Ultrafast dynamics of excited electronic states in nitrobenzene measured by ultrafast transient polarization spectroscopy

We investigate ultrafast dynamics of the lowest singlet excited electronic state in liquid nitrobenzene using Ultrafast Transient Polarization Spectroscopy (UTPS), extending the well-known technique of Optical-Kerr Effect (OKE) spectroscopy to excited electronic states. The third-order non-linear re...

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Bibliographic Details
Published in:arXiv.org 2019-12
Main Authors: Thurston, Richard, Brister, Matthew M, Tan, Liang Z, Champenois, Elio G, Bakhti, Said, Muddukrishna, Pavan, Weber, Thorsten, Belkacem, Ali, Slaughter, Daniel S, Shivaram, Niranjan
Format: Article
Language:English
Subjects:
Electron states
Excitation
Excitation spectra
Femtosecond pulses
Nitrobenzene
Nonlinear response
Polarization
Spectrum analysis
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Summary:We investigate ultrafast dynamics of the lowest singlet excited electronic state in liquid nitrobenzene using Ultrafast Transient Polarization Spectroscopy (UTPS), extending the well-known technique of Optical-Kerr Effect (OKE) spectroscopy to excited electronic states. The third-order non-linear response of the excited molecular ensemble is highly sensitive to details of excited state character and geometries and is measured using two femtosecond pulses following a third femtosecond pulse that populates the S1 excited state. By measuring this response as a function of time delays between the three pulses involved, we extract the dephasing time of the wave-packet on the excited state. The dephasing time measured as a function of time-delay after pump excitation shows oscillations indicating oscillatory wave-packet dynamics on the excited state. From the experimental measurements and supporting theoretical calculations, we deduce that the wave-packet completely leaves the S1 state surface after three traversals of the inter-system crossing between the singlet S1 and triplet T2 states.
ISSN:2331-8422
DOI:10.48550/arxiv.1912.12902