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Two-State System
Consider a system in which the time-independent Hamiltonian
possesses two eigenstates, denoted
where
.
Suppose, for the sake of simplicity, that the diagonal matrix
elements of the interaction Hamiltonian,
, are zero: that is,
|
(8.15) |
The off-diagonal matrix elements are assumed to oscillate sinusoidally
at some angular frequency
:
|
(8.16) |
where
and
are real.
Note that it is only the off-diagonal matrix elements that give rise to
the effect in which we are primarily interested--namely, transitions between states
1 and 2. (See Exercise 1.)
For a two-state system, Equation (8.11) reduces to
where
, and it is assumed that
. Equations (8.18) and
(8.19) can be combined to give a second-order differential equation
for the time variation of the amplitude
:
|
(8.19) |
Once we have solved for
, we can use Equation (8.19) to obtain the
amplitude
. Let us look for a solution in which the system is
certain to be in state 1 at time
. Thus, our initial
conditions are
and
. It is easily
demonstrated that the appropriate solutions are [51]
and
The probability of finding the system in state 1 at time
is
simply
. Likewise, the probability of finding the
system in state 2 at time
is
.
It follows that
Equation (8.23) is generally known as the Rabi formula [86].
Equation (8.23) exhibits all the features of a classic resonance [51].
At resonance, when the oscillation frequency of
the perturbation,
, matches the so-called Rabi frequency [86],
, we find
that
According to the previous result,
the system starts off at
in state
. After a time
interval
, it is certain to be in state 2. After a
further time interval
, it is certain to be in
state 1, and so on. In other words, the system periodically flip-flops between states
1 and 2 under the influence of the time-dependent perturbation. This
implies that the system alternatively absorbs energy from, and emits energy to,
the source of the perturbation.
The absorption-emission cycle also take place away from the resonance,
when
. However, the amplitude of oscillation of
the coefficient
is reduced. This means that the maximum value
of
is no longer unity, nor is the minimum value of
zero. In fact, if we plot the maximum value of
as a function
of the applied frequency,
, then we obtain a resonance curve
whose maximum (unity) lies at the resonance, and whose full-width
half-maximum (in angular frequency) is
. Thus, if the
applied frequency differs from the resonant frequency by substantially
more than
then the probability of the system making a transition from
state 1 to state 2 is very small (i.e.,
). In other words, the time-dependent
perturbation is only effective at causing transitions between states
1 and 2 if its angular frequency of oscillation lies in the approximate range
. Clearly, the weaker the perturbation
(i.e., the smaller
becomes), the narrower the resonance.
Next: Nuclear Magnetic Resonance
Up: Time-Dependent Perturbation Theory
Previous: General Analysis
Richard Fitzpatrick
2016-01-22