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Lead-free hybrid ferroelectric material based on formamidine: [NH2CHNH2]3Bi2I9Electronic supplementary information (ESI) available. CCDC 1855907 and 1855908. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8tc06458j

The extraordinary thermal stability of [NH 2 CHNH 2 ] 3 Bi 2 I 9 (FA 3 Bi 2 I 9 ) crystals, up to around 600 K, has been enhanced by using the evaporating method. DSC measurements have revealed reversible structural phase transitions: at 203 K (Phase I → Phase II), 173 K (II → III), 134.7 K (III → I...

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Main Authors: Szklarz, Przemys aw, G gor, Anna, Jakubas, Ryszard, Zieli ski, Piotr, Piecha-Bisiorek, Anna, Cichos, Jakub, Karbowiak, Miros aw, Bator, Gra yna, Ci man, Agnieszka
Format: Article
Language:English
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Summary:The extraordinary thermal stability of [NH 2 CHNH 2 ] 3 Bi 2 I 9 (FA 3 Bi 2 I 9 ) crystals, up to around 600 K, has been enhanced by using the evaporating method. DSC measurements have revealed reversible structural phase transitions: at 203 K (Phase I → Phase II), 173 K (II → III), 134.7 K (III → IV), 131.4 K (IV → V), and 120 K (V → VI). The crystal structures of FA 3 Bi 2 I 9 adopt the polar space groups P 6 3 mc at 220 K (Phase I) and Cmc 2 1 at 190 K (Phase II). The pyroelectric current ( I pyr ) measured in the temperature range covering all the phases of FA 3 Bi 2 I 9 confirmed their polar nature. The reversibility of the spontaneous polarization in each phase has been confirmed by the observed hysteresis loops. All the phase transitions are dielectrically active. The dielectric response ( *( ω , T ) close to 134.7 and 131.4 K) is characteristic of ferroelectrics with a critical slowing-down process. Optical bandgaps estimated from the UV-vis measurements and calculated using the DFT method are equal to 1.85 and 1.89 eV, respectively. On the basis of the structural, dielectric, and spectroscopic results, the molecular mechanisms of the phase transitions have been proposed. Novel room-temperature ferroelectric crystals with complex sequences of phase transitions.
ISSN:2050-7526
2050-7534
DOI:10.1039/c8tc06458j