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- W2326164023 abstract "Demands for low-power and high-efficiency electronic devices have spurred an increased interest in new ferroelectric oxides, which display spontaneous electric polarizations. There are only a few mechanisms, however, capable of producing ordered dipoles in solid-state materials. Using first-principles density functional calculations, we extend the current repertoire and identify the required rotational patterns conducive to “geometric” ferroelectricity in (A,A′)B2O6 perovskite oxides with A cation order along [001]-, [111]-, and [110]-directions. For the polar oxides, we show that electric polarizations arise through a geometric, “rotation-induced” mechanism and are greater than those induced by spin-driven mechanisms. We also discuss the energetics of each ordered arrangement and explain how competing centrosymmetric phases can lead to potential complications in thin-film growth of these materials. Finally, we generalize these results to a simple set of structural chemistry guidelines, which may be used to design other artificial oxides without inversion symmetry." @default.
- W2326164023 created "2016-06-24" @default.
- W2326164023 creator A5007838414 @default.
- W2326164023 creator A5035667249 @default.
- W2326164023 date "2013-11-05" @default.
- W2326164023 modified "2023-09-26" @default.
- W2326164023 title "Atomic Scale Design of Polar Perovskite Oxides without Second-Order Jahn–Teller Ions" @default.
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- W2326164023 doi "https://doi.org/10.1021/cm402550q" @default.
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