Abstract
β-Ga2O3, as an ultrawide band gap semiconductor, has emerged as the most promising candidate in solar-blind photodetectors. The practical application of β-Ga2O3, however, suffers from intrinsic defects and suboptimal crystal quality within the devices. In this work, high-quality β-Ga2O3 was successfully synthesized by employing the Zr-doping strategy, which has facilitated the development of ultrahigh-performance solar-blind photodetectors based on Cu2O/β-Ga2O3 heterostructures. Structural analyses indicate that the strong Zr-O covalent bond effectively stabilizes the material, thereby eliminating oxygen vacancy defects. The Cu2O/β-Ga2O3 heterostructure photodetector demonstrates an ultrahigh responsivity and detectivity coupled with an external quantum efficiency. Furthermore, the device exhibits a photocurrent-to-dark current ratio of 3 × 105, showcasing its superior capability in detecting low-intensity deep ultraviolet signals, markedly surpassing previous heterostructure ultraviolet photodetectors. These exceptional performances are attributed to the effective elimination of oxygen vacancy defects in β-Ga2O3 and the variation of band alignment at the interface, which facilitate rapid separation of photogenerated electron-hole pairs under reverse bias. This study not only provides an enhanced and easy route to mitigate oxygen vacancy defects in oxide materials but also propels further exploration into the next generation of flexible, high-performance, solar-blind ultraviolet photodetectors.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.