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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Published in | Chinese chemical letters Vol. 31; no. 6; pp. 1686 - 1689 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.06.2020
School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, China |
Subjects | |
Online Access | Get full text |
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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.
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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. |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2019.11.011 |