
c =
3kT m ne 2E 2m m 3kT
Thus
j =
12mkT
...(2.1.9)
These two expressions are independent of current. Hence at constant temperature the electrical conductivity (i.e., the ratio of the current density to the applied field) is a constant. In other words at constant temperature the applied p.d is directly proportional to the current. This is Ohms law.
2 k 3 e
FG IJ H K
W =L= T
is equal to 2.45 108 watt m/K2 comes to be a constant. However, for many
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metals, the Lorentz number varies with temperature at low temperatures. This is due to the fact all the electrons may not be participating in conduction process. W is the thermal conductivity of the metal. 4. Drudes classical free electron theory totally failed to explain the conduction mechanism in semiconductors and insulators. 5. The classical model could not explain the origin of Paulis paramagnetism. We shall now discuss one or two failures of classical free electron theory of metals with necessary theory. (i) Heat capacity of the electron gas: Classical free electron theory assumes that all the valence electrons can absorb thermal energy, move to higher energy states and contribute to heat capacity. According to the law of equipartition of energy, every free electron in a metal has an
3 KT. For a manovalent metal (copper) these will be NA (Avagadros number 2 of electrons = 6.02 1026) in one kmol. Hence the molar electronic specific heat is
average kinetic energy [Cv]el = with Thus i.e., U = [Cv]el =
dU dT 3 N kT 2 A
...(2.1.10)
This classical value of 1.5 R is about hundred times greater than the experimentally predicted value. (ii) Computation of mean free path: The microscopic expression for the resistivity (Eqn. 2.1.7) is ...(2.1.11) ne 2 The resistivity of the most useful metal copper at 20C is 1.69 108 ohm-m and the concentration of free electrons in copper, n = 8.5 1028/m3. Thus =
m ne 2 = 9.1 10 31
with =
3kT m
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The experimentally found value for is about ten times above this value. Classical theory could not explain this value.
...(2.1.13) ...(2.1.14)
But
J = E
ne2 m If is the mean free paths and vF the speed of free electrons whose kinetic energy is equal to Fermi energy since only electrons near Fermi level contribute to the conductivity. The average time between collisions is given by = vF
= i.e., =
ne 2 m vF
...(2.1.15)
The drift velocity for unit electric field is called mobility. i.e.,
vd eE e = = mE m E Thus the electric conductivity,
ne 2 ne 2 = ne = ...(2.1.16) m mv F From expression (2.1.16) it is obvious at a given temperature the only factor which varies from one metal to the other is densities of free electron.
= One must also note that the energy kT (where T is of the order of 300 k) can activate only the free electrons near the Fermi level to move to unoccupied states and contribute to specific heat. We may therefore require an energy EF called (very high compared with kT = 0.025 eV at 300 k) Fermi energy to make all the electrons to more to the unoccupied states corresponding to a temperature TF called Fermi temperture. The unique relation connecting the various parameters in quantum theory of free electron is 1 2 mv F = kTF EF = ...(2.1.17) 2
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2.1.6 Relation Between Thermal Conductivity and Electrical Conductivity (Wiedemann-Franz Law)
Figure 2.1.3 shows the view of a copper rod of appreciable length with unit area of cross-section in the steady state.
T+ Ste am dT dx T T dT dx
A H e a t flo w E E + dE dx
dE dx
Fig. 2.1.3 Flow of heat through a copper rod at the steady state
Let = AB = BC be the mean free path of the electron. The excess of energy carried by an electron from A to B is
transported by the process of conduction through unit area in unit time at the middle layer B is
LM OP N Q
1 nc is the number of free electrons flowing in a given direction through unit area in unit 6
The general expression for the quantity of heat energy transported through unit area for unit dT . Equating the two equations, one gets time is T dx
LM OP LM N Q N
LM OP = N Q
nc dE 3 dT
FG IJ FG dT IJ OP H K H dx K Q
FG IJ H K
T = But
nc dE 3 dT
FG IJ H K
dE is the energy required to raise the temperature by one degree and hence it is [cv]el. dT
T =
nc cv 3
el
Now
n cv 3
el
3k T m
...(2.1.18)
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But Thus
[cv]el = T =
3 k 2
with n = 1 electron
n 3 k 3 2
FG IJ H K
3k T nk = m 2
3k T m
Thus
nk T = 2
k T = 3 e
LM OP T NQ
R | S | T
12mk T ne
2
U | V | W
...(2.1.19)
This is called Wiedemann Franz law and the multiplying factor 3 (k/e)2 is called Lorentz number.
