Lecture #3b-- Photon emission in non-LTE



1) Sample problem
A sample problem is worked where we find the necessary dilution factor W for a 3-eV quasi-thermal radiation spectrum, to yield 50% ionization, in a gas where the density is 10^-16 particles per elementary state volume (the latter is the cube of the deBroglie wavelength of thermal electrons). We find W must be about 10^-14, so we need to be about 10^7 solar radii, or about 100 pc, from the O-star. It is pointed out that HII regions are rarely so large-- because we did not worry about exhausting all possible ionizing photons.
2) Concept of Emission Measure
If we have an optically thin box, then all the light emitted in the box will escape to be seen. Since the densities are far below critical, all the de-excitation will be radiative, so we need only worry about the excitation rates. Unless we are looking at flourescence, all the excitation will either be collisional (so proportional to density-squared) excitation, or it will be radiative recombination (also proportional to density-squared), so the excitation rate in the box is proportional to the density squared. The emission just depends on inherent radiative rates, so the total rate that light emerges will be proportional to the density-squared times the volume. This latter quantity is therefore called the "emission measure", and is elevated by clumping even if you have a fixed amount of stuff in the box.
3) Electronic vs. vibrational vs. rotational transitions
For a system to emit a photon, there must be something inside the system that is responding at the frequency of the photon, so that it can resonate with the photon it is making over many many cycles (each cycle is itself a very weak interaction, that's the flavor of "perturbation theory"). That also puts a constraint on the characteristic frequency the system can emit. For quantum systems of fixed size L, the uncertainty principle dictates that the emitted frequency be proportional to the mass of the charged particle doing the emitting (say an electron in a hydrogen atom). For classical oscillators, the frequency is inversely proportional to the square root of the mass, because the restoring force limits the amplitude of the oscillation in a way such that increasing the acceleration by reducing the mass will shorten the period, but not proportionally because the amplitude is also enhanced. For classical rotators, the frequency is inversely proportional to the mass, because the amplitude of the oscillation is fixed by the size of the molecule that is rotating.

When you go from the oscillations of the electron in an atom, to the vibrations of the nuclei themselves, you can treat the nuclei classically and say that their mass is up by a factor of 1843 so their frequency is down by the square root of that-- putting it in the near-infrared. If you look instead at the rotations of the nuclei around each other, you are down in frequency by the full 1843, so you are in the submillimeter regime.