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A Semiconducting Organic‐Inorganic Hybrid Metal Halide [(C6H15ClNO)2CdBr4] with Switchable Dielectric and Large Phase Transition Thermal Hysteresis
A semiconducting organic‐inorganic hybrid compound [(C6H15ClNO)2CdBr4] (1), which displays excellent switchable dielectric, has been successfully synthesized. Systematic characterizations including variable‐temperature structural analyses, DSC, TG, variable‐temperature dielectric measurements, solid...
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Published in: | ChemistrySelect (Weinheim) 2019-04, Vol.4 (13), p.3921-3925 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A semiconducting organic‐inorganic hybrid compound [(C6H15ClNO)2CdBr4] (1), which displays excellent switchable dielectric, has been successfully synthesized. Systematic characterizations including variable‐temperature structural analyses, DSC, TG, variable‐temperature dielectric measurements, solid‐state UV/Vis diffuse reflectance and photoluminescence were performed. DSC curve shows a couple of reversible heat anomaly peaks at 363/322 K on the heating/cooling process with a very large thermal hysteresis of ∼41 K, indicating the first‐order type of phase transition. Obvious dielectric switching occurs at about 364 K and 314 K also with a large thermal hysteresis of ∼50 K in the heating and cooling process, respectively. The large phase transition thermal hysteresis makes 1 a potential latent heat based thermal energy storage materials which can maintain the system over a wide temperature range. Variable‐temperature structural analyses show that the rotating or orientating movement of anion clusters is the mainly attribution for the phase transition of 1.
A semiconducting organic‐inorganic hybrid metal halide [(C6H15ClNO)2CdBr4] exhibits switchable dielectric and a large phase transition thermal hysteresis of ∼50 K due to temperature‐triggered rotating or orientating movement of anion clusters. |
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ISSN: | 2365-6549 2365-6549 |
DOI: | 10.1002/slct.201900598 |