Abstract
Tunable electronic properties of transition metal oxides and their interfaces offer remarkable functionalities for future devices. The interest in these materials has been boosted with the discovery of a 2D electron gas (2DEG) at SrTiO3 (STO)-based interfaces. For the majority of these systems, oxygen vacancies play a crucial role in the emergence of interface conductivity, ferromagnetism, and high electron mobility. Despite its great importance, controlling the density and spatial distribution of oxygen vacancies in a dynamic way remains extremely challenging. Here, lithography-like writing of a metallic state at the interface between SrTiO3 and amorphous Si using X-ray irradiation is reported. Using a combination of transport techniques and in operando photoemission spectroscopy, it is revealed in real time that the X-ray radiation induces transfer of oxygen across the interface leading to the on-demand formation of oxygen vacancies and a 2DEG in STO. The formed 2DEG stays stable in ambient conditions as the interface oxygen vacancies are stabilized by the capping of Si. The study provides a fundamental understanding of X-ray-induced redox reactions at the SrTiO3-based interfaces and in addition shows the potential of X-ray radiation for patterning stabile conductive pathways for future oxide-based electronic devices.
Original language | American English |
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Article number | 1900645 |
Journal | Advanced Functional Materials |
Volume | 29 |
Issue number | 25 |
DOIs | |
State | Published - 21 Jun 2019 |
Externally published | Yes |
Keywords
- functional oxides
- oxide interfaces
- oxide surfaces
- photoemission spectroscopy
All Science Journal Classification (ASJC) codes
- General Chemistry
- Condensed Matter Physics
- General Materials Science