Defect Engineering Centrosymmetric 2D Material Flexocatalysts

Abstract In this study, the flexoelectric characteristics of 2D TiO 2 nanosheets are examined. The theoretical calculations and experimental results reveal an excellent strain‐induced flexoelectric potential (flexopotential) by an effective defect engineering strategy, which suppresses the recombination of electron–hole pairs, thus substantially improving the catalytic activity of the TiO 2 nanosheets in the degradation of Rhodamine B dye and the hydrogen evolution reaction in a dark environment. The results indicate that strain‐induced bandgap reduction enhances the catalytic activity of the TiO 2 nanosheets. In addition, the TiO 2 nanosheets degraded Rhodamine B, with k obs being ≈1.5 × 10 −2 min −1 in dark, while TiO 2 nanoparticles show only an adsorption effect. 2D TiO 2 nanosheets achieve a hydrogen production rate of 137.9 µmol g −1 h −1 under a dark environment, 197% higher than those of TiO 2 nanoparticles (70.1 µmol g −1 h −1 ). The flexopotential of the TiO 2 nanosheets is enhanced by increasing the bending moment, with excellent flexopotential along the y ‐axis. Density functional theory is used to identify the stress‐induced bandgap reduction and oxygen vacancy formation, which results in the self‐dissociation of H 2 O on the surface of the TiO in the dark. The present findings provide novel insights into the role of TiO 2 flexocatalysis in electrochemical reactions.