Proton doping enhanced flexoelectricity and photocurrent in hydrogen-charged TiO2.

The intrinsic flexoelectric effect observed in oxide materials often falls below the desired threshold for practical applications. In this work, we demonstrate proton doping in insulating rutile TiO₂ crystal as an effective approach to significantly increase flexoelectricity by more than two orders of magnitude. We attribute the noteworthy enhancement of flexoelectricity to the dual impact of proton doping in oxide materials. First, proton doping serves to induce the presence of charge carriers, resulting in the generation of flexoelectric currents. Second, proton doping induces expansion and distortion of the lattice structure, leading to an amplified flexoelectric field when the crystal experiences a strain gradient. The formation of O–H bonding in TiO₂ crystal provides another route to break centrosymmetry according to lattice distortion of the TiO₂ lattice, resulting in a larger flexoelectric field. In addition, the introduction of proton doping in TiO₂ single crystals leads to a substantial increase in photocurrent by effectively flattening the interfacial Schottky junction. This phenomenon results in a three-order of magnitude enhancement of the photocurrent. Our work broadens the horizon of study on dielectric materials through proton doping and may also provide an approach that enables the utilization of dielectric materials in energy conversion applications. [ABSTRACT FROM AUTHOR]