First-order time-dependent perturbation theory on a Hydrogen atom

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SUMMARY

The discussion focuses on first-order time-dependent perturbation theory applied to a Hydrogen atom subjected to a pulsed electric field E(t)=E_{0}\delta(t). Key findings include the selection rule that dictates the final angular momentum quantum number l must equal 1 for a nonzero transition amplitude. It is established that the transition probability to an excited state is calculated using the formula P_{n<-m}=|<\psi^{0}_{n}|\hat{U}(t,t_{0})|\psi^{0}_{m}>|^{2}, leading to a total transition probability P_{total}=\sum^{\infty}_{n=2}P_{n<-1}. The discussion also highlights the necessity of using the radial wavefunction for the Hydrogen atom to derive the total transition probability.

PREREQUISITES
  • Understanding of first-order time-dependent perturbation theory
  • Familiarity with quantum mechanics concepts such as angular momentum quantum numbers
  • Knowledge of electric dipole transitions and selection rules
  • Ability to work with generalized Laguerre polynomials
NEXT STEPS
  • Study the derivation of the radial wavefunction for the Hydrogen atom, R_{nl}
  • Learn about the properties and applications of generalized Laguerre polynomials
  • Explore advanced topics in quantum mechanics, focusing on perturbation theory
  • Investigate the implications of electric dipole transitions in multi-electron systems
USEFUL FOR

Students and researchers in quantum mechanics, particularly those studying atomic physics and perturbation theory, as well as educators seeking to enhance their understanding of transition probabilities in quantum systems.

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Homework Statement



A Hydrogen atom is initially in its ground state and then subject to a pulsed electric field E(t)=E_{0}\delta(t) along the z direction. We neglect all fine-structure and hyperfine-structure corrections.

Homework Equations



1. It is important to use selection rules to avoid unnecessary calculations of many zero transition matrix elements. According to the selection rule associated with electric dipole transitions, what is the final angular momentum quantum number l in order to have a nonzero transition amplitude?

2. For an excited state |nlm&gt;, its angular part Y^{m}_{l}(\theta,\phi) will contain a term exp(im\phi). Based on this observation, show that the transition probability from the ground state to a final state would be zero if the quantum number m of the final state is not zero.

3. Calculate the transition probability to an arbitrary excited state using the first-order time-dependent perturbation theory. You don't need to evaluate the matrix elements of the dipole operator explicitly.

4. Can you calculate the total transition probability (that is, the sum of transition proba-
bilities to all excited states)? Note that here we cannot use Fermi's golden rule because
the final states are a collection of discrete states.

The Attempt at a Solution



1. Selection rules: \Delta l=1 ---> l=1

2. m=0

3. Transition probability from first order time-dependent perturbation theory:
P_{n&lt;-m}=|&lt;\psi^{0}_{n}|\hat{U}(t,t_{0})|\psi^{0}_{m}&gt;|^{2}=|&lt;\psi^{0}_{n}|\hat{U}_{I}(t,t_{0})|\psi^{0}_{m}&gt;|^{2}=(\frac{1}{hbar})^{2}|\int^{t}_{0}&lt;\psi^{0}_{n}|\hat{V}(t_{1})|\psi^{0}_{m}&gt;e^{i(E^{0}_{n}-E^{0}_{m})(t_{1}-t_{0})/hbar}dt_{1}|^{2}

where \psi_{m}=\psi_{1}=\psi_{100}
\psi_{n}=\psi_{n}=\psi_{n10}
\hat{V}(t)=-q\overline{r}\cdot E_{0}\delta(t)\widehat{z}
t_{0}=0
\omega_{nm}=\frac{(E^{0}_{n}-E^{0}_{m})}{hbar}

Then I have

P_{n1}=(\frac{|\overline{d}_{n1}\cdot\widehat{z}|E_{0}}{hbar})^{2}|\int^{t}_{0}\delta(t_{1})e^{i\omega_{n1}t_{1}}dt_{1}|^{2}=(\frac{|\overline{d}_{n1}\cdot\widehat{z}|E_{0}}{hbar})^{2}|e^{i\omega_{n1}t}|^{2}=(\frac{|\overline{d}_{n1}\cdot\widehat{z}|E_{0}}{hbar})^{2}

4. Total transition probability
P_{total}=\sum^{\infty}_{n=2}P_{n&lt;-1}=(\frac{E_{0}}{hbar})^{2}\sum^{\infty}_{n=2}|\vec{d_{n1}}\cdot \hat{z}|^{2}

where \vec{d_{n1}}\cdot \hat{z}=q&lt;n10|z|100&gt;

After this, I have to use the formula of radial wavefunction for Hydrogen atom
R_{nl}=\sqrt{(\frac{2}{na})^{3}\frac{(n-l-1)!}{2n[(n+1)!]^{3}}}e^{-r/na}(2r/na)^{l}[L^{2l+1}_{n-l-1}(2r/na)]
set l=1, and get the function of n, then plug into the formula for total transition probability which is a summation of n.

The problem is, that I can't find the formula of R_{nl} for n=n and l=1.
Can anyone show me how to continue my derivation?

Many thanks!
 
Last edited:
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In your expression

<br /> R_{nl}=\sqrt{(\frac{2}{na})^{3}\frac{(n-l-1)!}{2n[(n+1)!]^{3}}}e^{-r/na}(2r/na)^{l}[L^{2l+1}_{n-l-1}(2r/na)]<br />

you have the generalized Laguerre polynomials, which can be computed from

L^p_q(x) = \frac{ x^{-p} e^x}{q! } \frac{d^q}{dx^q}(e^{-x} x^{p+q}).

There are more relations that you can probably find in your textbook or at http://en.wikipedia.org/wiki/Laguerre_polynomial#Generalized_Laguerre_polynomials
 

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