| Literature DB >> 29219370 |
Yuan-Yuan Tang1, Peng-Fei Li1, Ping-Ping Shi1, Wan-Ying Zhang1, Zhong-Xia Wang1, Yu-Meng You1, Heng-Yun Ye1, Takayoshi Nakamura2, Ren-Gen Xiong1.
Abstract
Recently, a plastic crystal of quinuclidinium perrhenate (HQReO_{4}) was reported to have the feasibility of controlling the crystallographic orientation in the grown crystal, but the corresponding temperature window is only about 22 K (345-367 K). Such a narrow window and uncertain ferroelectricity at room temperature would extremely limit its application potential. In this report, we prepared a large area high-quality polycrystalline thin film of HQReO_{4} and for the first time observed ferroelectricity in the temperature range from 298 to 367 K. Density functional theory calculations revealed the origin of room-temperature ferroelectricity is ascribed to the collaborative flipping of HQ (protonated quinuclidine) and ReO_{4}^{-}, which is dynamically preferred in the presence of a N─H⋯O hydrogen bond. A local piezoresponse force microscopy measurement was also employed to study the mechanisms of multiaxial polarization rotation and domain dynamics. By extending the ferroelectric temperature window to room temperature and the extraordinary thin-film processability, HQReO_{4} would certainly become a suitable candidate for next generation ferroelectric materials.Entities:
Year: 2017 PMID: 29219370 DOI: 10.1103/PhysRevLett.119.207602
Source DB: PubMed Journal: Phys Rev Lett ISSN: 0031-9007 Impact factor: 9.161