This will be child’s play for harmonic oscillator,
{A.12}, and spherical harmonics, {A.15},
veterans. If you replace the angular terms in (3.15) by
, and then divide the entire equation by
, you
get
Since
is nondimensional, all terms in this equation must be.
In particular, the ratio in the third term must be the inverse of a
constant with the dimensions of length; so, define the constant
to be the Bohr radius
. It is convenient to also define a
correspondingly nondimensionalized radial coordinate as
.
The final term in the equation must be nondimensional too, and that
means that the energy
must take the form
, where
is a nondimensional energy. In
terms of these scaled coordinates you get
Similar to the case of the harmonic oscillator, you must have
solutions that become zero at large distances
from the nucleus:
gives the probability of finding the
particle integrated over all possible positions, and if
does
not become zero sufficiently rapidly at large
, this integral
would become infinite, rather than one (certainty) as it should. Now
the ODE above becomes for large
approximately
, which has solutions of the rough form
for positive
that do not
have the required decay to zero. Zero scaled energy
is
still too much, as can be checked by solving in terms of Bessel
functions, so you must have that
is negative. In classical
terms, the earth can only hold onto the moon since the moon’s
total energy is less than the potential energy far from the earth; if
it was not, the moon would escape.
Anyway, for bound states, you must have the scaled energy
negative. In that case, the solution at large
takes the
approximate form
. Only the
negative sign is acceptable. You can make things a lot easier for
yourself if you peek at the final solution and rewrite
as
being
(that is not really cheating, since you are not at this
time claiming that
is an integer, just a positive number.) In
that case, the acceptable exponential behavior at large distance takes
the form
where
. Split off this
exponential part by writing
where
must remain bounded at large
. Substituting
these new variables, the ODE becomes
If you do a power series solution of this ODE, you see that it must
start with either power
or with power
. The
latter is not acceptable, since it would correspond to an infinite
expectation value of energy. You could now expand the solution
further in powers of
, but the problem is that tabulated
polynomials usually do not start with a power
but with power zero
or one. So you would not easily recognize the polynomial you get.
Therefore it is best to split off the leading power by defining
, which turns the ODE into
Substituting in a power series
, you get
With
identified, you can identify the ODE as Laguerre's associated
differential equation, e.g. [20, 30.26], the
-th
derivative of Laguerre's differential equation,
e.g. [20, 30.1], and the polynomial solutions as the
associated Laguerre polynomials
,
e.g. [20, 30.27], the
-th derivatives of the
Laguerre's polynomials
, e.g. [20, 30.2]. To
normalize the wave function use an integral from a table book,
e.g. [20, 30.46].
Putting it all together, the generic expression for hydrogen eigenfunctions
are, drums please:
Do keep in mind that different references have contradictory
definitions of the associated Laguerre polynomials. This book follows
the notations of [20, pp. 169-172], who define
Combine the messy definition of the spherical harmonics
(A.28) with the uncertain definition of the Laguerre
polynomials in the formulae (A.30) for the hydrogen energy
eigenfunctions
above, and there is of course always a
possibility of getting an eigenfunction wrong if you are not careful.
Sometimes the value of the wave functions at the origin is needed.
Now from the above solution (A.30), it is seen that