PbS quantum dots (QDs) are attractive
near-infrared (NIR) materials,
but traditional synthetic methods require inert atmosphere and/or
high temperature. Herein we develop a facile, room-temperature synthetic
route for in situ halide passivated PbS QDs through
controllable reactions between lead halide, N,N′-diphenyl thiourea, and oleyamine (OLA) in toluene.
Contrast experiments and theoretical calculations reveal that the
OLA plays a bifunctional role as a mild base to initiate the formation
of PbS monomers and as a dynamic ligand to control the crystallization
of PbS QDs and further ligand exchange. The oleic acid-capped PbS
QDs exhibit high photoluminescence quantum yields up to 45%. The scaled-up
synthesis on multigram scales shows great batch-to-batch consistency.
We further demonstrate high-power NIR light-emitting diodes using
the PbS QDs as color converters, delivering NIR optical power of 9.2
mW at 160 mA. This work provides a simple and versatile synthetic
route for high-quality PbS QDs and boosts the applications of NIR
materials.