V2 R = E 2 Al
H =
bElg
l A
i.e.,
H = E2 Al W = E2
Thus heat developed per unit volume per second is But current density, j = E
...(2.1.20)
In an isotropic medium, consider a particular electron which at the instant t = 0, has carried out a collision with the lattice, and let the velocity components of the electron be vx, vy and vz. Now at the instant (t > 0), the electron has yet to collide with the lattice again, and assuming an electric field of intensity E is applied along the negative x-direction, the velocity components of the electron are
vx +
FG e IJ Et H mK
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LM e EtOP in velocity is due to the acceleration due to the field on the electron. Nm Q Thus the increase in energy of the electron over the field is O e U 1 LR m M Sv + Et V v P (W) = 2 MT N m W PQ 1 L L 2e O LeO O m MM P E v t + M P E t P (W) = 2 NN m Q N m Q QP M
The increment
2
2 x
2 2
The above expression may be averaged over a large number of electrons which have all lived through the period without having suffered a collision, but which presumbly have a random distribution of their velocities. Thus are finds (W)t =
1 e m 2 m
FG IJ H K
E 2t 2 =
e 2Et 2 2m
...(2.1.21)
If P (t) represents the probability that an electron moves for a ture t without suffering a collision, then P (t) = exp (t/c). For isotropic scattering, the average time between collisions, is equal to the relaxation time . Also, the probability that an electron will suffer a collision during a time dt is given by
dt dt = c
So, the probability that the electron makes a collisions between t and t + dt is given by
LMexp FG t IJ OP FG dt IJ N H KQ H K
Thus, the average energy increase of the electrons during the period between two collisions is equal to (W) =
t=0
= We known that
LM e E OP NM 2m QP
2 2
zb
W t exp
FG t IJ dt H K
dt
z
0
t e
z
0
x n e ax dx =
n an + 1
e2 E 2 2 m If n is the number of electrons present in unit volume, the total energy dissipated per unit volume per second
or W =
42
W = W =
n W
...(2.1.22)
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electrons form a cloud over the metal just as a cloud of vapour is formed over an evaporating liquid. Just as in the case of vapour, the electrons in the electron clould will be returning into the metal. When equilibrium sets in, the number of electrons emitted from the metal per second will be equal to the number of electrons returning to the metal per second. Consider one mole of electrons remembering that one mole of electrons will contain Avagadros number of electrons (NA). Let the pressure exerted by these electrons on the metal be P Let the . specific volumes of electrons in the metal be u and specific volume in the cloud by v. Let the heat energy absorbed by the NA electrons when they escape from the metal be W. Let us assume that Clausius-Clapeyrons equation in thermodynamics can be applied to the electrons. We then have
dP vu ...(2.1.23) dT where T is the temperature of the metal and the enclosure. In reality, u << v. We can, therefore, write the above quation as
W = T
dP ...(2.1.24) dT The energy W consists of two parts: (i) energy required to provide the work function, which may be written as NA , where is the work function per electron, and (ii) the work done by the ejected electrons is moving against the pressure Pexerted by the electron cloud over metal, which
W = Tv can be written as Pv [just as W = zero volume to a volume V]. Therefore W = NA + Pv ...(2.1.25) Let us ignose the electric repulsion between electrons and assume that the cloud behaves as a perfect gas. We have Pv = RT = NA kT where k is Boltzmanns constant. Therefore W = NA + NA KT = NA ( + kT) Therefore (Referring Eqn. 2.1.23) NA ( + kT) = Tv But
z
V 0
FG dP IJ H dT K
...(2.1.26)
Pv = RT = NA kT v =
NA ( + kT) = T
N A kT dP dT P
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i.e., or
+ kT = T
dP = dT
FG + kT IJ dT H KT K
2
kT 2 dP P dT
z z z
+ kT T2 dT kT 2 dT
dT + log e A
...(2.1.27)
+ log e T + log e A
Let Then
dT
log e
FG P IJ H AT K
= I
P = eI, or P = AT eI ...(2.1.28) AT If these are n electrons per unit volume of the gas, we have from the following general equation.
PV = RT = kA NA T if V = 1, NA = n and hence P = knT n = i.e., n =
AT e I P A I e = = kT kT k
1 3 mc 2 = kT 2 2 According to Knudsens cosine law, the number of electrons n0 crossing unit area per second is given by
n0 =
nc 6
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1 6
BeI
3kT m
1 6
3K Be I T m
n0 = c e I T c =
1 6
3k B = constant m
kT
Richardson first assumed that the work function is independent of temperature, then
kT n0 = c e(/KT)
I =
dT
2
j = D e/kT
...(2.1.29)
Equation (2.1.29) is the simplest form of Richardson and Dushman of themionic emission.
