H3+ cooling in planetary atmospheres
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Updated: Jun 4, 2026

Simulation of the Planetary Interior Differentiation Processes in the Laboratory
Published on: November 15, 2013
Steve Miller1, Tom Stallard, Henrik Melin
1Department of Physics and Astronomy, University College London, Gower Street, London WC1E 6BT, UK. s.miller@ucl.ac.uk
Abstract:
We review the role of H3+ in planetary atmospheres, with a particular emphasis on its effect in cooling and stabilising, an effect that has been termed the "H3+ thermostat" (see Miller et al., Philos. Trans. R. Soc. London, Ser. A, 2000, 58, 2485). In the course of our analysis of this effect, we found that cooling functions that make use of the partition function, Q(T) based on the calculated H3+ energy levels of Neale and Tennyson (Astrophys. J., 1995, 454, L169) may underestimate just how much energy this ion is radiating to space. So we present a new fit to the calculated values of Q(T) that is accurate to within 2% for the range 100 K to 10 000 K, a very significant improvement on the fit originally provided by Neale and Tennyson themselves. We also present a fit to Q(T) calculated from only those values Neale and Tennyson computed from first principles, which may be more appropriate for planetary scientists wishing to calculate the amount of atmospheric cooling from the H3+ ion.
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