Solution epitaxy of polarization-gradient ferroelectric oxide films with colossal photovoltaic current

Abstract

Solution growth of single-crystal ferroelectric oxide films has long been pursued for the low-cost development of high-performance electronic and optoelectronic devices. However, the established principles of vapor-phase epitaxy cannot be directly applied to solution epitaxy, as the interactions between the substrates and the grown materials in solution are quite different. Here, we report the successful epitaxy of single-domain ferroelectric oxide films on Nb-doped SrTiO₃ single-crystal substrates by solution reaction at a low temperature of ~200 ^oC. The epitaxy is mainly driven by an electronic polarization screening effect at the interface between the substrates and the as-grown ferroelectric oxide films, which is realized by the electrons from the doped substrates. Atomic-level characterization reveals a nontrivial polarization gradient throughout the films in a long range up to ~500 nm because of a possible structural transition from the monoclinic phase to the tetragonal phase. This polarization gradient generates an extremely high photovoltaic short-circuit current density of ~2.153 mA/cm² and open-circuit voltage of ~1.15 V under 375 nm light illumination with power intensity of 500 mW/cm², corresponding to the highest photoresponsivity of ~4.306×10⁻³A/W among all known ferroelectrics. Our results establish a general low-temperature solution route to produce single-crystal gradient films of ferroelectric oxides and thus open the avenue for their broad applications in self-powered photo-detectors, photovoltaic and optoelectronic devices.

Developing low-temperature solution epitaxy and elucidating its underlying mechanisms is highly desired for low-cost fabrication of single-crystal ferroelectric films. Here, the authors show that a polarization screening between ferroelectrics and substrates can tailor the interface energy and drive the solution epitaxy of polarization-gradient ferroelectric oxide films, demonstrating a remarkable photovoltaic effect.