Download Homework No. 10 (Spring 2016) PHYS 530A: Quantum Mechanics II

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts
no text concepts found
Transcript
Homework No. 10 (Spring 2016)
PHYS 530A: Quantum Mechanics II
Due date: Thursday, 2016 May 5, 4.30pm
1. (110 points.) The Hamiltonian for an hydrogenic atom is
H=
p2
Ze2
−
.
2µ
r
(1)
(a) Using
h̄ ∂
h̄
∇
and
H=−
(2)
i
i ∂t
in conjunction with the fact that Hamiltonian is a constant of motion, construct the
‘time-independent Schrödinger equation’ for hydrogenic wavefuntions to be
h̄2 2 Ze2
− ∇ −
ψn (r) = En ψn (r).
(3)
2µ
r
p=
(b) We shall confine our discussion to bound states (En < 0). Define
µZ 2 e4 1
En = −
2h̄2 n2
and
h̄2
a0 = 2 ,
µe
later being the (first) Bohr radius. Thus, derive
2Z
Z2 1
2
∇ +
ψn (r) = 2 2 ψn (r).
a0 r
a0 n
(c) The Laplacian in spherical polar coordinates is
1
∂
1 ∂2
1 ∂
1 ∂ 2∂
2
.
+
sin θ
+
∇ = 2 r
r ∂r ∂r r 2 sin θ ∂θ
∂θ sin2 θ ∂φ2
(4)
(5)
(6)
Since angular momentum is a constant of motion we can expand the wavefunctions
in the form
n−1 X
l
X
ψn (r) =
Rnl (r)Ylm (θ, φ),
(7)
l=0 m=−l
where the spherical harmonics satisfy
∂
1 ∂2
1 ∂
2
2
sin θ
+
= h̄2 l(l + 1)Ylm (θ, φ).
L Ylm (θ, φ) = −h̄
2
2
sin θ ∂θ
∂θ sin θ ∂φ
(8)
Thus, derive the differential equation for the radial part of the wavefunction as
1 d 2d
l(l + 1) 2Z
Z2
r
−
+
−
Rnl (r) = 0.
(9)
r 2 dr dr
r2
a0 r a20 n2
1
(d) In terms of the dimensionless variable
x=
derive
2Zr
a0
(10)
d2
2 d
l(l + 1) 1
1
+
−
+ −
Rnl (x) = 0.
dx2 x dx
x2
x (2n)2
(e) For x ≫ 1 argue that we have
1
d2
Rnl (x) = 0.
−
dx2 (2n)2
(11)
(12)
Solve this equation to learn the asymptotic behaviour of the radial wavefunction to
be
x
Rnl (x) ∼ e− 2n
for
x ≫ 1.
(13)
(f) For x ≪ 1 argue that we have
l(l + 1)
1 d 2 d
Rnl (x) = 0.
x
−
x2 dx dx
x2
(14)
Solve this equation to learn the limiting behaviour of the radial wavefunction to be
Rnl (x) ∼ xl
for
x ≪ 1.
(15)
(g) Use the above limiting forms to define
x
Rnl (x) = xl e− 2n L(x),
(16)
and derive, in terms of
x
,
n
2
d
d
y 2 + {(2l + 1) + 1 − y} + (n − l − 1) L(y) = 0.
dy
dy
y=
(17)
(18)
Compare this to the differential equation satisfied by the Laguerre polynomials,
(α)
Ln (y), the Laguerre equation,
2
d
d
y 2 + {α + 1 − y} + n L(α)
(19)
n (y) = 0.
dy
dy
Thus, derive
Rnl (r) = N
2Zr
na0
where N is a normalization constant.
2
l
Zr
− na
e
(2l+1)
0L
n−l−1
2Zr
na0
,
(20)
(h) The normalization constant N is, in principle, determined using
Z ∞
r 2 dr|Rnl (r)|2 = 1.
(21)
0
Verify that, the above statement does not, immediately, lead to the orthogonality
relation for Laguerre polynomials,
Z ∞
(n + α)!
(α)
dx xα e−x L(α)
.
(22)
n (x)Ln′ (x) = δnn′
n!
0
(i) Let us derive the Hellmann-Feynman theorem. Consider the energy eigenvalue equation
[H(λ) − E(λ)]|E, λi = 0
(23)
and its adjoint
hE, λ|[H(λ) − E(λ)] = 0.
Differentiate with respect to λ:
∂E ∂H
|E, λi + (E − H)|E, λi = 0,
−
∂λ
∂λ
and multiply with hE, λ| to obtain
∂H
∂E
∂H
= hE, λ|
|E, λi =
,
∂λ
∂λ
∂λ
(24)
(25)
(26)
which is the statement of the Hellmann-Feynman theorem.
(j) Use the Hellmann-Feynman theorem, by regarding λ as Z, in the hydrogenic atom
to evaluate
Z ∞
1
Z
1
=
.
(27)
r 2 dr |Rnl (r)|2 =
r n
r
a0 n2
0
(k) Use the orthogonality relation of Laguerre polynomials in Eq. (22) in Eq. (27) to
derive the normalization constant N as
3 s
2 Z 2 (n − l − 1)!
.
(28)
N= 2
n
a0
(n + l)!
Thus, derive the hydrogenic wavefunction
l
3 s
Zr
2Zr
2 Z 2 (n − l − 1)! 2Zr
− na
(2l+1)
ψnlm (r) = 2
Ylm (θ, φ). (29)
e 0 Ln−l−1
n a0
(n + l)!
na0
na0
3
Related documents