Solved Problems
Solved Problems
Harmonic
From the equation (1) if the energy E is less than the potential energy
V(x) then the right hand side will be negative. This means that the double
space derivative of the eigen function ψ will be negative.
In addition if E < V (x) then then ψ ” and ψ will have same sign. geometri-
cally this means that the curve will go away from the x axis. The situation
is shown in the diagram below.
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The green curve shows the situation when ∂∂xψ2 is positive and the red
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curve shows the situation when the ∂∂xψ2 is negative. In both cases the curve
moves away from the x axis.
But the condition of well behaved eigen functions requires that ψ should be
zero at x=∞.But it is not so here the net result is that
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Figure 1: variation of ψ with x in case E < V
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the wave function is not normalizable
The total energy E can never be less than the minimum value of poten-
tial. So the minimum energy can never be zero.
From the last article we saw that the the raising and lowering ladder
operators increase and decrease the energy in units of 6 hω. so if
we apply the lowering operator a− repeatedly on the eigen function we may
expect to reach a state whose energy will be less than zero!!!! But that is
not physically possible. So what is the result of a− ψ.Let us assume that we
reach a lowest state by repeated application of a− and that lowest state is ψ0
. By definition of lowering ladder operator we know that it will reduce the
energy. So we can easily guess that the repeated operation of the lowering op-
erator on the eigen function will take the system to the lowest possible state .
But What will be the lowest state of the one dimensional har-
monic oscillator??? let us consider that we have a state ψ0 which is the
lowest eigen state of the Harmonic oscillator . Now if we apply the ladder
operator to this state then it will result in zero as there can be no state less
than zero so
a− ψ0 = 0——(2)
from the previous articles we use the correct mathematical form of the low-
ering operator in equation (2) then
√ 1 ( d + mωx)ψ0 = 0—(3)
26hmω dx
equation (3) is a differential equation and is not much difficult to solve. The
solution comes out in the following steps
dψ0
dx
= − mω 6h
xψ0 —(4)
from the most basic course of differential equations you can solve (4) andthe
solution will 2be of the form
mωx
ψ0 = Ae− 26h —(5) Equation (5) gives the lowest state of the quantum me-
chanical SHO. The significant feature is that the equation (5) is that it is
well behaved wave function and it can be normalized . The normalization
of this wave function is done as shown below
R +∞
|A|2 −∞ |ψ|2 dx = 1—(6)
q
2 π6h
|A| mω
= 1(7)
3
14
A= mω
π6h
–(8)
14 mωx2
ψ0 (x) = mω
π6h
e− 26h —(9)
Q3. What is the energy of the lowest sate ψ0 and how to calcu-
late the lowest energy
It is quiet easy we use the only step is to use the Schrodinger equation
Hψ = Eψ in terms of the ladder operators. The Schrodinger equation then
becomes
6 hω(a+ a− + 12 )ψ0 = E0 ψ0 —-(10)
expanding the bracket on the left hand side of equation (10) we have
6 hω(a+ a− ψ0 + 21 ψ0 ) = E0 ψ0
using the fact a− ψ0 = 0 and comparing the left and right hand sides we have
1
E0 = 2
6 hω—(11)
equation (11) gives the energy of the lowest state (ground state) of the
quantum mechanical harmonic oscillator which is called the zero point en-
ergy
Q4. How can I calculate the energy of the first excited state of
the quantum mechanical SHO?
The process of calculating the energy and eigen states above the ground
state can be done by using the a+ raising ladder operator on the ground
state. The raising ladder operator takes the system to the next higher state
with higher energy. Let us take the ground stateψ0 and apply the ladder
operator to obtain the next higher states.