D , where r is the radius of the atoms. r Consequently, the electron has a fairly substantial amount of kinetic energy, of the order of several eV However, in the crystalline, metallic state, the electrons are essentially free to be anywhere in . the entire crystal. As a result, these is considerable reduction in kinetic energy. This is the source of metallic bonding. The bond between two metallic atoms is somewhat weaker than ionic or covalent bonds. This leads to relatively low melting points, for example, 63C for K. However, the cohesive energy of the metals is fairly large since each valence electron interacts with several ions. The metallic bonds are not directional where allows the planes of atoms to slide over each other quite easily. Hence metals are found to be ductile and malleable rather than brittle. The existence of essentially free electrons gives rise to high electrical and thermal conductivity for metals.
gives rise to an uncertainty in the momentum p Because of these favourable properties metals are widely used in many areas mechanical engineering and electrical engineering.
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2.3 SUPERCONDUCTIVITY
2.3.1 Introduction
Superconductivity is a phenomenon observed in some materials: there is disappearance of the electrical resistivity at temperatures approaching 0K. The discovery of this phenomenon was not an attempt of any body; but by charm of face. The phenomenon of superconductivity was discovered by Kamerlingh Onnes (1911), when he was measuring the resistivity of mercury at low temperature. He observed that the electrical resistivity of pure mercury drops abruptly to zero at about 4.2 K. He concluded that the mercury has passed into a new state which is called the superconductivity state. The materials that display this behaviour are called superconductors and the temperature at which they attain superconductivity is called critical temperature Tc. The resistivity-temperature behaviours are contrasted in Fig. 2.3.1. The critical temperature varies from superconductor to superconductor but lies between less than 1 K and approximately 20 K for metals and alloys. Recently it has been demonstrated that some complex ceramics have critical temperature approaching 100 K and above. Superconductivity is Adonis and the adolescence is retained even after one hundred years. Four times Nobel Prize was awarded for discoveries and inventions in this area, and many more are aiming.
S uperconductor Im pure m etal P erfectly pure m etal
o 0 Tc T(in K )
The resistivity of metal falls with temperature T as per the law T when T > D T5 when T < D, D being the Debye temperature, but the experiments do not lead to the conclusion 0 as T 0. It is because any trace of impurity or crystal defects prevent the metals becoming perfect conductors and gives rise to a residual resistivity, 0. Then the question is whether superconductivity is related to purity of the metal. An emphatic no is the answer. Superconductivity is a different phenomenon. If impurities are present in a superconductor, then fall of takes place in a very small region of temperature instead of sharply at Tc.
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with the vibrating ions in the crystal lattice. In the superconductivity state, the electrons tend to be scattered in pairs rather than individually. This gives rise to an exchange force (similar to the force between the atoms in a hydrogen molecule and the force between nucleans (in a nucleus), between the electrons. The force is attractive; and is very strong if the electrons are of opposite spins and momenta. In the superconducting state, the forces of attraction between the conduction electrons exceed the forces of electrostatic repulsion. The entire system of conduction electrons then becomes a bound system. No transfer of energy takes place from the system to the lattice ions. If an electric field is established the bound system of electrons gain additional kinetic energy and give rise to a current. But they do not transfer this energy to the lattice, so that they do not get slowed down. As a consequence of this, the substance does not possess any electrical resistivity. This theory was put forward, by John Bardeen, L. N. Cooper and J. R. Schriffer in 1957. The bound pairs of electrons is called Cooper pairs. Normally, the resistivity of a superconductor is measured by causing a current to flow in a ring shaped sample (one can start the current by induction after removing a magnetic flux linking the ring), and observing the current as a function of time. If the sample is in a normal state, the current damps out quickly because of the resistance of the ring. But if the ring has zero resistance, the current, once set up, flows indefinitely without any decrease in value. According to experiments conducted, the current remained constant in the ring even for several years.
Tc
T c1 Tem perature
T c2 T c T
b g LMM N
T2 Tc2
OP PQ
...(2.3.1)
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superconductor. Hence the maximum current flowing through the specimen at which this property is destroyed is called critical current. If a superconducting wire of radius r carries a current I, then as per
M a g n e tic lin es of fo rc e
I
r
Amperes law,
H dl = I
H2r = I
Ic = 2 rHc
...(2.3.2)
If I becomes Ic superconductivity will be destroyed. If in addition to current, transverse magnetic field H is applied, the value of critical current decreases.
