Oxygen vacancy engineering in pulsed laser deposited BaSnO$_3$ thin films on SrTiO$_3$

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Main Authors: Acevedo, Wilson Román, Aguirre, Myriam H., Noheda, Beatriz, Rubi, Diego
Format: Preprint
Published: 2025
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author Acevedo, Wilson Román
Aguirre, Myriam H.
Noheda, Beatriz
Rubi, Diego
author_facet Acevedo, Wilson Román
Aguirre, Myriam H.
Noheda, Beatriz
Rubi, Diego
contents We demonstrate the tunability of oxygen content in pulsed laser deposition (PLD)-grown barium stannate (BaSn$O_3$, BSO) thin films by precisely controlling the background oxygen pressure over a broad range from 0.0004 mbar to 0.13 mbar. The introduction of oxygen vacancies significantly alters the structural properties of BSO films, inducing a monotonic expansion of the out-of-plane lattice parameter and cell volume as the vacancy concentration increases. The progressive formation of oxygen vacancies was spectroscopically tracked using X-ray photoelectron spectroscopy (XPS), providing direct insight into the vacancy evolution. Furthermore, we show that the oxygen stoichiometry in BSO plays a critical role in modulating the sheet resistance of BSO/LaScO$_3$ heterostructures, enabling interface metallic electron conduction. This oxygen content control offers a robust strategy to tailor the electronic properties at the interface, highlighting its potential for oxide electronics and functional interface engineering.
format Preprint
id arxiv_https___arxiv_org_abs_2503_11957
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Oxygen vacancy engineering in pulsed laser deposited BaSnO$_3$ thin films on SrTiO$_3$
Acevedo, Wilson Román
Aguirre, Myriam H.
Noheda, Beatriz
Rubi, Diego
Materials Science
We demonstrate the tunability of oxygen content in pulsed laser deposition (PLD)-grown barium stannate (BaSn$O_3$, BSO) thin films by precisely controlling the background oxygen pressure over a broad range from 0.0004 mbar to 0.13 mbar. The introduction of oxygen vacancies significantly alters the structural properties of BSO films, inducing a monotonic expansion of the out-of-plane lattice parameter and cell volume as the vacancy concentration increases. The progressive formation of oxygen vacancies was spectroscopically tracked using X-ray photoelectron spectroscopy (XPS), providing direct insight into the vacancy evolution. Furthermore, we show that the oxygen stoichiometry in BSO plays a critical role in modulating the sheet resistance of BSO/LaScO$_3$ heterostructures, enabling interface metallic electron conduction. This oxygen content control offers a robust strategy to tailor the electronic properties at the interface, highlighting its potential for oxide electronics and functional interface engineering.
title Oxygen vacancy engineering in pulsed laser deposited BaSnO$_3$ thin films on SrTiO$_3$
topic Materials Science
url https://arxiv.org/abs/2503.11957