Temperature and Pressure Effects on Phase Transitions and Structural Stability in CsPb2Br5 and CsPb2Br4I Perovskite-Derived Halides

• Published in: Inorganic chemistry 2024-11, Vol.63 (46), p.22258-22272
• Main Authors: Chakroun, Yousra, Cherif, Wajdi, Rodrigues, Francielen S. M., Ktari, Lilia, López, Carlos A., Serrano-Sánchez, Federico, Alabarse, Frederico G., Ferrer, Mateus M., Rodrigues, João Elias F. S., Alonso, José A.
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X; 1520-510X
• DOI: 10.1021/acs.inorgchem.4c03920

All-inorganic perovskites exhibit outstanding light absorption properties in the visible range suitable for solar energy applications. We focus on the synthesis of CsPb2(Br,I)5 using mechanochemical procedures. Synchrotron X-ray diffraction (SXRD) data are essential for determining the crystallographic evolution in the 295–753 K temperature range. From room temperature to 573 K, the crystal structure is refined in a two-dimensional (2D) tetragonal framework (space group: I4/mcm) consisting of layers of face sharing [Pb­(Br,I)8] polyhedra. Above a transition temperature of T t = 630 and 621 K, identified from differential scanning calorimetry (DSC) curves for CsPb2Br5 and CsPb2Br4I, respectively, a cubic three-dimensional (3D) corner-sharing perovskite structure is identified, showing substantial Cs and (Br,I) deficiency. A more ionic character for Cs-halide versus Pb-halide is derived from the evolution of the anisotropic atomic displacements. An ultralow thermal conductivity of 0.35–0.18 W m–1 K–1 is related to the low Debye temperatures. From high-pressure SXRD studies, the change in B 0 can be attributed to a basic expansion of the unit-cell volume caused by the chemical pressure from iodine within the CsPb2Br5 framework. UV–vis–NIR spectroscopy revealed optical gaps of approximately 2.93 and 2.50 eV, respectively, which agrees with ab initio calculations.