Hydrogenic Atom emitting electron - probability of remaining in ground state

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SUMMARY

The discussion centers on the probability of a hydrogenic atom remaining in its ground state after the nucleus emits an electron, resulting in a change in charge from Ze to (Z + 1)e. The ground-state wavefunction is defined as ψ₀(r) = (1/√(πa³))exp(-r/a), with the constant a dependent on the atomic number Z. The probability calculation involves integrating the product of two wavefunctions, ψ₀(r,a) and ψ₀(r,â), where â = (az)/(z+1), over spherical coordinates. This approach confirms that the probability is derived from the overlap of the two states rather than a simple modulus squared of a single wavefunction.

PREREQUISITES
  • Understanding of quantum mechanics principles, specifically the Schrödinger equation.
  • Familiarity with hydrogenic atom models and wavefunctions.
  • Knowledge of spherical coordinates for volume integrals.
  • Basic proficiency in LaTeX for mathematical expressions.
NEXT STEPS
  • Study the derivation of the hydrogenic atom wavefunctions in quantum mechanics.
  • Learn about the time-dependent Schrödinger equation and its implications for wavefunction continuity.
  • Explore the concept of probability amplitudes and their role in quantum state measurements.
  • Investigate the use of spherical coordinates in quantum mechanical integrals.
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Students and professionals in quantum mechanics, particularly those studying atomic physics, as well as educators seeking to clarify concepts related to wavefunctions and probability calculations in quantum systems.

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Homework Statement



Hi all - I've done all but the last part of this problem, for which I have the solution, but I was hoping someone could explain why the solution is what it is :)

q:The Hamiltonian of a quantum system suddenly changes by a finite amount. Show that the wavefunction must change continuously if the time-dependent Schrödinger equation is to be valid throughout the change.

Show that the ground-state wavefunction for a hydrogenic atom (a bound state of one electron and a nucleus of charge Ze, with Z a positive integer) takes the form

\psi_{0}(r) = \frac{1}{\sqrt{\pi a^3}}exp(\frac{-r}{a})

and determine the dependence of the constant a on Z. Such a hydrogenic atom is in its ground state. The nucleus emits an electron, suddenly changing to one with charge (Z + 1)e. Compute the probability that if the energy is now measured, the atom will still be found in its ground state.

Now it's just the red bit I'm stuck on - I've done the rest, but to save rewriting the formula every time you use it, you can just call it \psi_{0}(r,a) if it's easier.

I have from the previous parts a=\frac{4 \pi \epsilon_{0} h^2}{z e^2 m}, where h is actually the 'h-bar' version of Planck's constant, but I'm not sure how to LaTeX that!

Now in the solution I have, the probability given is

\frac{1}{\sqrt{\pi a^3}}}\frac{1}{\sqrt{\pi \tilde{a}^3}}}\int_0^{\infty} exp(-\frac{r}{a})exp(-\frac{r}{\tilde{a}})r^2\, dr \,sin(\theta)\,d\theta\,d\phi

(possibly with some mod bars somewhere), the calculation of which is fairly simple - where '\tilde{a}' is \frac{a z}{z+1}, i.e. the new value of 'a' you'd have if z was z+1 - which makes the integral

\int_0^{\infty} \psi_{0}(r,a)\psi_{0}(r,\tilde{a})r^2\, dr \,sin(\theta)\,d\theta\,d\phi I believe.

Why is it this to begin with? It doesn't seem to be the standard 'probability is mod wavefunction squared' because there's one a and one \tilde{a} - can anyone explain?

One other thing, I'm not good with bra-ket notation(Dirac notation) so unless absolutely necessary words/other notation would be much more appreciated!

Thanks very much all :)
 
Last edited:
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It's very simple; if a particle is known to be in the (normalized) state \psi_1(\textbf{r}) (In the position basis), Then the probability of measuring it in a different (normalized) state \psi_2(\textbf{r}) is defined as

P(\psi_2)=\int_{\text{all space}}\left|\psi_1(\textbf{r})\psi_2(\textbf{r})\right|dV

In Bra-Ket notation, this is the same as P(\psi_2)=|\langle \psi_2|\psi_1\rangle|. You should have a similar definition in your text.

Your wavefunctions are real-valued, so taking the norm of their product is trivial, and the volume integral is done in spherical coordinates.
 

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