Halide
segregation is a critical bottleneck that hampers the application
of mixed-halide perovskite nanocrystals (NCs) in both electroluminescent
and down-conversion red-light-emitting diodes. Herein, we report a
strategy that combines precursor and surface engineering to obtain
pure-red-emitting (peaked at 624 nm) NCs with a photoluminescence
quantum yield of up to 92% and strongly suppresses the halide segregation
of mixed-halide NCs under light irradiation. Red-light-emitting diodes
(LED) using these mixed-halide NCs as phosphors exhibit color-stable
emission with a negligible peak shift and spectral broadening during
operation over 240 min. By contrast, a dramatic peak shift and spectral
broadening were observed after 10 min of operation in LEDs based on
mixed-halide NCs synthesized by a traditional method. Our strategy
is critical to achieving photo- and band-gap-stable mixed-halide perovskite
NCs for a variety of optoelectronic applications such as micro-LEDs