A first-principles study of H2O adsorption and dissociation on the SrTiO3(100) surface

• Published in: Molecular simulation 2010-06, Vol.36 (7-8), p.604-617
• Main Authors: Hinojosa, Beverly Brooks, Van Cleve, Tim, Asthagiri, Aravind
• Format: Article
• Language: English
• Subjects: Adsorption; Density functional theory; Energy of dissociation; Mathematical analysis; oxide surfaces; Short range order; Simulation; SrTiO; Surface chemistry; Titanium dioxide; water
• ISSN: 0892-7022; 1029-0435
• DOI: 10.1080/08927021003762746

We use density functional theory (DFT) to examine the adsorption of H 2 O on the SrO- and TiO 2 -terminated SrTiO 3 (100) surface. At coverages of 0.5 monolayer (ML), we find that water preferentially binds associatively on the TiO 2 termination by 0.2 eV/H 2 O and negligible differences in energy between associated and dissociated H 2 O on the SrO termination. These results are in agreement with an earlier hybrid Hartree-Fock-DFT study and the general conclusions from several experimental studies. But at coverages below 3/8 ML, our DFT calculations predict a crossover to preference for dissociative H 2 O on the TiO 2 termination. On the SrO termination, the use of larger surface supercells (2 × 2) allows for the stabilisation of mixed adsorption configuration at 1/2 ML and subsequent decrease in coverage results in dissociative water configurations. We explored dimer configurations of molecular H 2 O and HO-H 2 O complexes at 1/4 ML coverage but these configurations are less stable than the isolated dissociated state. The energy barrier for dissociation of H 2 O on the TiO 2 termination at 1/8 ML coverage is found to be 0.08 eV, which suggests that the dissociated state is both favoured energetically and kinetically at low coverages and temperatures. These low coverage results from our DFT study conflict with existing experimental studies and we present scenarios that can be explored both experimentally and theoretically to resolve this discrepancy.