Red-light-emitting
InP/ZnSexS1–x core/shell quantum dots (QDs) were prepared by one-pot
synthesis with optimal hydrogen fluoride (HF) treatment. Most of the
surficial oxidative species could be removed, and the dangling bonds
would be passivated by Zn ions for the InP cores during HF treatment,
which would be beneficial to the subsequent ZnSexS1–x shell coating. Three-dimensional
time-resolved photoluminescence spectra of the QD samples were analyzed
by singular value decomposition global fitting to determine the radiative
and nonradiative lifetimes of charge carriers. A proposed model illustrated
that the charge carriers in the InP/ZnSexS1–x QDs with interfacial oxidative
layer removal would evidently recombine through radiative pathways,
mainly from the conduction band to the valence band (lifetime, 33
ns) and partially from the trap states (lifetime, 150 ns). This work
offers the important physical insight into the charge carrier dynamics
of low-toxicity QDs which have the desired optical properties for
optoelectronic applications.