A novel ferroelectric based on quinuclidine derivatives

One phase transition material [(CH3)2CH-C3H17N][CoBr4] was synthesized and underwent the phase transitionsfrom space group C2/c to Cc. The structural phase transition of 1 was ascribed to the distortion of [(CH3)2CH-C3H17N]2+ cation. The change of the dielectric permittivity and the spontaneous pola...

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Bibliographic Details
Published inChinese chemical letters Vol. 31; no. 6; pp. 1686 - 1689
Main Authors Deng, Siyu, Li, Junyi, Chen, Xiang, Hou, Yunlong, Chen, Lizhuang
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.06.2020
School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, China
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Summary:One phase transition material [(CH3)2CH-C3H17N][CoBr4] was synthesized and underwent the phase transitionsfrom space group C2/c to Cc. The structural phase transition of 1 was ascribed to the distortion of [(CH3)2CH-C3H17N]2+ cation. The change of the dielectric permittivity and the spontaneous polarization gives compound 1 greater application potential for low temperature ferroelectrics. [Display omitted] The compound [(CH3)2CH-C3H17N][CoBr4] (1) based on quinuclidine derivatives was achieved by the solution synthetic method and characterized by elemental analysis, infrared spectroscopy, single-crystal X-ray structural analysis and dielectric measurement, respectively. Variable-temperature single-crystal X-ray diffraction suggested that the compound underwent the phase transition from the space group C2/c to Cc. The polarization curve was measured using the Sawyer-Tower circuit. The structural phase transitions of 1 was ascribed to the distortion of a [(CH3)2CH-C3H17N]2+ cation from this inorganic–organic hybrid material [(CH3)2CH-C3H17N][CoBr4]. The strong change in dielectric anomalies makes compound 1 a suitable candidate for promising switchable dielectric materials. This work represents a feasible strategy thought for the targeted harvesting of low temperature ferroelectrics.
ISSN:1001-8417
1878-5964
DOI:10.1016/j.cclet.2019.11.011