Polarization loss in the organic ferroelectric trialkylbenzene-1,3,5-tricarboxamide (BTA)

We investigate the polarization loss in the archetypical molecular organic ferroelectric trialkylbenzene-1,3,5-tricarboxamide (BTA). We prove that the polarization loss is due to thermally activated R-relaxation, which is a collective reversal of the amide dipole moments in ferroelectric domains. By...

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Hauptverfasser: Gorbunov, Andrey V. (VerfasserIn) , Meng, Xiao (VerfasserIn) , Urbanavičiūtė, Indrė (VerfasserIn) , Putzeys, Tristan (VerfasserIn) , Wübbenhorst, Michael (VerfasserIn) , Sijbesma, Rint P. (VerfasserIn) , Kemerink, Martijn (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2017
In: Physical chemistry, chemical physics
Year: 2016, Jahrgang: 19, Heft: 4, Pages: 3192-3200
ISSN:1463-9084
DOI:10.1039/C6CP08015D
Online-Zugang:Verlag, Volltext: https://doi.org/10.1039/C6CP08015D
Verlag, Volltext: https://pubs.rsc.org/en/content/articlelanding/2017/cp/c6cp08015d
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Verfasserangaben:A.V. Gorbunov, X. Meng, I. Urbanaviciute, T. Putzeys, M. Wübbenhorst, R.P. Sijbesma and M. Kemerink
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Zusammenfassung:We investigate the polarization loss in the archetypical molecular organic ferroelectric trialkylbenzene-1,3,5-tricarboxamide (BTA). We prove that the polarization loss is due to thermally activated R-relaxation, which is a collective reversal of the amide dipole moments in ferroelectric domains. By applying a weak electrostatic field both the polarization loss and the R-relaxation are suppressed, leading to an enhancement of the retention time by at least several orders of magnitude. Alternative loss mechanisms are discussed and ruled out. By operating the thin-film devices slightly above the crystalline to liquid crystalline phase transition temperature the retention time of one compound becomes more than 12 hours even in absence of supportive bias, which is among the longest reported so far for organic ferroelectric materials.
Beschreibung:First published on 23 Dec 2016
Gesehen am 03.12.2019
Beschreibung:Online Resource
ISSN:1463-9084
DOI:10.1039/C6CP08015D