Charge Transfer between Quantum Dots and Redox Molecules Is Not Auger-Assisted
Yan B. Vogel (TU Delft - ChemE/Materials for Energy Conversion and Storage)
Willemijn Boeije (TU Delft - ChemE/Opto-electronic Materials)
Lotte van Steekelenburg (TU Delft - QN/Kavli Nanolab Delft)
Demi Vollebregt (TU Delft - Applied Sciences)
Reinout Ubbink (TU Delft - ChemE/Opto-electronic Materials)
Hua Chen (TU Delft - ChemE/Opto-electronic Materials)
Wolter F. Jager (TU Delft - ChemE/Advanced Soft Matter)
Ferdinand Grozema (TU Delft - ChemE/Opto-electronic Materials)
Arjan J. Houtepen (TU Delft - ChemE/Opto-electronic Materials)
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Abstract
Charge transfer between quantum dots (QDs) and redox molecules is not well described by the Marcus theory, the hall-mark theory for charge transfer in molecular systems. The Marcus inverted region, where the rate decreases with increasing the free energy difference, has never been observed in QDs. The previously reported hypothesis for the absence of the Marcus inverted region in QDs is an Auger-assisted charge transfer pathway, which we refer to as the "Auger hypothesis". Here, we show that the Auger hypothesis does not hold to experimental tests. We measured the rate constants for two processes where Auger is either allowed or not: charge separation and charge recombination. We used ultrafast transient absorption spectroscopy to probe the rate of charge separation and recombination between PbS QDs and ferrocene derivatives ligands bound to their surface. We find that the rate constant for both charge separation and recombination increases by increasing the free energy difference, is temperature-independent, and increases with the number of molecular acceptors. All these results are against theoretical predictions for an Auger-assisted charge transfer pathway.
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