I
Now
...(2.3.3)
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B=0
B 0
Fig. 2.3.5 Meisnner Effect
B=0
The perfect diamagnetism is an account of some special bulk magnetic property of the superconductor. If there is no magnetic field inside the superconductor, it can be said that its relative permeability r is zero. Here the mechanism of diamagnetism is not considered.
0 H
M =H M
The general equation connecting magnetic induction and magnetic field is or B = o (H + M) H + M = and also i.e.,
H + M = 0 M = H
M = 1 H
...(2.3.4)
It must be noted that superconductivity is not only a strong diamagnetism but also a new type of diamagnetism. Critical field: Superconductivity can be destroyed by the application of a strong magnetic field called critical field, Hc even at T < Tc. The critical field depends on temperature and decreases as the temperature rises from T = 0 K to T = Tc.
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i.e.,
Hc (T) = H c 0 1
L T O b g MM FGH T IJK PP Q N
2 c
...(2.3.5)
Figure 2.3.7 shows Hc vs Tc for some selected superconductors and the phase diagram.
A p plied m agnetic field strength C ritical m agn etic field 6 10
4
Hc N orm al
Pb 3 10 Sn Al 2 10 1 10 3 7 8
4
P S uperconductivity
0
(a)
T(K )
Tc
4 T(K )
(b)
Fig. 2.3.7 (a) Phase diagram of a superconductor (b) Critical fields of superconductors
2.3.6 Superelectrons
According to Two-fluid Model (a model introduced for explaining the electrodynamic property of superconductors), the conduction electrons in a superconducting substance fall into two classes: Superelectrons and normal electrons: The superelectrons experience no scattering, have zero entropy (perfect order), etc. The normal electrons behave in the usual fashion discussed in the free electron study chapter. The number of superelectrons depends on the temperature as stated below: ns = n 1
LM F T I OP MN GH T JK PQ
4 c
...(2.3.6)
1 ns n
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This is plotted in Fig. 2.3.7. Thus at 0 K, all the electrons are superelectrons, but as T increases, the superelectrons decrease in number, and they become normal electrons at T = Tc.
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2.3.9 Squid
Squid is an acronym for superconducting quantum interference device and the arrangement is as shown in Fig. 2.3.9. All squids make use of the fact that the maximum current in superconducting ring that contains a Josephson junction varies periodically as the magnetic flux through the ring changes. This periodicity is interpreted as an interference effect involving the wave functions of the cooper pairs. It consists of a ring superconducting material having two side arms A and B which act as entrance and exist for the supercurrent respectively.
P
l1
B A B
l2
Josephson junction
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The insulating layers P and Q may have different thicknesses and let the currents through these layers be I1 and I2 respectively. The variations I1 and I2 versus the magnetic field is shown in Fig. 2.4.1. Both I1 and I2 vary periodically with the magnetic field, the periodicity of I1 being greater than that of I2. The variation of I2 is an interference effect of the two junctions while I1 is the diffraction effect that arises from the finite dimension of each junction. Since the current is sensitive to very small changes in the magnetic field, the SQUID can be used as a very sensitive galvanometer.
