Dissociation energy of the hydrogen molecule at 10 accuracy
arXiv:1804.11143 · doi:10.1103/PhysRevLett.121.013001
Abstract
The ionization energy of ortho-H has been determined to be cm from measurements of the GK(1,1)--X(0,1) interval by Doppler-free two-photon spectroscopy using a narrow band 179-nm laser source and the ionization energy of the GK(1,1) state by continuous-wave near-infrared laser spectroscopy. (H) was used to derive the dissociation energy of H, (H), at cm with a precision that is more than one order of magnitude better than all previous results. The new result challenges calculations of this quantity and represents a benchmark value for future relativistic and QED calculations of molecular energies.
6 pages, 5 figures
References in corpus (8)
- CODATA Recommended Values of the Fundamental Physical Constants: 2014
- Born-Oppenheimer potential for H
- Fundamental transitions and ionization energies of the hydrogen molecular ions at the few ppt level
- Toward a determination of the proton-electron mass ratio from the Lamb-dip measurement of HD
- Complete corrections to the ground state of H
- Relativistic corrections for the ground electronic state of molecular hydrogen
- Schrödinger equation solved for the hydrogen molecule with unprecedented accuracy
- Elimination of the Translational Kinetic Energy Contamination in pre-Born-Oppenheimer Calculations
Cited by in corpus (29)
- Benchmarking theory with an improved measurement of the ionization and dissociation energies of H
- Rovibrational energy levels of the hydrogen molecule through nonadiabatic perturbation theory
- Nonadiabatic QED correction to the dissociation energy of the hydrogen molecule
- Lamb-dips and Lamb-peaks in the saturation spectrum of HD
- Nonadiabatic relativistic correction in H, D, and HD
- Quantum control of molecules for fundamental physics
- Dissociation Energy of Molecular Hydrogen Isotopologues
- A terahertz vibrational molecular clock with systematic uncertainty at the level
- Molecule-specific Uncertainty Quantification in Quantum Chemical Studies
- Precision measurement of the fundamental vibrational frequencies of tritium-bearing hydrogen molecules: T, DT, HT
- Precision Measurements in Few-Electron Molecules: The Ionization Energy of Metastable He and the First Rotational Interval of He
- Effective non-adiabatic Hamiltonians for the quantum nuclear motion over coupled electronic states
- Precise computation of rovibronic resonances of molecular hydrogen: inner-well rotational states
- Quantum System Partitioning at the Single-Particle Level
- Improved Ionization and Dissociation Energies of the Deuterium Molecule
- Explicitly correlated Gaussian functions with shifted-center and projection techniques in pre-Born-Oppenheimer calculations
- H as a five-body problem described with explicitly correlated Gaussian basis sets
- Photolysis production and spectroscopic investigation of the highest vibrational states in H (X )
- 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
- Determining Absolute Neutrino Mass using Quantum Technologies
- Density functional theory beyond the Born-Oppenheimer approximation: accurate treatment of the ionic zero-point motion
- Precision measurement of quasi-bound resonances in H and the H + H scattering length
- Shape resonances in H as photolysis reaction intermediates
- Chirp-compensated pulsed titanium-sapphire laser system for precision spectroscopy
- Two-photon Doppler-free ultraviolet laser spectroscopy on sulphur atoms
- Lamb-peak spectrum of the HD (2-0) P(1) line
- Intensity-dependent precision two-photon Doppler-free spectroscopy of Xe using narrow-bandwidth long-pulse deep-UV laser radiation