Due to comments below this answer I note the term "degenerate states" was subjective so firstly I'll give a formal definition:
Degenerate states results when two (or more) different eigenstates to an eigenvalue equation correspond to the same eigenvalue.
I'm tasked with the following question on a problem sheet set by my lecturer:
Do degenerate states always have the same energy?
The answer given was:
False (they have the same eigenvalue of any operator, not necessarily energy)
My interpretation of the quotation above is as follows: The eigenvalues of any operator can be the same but the energy can be different. At the moment it is my understanding that Eigenvalues=Energy Eigenvalues=Energies. Is there a distinction between these terms when considering the Hamiltonian? If my interpretation of the answer is wrong could someone please explain what the correct interpretation is? If you are able to do this there is no need to read any more of the content below until you reach the line, where below is my main question.
I do not understand how this answer can be false, so I will use the eigenvalues to the two dimensional Simple Harmonic Oscillator as an example that I believe contradicts the answer statement:
The TISE eigenvalue equation for the SHO is $$\hat Hu(x,y)=\left[-\frac{\hbar^2}{2m}\left(\frac{\partial^2}{\partial x^2}+\frac{\partial^2}{\partial y^2}\right)+\frac{m\,{\omega_{x}}^2x^2}{2}+\frac{m\,{\omega_{y}}^2y^2}{2}\right]u(x,y)=E\,u(x,y)\tag{1}$$
Using separation of variables $u(x,y)=X(x)Y(y)$ such that $(1)$ becomes
$$-\frac{\hbar^2}{2m}\left(Y\frac{\partial^2X}{\partial x^2}+X\frac{\partial^2Y}{\partial y^2}\right)+\frac{m\,{\omega_{x}}^2x^2}{2}XY+\frac{m\,{\omega_{y}}^2y^2}{2}XY=EXY$$
and dividing throughout by $XY$ gives
$$\left(-\frac{\hbar^2}{2m}\frac{1}{X}\frac{\partial^2X}{\partial x^2}+\frac{m\,{\omega_{x}}^2x^2}{2}\right)+\left(-\frac{\hbar^2}{2m}\frac{1}{Y}\frac{\partial^2Y}{\partial y^2}+\frac{m\,{\omega_{y}}^2y^2}{2}\right)=E$$
Where $E=E_x+E_y$, I can now write equations involving $x$ and $y$:
$$-\frac{\hbar^2}{2m}\frac{\partial^2X}{\partial x^2}+\frac{m\,{\omega_{x}}^2x^2}{2}X=E_xX\tag{a}$$
$$-\frac{\hbar^2}{2m}\frac{\partial^2Y}{\partial y^2}+\frac{m\,{\omega_{y}}^2y^2}{2}Y=E_yY\tag{b}$$
Since $(\mathrm{a})$ and $(\mathrm{b})$ are one dimensional SHO eigenstate equations in $x$ and $y$ respectively; then we immediately know the eigenvalues:
$$E_x=\left(n_x + \frac12\right)\hbar\,\omega_x\quad\text{&}\quad E_y=\left(n_y + \frac12\right)\hbar\,\omega_y$$
Hence, the total energy $E$ is
$$E=E_x+E_y=\left(n_x + \frac12\right)\hbar\,\omega_x+\left(n_y + \frac12\right)\hbar\,\omega_y\tag{2}$$
So we now need two quantum numbers $n_x$ and $n_y$ to label eigenstates $$u_{{n_{x}}{n_{y}}}\equiv u_{n_{x}}(x)\,u_{n_{y}}(y)\tag{c}$$
Now suppose we are given a Central Potential such that $\omega_{x}=\omega_{y}=\omega_0$
Then $$V(x,y)=\frac{m\,{\omega_{x}}^2x^2}{2}+\frac{m\,{\omega_{y}}^2y^2}{2}=\frac{m\,{\omega_0}^2(x^2+y^2)}{2}=\frac{m\,{\omega_0}^2r^2}{2}=V(r)\tag{3}$$
As a result of $(2)$ and $(3)$ the energies are now given by
$$E=E_x+E_y=(n_x+n_y+1)\hbar\,\omega_0$$
The ground state clearly has $n_x=n_y=0$, for which $E_0=\hbar\,\omega_0$. However, there are now two first excited states, given by $n_x=1,n_y=0$ and $n_x=0,n_y=1$, both of which have $\fbox{$\color{blue}{E_1=2\hbar\,\omega_0}$}$. So from the definiton $(\mathrm{c})$ I have two degenerate states: $u_{10}$ and $u_{01}$ with eigenvalue equations $$\hat H u_{10}=E_1 u_{10}$$ and $$\hat H u_{01}=E_1 u_{01}$$
So I have found a case where same eigenvalues $E_1$ are the same energy.
Is this just a one-off coincidence, or can anyone provide me with an example where the energies are different but the Eigenvalues are the Same?
More importantly suppose we have a free particle with $$E=\frac{{\hbar}^2 k^2}{2m}$$
and a wavefunction $\psi$ satisfying $$\frac{d^2 \psi}{dx^2}+k^2\psi=0\tag{4}$$
$(4)$ has two possible solutions: $$\psi_1(x)=Ae^{ikx}\quad\text{and}\quad\psi_2(x)=Ae^{-ikx}$$
Applying the momentum operator $$\hat p=-i\hbar\frac{d}{dx}$$ to the two wavefunctions that solve $(4)$ gives for $\psi_1(x)$ $$\hat p\psi_1(x)=-i\hbar\frac{d}{dx}\left(Ae^{ikx}\right)=-i\hbar(ik)Ae^{ikx}=(\hbar k)Ae^{ikx}=\color{red}{(\hbar k)}\psi_1(x)$$ Similarly for $\psi_2(x)$ $$\hat p\psi_2(x)=\color{red}{-(\hbar k)}\psi_2(x)$$
So I have two degenerate states: $\psi_1(x)$ and $\psi_2(x)$ that apparently share eigenvalues.
But $$\color{red}{\hbar k} \ne \color{red}{-\hbar k}$$ If the eigenvalues are different how can the states be degenerate?
Or put in another way; since $\psi_1(x)$ and $\psi_2(x)$ no longer have the same eigenvalue this violates the definition of degenerate states in the first quotation at the beginning of this post.
EDIT:
It was my understanding that the minus sign belongs to the eigenvalue.
Do we simply consider the absolute value of the eigenvalue so that $\color{red}{\hbar k}$ will be the same for $\psi_1(x)$ and $\psi_2(x)$?