Abstract

Electronic coherence has attracted considerable attention for its possible role in dynamical processes in molecular systems. However, its detection is challenged by inhomogeneous line broadening and interference with vibrational coherences. In particular, reports of 'persistent' coherent exciton superpositions at room temperature remain controversial, as the related transitions give typically shorter optical dephasing times of about 10-20 fs. To rationalize these reported long-lived coherences, several models have been proposed, involving strong correlation in the mechanisms of decoherence or that electronic coherences may be sustained by resonant vibrational modes. Here we report a decisive example of electronic coherence occurring in a chemical system in a 'warm and wet' (room-temperature solution) environment, colloidal semiconductor nanoplatelets, where details are not obscured by vibrational coherences nor ensemble dephasing. Comparing the exciton and optical coherence times evidences a partial correlation of fluctuations underlying dephasing and allows us to elucidate decoherence mechanisms occurring in these samples.

Highlights

  • Electronic coherence has attracted considerable attention for its possible role in dynamical processes in molecular systems

  • Models were proposed where the electronic coherence is sustained by interaction with a resonant vibrational mode[14,15,16]

  • It is evident that the pure homogeneous line broadening of the colloidal NPLs enables clear observation of the electronic coherence that is hidden by inhomogeneous dephasing in the case of the CdSe colloidal quantum dots

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Summary

Introduction

Electronic coherence has attracted considerable attention for its possible role in dynamical processes in molecular systems. We use 2D electronic spectroscopy (2DES) to study the exciton superposition and dephasing in colloidal nanoplatelets (NPLs) at room temperature.

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