Low-dimensional hybrid organic-inorganic metal halide perovskites exhibit appealing charge and thermal transport properties, paired with better chemical and thermal stabilities. These systems show highly anisotropic thermal expansion effects, indicating potential applications in optoelectronics and thermoelectrics.
Low-dimensional hybrid organic-inorganic metal halide perovskites are rapidly emerging as a fascinating sub-class of the three-dimensional parent structures, thanks to their appealing charge and thermal transport properties, paired to better chemical and thermal stabilities. Extensive investigations of the thermal behavior in these systems are of paramount relevance to understand their optoelectronic and thermoelectric applications. Herein, we present a complete thermophysical characterization of imidazolium lead iodide, (IMI)PbI3, a 1D pseudo-perovskite with chains of face-sharing octahedra, and histammonium lead iodide, (HIST)PbI4, a 2D layered perovskite with corner-sharing octahedra. Upon heating, the two compounds show highly anisotropic thermal expansion effects and high thermal stability until 250-300 degrees C. The thermal diffusivity of pelletized powders was measured with the laser flash technique from room temperature up to 225 degrees C. To account for the reduced density of the pelletized powders with respect to the bulk, the diffusivity data in different atmospheres were modeled as a function of the volume fraction and dimensionality of the pores, allowing to extrapolate the thermal conductivity of the bulk materials. The two compounds exhibit an ultralow thermal conductivity of 0.15 W/m K, two to three times lower than that reported on 3D MAPbI(3) using the same technique. This finding suggests the primary role of the organic molecules within the hybrid systems, regardless of the octahedra connectivity and dimensionality.
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