Abstract
Photodissociation dynamics of H(2)O via the D state by two-photon absorption have been investigated using the H-atom Rydberg tagging time-of-flight technique. The action spectrum of the D<--X transition band has been measured. The predissociation lifetime of the D state is determined to be about 13.5 fs. The quantum state-resolved OH product translational energy distributions and angular distributions have also been measured. By carefully simulating these distributions, quantum state distributions of the OH product as well as the state-resolved angular anisotropy parameters were determined. The most important pathway of the H(2)O dissociation via the D state leads to the highly rotationally excited OH(X,v=0) products. Vibrationally excited OH(X) products (up to v=10) and electronically excited OH(A,v=0,1,2) have also been observed. The OH(A)/OH(X) branching ratios are determined to be 17.9% at 244.540 nm (2omega(1)=81,761.4 cm(-1)) and 19.9% at 244.392 nm (2omega(2)=81,811 cm(-1)), which are considerably smaller than the value predicted by the theory. These discrepancies are attributed to the nonadiabatic coupling effect between the B and D surfaces at the bent geometry.
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