Dielectric phase transition of an A2BX4-type perovskite with a pentahedral to octahedral transformation

Abstract

Organic–inorganic hybrid compounds that undergo reversible dielectric phase transitions are a very attractive class of smart materials due to their wide applications in data storage, data communication and signal sensing. Here, a piperidine ring, C₅H₁₁N, was introduced into the inorganic lead halide perovskite scaffold to obtain three hybrid perovskite compounds, [C₅H₁₂N]₂PbCl₄ (1), [C₅H₁₂N]₂PbBr₄ (2), and [C₅H₁₂N]PbI₃ (3). When compound 2 and compound 3 feature static two-dimensional (2D) and one-dimensional (1D) perovskite structures, respectively, it is striking that compound 1 shows a reversible pentahedral to octahedral transformation. It undergoes an above-room-temperature dielectric phase transition at T_c ≅ 352 K, wherein the high dielectric constant is more than twice the low dielectric constant. Structural analysis shows that 1 undergoes a phase transition from the space group Pnma at the low temperature phase (LTP) to C2/c at the high temperature phase (HTP). The phase transition originates from the order–disorder conversion of piperidinium cations. It is interesting to note that, the Pb²⁺ cations in the inorganic moieties change from five-coordinate at the LTP to six-coordinate at the HTP. The discovery of dielectric phase transition hybrid organic–inorganic lead halide perovskite materials further enhances the potential applications of high temperature responsive dielectric switchable materials.