(b) Cu (d) Al
1 d dT
(b)
(c)
d dT
(d)
1 d dT
1 E
(b) j E (d) j
(c) j E
1 E2
2.4 R1 is the resistance of a copper wire of length l cm and radius r cm. If R2 is the resistance of another R copper wire of length l2 cm and radius 2r cm. Now 2 is R1 (a) (c)
l 2 l 4
(b) (d)
l2 4
l r
2.5 The length of copper wire is halved and diameter is doubled, the resistivity of copper (a) reduces by 50% (c) decreases by 60% (b) increases by 25% (d) remains the same
2.6 In the absence of an external field, the root mean square velocity c follows: (a) c T (c) c T 2 (b) c (d) c
1 T
1 T4
2.7 The resistance of an aluminium wire of length l1 and radius r1 is R1 ohm. If the length is halved and the radius doubled, the corresponding resistance R2 is
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2.8 The mobility of electron in a metal is 0.00132 m2/V-sec subjected to a field 50 V/m. The drift velocity of the electron is (a) 0.066 m/sec (c) 66 m/sec (b) 6.66 m/s (d) 6.6 107 m/sec
2.9 At Fermi temperature the number of electrons excited from the occupied states to the unoccupied states is (a) 10% (c) 50% 2.10 The formula for Fermi velocity is (a) vF =
kTF 2m
(b) vF =
12 F
2kTF m
m 2kTF
(c) vF =
LM kT OP N 2m Q
(d) vF =
2.11 If the mobility of the electrons in a metal increases, the resistivity (a) decreases (c) first increases and then decreases (a) is the same for all metals (b) it varies exponentially (c) it is different for different metals (d) depending on the electronic structure of the metal 2.13 Depositing a layer of thorium on tungsten will (a) lower the work function (b) raise the work function (c) no effect on the work function 2.14 The Fermi energy of a metal is 1.4 eV, the Fermi temperature of the metal is approximately (a) 1.6 103 K (c) 1.6 105 K 2.15 Superelectrons become normal electrons at (a) zero degree kelvin (c) the critical temperature (b) 0C (d) Debye temperature (b) 1.6 104 K (d) 1.6 106 K (b) increases (d) first decreases and then increases
2.16 If the temperature of a metal is reduced to a value below the critical temperature, the value of the critical magnetic field will (a) increase (c) may increase or decrease (b) decrease (d) keeps a constant value
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l r 2
and
R2 =
l 2
2r
R2 l 2 = R1 4 r 2
F r I GH l JK
2
b g
l 2 4 r 2
l 4
if the volume is 1 m3
c2 =
c =
3kT m
T
vd E
Hence 2.8
vd = E = 0.00132 50 vd = 0.066 m/s 2.14 EF = kTF 1.4 1.6 10 19 EF = TF = 1.38 1023 k TF = 1.62 104 K.
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collisions with the atoms in the lattice. The resulting current is proportional to the average velocity of the free electrons. The velocity is determined by the applied electric field and also the collision frequency. Thus both thermal and electrical behaviour of matter depend on the free electrons in it. 2.2 Discuss some of the important factors which reduce electron mobility or scattering which in turn reduce the mobility. Ans. (i) Thermal agitation: Increase in temperature increases the resistance or scattering which in turns reduce the mobility. (ii) Plastic deformation: Internal stresses are caused by cold working which distort the energy levels at which electron transfer takes place. This is the other reason. (iii) Impurities: Lattice distortion and impurities cause irregularities and hence reduce the mean free path of the electrons and thus reduce the mobility of the electron. 2.3 Distinguish between the two velocities associated with the electron in metals. Ans. The velocity, vd =
known as random velocity ( ) due to the random motion of the electron (thermal motion). Just as c in an ordimary gas, the electrons have random motion even in the absence of the field. This is due to the fact that the electrons move about and occasionally scatter and change direction. The random motion, which contributes zero current, exists also in the presence of the field, but in this case there is an additional velocity opposite to the field. 2.4 Where metals and alloys are preferred? Ans. Metals are chosen in places where high conductivity and large temperature coefficient of resistance is desired. Alloys are chosen for heating purposes by I2R dissipation and for low temperature coefficient of resistance. 2.5 Why electrons and neutrons are diffracted easily by metallic crystals? Ans. Both neutrons and electrons have wave characteristics and the wavelength is of the order of grating elements in crystals. 2.6 Discuss briefly the important properties of superconducting materials. Ans. (i) At room temperature, superconducting materials have greater resistivity than other elements. (ii) The transition temperature Tc is different for different isotopes of an element. If decreases with increasing atomic weight of the isotopes. (iii) The superconducting property of a superconducting element is not lost by impurities to it but the critical temperature is lowered. (iv) There is no change in the crystal structure as revealed by x-ray diffraction studies. This means that superconductivity may be more concerned with the conduction electrons than with the atoms themselves. (v) The thermal expansion and elastic properties do not change in the transition. (vi) All thermoelectric effects disappear in superconducting state. (vii) When a sufficiently strong magnetic field is applied to a superconductor below the critical temperature, its superconducting property is destroyed. At any given temperature below Tc, there is a critical magnetic field Hc such that the superconducting property is destroyed by the application of a magnetic field. The value of Hc decreases as the temperature increases. 2.7 How will you know that a metal has become a superconductor? Ans. The simple method to study this problem is discussed below: A superconducting metal is connected with a source of electricity. A voltmeter is connected across as shown in figure. When the material is in normal conducting state a p.d is maintained at the ends
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of the wire or conductor. When the material is cooled below its critical temperature Tc, the potential disappears as shown in the figure below:
V V (a) V
V=0
(b)
2.8 Show that the following two definitions of the resistivity are equivalent. (a) resistance of a bar = (b) = Ans. (a) (b) Ohms law: V = IR R = V = E = =
V l = I a Il a
...(1)
V I = = j l a E j or =
j E
...(2)
REVIEW QUESTIONS
2.1 Outline free electron model of metals. Derive an expression for the electrical conductivity of a metal on the basis of classical free electron theory of metals. 2.2 What are the assumptions introduced by Drude-Lorentz to explain classical free electron theory of metals? Discuss the achievements and failures of this model. 2.3 Discuss the failures of classical theory of free electrons with special reference to specific heat and mean free path. 2.4 Obtain Wiedemann-Franz law. Give the significance of Lorentz number. 2.5 Enumerate the heat developed in a current carrying conductor and get the expression for the total energy dissipated per unit volume per second.
