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Published on: March 24, 2019
Electronic subband reconfiguration in a d0-perovskite induced by strain-driven structural transformations
V Laukhin1, O Copie, M J Rozenberg
1Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus de la UAB, Bellaterra 08193, Catalonia, Spain.
Applying pressure to strontium titanate (SrTiO3) alters its electronic band structure, significantly boosting electron mobility. This discovery explains strain-induced transport enhancements in perovskites.
Area of Science:
- Solid State Physics
- Materials Science
- Condensed Matter Physics
Background:
- Transport in lightly n-doped strontium titanate (SrTiO3) is characterized by the interplay of light and heavy electron bands.
- Understanding the electronic properties of perovskite materials is crucial for developing advanced electronic devices.
Purpose of the Study:
- To investigate the effects of quasi-isotropic pressure on the electronic band structure of SrTiO3.
- To elucidate the mechanism behind strain-induced mobility enhancements in SrTiO3.
- To compare the pressure-induced electronic reconfiguration in SrTiO3 with that in potassium tantalate (KTaO3).
Main Methods:
- Application of moderate quasi-isotropic pressures to SrTiO3 samples.
- Analysis of subtle changes in subband positions and band inversion using experimental techniques (details not specified in abstract).
- Comparative study with KTaO3 to highlight material-specific responses.
Main Results:
- A few meV shift in subband positions and band inversion occurring at approximately 1 kbar in SrTiO3.
- Suppression of these pressure-induced effects in KTaO3, indicating material specificity.
- Strain-induced structural transformations in SrTiO3 leading to remarkable electron mobility enhancements of up to ~300%.
Conclusions:
- The electronic reconfiguration in SrTiO3 under pressure is driven by strain-induced structural changes.
- These findings provide a microscopic explanation for the observed transport enhancement under strain in perovskites.
- The study highlights the significant role of internal structural degrees of freedom in modulating the electronic properties of perovskites.
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