4.7 Article

Fast switching of spontaneous polarization in a microporous molecular rotor ferroelectric

Journal

INORGANIC CHEMISTRY FRONTIERS
Volume 10, Issue 1, Pages 61-66

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qi02167f

Keywords

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Funding

  1. National Natural Science Foundation of China [11834002, 22175079, 22205087, 21875093]
  2. Jiangxi Provincial Key Laboratory of Functional Molecular Materials Chemistry [20212BCD42018]
  3. Natural Science Foundation of Jiangxi Province [20204BCJ22015, 20202ACBL203001]

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This research reports a microporous structural molecular rotor ferroelectric material with fast switching spontaneous polarization (P-s), high operational performance, and stability, which shows potential application in the next-generation non-volatile memory devices.
The fast switching feature of spontaneous polarization (P-s) is one of the basis for ferroelectric applications in the field of data storage. However, most molecular ferroelectrics exhibit low operating performance in polarization switching. Herein, we report fast switching P-s (25 kHz, 293 K) and low coercive field (0.55 kV cm(-1), 353 K) for a microporous structural molecular rotor ferroelectric [CdL4](2+)[NO3-](2) (L = beta-alanine). In particular, the high switching frequency of P-s remains steady with high operational cycles (4.66 x 10(7)). Single-crystal structures analysis and density functional theory (DFT) calculations reveal the fast switching of P-s originating from the fast static-rotating-static process of NO3-. This molecular rotor-type ferroelectric material provides more possibilities to develop next-generation non-volatile memory devices.

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