Past exam of the further quantum theory course of the University of Oxford / 2023 / 3 / e

A tall, broad central potential barrier has $\varphi \gg 1$. Let $\sigma =+1$ denote even parity and $\sigma =-1$ odd parity, and write $\theta =(n+\frac{1}{2})\pi +{\delta }_{\sigma }$, where $n=0,1,\dots$. Since $\tan [(n+\frac{1}{2})\pi +\delta ]=-\cot \delta$, the condition in part (d) givesThus the leading correction to the isolated-well Bohr-Sommerfeld quantization condition isThis is an implicit condition, with all action integrals evaluated at the corrected energy. To convert it into an explicit leading energy correction, let $E_n^{(0)}$ solve $\theta (E_n^{(0)})=(n+\frac{1}{2})\pi$ and define the full classical oscillation period in one well by $\mathcal{T}(E)=2m{\int }_{x_1}^{x_2}dx/p(x)$. Differentiation of the action integral has no endpoint terms because $p(x_1)=p(x_2)=0$, and givesConsequently, to leading exponentially small order within the WKB approximation,The even member lies below its odd partner. For an approximately harmonic oscillator well, $\mathcal{T}\simeq 2\pi /\omega$, giving the familiar double-well tunneling splitting $\Delta E\simeq (\hslash \omega /\pi )e^{-\varphi }$. The explicit energy formula retains only its leading exponential correction; varying $\varphi$ and ${\theta }^{\prime }$ with the shifted energy also contributes at higher orders.

The ground state has an even, everywhere same-sign wavefunction with a peak in each well and a small nonzero value beneath the central potential barrier. Its derivative vanishes at zero. The first excited state is odd, has opposite-sign lobes in the two wells, and has exactly one interior node of a wavefunction, at zero. Both wavefunctions decay outside the wells. In terms of localized normalized wavefunctions ${\phi }_L,{\phi }_R$, with overlap $s=⟨{\phi }_L|{\phi }_R⟩$, their qualitative shapes are the lowest parity states of a symmetric double well:The overall sign of the odd wavefunction is arbitrary. The sketch uses localized Gaussian profiles to show the parity and the central node of a wavefunction, rather than claiming exact energy eigenfunctions for an unspecified potential energy.