Apr 8, 2025
11:45am - 12:00pm
Summit, Level 3, Room 343
Stephen O'Leary2,Matthew Pelton1,Yana Wang2,Igor Fedin3,Dmitri Talapin4
University of Maryland, Baltimore County1,University of British Columbia2,The University of Alabama3,The University of Chicago4
Stephen O'Leary2,Matthew Pelton1,Yana Wang2,Igor Fedin3,Dmitri Talapin4
University of Maryland, Baltimore County1,University of British Columbia2,The University of Alabama3,The University of Chicago4
We present time-resolved photoluminescence spectroscopy of a series of colloidal CdSe/CdS core/shell nanoplatelets with different core and shell thicknesses. Carrier numbers are determined from the integrated photoluminescence intensities, and carrier temperatures are determined from the high-energy exponential tail on the photoluminescence spectra. For times between 10 ps and 1 ns and for shell thicknesses up to 4 monolayers, the measured carrier relaxation dynamics are well described by a simple model of Auger reheating: biexcitonic Auger recombination continually increases the average energy of the carriers (while decreasing their number), and this reheating sets a bottleneck to cooling through electron-phonon coupling. For times between 1 and 10 ps, the relaxation dynamics are consistent with electron-phonon coupling, where the bottleneck is now the decay of the LO-phonon population. For shell thicknesses greater than 4 monolayers, the simple Auger-reheating model cannot quantitatively account for the measurement results. The implications of these results will be presented.