Abstract
Strongly correlated perovskite oxides exhibit a plethera of intriguing phenomena and stimulate a great potential for multifunctional device applications. Utilizing tunable uniaxial strain, rather than biaxial or anisotropic strain, delivered from the crystallography of a single crystal substrate to modify the ground state of strongly correlated perovskite oxides has rarely been addressed for phase-space control. Here, we show that the physical properties of La2/3Ca1/3MnO3 (LCMO) films are remarkably different depending on the crystallographic orientations of the orthorhombic NdGaO3 (NGO) substrates. More importantly, the antiferromagnetic charge-ordered insulating (COI) phase induced in the (100) or (001)-oriented LCMO films can be dramatically promoted (or suppressed) by a uniaxial tensile (or compressive) bending stress along the in-plane [010] direction. By contrast, the COI phase is nearly unaffected along the other transverse in-plane directions. Results from scanning transmission electron microscopy reveal that the (100)-or (001)-oriented LCMO films are uniaxially tensile strained along the [010] direction, while the LCMO/NGO(010) and LCMO/NGO(110) films remaining as a bulklike ferromagnetic metallic state exhibit a different strain state. Density functional theory calculations further reveal that the cooperatively increased Jahn-Teller distortion and charge ordering may be indispensible for the inducing and promoting of the COI phase. These findings provide a path to understand the correlation between local and extended structural distortions imparted by coherent epitaxy and the electronic states for quantum phase engineering.
Original language | English (US) |
---|---|
Pages (from-to) | 1131-1140 |
Number of pages | 10 |
Journal | Nano letters |
Volume | 20 |
Issue number | 2 |
DOIs | |
State | Published - Feb 12 2020 |
Funding
This work is supported by the National Basic Research Program of China (Grants 2016YFA0401003 and 2017YFA0403502), the National Natural Science Foundation of China (Grants 11974326, 11804342, 51872278, and 11574281), Hefei Science Center of Chinese Academy of Sciences (Grant 2018ZYFX002), China Postdoctoral Science Foundation (2018M632557), and Anhui Province Key Laboratory of Condensed Matter Physics at Extreme conditions. E.J.G. was supported by Hundred Talent Program from Chinese Academy of Sciences. M.G. and J.M.R. were supported by the U.S. Department of Energy (DOE) under Grant DE-SC0012375. DFT calculations were performed on the CARBON cluster at the Center for Nanoscale Materials and the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by the National Science Foundation (ACI-1548562). Use of the Center for Nanoscale Materials, an Office of Science user facility, was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract No. DE-AC02-06CH11357. In addition, a portion of this work was performed on the Steady High Magnetic Field Facility, the High Magnetic Field Laboratory, Chinese Academy of Sciences.
Keywords
- density functional theory calculations
- manganite thin films
- phase separation
- scanning transmission electron microscopy
- uniaxial strain engineering
ASJC Scopus subject areas
- Condensed Matter Physics
- Mechanical Engineering
- Bioengineering
- General Chemistry
- General Materials Science