Understanding the electronic structure of Y2Ti2O5S2 for green hydrogen production: a hybrid-DFT and GW study

Abstract

Utilising photocatalytic water splitting to produce green hydrogen is the key to reducing the carbon footprint of this crucial chemical feedstock. In this study, density functional theory (DFT) is employed to gain insights into the photocatalytic performance of an up-and-coming photocatalyst Y₂Ti₂O₅S₂ from first principles. Eleven non-polar clean surfaces are evaluated at the generalised gradient approximation level to obtain a plate-like Wulff shape that agrees well with the experimental data. The (001), (101) and (211) surfaces are considered further at hybrid-DFT level to determine their band alignments with respect to vacuum. The large band offset between the basal (001) and side (101) and (211) surfaces confirms experimentally observed spatial separation of hydrogen and oxygen evolution facets. Furthermore, relevant optoelectronic bulk properties were established using a combination of hybrid-DFT and many-body perturbation theory. The optical absorption of Y₂Ti₂O₅S₂ weakly onsets due to dipole–forbidden transitions, and hybrid Wannier–Mott/Frenkel excitonic behaviour is predicted to occur due to the two-dimensional electronic structure, with an exciton binding energy of 0.4 eV.