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(Chris Devlin) #1

28 The hydrogen atom


Table 2.2 Radial hydrogenic wavefunctionsRn,lin terms of the variableρ =
Zr/(na 0 ), which gives a scaling that varies withn. The Bohr radiusa 0 is defined in
eqn 1.40.

R 1 , 0 =

(
Z
a 0

) 3 / 2
2e−ρ

R 2 , 0 =

(
Z
2 a 0

) 3 / 2
2(1−ρ)e−ρ

R 2 , 1 =

(
Z
2 a 0

) 3 / 2
2

3

ρe−ρ

R 3 , 0 =

(
Z
3 a 0

) 3 / 2
2

(
1 − 2 ρ+
2
3
ρ^2

)
e−ρ

R 3 , 1 =

(
Z
3 a 0

) 3 / 2
4


2
3
ρ

(
1 −
1
2
ρ

)
e−ρ

R 3 , 2 =

(
Z
3 a 0

) 3 / 2
2


2
3


5

ρ^2 e−ρ

Normalisation:

∫∞

0

R^2 n,lr^2 dr=1

These show a general a feature of hydrogenic wavefunctions, namely
that the radial functions forl= 0 have a finite value at the origin, i.e.
the power series inρstarts at the zeroth power. Thus electrons with
l= 0 (called s-electrons) have a finite probability of being found at the
position of the nucleus and this has important consequences in atomic
physics.
Inserting|E|from eqn 2.20 into eqn 2.17 gives the scaled coordinate

ρ=

Z

n

r
a 0

, (2.21)

where the atomic number has been incorporated by the replacement
e^2 / 4 π 0 →Ze^2 / 4 π 0 (as in Chapter 1). There are some important prop-
erties of the radial wavefunctions that require a general form of the
solution and for future reference we state these results. The probability
density of electrons withl= 0 at the origin is

|ψn,l=0(0)|^2 =

1

π

(

Z

na 0

) 3

. (2.22)

For electrons withl= 0 the expectation value of 1/r^3 is

1
r^3


=

∫∞

0

1

r^3

Rn,l^2 (r)r^2 dr=

1

l

(

l+^12

)

(l+1)

(

Z

na 0

) 3

. (2.23)

These results have been written in a form that is easy to remember;
they must both depend on 1/a^30 in order to have the correct dimensions
and the dependence onZfollows from the scaling of the Schr ̈odinger
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