Exciton and biexciton transient absorption spectra of CdSe quantum dots with varying diameters

Katherine E Shulenberger; Skylar J Sherman; Madison R Jilek; Helena R Keller; Lauren M Pellows; Gordana Dukovic

doi:10.1063/5.0179129

Exciton and biexciton transient absorption spectra of CdSe quantum dots with varying diameters

J Chem Phys. 2024 Jan 7;160(1):014708. doi: 10.1063/5.0179129.

Authors

Katherine E Shulenberger¹, Skylar J Sherman¹, Madison R Jilek¹, Helena R Keller², Lauren M Pellows¹, Gordana Dukovic^{1

2

3}

Affiliations

¹ Department of Chemistry, University of Colorado Boulder, 215 UCB, Boulder, Colorado 80309, USA.
² Materials Science and Engineering, University of Colorado Boulder, 613 UCB, Boulder, Colorado 80303, USA.
³ Renewable and Sustainable Energy Institute (RASEI), University of Colorado Boulder, 027 UCB, Boulder, Colorado 80309, USA.

PMID: 38174790
DOI: 10.1063/5.0179129

Abstract

Transient absorption (TA) spectroscopy of semiconductor nanocrystals (NCs) is often used for excited state population analysis, but recent results suggest that TA bleach signals associated with multiexcitons in NCs do not scale linearly with exciton multiplicity. In this manuscript, we probe the factors that determine the intensities and spectral positions of exciton and biexciton components in the TA spectra of CdSe quantum dots (QDs) of five diameters. We find that, in all cases, the peak intensity of the biexciton TA spectrum is less than 1.5 times that of the single exciton TA spectrum, in stark contrast to a commonly made assumption that this ratio is 2. The relative intensities of the biexciton and exciton TA signals at each wavelength are determined by at least two factors: the TA spectral intensity and the spectral offset between the two signals. We do not observe correlations between either of these factors and the particle diameter, but we find that both are strongly impacted by replacing the native organic surface-capping ligands with a hole-trapping ligand. These results suggest that surface trapping plays an important role in determining the absolute intensities of TA features for CdSe QDs and not just their decay kinetics. Our work highlights the role of spectral offsets and the importance of surface trapping in governing absolute TA intensities. It also conclusively demonstrates that the biexciton TA spectra of CdSe QDs at the band gap energy are less than twice as intense as those of the exciton.