Enhanced hybrid improper ferroelectricity in Fe/Nb cosubstituted Ca3Mn2O7 ceramics
Enhanced hybrid improper ferroelectricity in Fe/Nb cosubstituted Ca3Mn2O7 ceramics
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Fe/Nb 共取代 Ca3Mn2O7 陶瓷中增强的杂化不当铁电性
DOI:
10.1111/jace.17791
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发表时间:
2021
影响因子:
3.9
通讯作者:
Chen Xiang Ming
中科院分区:
文献类型:
--
作者:
Chen Bu Hang;Sun Tu Lai;Wei Li Yu;Liu Xiao Qiang;Wen Wen;Tian He;Li Jiang Yu;Chen Xiang Ming
The prototypical Ruddlesden‐Popper compound Ca3Mn2O7has been predicted to possess hybrid improper ferroelectricity, where the polarization is induced by the condensation of two oxygen octahedral distortion modes. Nevertheless, it is a big challenge to switch the polarization at room temperature in Ca3Mn2O7since the presence of intermediate nonpolarAcaaphase generally leads to the complex domain morphology. Here, the effects of Fe/Nb cosubstitution on hybrid improper ferroelectricity in Ca3Mn2O7are reported, and easy polarization switching at room temperature is achieved in Ca3[Mn0.5(Fe0.5Nb0.5)0.5]2O7. The ferroelectric phase transition occurs directly fromI4/mmmtoA21amat a temperature far above room temperature without intermediate nonpolarAcaaphase. The distinct transition pathway forms the alternating 180°‐type ferroelectric domains rather than the irregular 90°‐type ferroelastic domains stacked along [001], resulting in easy polarization switching at room temperature. Moreover the enhanced ferroelectric polarization (Pr~2.0 μC/cm2) is obtained due to the increased anti‐ferrodistortive displacements of Ca cations atA‐site, arising from the larger amplitudes of oxygen octahedral distortions. Chemical pressure is emphasized here for the tunability of phase transition, domain morphology, and ferroelectric characteristics, and it provides a useful approach for designing and creating high‐performance improper ferroelectrics.