Origin of Vibronic Coherences During Carrier Cooling in Colloidal Quantum Dots

Recent two-dimensional electronic spectroscopy experiments [] indicate the creation of coherent vibronic wavepackets in the first femtoseconds of hot carrier cooling in hexadecylamine-passivated CdSe quantum dots. Here we present a quantum chemical study of the origin of these coherences in a CdSe nanocrystal. We find that coherent wavepacket motions along vibrational coordinates with alkylamine character promote nonradiative relaxation through conical intersections between the exciton states of the inorganic core. Electronic excitations in the core are found to pass energy to the vibrations of the ligands via two distinct mechanisms: excitation of core phonon modes that are coupled to the ligand vibrations and direct excitation of ligand vibrations by delocalization of the exciton onto the ligands, both of which naturally arise within a photochemical framework based on many-electron potential energy surfaces. If these findings are demonstrated to be general, vibronic coherences may be leveraged to control photophysical outcomes in colloidal quantum dots.