Efficient Quantum Dot Light-Emitting Diodes Based on Trioctylphosphine Oxide-Passivated Organometallic Halide Perovskites.

Metal halide perovskite quantum dots (QDs) have attracted significant research interest in the next-generation display and solid illumination fields due to their excellent optical properties of high photoluminescence quantum efficiency, high color purity, obvious quantum confinement effect, and large exciton binding energy. A large amount of surface defects and nonradiative recombination induced by these defects are considered as major problems to be resolved urgently for practical applications of perovskite QDs in high-efficiency light-emitting diodes (LEDs). Herein, we report an efficient passivation of green perovskite QD CHNHPbBr with trioctylphosphine oxide (TOPO). By simply adding the appropriate amount of TOPO into the nonpolar toluene solvent to synthesize CHNHPbBr QDs, the surface defects of these as-synthesized perovskite QDs are obviously reduced, along with an increased photoluminescence lifetime and suppressed nonradiative recombination. Further investigation indicates that electronegative oxygen from TOPO (Lewis base) bonds with uncoordinated Pb ions and labile lead atoms in perovskite. With TOPO passivation, the green perovskite QD LEDs based on CHNHPbBr show significant performance improvement factors of 93.5, 161.1, and 168.9% for luminance, current efficiency, and external quantum efficiency, respectively, reaching values of 1635 cd m, 5.51 cd A, and 1.64% in the eventual optimized devices. Furthermore, the presence of TOPO dramatically improves stabilities of CHNHPbBr QDs and related devices. Our work provides a robust platform for the fabrication of low-defect-density perovskite QDs and efficient, stable perovskite QD LEDs.