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The photocatalytic activity of TiO2 for water splitting has been known for decades, yet the adsorption structure and hydrogen bonding of water at the interface with TiO2 have remained controversial. We investigate the prototypical aqueous interface with anatase TiO2 (101) using ab initio molecular dynamics (AIMD) with the strongly constrained and appropriately normed (SCAN) density functional, recently shown to provide an excellent description of the properties of bulk liquid water. We find that water forms a stable bilayer of intact molecules with ice-like dynamics and enhanced dipole moment and polarizability on the anatase surface. The orientational order and H-bond environment of interfacial water are reflected in the computed sum frequency generation (SFG) spectrum, which agrees well with recent measurements in the OH stretching frequency range (3000–3600 cm–1). Additional AIMD simulations for a model interface with 66% of dissociated water in the contact layer show that surface hydroxyls disrupt the...

The photocatalytic activity of TiO