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 language | English |
|---|---|
| Pages (from-to) | 18863-18872 |
| Number of pages | 10 |
| Journal | ACS Nano |
| Volume | 20 |
| Issue number | 26 |
| DOIs | |
| State | Published - 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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