Lecture 17
Lecture 17
Next time:
We rule out any comfortable explanations
Particle Waves
• Light
– is a wave. It exhibits interference (Young, 1814).
– now it is seen to have some particle properties:
photoelectric effect & Compton scattering
• Electrons
– Appear at fluorescent screen (CRT) at a point, like particles.
– Have wave properties: Interference (Davisson, ~1922).
• Our old particles have frequency, wavelength…
• Our old waves have discrete lumps of energy, momentum….
– The old dualism (world made of particles interacting by fields) is gone-
everything consists of quantum objects which have both wave-like and
particle-like aspects, which become relevant in different situations.
• The common claim that these objects are both waves and particles is false- they're
just something else, with a resemblance to both classical waves and classical
particles, but also with properties of neither.
• We seem to be saying something very incoherent. A wave cannot have a
wavelength, even approximately, unless it is spread out over distances large
compared with the wavelength. A particle is supposed to have a particular position.
How can we say "the momentum of the particle is given by its wavelength?"
The wave and its equation
• The electron is described by a wave function, Ψ(r,t), which obeys a
differential equation. The non-relativistic version is called
Schrödinger’s equation. 2 2
V(r ) i
2m t
• First term, (squared momentum), depends on how Ψ wiggles in
space. Like 1/wavelength squared, p2/2m
– Second term, (potential energy), due to various neighbors
(whose positions are presumed fixed in our reference frame).
– Third term (total energy) is how fast ψ changes in time:
frequency. E=hf.
• This equation is linear, which means that the principle of
superposition works:
– Adding any two solutions produces another solution.
Quantum Theory
• The SE is non-relativistic quantum mechanics. Dirac generalized to be
relativistic. We will discuss it in a few weeks.
• It describes electrons, neutrons, protons. For photons we need a little
more.
• When the SE can be solved, it is always right. The most precise physical
theory known.
All of the physical laws necessary for the mathematical theory of a large part
of physics and the whole of chemistry are completely known and it is only
necessary to find practical methods to solve the equations” Dirac 1929.
• Condensed matter physics, chemistry, microbiology,… are all reduced to
mathematics. We understand how to use and rely QM in the modern
world. (transitor, laser, chemistry, ....)
But what does it mean? What is the wavefunction?
Born’s probability interpretation
• Recall that the intensity (energy density) of a wave goes as the square of
the amplitude (for light the magnitude of the electric field, for water
ripples the height change).
• Quantum mechanics says that if we consider an ensemble (collection) of
identically prepared electrons, each described by similar wave functions,
Ψ(x,t).
• | Ψ (x,t)| 2 ΔV is the probability that an electron would be found in the
little volume ΔV near point x at time t, if an experiment is done that could
locate it that accurately.
• Because |Ψ2| gives a probability density, when we have a large ensemble
it tells us the rate at which electrons arrive at the spot of interest on the
screen. In the places where the two waves interfere destructively, the
probability is less than the sum of the two individual probabilities, and may
even be zero.
• There is a fundamental loss of determinism.
An important mathematical property of waves
• The wavelength of a wave, describes a sinusoidal function of position, sin(kx),
where k = 2π/λ. The sine function oscillates for all x between ± ∞. Thus, if we limit
the spatial extent of the wave, it is no longer a simple sine wave and is not
described by a single wavelength.
x
Superposition lets us write a spatially limited wave as the sum of a many sine
waves of various wavelengths. (“Fourier decomposition”) Fourier analysis shows
that if the wave is limited to a spatial region Δx, the spread of k values in the sum is
approximately 1/Δx. One can prove that Δx Δk ≥ 1/2. Δ means “the spread of,” or
“the uncertainty of.”
• Classically, position and momentum were specified by separate vectors. In QM they
are both specified by Ψ(r,t), but Ψ(r,t) cannot both wiggle at a steady rate in space
and be confined to one point in space, so it cannot specify precisely both r and p.
• A quantum state cannot have both precise px and precise x.
Heisenberg’s uncertainty principle
• Our Fourier analysis of the wave, gives: Δx Δp ≥ .
2
• One often reads that the uncertainty principle is merely a statement about our lack of
knowledge of the electron’s position and momentum, but that’s false. Exact position
and momentum are not attributes that any object ever has at the same time.
Assuming otherwise leads to incorrect predictions.
• Why call that an “uncertainty”? A water wave also has a spread in positions and
directions. This is uncertainty, not just classical spread, because various measurements
(e.g. letting the electron hit a screen) don’t give results with the whole spread. We only
see part of the spread, and are uncertain which part it will be. For the water wave we
are certain to see the whole spread.
• Note the difference between this QM unmeasurability and previous unobservables,
such as the ether. If we assume that the ether exists, we open up the possibility of
making various hypotheses about how to find it, none of which work. So, for simplicity,
we say it doesn't exist. If we say that precise x and p simultaneously exist (at least in
the usual meaning of those words) we will directly run into predictions which violate
both QM and experience, since interference is found between parts of the wave at
different x's and p's, leaving it very hard to see how those variables could have had
only single values.
Trajectories?
• The uncertainty principle means there are no classical trajectories
• Suppose we try to make an accurate measurement
of the path of our electron by passing it through a
bunch of slits or otherwise determining the position
to some accuracy, e.g. by looking via light
What happens if we try to
improve the accurately by
narrowing the slits? The
uncertainty principle foils us.
We are limited by the quantum nature of the photon. The spot on the camera film
is limited by diffraction as the light passes through the lens. If we make the lens
bigger, then we don’t know which direction the photon was going after it bounced
off the electron. Similarly, reducing the wavelength reduces Δx, but the photon
now has more momentum, and thus a larger Δp.
Thus, we can have small Δx or Δp, but not both.
Every type of object, or none, must share the uncertainty rule, otherwise
you could unravel the uncertainty of one type with microscopes using a
less uncertain type.
Not everything is imprecise
• We can predict the frequencies (energies) of photons emitted from
hydrogen and helium atoms to 10 decimal places.
• But we don’t know when the photon will arrive.
• But if you recombine the sy= 1/2 and the sy= 1/2 beams without measuring, i.e. without
letting them interact with some sort of detector, the resulting beam is still all s x= +1/2.
• Each sx= +1/2 was BOTH sy= +1/2 and sy= -1/2, and follows BOTH pathways . Only a
"measurement" makes it choose one or the other. Apparently sy is not specified by a
hidden variable, since each sx= +1/2 neutron seems to have both values of sy.
The Copenhagen Interpretation
(Bohr 1930)