CsCuCl3 perovskite-like compound under extreme conditions

Halide perovskite has attracted intense research interest owing to its multifaceted and versatile applications in optoelectronics. This intrigue is further fueled by their propensity to undergo intricate structural modifications under extreme conditions, thereby instigating property changes. Within this context, our study delves deep into the intricate interplay of structural and vibrational attributes within the inorganic-metal halide perovskite-like CsCuCl3. Our approach employs Raman spectroscopy and Synchrotron Powder X-Ray Diffraction (SPXRD) techniques harnessed under the dual conditions of low temperatures and high pressures. We have observed a distinct spin-phonon coupling mechanism by employing Raman spectroscopy at low temperatures; this coupling has been manifested as a renormalization phonon phenomenon that occurs notably at T* = 15 K. The correlation between spin and phonon dynamics becomes pronounced through a notable hardening of phonon temperature dependence, a behavior intricately linked to the material antiferromagnetic transition at TN = 10.7 K. The SPXRD under high pressure showed a first-order structural phase transition (SPT) at the critical pressure Pc = 3.69 GPa, leading to the transformation from the hexagonal P6522 to a base-centered monoclinic cell. Notably, the coexistence of both phases is discernible within the pressure range from 2.79 to 3.57 GPa, indicating that the SPT involves the reorganization of the internal [Cu2Cl9]5- dimer unit, with the Cl-Cu-Cl bending contributing more than stretching modes. Furthermore, we demonstrate that the SPT is reversible, but residual strain pressure influences the modification of the critical pressure Pc value upon pressure decrease.