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Solids and conductivity

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Title: Solids and conductivity


1
Solids and conductivity
  • At long distances, the electric field from one
    atom polarizes another, that is distorts it
    slightly, inducing an electric dipole that
    attracts the other atom, and vice versa.
  • At short distances, the electron wave functions
    start to overlap, and the Pauli exclusion
    principle kicks in, and the atoms repel each
    other- all this seen in molecules.
  • If there are many atoms close to each other, and
    there is enough time for them to find the lowest
    energy state, there must always be some
    geometrical configuration that is most stable.

2
  • If this configuration is most stable, it will be
    so everywhere, and we will have the same
    configuration over the whole sample called long
    range order.
  • If we start in a small region with a relatively
    stable configuration, different from the lowest
    energy state, it will spread throughout the
    sample, and we have a metastabel state which will
    be stable for nearly infinite time- it would have
    to tunnel to the more stable state.
  • If we start from a disordered state and cool
    quickly, we can get disordered cold states that
    are not as stable, but still live practically
    forever, like glass, amorphous with great
    viscosity of flow.

3
  • We dont need to study the different
    configurations, leading to crystals of different
    symmetry. The only property we need for our
    study of conductivity is the fact that the
    molecules are fixed in a regular pattern.
  • CONDUCTIVITY we will investigate
  • electrical conductivity
  • semiconductivity
  • superconductivity
  • Classical electrical conductivity (look back to
    Chapter 22-5 in the Tipler book, to combine with
    Chapter 39-2
  • (Developed first in lectures at Columbia by H.
    Lorentz in 1909.)

4
  • Assume that in some materials that there are some
    electrons that are not attached to a particular
    molecule, but can move more or less freely in the
    material. We call them non-localized. These
    must be electrons that sit in the outer shells of
    atoms, and cant decide which atom they are
    attached to.
  • When an electric field is applied to the
    material, these electrons start to accelerate,
    with a force eE, so an acceleration aF/meE/m.
    If they were completely free, they would continue
    to accelerate across the whole material and the
    time to arrive at the far side would be
    proportional to ?1/E, from sat²/2 .

5
  • Then the total current would be
    where A is the area of the conductor. This is
    not Ohms law, which tells us that the current
    varies as E. One concludes that electrons dont
    accelerate freely all the way across the
    material, but only for a short distance,
    presumably until they hit one of the fixed atoms
    and bounce off in a random direction (scatter)

6
  • Then the average drift velocity of a random
    electron, making a collision after the average
    time ? is We can express ? in terms
    of the mean free path and the average electron
    velocity
  • and can get the average velocity from the
    thermal velocity with the thermal kinetic energy,
    for three degrees of freedom (xyz) this is
    3/2(kT), so
  • and it is striking that this average
    velocity is typically 1010 times vd, so the
    average is not affected by E

7
  • Since vav doesnt change with E, neither will ?
    or ? and none of the constants in the equation
    for the drift velocity will
    depend on E, and we get the
    linear current with E that the experimental Ohms
    Law finds. To fill in the details, note

8
  • From the picture of the crystal, it is clear that
    since the spacing of atoms is such that that just
    touch in some sense, the value of ? must be
    about equal to the lattice spacing between atoms
    in the crystal, a few tenths nanometer.
  • This all seems pretty reasonable
  • it gives Ohms Law
  • it gives a resistivity that is too big, but only
    by an order of magnitude at room temperature, but
  • it says that the resistivity should go down as
    the temperature is increased and the drift
    velocity increases, not so

9
  • Look at resistivity over a wide range of
    temperature
  • This looks seriously wrong. Also, the
    resistivity at low temperature is very dependent
    on tiny admixtures of impurities, a sign that the
    low resistivity in pure crystals is related to a
    very long mean free path- also, why are there
    insulators?

10
  • Another question, is there channeling?
  • If we rotate the crystal, we should see more
    conductivity when the direction of measurement
    lines up with a path down the channels in the
    crystal. We do not, but if we look at gt1000Volt
    particles, we do see channeling.

11
  • Another hint as to what is wrong comes from the
    heat capacity of metals and insulators. In both,
    we should see the heat capacity of the nuclei
    vibrating around their locations on the
    crystalline lattice (3R in gas law constant
    units) and in insulators, no more, if there are
    no free electrons to move around. This is
    observed. In metals, we should expect an
    additional ½kT for motion in each direction
    (xyz). Not observed! There is an excess of only
    about 0.02R. Evidently, there are very few free
    electrons, but the conductivity at low
    temperatures is way greater than that given by
    our classical theory! Those few must be working
    very hard!

12
  • The only way an electron can work harder to make
    more conductivity is to move further before it
    scatters, but it has to move in this forest of
    atoms. How?
  • The wave packet of the electron diffracts through
    the forest because of the periodic nature of
    the lattice, it can go on forever, if the lattice
    is perfect. Thermal motions and impurities make
    the lattice imperfect.

13
  • This long distance before the electron explains
    how we can get so much conductivity with few free
    electrons and wave doesnt channel. Now let us
    look at the distribution of the electrons. The
    key is going to be the Pauli Principle. Use the
    particle in a box again to get a
    one-dimensional version of the energy
    distributions of the electron.
  • Recall that the energy levels in a box are
  • and we know that we can only put two electrons in
    a state with a given n, one with spin up, one
    with spin down, according to the Pauli Principle

14
  • Calculate the energy for N electrons in the box,
    which we call the Fermi energy
  • and for copper this is 1.8eV, or about
    80,000Kelvin. Hot! So most electrons are frozen.
    At room temperature a few electrons are
    thermally excited

15
  • Now we must look more carefully at the wave
    properties of the electrons in the periodic
    potential of the lattice of atoms, to find out
    the story on conductors, insulators and
    semiconductors. There are two ways 1. Start
    with free atoms and calculate what happens when N
    atoms are brought close together. (this is done
    in the book.) 2. Start with free electrons,
    calculate the solutions in a periodic potential.
  • Free atom atomic levels with quantum numbers
    (n,l) are split up into N levels by the effects
    of distant atoms. Ngtgtgt1, so consider them a
    continuous band., labeled by (n,l). Example Na
    n3, l0.

