Precision measurement of quasi-bound resonances in H2 and the H + H scattering length

Abstract

Quasi-bound resonances of H2 are produced via two-photon photolysis of H2S molecules as reactive intermediates or transition states, and detected before decay of the parent molecule into three separate atoms. As was previously reported [K.F. Lai et al., Phys. Rev. Lett. 127, 183001 (2021)] four centrifugally bound quantum resonances with lifetimes of multiple μs, lying energetically above the dissociation limit of the electronic ground state X1g+ of H2, were observed as X(v,J) = (7,21)*, (8,19)*, (9,17)*, and (10,15)*, while also the short-lived ( 1.5 ns) quasi-bound resonance X(11,13)* was probed. The present paper gives a detailed account on the identification of the quasi-bound or shape resonances, based on laser detection via F-X two-photon transitions, and their strongly enhanced Franck-Condon factors due to the shifting of the wave function density to large internuclear separation. In addition, the assignment of the rotational quantum number is verified by subsequent multi-step laser excitation into autoionization continuum resonances. Existing frameworks of full-fledged ab initio computations for the bound region in H2, including Born-Oppenheimer, adiabatic, non-adiabatic, relativistic and quantum-electrodynamic contributions, are extended into the energetic range above the dissociation energy. These comprehensive calculations are compared to the accurate measurements of energies of quasi-bound resonances, finding excellent agreement. Etc.

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