All-Inorganic Quantum-Dot LEDs Based on a Phase-Stabilized α-CsPbI3 Perovskite

The all-inorganic nature of CsPbI3 perovskites allows to enhance stability in perovskite devices. Research efforts have led to improved stability of the black phase in CsPbI3 films; however, these strategies-including strain and doping-are based on organic-ligand-capped perovskites, which prevent perovskites from forming the close-packed quantum dot (QD) solids necessary to achieve high charge and thermal transport. We developed an inorganic ligand exchange that leads to CsPbI3 QD films with superior phase stability and increased thermal transport. The atomic-ligand-exchanged QD films, once mechanically coupled, exhibit improved phase stability, and we link this to distributing strain across the film. Operando measurements of the temperature of the LEDs indicate that KI-exchanged QD films exhibit increased thermal transport compared to controls that rely on organic ligands. The LEDs exhibit a maximum EQE of 23% with an electroluminescence emission centered at 640 nm (FWHM: approximate to 31 nm). These red LEDs provide an operating half-lifetime of 10 h (luminance of 200 cd m(-2)) and an operating stability that is 6x higher than that of control devices.

Automated summary

The all-inorganic nature of CsPbI3 perovskites enhances stability in perovskite devices. Inorganic ligand exchange leads to CsPbI3 QD films with superior phase stability and increased thermal transport. LEDs with KI-exchanged QD films exhibit increased thermal transport and higher operating stability compared to control devices.