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2.6 Discuss the properties of metals and insulators bringing in the important applications of them. 2.7 Give an account of the phenomenon of superconductivity. 2.8 Discuss the significance of critical temperature, critical magnetic field and critical current density in superconductors. 2.9 Distinguish between type I and type II superconductors with suitable diagrams. 2.10 List out the various applications of superconductors.
...(1)
m ne2
e = m ne
FG I IJ l H lK a
= I nea
FG IJ FG I IJ H ne K H a K
vd = 1.99 104 m/s. 2.2 In the first case a copper wire of cross-sectional area 104 m2 and in which there is a current of 200 ampere is considered. If the free electron density of copper is 8.5 1025/m3, compute the drift velocity. If a p.d. of 1 volt is applied across 20 metre of this wire, express the new drift velocity in terms of the one calculated in the previous case. Relaxation time is 1014 sec. Sol. Case 1: If I is the current flowing, then I = n A vd e vd =
I 200 = nAe 8.5 1028 1.6 10 19 10 4
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vd v1 d
= 1.67 Ans.
2.3 Calculation of Fermi energy for some monovalent element yield the following results: Metal EF (eV) Cu 7.04 Li 4.72 Rb 1.82 Cs 1.53 Ag 5.51 K 2.12
If the Fermi velocity of the electron in one of the metals of the above series is 0.73 106 m/s, identify the metal. Also compute its Fermi temperature. Sol. i.e.,
1 2 m vF = E F 2
EF =
FG 1 IJ H 2K
TF = 1.75 104 K
2.4 For a specimen of V3 Ga, the critical fields are respectively 1.4 105 and 4.2 105A/m for 14 K and 13 K. Calculate the transition temperature and critical fields at 0 K and 4.2 K. Sol. The general formula is Hc (T) = H c 0 1
1.4 105 = H c
4.2
105
= Hc
L T b g MM FGH T IJK N L b0g MM1 FGH 14 IJK N T L b0g MM1 FGH 13 IJK N T
c c c
OP PQ OP PQ OP PQ
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1 = 3
eT eT
2 c 2 c
14 2
2
j 13 j
Tc2 Tc2
1.4 105 = H c 0 1
b g LMM N
14 2 14.47
2
OP PQ
= Hc (0) 0.16
Hc =
2.5 The resistivity of a superconductor becomes zero. Consequently the flux density is zero due to this abrupt change. Prove that the superconductor behaves as perfect diamagnetic. Sol. The general equation is B = 0 (H + M) Since B = 0 H = M or = Thus or
M = (r H
1
M = 1 H
1)
or
= 1 H
...(1)
1 = r r = 0
...(2)
Equations 1 and 2 show the possibility of perfect diamagnetism. Some Important Tables Table I: Critical field of some elements Element Al Cd Ga Pb Hg () Hg () Ta Sn BC (0) in 102 Wb/m2 0.99 0.30 0.51 0.51 4.13 3.40 8.30 3.06
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Table II. Properties of some selected superconducting elements Element Aluminium Cadmium Gallium Indium Tin Mercury Iridium Lead Tc (K) 1.196 0.52 1.09 3.4 3.72 4.12 0.11 7.175 Ho (A/m) 0.79 104 0.22 104 0.4 104 2.2 3.3 6.5 104 104 104 2.4 104 0.13 104 Type 1 1 1 1 1 1 1 1 Element Zinc Tantalum Thlium Niobium Rhenium Thorium Zirconium Osmium Tc K 0.9 4.5 2.4 9.3 1.7 1.4 0.8 0.7 Ho A/m 0.42 104 6.6 104 1.4 104 15.6 1.3 0.5 104 104 104 1.6 104 0.37 104 Type 1 11 11 11 11 11 11 11
GGG