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Title: The enhanced ferroelectricity in Sr1-δTiO3/BaTiO3 superlattices with Sr deficiency

Journal Article · · Journal of Physics. D, Applied Physics
ORCiD logo [1];  [2];  [1];  [1];  [1];  [3];  [4];  [1]
  1. Univ. of Science and Technology of China, Hefei (China)
  2. Univ. of Science and Technology of China, Hefei (China); Argonne National Lab. (ANL), Argonne, IL (United States)
  3. Argonne National Lab. (ANL), Argonne, IL (United States)
  4. Univ. of Science and Technology of China, Hefei (China); Shanghaitech Univ. (China)

Here we report the tunable ferroelectricity in superlattices of (Sr1-δTiO3)n/(BaTiO3)8 with δ ≈ 5% and the maximally enhanced ferroelectricity is found in the n = 6 superlattice. The room-temperature remnant polarization of n = 6 is enhanced by 70% and 1120% compared to those of BaTiO3 and Sr1-δTiO3 thin films, respectively. The ferroelectric transition temperature of n = 6 is 40 K higher than that of the BaTiO3 film, and is independent of the measurement frequency. The dependence of remnant field 2Pr on n coincides well with the n dependence of γ/α, which is ratio between out-of-plane and in-plane octahedral rotation angles. It thus suggests a strong correlation between the octahedral rotation pattern and the ferroelectric distortion. Furthermore, our study demonstrates the importance of constructing superlattices to enhance the ferroelectric properties of the defect-engineered materials to be better than the pristine materials.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES); National Natural Science Foundation of China (NSFC); National Key Research and Development Program of China; Fundamental Research Funds for the Central Universities
Grant/Contract Number:
AC02-06CH11357; 51627901; 11574287; 2016YFA0401004; WK2340000088; 2016389
OSTI ID:
1787327
Journal Information:
Journal of Physics. D, Applied Physics, Vol. 53, Issue 31; ISSN 0022-3727
Publisher:
IOP PublishingCopyright Statement
Country of Publication:
United States
Language:
English

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