Clarification on Energy Levels for a Hyperbolic Wave Function in Introductory Quantum Theory

I am working through an introductory problem that is part of an undergraduate course for Quantum Theory. I am self-studying currently. $$\DeclareMathOperator{\sech}{sech} \DeclareMathOperator{\tanh}{tanh}$$

A particle of mass $$m$$ moving on the $$x$$-axis has a ground-state wave function $$\psi_1(x)=\sech^2(x).$$ Show that the potential is $$V(x)=-\frac{3\hbar^2}{m}\sech^2(x).$$ If $$\psi(x)=\sech(x)\tanh(x)$$ is an excited state wave function for the particle, what is the energy of this state?

Both answers seem to follow straightforwardly from the stationary state Schrödinger Equation, and I have obtained $$E=-\frac{\hbar^2}{2m}$$ for the second part (hopefully correct).

From all examples I can find, the energy levels will typically be related by $$E_1n^2=E_n.$$

My question is what is the precise $$n$$ giving the energy level that has been found? My guess would be the second, since the relation $$\frac{1}{n^2}E_1=E_n$$ could make sense given that the ground state is the inverse of a standard hyperbolic function, and the examples I have covered lead to linear combinations of either $$\cos$$ & $$\sin$$, or $$\cosh$$ & $$\sinh$$, but I do not feel I am in a position this early on to understand how to explain such a result rigorously.

Please note I have only covered some fundamentals of Quantum Theory, namely:

$$\;\;\;\;\;\;\;\;\;\;\;\;\bullet$$ 'derivation' of Schrodinger's Equation

$$\;\;\;\;\;\;\;\;\;\;\;\;\bullet$$ modelling the wave function as a probability density funtion

$$\;\;\;\;\;\;\;\;\;\;\;\;\bullet$$ simple examples based around 'a particle in a box' (1D and 3D)

You were given the information that $$\psi_1$$ is the wavefunction of a ground state. Ground state, by definition, is the lowest energy stationary state. All stationary states have to fulfill the Time-independent Schrödinger Equation (TISE), so $$\psi_1$$ also has to. The final piece of the puzzle is that the Hamiltonian of a scalar particle in a potential is $$H = -\frac{\hbar^2}{2m} \, \frac{\mathrm d^2}{\mathrm dx^2} + V(x) \: ,$$ where $$V(x)$$ is the unknown function. And now it's just algebra: \begin{align} H \, \psi_1 &= E_1 \, \psi_1 \tag{TISE} \\ - \frac{\hbar^2}{2m} \, \frac{\mathrm d^2}{\mathrm dx^2} \, \psi(x) + V(x) \, \psi_1 &= E_1 \, \psi_1 \\[5pt] - \frac{\hbar^2}{2m} \, \frac{\mathrm d^2}{\mathrm dx^2} \, \operatorname{sech}^2(x) + V(x) \, \operatorname{sech}^2(x) &= E_1 \, \operatorname{sech}^2(x) \\[5pt] - \frac{\hbar^2}{2m} \big( 4 \operatorname{sech}^2(x) - 6 \operatorname{sech}^4(x) \big) -E_1 \, \operatorname{sech}^2(x) &= - V(x) \, \operatorname{sech}^2(x) \tag{1} \label{wolfram} \\[5pt] \frac{\hbar^2}{2m} \big( 4 - 6 \operatorname{sech}^2(x) \big) + E_1 &= V(x) \\[5pt] -\frac{3\hbar^2}{m} \operatorname{sech}^2(x) + \Big( E_1 + \frac{2\hbar^2}{m} \Big) &= V(x) \\[5pt] \end{align} At the step marked \eqref{wolfram} I used WolframAlpha (link). Since we weren't told the value of the ground-state energy $$E_1$$, we can fix it on any value we wish, choosing $$E_1 = -2\hbar^2/m$$ in particular gives us $$V(x) = -\frac{3\hbar^2}{m} \operatorname{sech}^2(x) \: .$$ Now we know the entire Hamiltonian and, in principle, we can find all of its energies and stationary states by solving the TISE, this time with $$E$$ and $$\psi$$ as unknowns. However, you have it easy, since you're already been told what $$\psi$$ is, so you just solve for $$E$$: $$\frac{\hbar^2}{m} \Bigg( {- \frac{1}{2}} \frac{\mathrm d^2}{\mathrm dx^2} \, -3 \operatorname{sech}^2(x) \Bigg) \, \operatorname{sech}(x) \, \operatorname{tanh}(x) = E \, \operatorname{sech}(x) \, \operatorname{tanh}(x) \: .$$ I trust you can pull this off ;)
Notice that we aren't using the equation $$E_1n^2=E_n$$. Why? Because it doesn't hold – at least not generally! It is an equation that holds for the energies of a hydrogen atom, but not for a general Hamiltonian. And even the hydrogen atom Hamiltonian has energies $$E>0$$ for which the equation is useless. To find the energies of a generic system, you just have to find the spectrum of $$H$$, there is no short way around it.
• $\DeclareMathOperator{\sech}{sech}$ Thank you for this! I've just realised the mistake is that I accidentally put $\psi(x)=\sech(x)$ when it should have been $\psi(x)=\sech^2(x)$. Sep 1, 2021 at 17:59
• I've edited the answer to have $\psi(x) = \operatorname{sech}^2(x)$. If this answers your question, please don't forget to mark it as the correct answer :)