A potential surface is reported for H2O at a fixed bond angle of 105°. The surface covers an extended range, including the dissociation channels OH(2Π) + H(2S) and O(3P) + 2H( 2S). Using a double-zeta basis set and multireference CI technique, followed by a fitting procedure using rotated Morse curves, the following results were obtained: H2O(1A1)→OH( 2Π) + H(2S), ΔE = 4.50 eV (expt. 5.47); H 2O(1A1)→O(3P) + 2H( 2S), ΔE = 8.03 eV (expt. 10.08). A double-zeta + polarization basis set leads to improved results (5.18 and 9.44 eV). The shape of the surface is well described by rotated Morse curves. A simple scaling procedure brings the computed surface into close coincidence (within ∼0.2 eV) with a surface based on an experimental force field. The scaled RMCS-CI approach may be useful for other triatomic systems to provide an accurate surface at a reasonable cost.

Additional Metadata
Journal The Journal of Chemical Physics
Citation
Wright, J.S, & Shih, S.-K. (Shing-Kuo). (1980). RMCS-CI potential surface for H2O→OH+H. The Journal of Chemical Physics, 73(10), 5204–5211.