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differentiating the equation (13) we have
r
1 − 26h mωx2
ψ1 = A1( mω
π6h ) 4 2mω
6h xe —-(14)
Your question is correct if this is so then the problem will be gigantic with
almost no solution. What we need to do is to formulate a general expres-
sion where we can do the calculation of higher states and energy easily by
changing a given parameter. From the previous question we saw how the
first excited state was obtained from the ground state by operating the rais-
ing ladder operator a+ once so we can generalize that the nth state can be
obtained as
ψn(x) = An(a+)nψ0(x)—-(15)
Now if we come to the energy then we saw that the lowest state has energy
E = 21 6 hω. If we apply the operator a+ once then energy will increase by
one unit of 6 hω. Thus for the energy of the nth state
En = (n + 12 ) 6 hω—-(16)
a±ψn = constantψ±—(17)
let us elaborate this in detail.
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a+ψn(x) = cnψn+1(x)—(18)
a−ψn(x) = dnψn−1(x)—(19)
the question is
Let the functions are f(x) and g(x). We have our latter operators as usual
a± . The mathematical concept that is used is
R +∞ ∗
R +∞ ∗
−∞ f (a ± g)dx = −∞ (a∓ f ) gdx
—-(18)
the * stands for complex conjugates of the functions.
In the language of mathematics a± and a∓ are said to be Hermitian Con-
jugate of each other
R +∞ R +∞
−∞ f ∗(a ± g)dx = 1
26hmω −∞
d
(∓ 6 h dx + mωx)gdx
It has to be kept in mind that the functions f(x) and g(x) are similar to
eigen functions and these functions must vanish at x = ±∞
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∗ dg
R
Integration by by parts gives f ( dx ) to − ( df )∗ gdx
R
dx
this property leads to the result
R +∞ R +∞
f ∗(a±g)dx = √ 1 d
[(± 6 h dx +mωx)f ]∗gdx =
R−∞
+∞
26hmω −∞
−∞ (a∓ + f )∗gdx——–(21)
a+a−ψn = nψn—-(23)
a−a+ψn = (n + 1)ψn—(24)
the normalization condition now becomes
R +∞ ∗ 2 R +∞ 2 R +∞ 2
−∞ (a+ ψ n ) (a + ψn )dx = |c n | ∞ |ψn+1 | dx = (n+1) −∞ |ψn | dx—
(25)
R +∞ ∗ 2 R +∞ 2 R +∞ 2
−∞ (a − ψ n ) (a − ψn )dx = |d n | ∞ |ψ n−1 | dx = (n) −∞ |ψn | dx—
(26)
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comparing we have the result
|cn |2 = n + 1—(27)
|dn |2 = n—(28)
thus we
√are now in a position to solve the problems of the constants
a+ ψn = n + 1ψn+1 —(29)
√
a− ψn = nψn−1 –(30)
Q7. All these mathematics is puzzling !! is there any use of these equa-
tions?
We have obtained a miraculous result that will make our work magically
easy. Suppose you are given the lowest state or ground state ψ0 and I ask
you to obtain the first excited state. The solution is damn easy
similarly we can find the second excited state from the first excited state
ψ2 = √1 a1 ψ1 –(31)
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now we can evaluate any higher state from the ground state using the formula
ψn = √1 (a+ )n ψ0 —(32)
n!
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equation (23) means that you have to apply the ladder operator twice,we
will do it one by one first we evaluate ψ1
ψ1 = a+ψ0
mωx2 1
d
ψ1 = (− 6 h dx + mωx)e 26h ( mω
π6h ) —-(33)
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2 mωx2
1 mω 14 − mωx
ψ1 = 26hmω 26h ) [−
( 6 h(−2xmωe 26h ) + mωe 26h ]
—-(34)
− −mωx2 1
√ 1 ( mω mω
ψ1 = e π6h ) [2 6 hx 26h + mωx]
26h 4
26hmωx
—–(35)
− −mωx2 2
ψ1 = √ 1
26hmωx
e 26h 2mωxe−( mωx
26h ) —–(36)
(i) ψ0
now we need to find the variation of ψ0 with x .The most oblivious thing
is that at x = 0 the function is maximum. Is it all that we require ? No
we require something more to sketch the variation of ψ with x. The best
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quantity that can serve our purpose is expectation value. The expectation
values of position can help us in sketching the exact variations of the func-
tions .
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0.8
0.6
0.4
0.2
0
−2 −1 0 1 2 3
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