Benchmarking theory with an improved measurement of the ionization and dissociation energies of H
arXiv:1902.09471 · doi:10.1103/PhysRevLett.122.103002
Abstract
The dissociation energy of H represents a benchmark quantity to test the accuracy of first-principles calculations. We present a new measurement of the energy interval between the EF state and the 54p1 Rydberg state of H. When combined with previously determined intervals, this new measurement leads to an improved value of the dissociation energy of ortho-H that has, for the first time, reached a level of uncertainty that is three times smaller than the contribution of about 1 MHz resulting from the finite size of the proton. The new result of 35999.582834(11) cm is in remarkable agreement with the theoretical result of 35999.582820(26) cm obtained in calculations including high-order relativistic and quantum electrodynamics corrections, as reported in the companion article (M. Puchalski, J. Komasa, P. Czachorowski and K. Pachucki, submitted). This agreement resolves a recent discrepancy between experiment and theory that had hindered a possible use of the dissociation energy of H in the context of the current controversy on the charge radius of the proton.
References in corpus (1)
Cited by in corpus (31)
- Near-ultraviolet photon-counting dual-comb spectroscopy
- The proton structure in and out of muonic hydrogen
- Molecule-specific Uncertainty Quantification in Quantum Chemical Studies
- Non-adiabatic, Relativistic, and Leading-order QED Corrections for Rovibrational Intervals of He ()
- Precision measurement of the ionization energy and quantum defects of 39K I
- High-Precision Ramsey-Comb Spectroscopy Based on High-Harmonic Generation
- Precision Measurements in Few-Electron Molecules: The Ionization Energy of Metastable He and the First Rotational Interval of He
- All-order relativistic computations for atoms and molecules using an explicitly correlated Gaussian basis
- Variational Dirac-Coulomb explicitly correlated computations for atoms and molecules
- Improved Ionization and Dissociation Energies of the Deuterium Molecule
- Slow decay processes of electrostatically trapped Rydberg NO molecules
- Hyperfine components of all rovibrational quadrupole transitions in the H and D molecules
- Rotational level spacings in HD from vibrational saturation spectroscopy
- The Bethe-Salpeter QED wave equation for bound-state computations of atoms and molecules
- Stochastic Variational Approach to Small Atoms and Molecules Coupled to Quantum Field Modes
- Excitation and characterization of long-lived hydrogenic Rydberg states of nitric oxide
- Born-Oppenheimer potentials for , , and states of the hydrogen molecule
- Nonrelativistic energy of tritium-containing hydrogen molecule isotopologues
- Pre-Born-Oppenheimer energies, leading-order relativistic and QED corrections for electronically excited states of molecular hydrogen
- Precision millimetre-wave spectroscopy and calculation of the Stark manifolds in high Rydberg states of para-H
- Precision measurement of quasi-bound resonances in H and the H + H scattering length
- Demonstration of Ramsey-Comb Precision Spectroscopy in Xenon at Vacuum Ultraviolet Wavelengths Produced with High-Harmonic Generation
- Shape resonances in H as photolysis reaction intermediates
- Electrostatic trapping of N molecules in high Rydberg states
- Precision Spectroscopy of the Fine Structure in the and States of the Helium Dimer
- Spectroscopic study of the F outer well state in H, HD and D
- Analysis of the first infrared spectrum of quasi-bound H2 line emission in Herbig-Haro 7
- Nonadiabatic corrections to electric quadrupole transition rates in H
- Laser Excitation of Muonic 1S Hydrogen Hyperfine Transition: Effects of Multi-pass Cell Interference
- Deformed Explicitly Correlated Gaussians
- Lamb-peak spectrum of the HD (2-0) P(1) line