16
  • That n3, l0 band of the outermost electron
    could hold two electrons, one spin up, one spin
    down. Na has only one electron in that state, so
    only half the states are filled. We say that the
    band is half filled. Then, since the states in
    the band are essentially a continuum, the
    slightest increase in energy of the topmost
    electron in the band can move it into a new state
    with no objection by the Pauli Principle. It can
    be moved easily by an electric field in
    particular, so Na is a conductor. In contrast
    take NaCl in solid form. The outer electron goes
    in the outer shell of Cl for binding the crystal,
    so we have a Na ion and a Cl- ion. Both are
    filled shells, so there is no nearby state

17
  • To move an electron up to the next state, or band
    in the crystal, we have to go to the state of
    (Na), and excited state, and that takes several
    eV. In between there are no states, and we say
    that there is a band gap or forbidden band. We
    draw the two energy level pictures
  • Na (conductor) NaCl (insulator)

18
  • The free electron method uses the Bloch-Floquet
    theorem which says that the solutions of the wave
    equation in a periodic potential must be of the
    form
  • the u(x) must satisfy a boundary condition, we
    usually bend the crystal in a circle of N periods
    and demand that

19
  • What is special about kan? ?
  • This corresponds to electron wavelengths of 2a/n,
    or twice the lattice spacing coresponds to an
    integer multiple of the free particle wavelength,
    and a free particle with this wavelength would be
    reflected by the lattice.
  • This corresponds to the stop bands in a
    periodically loaded waveguide. The width of the
    stop band depends on the details of the
    interaction.

20
  • Semiconductors are just insulators with a small
    forbidden band gap, if they are intrinsic
    superconductors with NO impurities, or
    extrinsic with impurities giving states with
    energies in the forbidden band

21
  • In the n-type a little thermal exitation of the
    impurity (often Arsenic) introduces an electron
    into the conduction band, so we get electron
    conduction
  • In the p-type, an electron from the valence band
    is easily excited into the impurity (typically
    Gallium) leaving a little bubble in the filled
    valence band that acts like a positive
    electron--it is called a hole
  • notice that the conductivity goes up with
    temperature in a semiconductor, unlike the metal
    dependence, because of the increased thermal
    exitation with temperature

22
  • What if we make a junction of a p-type and an
    n-type??

23
  • Field Effect Transitor
  • The drain is reverse biased, just enough to
    nearly pinch off the current source-to-drain,
    while the gate voltage is trying to open it up.
    Very like a vacuum tube triode!
  • Good because 1) gate controls s-to-d current
    with no dc current (high impedance) 2) easy to
    make by planar process

24
  • Almost 100 years ago, K. Onnes succeeded in
    liquefying Helium, finding it boiled at 4.2K.
    Many remarkable discoveries of quantum properties
    of Liquid Helium followed, but one discovery was
    Superconductivity. He found that below a certain
    termperature, lead and tin, and some other metals
    lost all resistance. How can it be? BCS
    (three guys) explained it as one electron
    distorting the lattice slightly, and another one
    with opposite spin joins (and aids) it, to form a
    pair Cooper pair. Pauli Principle tells us
    that no more than a pair can play this game.
  • Well exaggerate for a picture

25
  • Distortion of the lattice creates a well
  • The more wobbly the lattice, the easier it is
    distorted to form a well, and the more the
    electron pair is bound against thermal
    disturbances (high Tcritical) and against
    disruption by a magnetic field (high Bcritical),
    so you create alloys more wobbly until they
    become unstable gt Tcritical about 20K, with a
    well thousands of atoms across.

26
  • Thousands of atoms across that is a macroscopic
    state. It is not so easy to break that pair of
    electrons apart, that is why the critical
    temperature is high. It is very hard for just
    one electron to be scattered by an irregularity
    in the lattice, since the electrons are averaging
    over billions of atoms in the lattice. We saw
    before in normal metals that the mean free path,
    and the conductivity, go to infinity except for
    scattering. There is no scattering in the
    superconducting state, so the resistance is zero.
    Experiments have looked for decay of currents
    for years and seen none in good superconductors.

27
  • Since these Cooper pairs are both pure quantum
    states and macroscopic, it is easier to see real
    quantum states than with microscopic states, and
    relatively easy to build applied quantum devices.
  • Brian Josephson, while a Cambridge undergraduate,
    realized one could observe interference between
    two Cooper pairs in a macroscopic junction
    tunneling between two superconducting metal
    samples.
  • As the phase is changed between the two pairs,
    for example by putting on a small magnetic field,
    the tunneling rate changes in an oscillatory way

28
  • Superconducting Quantum Interference Device
  • or SQUID
  • this gadget will detect magnetic field below
  • 10-14 T 10-10 Gauss, if you keep the
    environmental noise down (special rooms) -see
    nice article in book on measure currents in the
    human brain

29
  • This finishes our exploration of quantum physics
    and engineering. (Nuclei and particles have
    interaction that are quantal, but the particles
    usually have high energy and act like particles
    indeed.)
  • We have tried to show how many common properties
    of atoms and solids have quantum effects which
    dominate their behavior, so the phenomena that
    seem strange are key to understanding much or our
    environment.
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