Enhanced photoelectrochemical performance of anatase TiO2 by metal-assisted S–O coupling for water splitting

In this study, hybrid density functional theory calculations have been used to investigate the electronic structures of (Mg, S), (2Al, S), (Ca, S), and (2Ga, S) codoped anatase TiO2, aiming at improving their photoelectochemical performance for water splitting. It is found that the acceptor metals (Mg, Al, Ca, and Ga), assisting the coupling of the incorporated S with the neighboring O in TiO2, lead to the fully occupied energy levels in the forbidden band of TiO2, which is driven by the antibonding state π* of the S–O bond. It is also found that the metal-assisted S–O coupling can prevent the recombination of the photo-generated electron–hole pairs and effectively reduce the band gap of TiO2. Among these systems, the (Mg, S) codoped anatase TiO2 has the narrowest band gap of 2.206 eV, and its band edges match well with the redox potentials of water. We propose that this metal-assisted S–O coupling could improve the visible light photoelectrochemical activity of anatase TiO2.

► Hybrid density functional theory calculations of codoped anatase TiO2.
► Metal-assisted S–O coupling can effectively reduce the band gap of TiO2.
► Band edges of codoped TiO2 match well with the redox potentials of water.
► (Mg, S) codoped TiO2 has the band gap of 2.206 eV.