Precision measurement of the fundamental vibrational frequencies of tritium-bearing hydrogen molecules: T2, DT, HT (original) (raw)

2020, Physical Chemistry Chemical Physics

High-resolution coherent Raman spectroscopic measurements of all three tritium-containing molecular hydrogen isotopologues T 2 , DT and HT were performed to determine the ground electronic state fundamental Q-branch (v = 0 → 1, ∆J = 0) transition frequencies at accuracies of 0.0005 cm −1. An over hundred-fold improvement in accuracy over previous experiments allows the comparison with the latest ab initio calculations in the framework of Non-Adiabatic Perturbation Theory including nonrelativisitic, relativisitic and QED contributions. Excellent agreement is found between experiment and theory, thus providing a verification of the validity of the NAPT-framework for these tritiated species. While the transition frequencies were corrected for ac-Stark shifts, the contributions of non-resonant background as well as quantum interference effects between resonant features in the nonlinear spectroscopy were quantitatively investigated, also leading to corrections to the transition frequencies. Methods of saturated CARS with the observation of Lamb dips, as well as the use of continuous-wave radiation for the Stokes frequency were explored, that might pave the way for future higher-accuracy CARS measurements.

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Precision measurements and test of molecular theory in highly-excited vibrational states of H$_2$ (v=11)(v=11)(v=11)

arXiv (Cornell University), 2016

Accurate EF 1 Σ + g − X 1 Σ + g transition energies in molecular hydrogen were determined for transitions originating from levels with highly-excited vibrational quantum number, v = 11, in the ground electronic state. Doppler-free two-photon spectroscopy was applied on vibrationally excited H * 2 , produced via the photodissociation of H 2 S, yielding transition frequencies with accuracies of 45 MHz or 0.0015 cm −1. An important improvement is the enhanced detection efficiency by resonant excitation to autoionizing 7pπ electronic Rydberg states, resulting in narrow transitions due to reduced ac-Stark effects. Using known EF level energies, the level energies of X(v = 11, J = 1, 3 − 5) states are derived with accuracies of typically 0.002 cm −1. These experimental values are in excellent agreement with, and are more accurate than the results obtained from the most advanced ab initio molecular theory calculations including relativistic and QED contributions.

Tables 3-10 of transition frequencies from Non-adiabatic effects in the H+3 spectrum

2019

The effect of non-adiabatic coupling on the computed rovibrational energy levels amounts to about 2 cm<sup>−1</sup> for H<sup>+</sup><sub>3</sub> and must be included in high-accuracy calculations. Different strategies to obtain the corresponding energy shifts are reviewed in the article. A promising way is to introduce effective vibrational reduced masses that depend on the nuclear configuration. A new empirical method which uses the stockholder atoms-in-molecules approach to this effect is presented and applied to H<sup>+</sup><sub>3</sub>. Furthermore, a highly accurate potential energy surface for the D<sup>+</sup><sub>3</sub> isotopologue, which includes relativistic and leading QED terms, is constructed and used to analyse the observed rovibrational frequencies for this molecule. Accurate band origins are obtained that improve existing data.This article is part of the discussion meeting issue &...

Ab initio rotation-vibration energy levels of triatomics to spectroscopic accuracy

Spectrochimica Acta - Part A Molecular and Biomolecular Spectroscopy, 2002

The factors that need to be taken into account to achieve spectroscopic accuracy for triatomic molecules are considered focusing on H 3 + and water as examples. The magnitude of the adiabatic and non-adiabatic corrections to the Born-Oppenheimer approximation is illustrated for both molecules, and methods of including them ab initio are discussed. Electronic relativistic effects are not important for H 3 + , but are for water for which the magnitude of the various effects is discussed. For H 3 + inclusion of rotational non-adiabatic effects means that levels can be generated to an accuracy approaching 0.01 cm − 1 ; for water the error is still dominated by the error in the correlation energy in the electronic structure calculation. Prospects for improving this aspect of the calculation are discussed.

Non-adiabatic effects in the H 3 + spectrum

Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences, 2019

The effect of non-adiabatic coupling on the computed rovibrational energy levels amounts to about 2 cm −1 for H 3 + and must be included in high-accuracy calculations. Different strategies to obtain the corresponding energy shifts are reviewed in the article. A promising way is to introduce effective vibrational reduced masses that depend on the nuclear configuration. A new empirical method that uses the stockholder atoms-in-molecules approach to this effect is presented and applied to H 3 + . Furthermore, a highly accurate potential energy surface for the D 3 + isotopologue, which includes relativistic and leading quantum electrodynamic terms, is constructed and used to analyse the observed rovibrational frequencies for this molecule. Accurate band origins are obtained that improve existing data. This article is part of a discussion meeting issue ‘Advances in hydrogen molecular ions: H 3 + , H 5 + and beyond’.

Vibrationally selective radiative and non-radiative transitions in gaseous hydrogen molecules

Spectrochimica Acta Part A-molecular and Biomolecular Spectroscopy, 2011

An efficient vibrationally selective technique to build-up the v″ = 1 vibrational levels in gaseous hydrogen is demonstrated using stimulated Raman pumping (SRP). Both photo-acoustic Raman spectroscopy (PARS) and coherent anti-Stokes Raman spectroscopy (CARS) are used to study non-radiative and radiative (v″ = 0 and v″ = 1) transitions in gaseous H2 molecules. The population fraction in the v″ = 1 vibrational level has been estimated using combined photo-acoustic and coherent anti-Stokes Raman spectroscopy with stimulated Raman pumping.► Environmental pollution problems: continuous monitoring of the leakage of inflammable gases is also required, such as H2, CH4 and H2S, chemical plants and along gas pipe-lines for health and safety reasons. ► PARS and CARS laser spectroscopic technique with SRP. ► It is particularly advantageous since a tunable infra-red laser is not required. ► Application in Combustion diagnostic Engineering and Technology.

Fundamental Vibration of Molecular Hydrogen

Physical Review Letters, 2013

The fundamental ground tone vibration of H 2 , HD, and D 2 is determined to an accuracy of 2 Â 10 À4 cm À1 from Doppler-free laser spectroscopy in the collisionless environment of a molecular beam. This rotationless vibrational splitting is derived from the combination difference between electronic excitation from the X 1 AE þ g , v ¼ 0, and v ¼ 1 levels to a common EF 1 AE þ g , v ¼ 0 level. Agreement within 1 between the experimental result and a full ab initio calculation provides a stringent test of quantum electrodynamics in a chemically bound system.

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