Halide Ion Mixing across Colloidal 2D Ruddlesden‐Popper Perovskites: Implication of Spacer Ligand on Mixing Kinetics

Abstract

AbstractHalide ion exchange seen in metal halide perovskites provide a substantial opportunity to control their halide composition and corresponding optoelectronic properties. Halide ion mixing across colloidal 3D perovskite nanocrystals have been extensively studied while the mixing within colloidal 2D counterparts remain underexplored. In this study, the halide ion exchange kinetics across colloidally stable 2D Ruddlesden‐Popper layered bromide (Br) and iodide (I) perovskites using two different spacer ligands such as aromatic phenethylammonium (PEA) versus linear butyammonium (BA) is demonstrated. The halide exchange kinetic rate constant (k), as determined by tracking time‐dependent absorbance changes, indicates that Br/I halide mixing in 2D PEA‐based perovskites (2.7 × 10−3 min−1) occurs at an order of magnitude slower than in 2D BA‐based perovskites (3.3 × 10−2 min−1). Concentration (≈1 mM to 100 mM) and temperature‐dependent (50 to 80 °C) kinetic studies further allow for the determination of activation barrier for halide ion mixing across the 2D layered perovskites with 75.2 ± 4.4 kJ mol−1 (2D PEA) and 57.8 ± 7.8 kJ mol−1 (2D BA), respectively. The activation energy reveals that the type of spacer cations plays a crucial role in controlling the halide ion mobility and halide stability due mainly to the internal ligand chemical interaction within 2D structures.