Dissociation Energy of Molecular Hydrogen Isotopologues
arXiv:1909.01985 · doi:10.1103/PhysRevA.100.020503
Abstract
The nonrelativistic energy together with relativistic and quantum electrodynamic corrections for all the molecular hydrogen isotopologues (D, T, HD, HT, DT) were evaluated without expansion in the electron-nucleus mass ratio. The obtained results significantly improve the uncertainty of theoretical predictions, reaching a value below 1 MHz for the total dissociation energy. We observe good agreement with the experimental value for D and discrepancy for the HD molecule, while no experimental values for the dissociation energy of molecules involving tritium have yet been obtained.
7 pages. arXiv admin note: text overlap with arXiv:1812.02980
References in corpus (2)
Cited by in corpus (14)
- Rovibrational energy levels of the hydrogen molecule through nonadiabatic perturbation theory
- Analysis methods for the first KATRIN neutrino-mass measurement
- Precision measurement of the fundamental vibrational frequencies of tritium-bearing hydrogen molecules: T, DT, HT
- Improved Ionization and Dissociation Energies of the Deuterium Molecule
- Hyperfine components of all rovibrational quadrupole transitions in the H and D molecules
- Leading-order QED effects in the ground electronic state of molecular hydrogen
- Rotational level spacings in HD from vibrational saturation spectroscopy
- Nonrelativistic energy of tritium-containing hydrogen molecule isotopologues
- A Study of New Physics Searches with Tritium and Similar Molecules
- Nuclear magnetic shielding in HD and HT
- Precision measurement of quasi-bound resonances in H and the H + H scattering length
- Ab initio QED calculations in diatomic quasimolecules
- Quantum Monte Carlo study of three-dimensional Coulomb complexes: trions and biexcitons; hydrogen molecules and ions; helium hydride cations; and positronic and muonic complexes
- Integrals for lower bounds to the exact energy