In recent years, the realization of highly efficient
perovskite
light-emitting diodes (PeLEDs) based on two-dimensional perovskite
nanoplates, featuring unique quantum-well structures and substantial
exciton binding energies, has been a notable achievement. However,
the perovskite emissive layer synthesized through solution processing
has exhibited numerous defects, and the propensity for the formation
of a wide-band gap low-dimensional phase has posed limitations on
the advancement of PeLEDs. In this study, the small organic molecule
trimorpholinophosphine oxide, containing PO bond, was employed
for passivating the uncoordinated Pb2+ cations, while an
antisolvent treatment using chlorobenzene was implemented to further
optimize the phase distribution based on the PPA2FAn–1PbnBr3n+1 perovskite film. This synergetic strategy
effectively reduced the defect density and enhanced the energy transfer
efficiency. Consequently, highly efficient PeLEDs were achieved, demonstrating
a remarkable external quantum efficiency of 14.14% and a luminance
of 17,196.7 cd/m2, representing more than 5.06 and 1.77
times superior performance compared to the original devices, respectively.
This study presents an approach for the defect passivation and phase
distribution control in perovskites nanoplates.