An one-dimensional organic-inorganic hybrid perovskite material [3.3.0-dabco]PbBr3 (1) was synthesized by reaction of 1,5-diazabicyclo[3.3.0]octane (3.3.0-dabco) with PbBr2 in concentrated HBr aqueous solution. The differential scanning calorimetry, dielectric measurements, and variable-temperature...
Two 3D organic–inorganic hybrid perovskite ferroelectrics [3.2.2-dabcn]RbX3 (X = Br for 1; X = I for 2) with Curie temperatures at 342 K and 293 K were designed and prepared by reaction of 1,5-diazabicyclo[3.2.2]nonane with RbX.
The emergence of (CH3NH3)PbI3 has brought the development of three‐dimensional (3D) organic‐inorganic hybrid perovskite (OIHP) structures with ABX3 type to a higher level; however, most 3D frameworks are constructed by corner‐sharing of BX6 octahedra. Herein, we substituted the spherical molecule 1,4‐diazabicyclo[2.2.2]octane (2.2.2‐dabco) with 1,4‐diazabicyclo[3.2.2]nonane (1,4‐3.2.2‐dabcn) as a template to react with RbX (X=Br, I) in the corresponding HX acids under the consideration of reducing the molecular symmetry. Two 3D OIHP compounds [1,4‐3.2.2‐H2dabcn]RbI3⋅H2O (1) and [1,4‐3.2.2‐H2dabcn]RbBr3 (2) crystallized in non‐centrosymmetric point group mm2 before the phase transition point were isolated. Among them, the 3D inorganic framework of 1 is constructed by sharing the corner of [RbI6] octahedra, while that of 2 is constructed by sharing the corner and face of [RbBr6] octahedra to acquire large cavities to accommodate the organic amine cation [1,4‐3.2.2‐H2dabcn]2+; this 3D framework type is unprecedented in the OIHPs. As expected, compounds 1 and 2 exhibit reversible phase transition, dielectric and second harmonic generation (SHG) and ferroelectric properties, in which the phase transition temperature of 2 at 374 K is much higher than compound 1 at 280 K.
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