THE DISSOCIATIN ENERGY OF THE HYDROGEN MOPLECULE

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1992

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Ohio State University

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Fluorescence-excitation spectroscopy has been used to measure the threshold for the second dissociation limit of Double exponent: use braces to clarifyH_{2}(B^{\prime}^{1}\Sigma{_{u}}^{\prime}) = H (1s) + H (2s)H_{2}(B^{\prime}^{1}\Sigma{_{u}}^{\prime}) = H (1s) + H (2s) at 118377.06±0.04cm−1, and to determine a precise value for the dissociation energy of the ground electronic state. Coherent radiation near 84.5nm was used to excite a beam of hydrogen gas, and tuned over this threshold region. Metastable 2s atoms formed in the dissociation process were detected by quenching with an electric field, delayed -- 200 ns after the excitation pulse. This delay time was sufficient to allow molecules excited in the B and B^{\prime} states to decay by radiation, long before the 2s atoms were quenched to produce Lyman-α radiation. This it was possible to observe the dissociation limit clearly, without overlapping molecular features, and to derive a value for the dissociation energy of H2, namely, Do(H2)=36118.11±0.08cm−1. This is in good agreement with the latest theoretical value1 of 36118.09±0.10cm−1, which includes nonadiabatic, relativistic, and radiative corrections. When the present value is combined with recent experimental values of the ionization potentials of H and H2 it yields D0 (H2+)=21379.36±0.08cm−1, also in good agreement with theory.

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1 W. Kolos, K. Szalewicz, and H.J. Monkhorst, J. Chem. Phys. 84, 3278 (1986).


Author Institution: Department of Physics, University of Toronto; D'{e}partment de Physique Atomique et Moleculaire, Universit'{e} de Rennes I, 35042 Rennes, France

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