posted on 2021-06-27, 17:13authored byEtienne Socie, Brener R. C. Vale, Aaron T. Terpstra, Marco A. Schiavon, Jacques-E. Moser
Strongly confined,
fully inorganic cesium lead halide perovskite
nanocrystals are of great promise for light-emitting devices in the
blue spectral range owing to their high photoluminescence quantum
yields. A combination of broadband fluorescence up-conversion and
transient absorption spectroscopies was used to study early exciton
dynamics in quasi-1D CsPbBr3 nanoplatelets (3 × 4
× 23 nm3, NPls). This allowed to reveal emitting band-edge
states in the NPls that form instantaneously upon photoexcitation
and then relax within the first picosecond to lower energy confined
hole states (CHSs). The influence of the pump excitation intensity
on the latter process was further scrutinized. The band-edge population
lifetime was found to increase with the rise of the photon fluence
due to CHS filling. When the concentration of NPls in solution becomes
very high, nanoparticles overlap, resulting in a decrease in their
external absorption cross-section and an increase in the emission
Stokes shift due to photon reabsorption.