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 | English |
|---|---|
| Article number | 1900645 |
| Journal | Advanced Functional Materials |
| Volume | 29 |
| Issue number | 5 |
| Number of pages | 5 |
| ISSN | 1616-301X |
| DOIs | |
| Publication status | Published - 2019 |
Keywords
- Functional oxides
- Oxide interfaces
- Oxide surfaces
- Photoemission spectroscopy