| Literature DB >> 30775915 |
Zhenyue Wu1,2, Xitao Liu1, Chengmin Ji1, Lina Li1, Sasa Wang1,2, Yu Peng1,2, Kewen Tao1, Zhihua Sun1, Maochun Hong1, Junhua Luo1.
Abstract
Antiferroelectric materials have been regarded as a promising candidate for electronic energy storage devices, due to their natural double polarization versus electric field ( P- E) hysteresis loops. Currently, two-dimensional organic-inorganic hybrid perovskites with structural diversity and tunability, have received blooming interests, whereas above-room-temperature antiferroelectrics are still unreported in this perovskite system. Herein, for the first time, we successfully acquire a two-dimensional Ruddlesden-Popper hybrid perovskite antiferroelectric, ((CH3)2CHCH2NH3)2CsPb2Br7 (1), which shows an above-room-temperature Curie temperature at 353 K, trigging by the synergistic dynamic motion of inorganic Cs atoms and organic isobutylammonium cations. Intriguingly, the antiferroelectricity of 1 existing over a wide temperature range of 298-353 K are revealed by the distinct double P- E hysteresis loops. Besides, 1 possesses remarkable energy storage efficiency up to 69%, comparable to those of some reported inorganic antiferroelectric ceramics, promoting 1 potential application in energy storage devices. This work provides an avenue to construct novel antiferroelectric materials for high-performance electronic device applications.Entities:
Year: 2019 PMID: 30775915 DOI: 10.1021/jacs.8b13827
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419