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A radiative lifetime depends on the available electromagnetic modes as well as on the atomic transition. In the ideal parallel-perfect conductor geometry of polarization-selective spontaneous emission between conducting plates, an in-plane transition dipole has no coupled propagating electric dipole radiation mode below the relevant waveguide cutoff frequency.

If that idealized electric dipole transition is the only decay channel, its rate is zero and the corresponding lifetime diverges. This is a statement about a restricted channel and geometry, not a general prediction of an immortal excited atom. Finite plates, absorbing surfaces, dipole misalignment and other allowed transitions can restore decay. A normal transition dipole can couple to the surviving transverse electromagnetic mode.

Define $\hslash {\omega }_0=E_2-E_1$ and use radiation energy density $u(\omega )$ per unit angular frequency, excluding the zero-point contribution. The Angular-frequency Einstein coefficients give rates per atom: $B_{12}u({\omega }_0)$ for absorption, $B_{21}u({\omega }_0)$ for stimulated emission, and $A_{21}$ for spontaneous emission. Stimulated emission adds a photon to the stimulating mode; spontaneous emission persists with no incident photons.

In thermal equilibrium the Boltzmann distribution gives $N_2/N_1=e^{-\hslash {\omega }_0/(k_{\mathrm{B}}T)}$. Balancing up and down rates yieldsMatching the Planck law for every temperature fixesNo degeneracy factor is needed for these nondegenerate levels.^[ref]

For plates of large area $A$ and spacing $d$, the surviving low-frequency transverse electromagnetic mode has one polarization, $\mathbf{E}\parallel \hat{\mathbf{z}}$, and in-plane wavevector. Periodic in-plane counting givesMultiplying this single-polarization two-dimensional photon density of states by $\hslash \omega$ and the Bose-Einstein distribution produces the thermal radiation between parallel conducting plates:The same rate balance therefore givesThese $B$ coefficients refer to the radiation polarization in their respective environments: isotropic free-space $B$ must not automatically be equated to the coefficient for a specified $z$-polarized field.

For hydrogen, take the quantization axis along $z$, neglect spin-orbit coupling, and assume perfect plates, a wide in-plane region and an unmodified atomic wavefunction: $a_{\mathrm{B}}\ll d\ll c/{\omega }_0$, with negligible surface-induced mixing or shifts. The electric-dipole selection rules for hydrogen require $\Delta l=\pm 1$; the allowed $z$ field has $\Delta m_{\ell }=0$. Hence the polarization-selective spontaneous emission between conducting plates givesThe thin-cavity enhancement of a normal electric dipole applies: the $2p_0\to 1s$ dipole points along $z$ and couples to the enhanced mode density. For $m_{\ell }=\pm 1$, the transition dipoles lie in the $x$–$y$ plane and couple to none of these low-frequency modes: the electric-dipole decay rate is zero in the ideal model, so this channel's lifetime is infinite. Real finite, imperfect plates and additional decay or mixing channels limit the lifetime. The order-one orientation factor for the allowed transition does not change the requested lifetime scaling.