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So what does it look like? The Schrödinger equation for single-electron
Coulomb systems in spherical coordinates is
This type of equation is an example of a partial differential equation,
which is no simple task to solve. However, solving it gives both the
allowed values of the angular momentum discussed above and
the allowed energies
, which agree with the simpler Bohr model.
Thus, we do not need to assume anything except the validity of the
Schrödinger equation, and the allowed values of energy and angular
momentum, together with the corresponding wave functions, all
emerge from the solution.
Obviously, we are not going to go through the solution of the Schrödinger
equation, but we can understand something about its mechanics and
the solutions from a few simple considerations. Remember that the
Schrödinger equation is set up starting from the classical energy, which we
said takes the form
which we can write as
where
The term
is actually dependent only on
and
, so it is purely angular.
Given the separability of the energy into radial and
angular terms, the wave function can be decomposed into
a product of the form
Solution of the angular part for the function
yields
the allowed values of the angular momentum
and the
-component
. The functions
are
then characterized by the integers
and
, and are
denoted
. They are known as
spherical harmonics. Here we present just a few
of them for a few values of
.
for
, there is just one value of
,
, and, therefore,
one spherical harmonic, which turns out to be a simple constant:
For
, there are three values of
,
, and, therefore,
three functions
. These are given by
Remember that
For
, there are five values of
,
, and, therefore,
five spherical harmonics, given by
The remaining function
is characterized by the integers
and
, as this function satisfies the radial part
of the Schrödinger equation, also known as the radial Schrödinger equation:
Note that, while the functions
are not
particular to the potential
, the radial functions
are particular for the Coulomb potential. It is the solution of the
radial Schrödinger equation that leads to the allowed energy levels.
The boundary conditions that lead to the quantized energies
are
and
.
The radial parts of the wave functions that emerge are given by (for the
first few values of
and
):
where
is the Bohr radius
The full wave functions are then composed of products of the
radial and angular parts as
At this points, several comments are in order. First, the
integers
that characterize each state are known as
the quantum numbers of the system. Each of them corresponds
to a quantity that is classically conserved. The number
is known as the principal quantum number, the
number
is known as the angular quantum number,
and the number
is known as the magnetic quantum
number.
As with any quantum system, the wave functions
give the probability amplitude for finding the electron
in a particular region of space, and these amplitudes are used
to compute actual probabilities associated with measurements
of the electron's position. The probability of finding the
electron in a small volume element
of space around the
point
is
What is
? In Cartesian coordinates,
is the volume of a small
box of dimensions
,
, and
in the
,
, and
directions. That is,
In spherical coordinates, the volume element
is a small element
of a spherical volume and is given by
which is derivable from the transformation equations.
If we integrate
over a sphere of radius
, we should obtain
the volume of the sphere:
which is the formula for the volume of a sphere of radius
.
Example: The electron in a hydrogen atom (
) is in the
state with quantum numbers
,
and
. What is
the probability that a measurement of the electron's
position will yield a value
?
The wave function
is
Therefore, the probability we seek is
Let
. Then
After integrating by parts, we find
which is relatively large given that this is at least
two Bohr radii away from the nucleus!
The part of the probability involving the product
is known as the radial probability distribution function
or simply the radial distribution function.
is the probability that a measurement of
the electron's position yields a value in a radial shell
of thickness
and radius
as shown in the figure below:
Figure:
Illustration of a radial shell for the
radial distribution with
,
.
|
|
What the radial probability distribution shows is that the
electron cannot be sucked into the nucleus because
. Hence, as we shrink the radial shell into
the nucleus, the probability of finding the electron in that
shell goes to 0.
Another point concerns the number of allowed states for each
allowed energy. Remember that each wave function corresponds to
a probability distribution in which the electron can be found
for each energy. The more possible states there are, the more varied
the electronic properties and behavior of the system will be.
For
, there is one energy
and only one wave function
.
For
, there is one energy
and four possible
states, corresponding to the following allowable values
of
and
Thus, there are four wave functions
,
,
, and
.
Whenever there is more than one wave function corresponding
to a given energy level, then that energy level is said
to be degenerate. In the above example, the
energy level is fourfold degenerate.
Next: Physical character of the
Up: lecture_8
Previous: Angular momentum
Mark E. Tuckerman
2008-10-08