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Probing Ultrafast Excitonic Coherences and Charge-Generation Pathways in Quantum-Dot Photocells via Photocurrent-Detected Two-Dimensional Electronic Spectroscopy

  • Hadar Manis Levy
  • , Matilde Doardo
  • , James R. Hamilton
  • , Carlo Nazareno Dibenedetto
  • , Thibault Degousée
  • , Jan A. Mol
  • , Marinella Striccoli
  • , Francoise Remacle
  • , Elisabetta Collini*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Understanding how coherent excitonic states influence charge generation is essential for optimizing quantum-dot (QD) optoelectronic devices. Here, we apply photocurrent-detected two-dimensional electronic spectroscopy (PC-2DES) to a functioning CdSe QD photocell to track excitonic interactions and charge-separation dynamics under operational conditions. Selective excitation of the |1S⟩ manifold reveals strong contributions from red-shifted, delocalized excitons that dominate the photocurrent but contribute only weakly in optically detected 2DES. Global analysis uncovers three dynamical components, including a sub-100 fs process associated with photocurrent growth at specific spectral coordinates, consistent with rapid population transfer through delocalized states and possible trion formation. Unlike optical detection, PC-2DES suppresses longitudinal optical phonon signatures, enabling clear observation of higher-frequency beatings attributed to interdot electronic coherences. These results demonstrate the utility of PC-2DES for probing coherent charge-generation pathways in QD solids and for guiding the design of coherence-enabled optoelectronic devices.

Original languageEnglish
Pages (from-to)18863-18872
Number of pages10
JournalACS Nano
Volume20
Issue number26
DOIs
StatePublished - 7 Jul 2026

Bibliographical note

Publisher Copyright:
© 2026 The Authors. Published by American Chemical Society.

Keywords

  • charge separation
  • excitonic coherence
  • interdot coupling
  • photocurrent-detected 2DES
  • quantum-dot photocells
  • ultrafast spectroscopy

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