Resonant Band-Edge Emissive States in Strongly Confined CsPbBr3 Perovskite Nanoplatelets

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 x 4 x 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.

Automated summary

The study investigated early exciton dynamics in strongly confined all-inorganic cesium lead halide perovskite nanocrystals, revealing the formation and relaxation process of emitting band-edge states and confined hole states. Increasing pump excitation intensity led to longer band-edge population lifetime due to confined hole state filling.