Given the potential find the eigenfunction

In summary, the task involves identifying the eigenfunction associated with a given operator or matrix, which typically entails solving an equation that relates the operator to a scalar multiple of the eigenfunction itself. This process is fundamental in various fields such as quantum mechanics and linear algebra, as eigenfunctions provide insight into the behavior of systems represented by linear transformations.
  • #1
Ashphy
6
0
Homework Statement
Given the potential find the eigenfunction
Relevant Equations
$$V(x)=\begin{cases}0; x>0\\ \infty;x<0 \end{cases}$$
Hi, this was one of the oral exam questions my teacher asked so i tried to solve it. Consider y>0 the energy spectrum here is continuous and non degenerate while for y<0 the spectrum is discrete and non degenerate because E<0.
for y>0 i thought of 2 cases
case 1 there is no wave function for x<0 because of infinite potential so the general solution must be $$\psi(x)=Ae^{ikx}+Be^{-ikx}$$ then i apply continuity of the function and continuity of the derevative to finde theat A=-B such $$\psi(x)=A(e^{ikx}-e^{-ikx})=-2iAsinkx$$ but this is not normalizable since the integral is divergent so i consider the case 2 such i have an oscillating wave function for x>0 and an exponentially decreasing function for x<0 and then i go ahead and find C (constant associated to the real exponential for x<0) and B in function of A but then again it is not normalizable. What am i doing wrong? if anyone could please tell me if there is a better approach to the problem it would be really helpful, thank you
 
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  • #2
I assume you haven't seen anything like this before? Non-normalizable solutions for a free particle?
 
  • #3
no i have not, i just recently started studying potentials and as of my class notes i have written that acceptable wave eigenfunctions must be normalizable, is it not so?
 
  • #4
Because plane-wave states are not properly normalisable we employ the trick of normalising them in a large (relative to potential range) cubic box of side L with periodic boundary conditions. We then take the limit L→∞ at the end of the calculation. Of course we no longer have a strictly continuous spectrum of eigenstates, except in the limit.
Note that this is equivalent to solving the problem of a well and letting one wall "go out to infinity". One becomes used to such chicanery because of its utility.
 
  • #5
Ashphy said:
no i have not, i just recently started studying potentials and as of my class notes i have written that acceptable wave eigenfunctions must be normalizable, is it not so?
To be viable physical solutions, they must be normalizable. What you've found is only part of the story. To normalize such wavefunctions you have to bundle them up into a wave-packet.

That said, the non-normalizable eigenfunctions can still be useful for studying quantum behaviour - such as reflection and transmission coefficients.

You didn't do anything wrong, by the way. This should have been covered in your course.
 
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  • #6
PeroK said:
To be viable physical solutions, they must be normalizable. What you've found is only part of the story. To normalize such wavefunctions you have to bundle them up into a wave-packet.

That said, the non-normalizable eigenfunctions can still be useful for studying quantum behaviour - such as reflection and transmission coefficients.

You didn't do anything wrong, by the way. This should have been covered in your course.
thank you for that, i may be missing notes, is there any good book where i can find more?
 
  • #7
hutchphd said:
Because plane-wave states are not properly normalisable we employ the trick of normalising them in a large (relative to potential range) cubic box of side L with periodic boundary conditions. We then take the limit L→∞ at the end of the calculation. Of course we no longer have a strictly continuous spectrum of eigenstates, except in the limit.
Note that this is equivalent to solving the problem of a well and letting one wall "go out to infinity". One becomes used to such chicanery because of its utility.
Thank you! i would have never thought.
so in this case do i just take my solutions for the potential well,with $$ \psi=\sqrt{2/L}sin(\frac{n\pi x}{L}) \\L\to\infty $$ doesn't it make ##\psi=0## ?
 
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  • #8
Typically when you need to calculate a real world number (one that corresponds to a measurable quantity) the answer will not depend explicitly on the "size of the box" and the limit doesn't matter. We are imperfect beings.........
 
  • #11
hutchphd said:
Typically when you need to calculate a real world number (one that corresponds to a measurable quantity) the answer will not depend explicitly on the "size of the box" and the limit doesn't matter. We are imperfect beings.........
following your tip i tried to solve it like so: Let the general solution to a finite well from 0 to L be ##\psi=Bsin(kx)+Acos(kx)## then i apply the periodic condition such $$\begin{cases}\psi(0)=\psi(L)\\ \psi '(0)=\psi '(L)\end{cases},$$ Solving the system gives $$\begin{cases}B=A\frac{1-coskL}{sinkL}\\coskL=n\pi\end{cases}$$ so i find the condition ##k=\frac{n\pi}{L};\;E=\frac{n^2\pi^2\hbar^2}{2mL^2}## which seem reasonable but then if i substitute k in B and i find an indeterminate form of ##\frac{0}{0}## so i thought i'd put B=0 (i feel that's wrong) and find ##\psi=Acos(\frac{n\pi x}{L})## that gives ##\psi=A## for ##L\to\infty## which seems wrong. Is this reasonable? am i approaching it correctly?
 

FAQ: Given the potential find the eigenfunction

What is an eigenfunction?

An eigenfunction is a special type of function that, when acted upon by a given linear operator, yields the original function multiplied by a constant, known as the eigenvalue. In mathematical terms, if \( \hat{L} \psi = \lambda \psi \), then \( \psi \) is the eigenfunction and \( \lambda \) is the eigenvalue.

How do you find the eigenfunction given a potential in quantum mechanics?

To find the eigenfunction given a potential in quantum mechanics, you typically solve the Schrödinger equation. For a time-independent potential, the equation is \( \hat{H} \psi = E \psi \), where \( \hat{H} \) is the Hamiltonian operator, \( \psi \) is the eigenfunction, and \( E \) is the eigenvalue (energy). The Hamiltonian usually includes the potential term, and solving this differential equation will yield the eigenfunctions.

What role does the potential play in determining the eigenfunctions?

The potential in the Schrödinger equation influences the form of the eigenfunctions. Different potentials lead to different differential equations, which in turn yield different sets of eigenfunctions. For example, a simple harmonic oscillator potential results in eigenfunctions that are Hermite polynomials, while a Coulomb potential leads to eigenfunctions that are spherical harmonics and radial functions.

Can you always find an analytical solution for the eigenfunctions given any potential?

No, it is not always possible to find an analytical solution for the eigenfunctions for any given potential. For many complex or irregular potentials, analytical solutions are not feasible, and numerical methods must be used to approximate the eigenfunctions and eigenvalues.

What are common methods to solve for eigenfunctions numerically?

Common numerical methods to solve for eigenfunctions include finite difference methods, the shooting method, and variational techniques. Additionally, eigenvalue problems can be tackled using matrix diagonalization methods when the problem is discretized. Software packages like MATLAB, Mathematica, and various quantum chemistry programs often have built-in functions to handle these calculations.

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