4.8 Article

Cooperative Couplings between Octahedral Rotations and Ferroelectricity in Perovskites and Related Materials

期刊

PHYSICAL REVIEW LETTERS
卷 120, 期 19, 页码 -

出版社

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.120.197602

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资金

  1. NSFC [11374056]
  2. Special Funds for Major State Basic Research [2015CB921700]
  3. Program for Professor of Special Appointment (Eastern Scholar), Qing Nian Ba Jian Program
  4. Fok Ying Tung Education Foundation
  5. Department of Energy, Office of Basic Energy Sciences [DE-SC0002220]
  6. ONR [N00014-12-1-1034, N00014-17-1-2818, N00014-15-1-2881]
  7. Air Force Office of Scientific Research [FA9550-16-1-0065]
  8. Luxembourg National Research Fund through the inter-mobility [15/9890527, P12/4853155]
  9. NSF [0722625]
  10. Department of Defense

向作者/读者索取更多资源

The structure of ABO(3) perovskites is dominated by two types of unstable modes, namely, the oxygen octahedral rotation (AFD) and ferroelectric (FE) mode. It is generally believed that such AFD and FE modes tend to compete and suppress each other. Here we use first-principles methods to show that a dual nature of the FE-AFD coupling, which turns from competitive to cooperative as the AFD mode strengthens, occurs in numerous perovskite oxides. We provide a unified model of such a dual interaction by introducing novel high-order coupling terms and explain the atomistic origin of the resulting new form of ferroelectricity in terms of universal steric mechanisms. We also predict that such a novel form of ferroelectricity leads to atypical behaviors, such as an enhancement of all the three Cartesian components of the electric polarization under hydrostatic pressure and compressive epitaxial strain.

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