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Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)]

[Image: see text] The preparation of materials featuring more than one ferroelectric phase represents a promising strategy for controlling electrical properties arising from spontaneous polarization, since it offers an added advantage of temperature-dependent toggling between two different ferroelec...

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Autores principales: Rok, Magdalena, Starynowicz, Przemysław, Ciżman, Agnieszka, Zaręba, Jan K., Piecha-Bisiorek, Anna, Bator, Grażyna, Jakubas, Ryszard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482396/
https://www.ncbi.nlm.nih.gov/pubmed/32799526
http://dx.doi.org/10.1021/acs.inorgchem.0c00830
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author Rok, Magdalena
Starynowicz, Przemysław
Ciżman, Agnieszka
Zaręba, Jan K.
Piecha-Bisiorek, Anna
Bator, Grażyna
Jakubas, Ryszard
author_facet Rok, Magdalena
Starynowicz, Przemysław
Ciżman, Agnieszka
Zaręba, Jan K.
Piecha-Bisiorek, Anna
Bator, Grażyna
Jakubas, Ryszard
author_sort Rok, Magdalena
collection PubMed
description [Image: see text] The preparation of materials featuring more than one ferroelectric phase represents a promising strategy for controlling electrical properties arising from spontaneous polarization, since it offers an added advantage of temperature-dependent toggling between two different ferroelectric states. Here, we report on the discovery of a unique ferroelectric–ferroelectric transition in diisopropylammonium tetrabromocadmate (DPAC, (C(6)H(16)N)(2)[CdBr(4)]) with a T(c) value of 244 K, which is continuous in nature. Both phases crystallize in the same polar orthorhombic space group, Iab2. The temperature-resolved second-harmonic-generation (SHG) measurements using 800 nm femtosecond laser pulses attest to the polar structure of DPAC on either side of the phase transition (PT). The dc conductivity parameters were estimated in both solid phases. The anionic substructure is in the form of [CdBr(4)](2–) discrete complexes (0D), while in the voids of the structure, the diisopropylammonium cations are embedded. The ferroelectric properties of phases I and II have been confirmed by the reversible pyroelectric effect as well as by P–E loop investigations. On the basis of the dielectric responses, the molecular mechanism of the PT at 244 K has been postulated to be of mixed type with an indication of its displacive nature.
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spelling pubmed-74823962020-09-11 Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)] Rok, Magdalena Starynowicz, Przemysław Ciżman, Agnieszka Zaręba, Jan K. Piecha-Bisiorek, Anna Bator, Grażyna Jakubas, Ryszard Inorg Chem [Image: see text] The preparation of materials featuring more than one ferroelectric phase represents a promising strategy for controlling electrical properties arising from spontaneous polarization, since it offers an added advantage of temperature-dependent toggling between two different ferroelectric states. Here, we report on the discovery of a unique ferroelectric–ferroelectric transition in diisopropylammonium tetrabromocadmate (DPAC, (C(6)H(16)N)(2)[CdBr(4)]) with a T(c) value of 244 K, which is continuous in nature. Both phases crystallize in the same polar orthorhombic space group, Iab2. The temperature-resolved second-harmonic-generation (SHG) measurements using 800 nm femtosecond laser pulses attest to the polar structure of DPAC on either side of the phase transition (PT). The dc conductivity parameters were estimated in both solid phases. The anionic substructure is in the form of [CdBr(4)](2–) discrete complexes (0D), while in the voids of the structure, the diisopropylammonium cations are embedded. The ferroelectric properties of phases I and II have been confirmed by the reversible pyroelectric effect as well as by P–E loop investigations. On the basis of the dielectric responses, the molecular mechanism of the PT at 244 K has been postulated to be of mixed type with an indication of its displacive nature. American Chemical Society 2020-08-15 2020-09-08 /pmc/articles/PMC7482396/ /pubmed/32799526 http://dx.doi.org/10.1021/acs.inorgchem.0c00830 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Rok, Magdalena
Starynowicz, Przemysław
Ciżman, Agnieszka
Zaręba, Jan K.
Piecha-Bisiorek, Anna
Bator, Grażyna
Jakubas, Ryszard
Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)]
title Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)]
title_full Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)]
title_fullStr Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)]
title_full_unstemmed Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)]
title_short Advances and Property Investigations of an Organic–Inorganic Ferroelectric: (diisopropylammonium)(2)[CdBr(4)]
title_sort advances and property investigations of an organic–inorganic ferroelectric: (diisopropylammonium)(2)[cdbr(4)]
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482396/
https://www.ncbi.nlm.nih.gov/pubmed/32799526
http://dx.doi.org/10.1021/acs.inorgchem.0c00830
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