Mixed-Layered Lead Halide Frameworks with High Stability and Efficient Room-Temperature Phosphorescence.

Abstract

Room-temperature phosphorescent (RTP) materials play a crucial role in optical anticounterfeiting science and information security technologies. Ionically bonded organic metal halides have emerged as promising RTP material systems due to their excellent self-assembly and unique photophysical property, but their intrinsic instability largely hinders their advanced practical applications. Herein, we employ a coordination-driven synthetic strategy utilizing organocarboxylates for the synthesis of two isostructural layered lead halide frameworks. The frameworks adopt a new mixed-layered topology, consisting of alternating [Pb10X9]11+ (X = Cl-/Br-) layers and [Pb6XO3]11+ (X = Cl-/Br-) layers that are coordinatively sandwiched by organocarboxylate layers. The frameworks exhibit long-lived green afterglow emission with the long lifetime of up to 45.89 ms and the photoluminescence quantum yield (PLQY) of up to 43.13%. The Pb2+-carboxylate coordination accelerates the metal-to-ligand charge transfer from the light-harvesting lead halide layers to the phosphorescent organic component, promoting efficient spin-orbit coupling and intersystem crossing. Moreover, the coordination networks exhibit good structural robustness under ambient conditions for at least 12 months, as well as stability in boiling water, acidic and basic aqueous environments. The highly efficient afterglow and high structural integrity enable multiple anticounterfeiting applications across diverse chemical environments.