Complete Suppression of Detrimental Polymorph Transitions in All-Inorganic Perovskites via Nanoconfinement

Reducing the size of metal halide perovskite crystals to the nanoscale has been demonstrated to stabilize high-performance metastable polymorphs at room temperature. Cesium lead iodide (CsPbI3), for example, typically exists as the insulating δ-phase at room temperature but can adopt the narrow-bandgap γ-phase when the crystal size is reduced to the nanometer length scale. Here we advance a fundamental understanding of the role of nanoconfinement in CsPbI3 polymorph stabilization through a combination of X-ray diffraction and temperature-dependent photoluminescence. Using a wet annealing method to directly form γ-CsPbI3 from solution in the cylindrical nanopores of anodized aluminum oxide, we discovered that nanoconfinement lowers the δ−γ solid-state phase transition temperature from 448 K in the bulk to 370 K. Once formed, nanoconfined γ-CsPbI3 crystals were found to be stable across the temperature range of 4–610 K and upon an unprecedented one year of air exposure at room temperature. Taking advantage of the nanoconfinement-induced suppression of phase transitions, we report for the first time a detailed analysis of electron–phonon interactions in γ-CsPbI3 via temperature-dependent photoluminescent measurements. In-depth analysis of the temperature-dependent peak broadening revealed electron–phonon interactions to be dominated by Fröhlich scattering, similar to that observed in inorganic–organic hybrid perovskite systems. Photoluminescence mapping further confirmed that nanoconfined γ-CsPbI3 crystals exhibit spatial uniformity on the tens of micrometers length scale, suggesting nanoconfinement as a promising strategy to form stable, high-performance perovskite films from solution for light-emitting and light-harvesting applications.