Excited state dynamics in SO2. I. Bound state relaxation studied by time-resolved photoelectron-photoion coincidence spectroscopy.

Excited state dynamics in SO2. I. Bound state relaxation studied by time-resolved photoelectron-photoion coincidence spectroscopy. Wilkinson, I., Boguslavskiy, A. E, Mikosch, J., Bertrand, J. B, Wörner, H. J., Villeneuve, D. M, Spanner, M., Patchkovskii, S., & Stolow, A. The Journal of chemical physics, 140(20):204301, May, 2014.

Paper doi abstract bibtex

The excited state dynamics of isolated sulfur dioxide molecules have been investigated using the time-resolved photoelectron spectroscopy and time-resolved photoelectron-photoion coincidence techniques. Excited state wavepackets were prepared in the spectroscopically complex, electronically mixed ([Formula: see text])(1)B1/(Ã)(1)A2, Clements manifold following broadband excitation at a range of photon energies between 4.03 eV and 4.28 eV (308 nm and 290 nm, respectively). The resulting wavepacket dynamics were monitored using a multiphoton ionisation probe. The extensive literature associated with the Clements bands has been summarised and a detailed time domain description of the ultrafast relaxation pathways occurring from the optically bright ([Formula: see text])(1)B1 diabatic state is presented. Signatures of the oscillatory motion on the ([Formula: see text])(1)B1/(Ã)(1)A2 lower adiabatic surface responsible for the Clements band structure were observed. The recorded spectra also indicate that a component of the excited state wavepacket undergoes intersystem crossing from the Clements manifold to the underlying triplet states on a sub-picosecond time scale. Photoelectron signal growth time constants have been predominantly associated with intersystem crossing to the ([Formula: see text])(3)B2 state and were measured to vary between 750 and 150 fs over the implemented pump photon energy range. Additionally, pump beam intensity studies were performed. These experiments highlighted parallel relaxation processes that occurred at the one- and two-pump-photon levels of excitation on similar time scales, obscuring the Clements band dynamics when high pump beam intensities were implemented. Hence, the Clements band dynamics may be difficult to disentangle from higher order processes when ultrashort laser pulses and less-differential probe techniques are implemented.

@article{Wilkinson2014,
	title = {Excited state dynamics in {SO2}. {I}. {Bound} state relaxation studied by time-resolved photoelectron-photoion coincidence spectroscopy.},
	volume = {140},
	issn = {1089-7690},
	url = {http://www.ncbi.nlm.nih.gov/pubmed/24880274},
	doi = {10.1063/1.4875035},
	abstract = {The excited state dynamics of isolated sulfur dioxide molecules have been investigated using the time-resolved photoelectron spectroscopy and time-resolved photoelectron-photoion coincidence techniques. Excited state wavepackets were prepared in the spectroscopically complex, electronically mixed ([Formula: see text])(1)B1/(Ã)(1)A2, Clements manifold following broadband excitation at a range of photon energies between 4.03 eV and 4.28 eV (308 nm and 290 nm, respectively). The resulting wavepacket dynamics were monitored using a multiphoton ionisation probe. The extensive literature associated with the Clements bands has been summarised and a detailed time domain description of the ultrafast relaxation pathways occurring from the optically bright ([Formula: see text])(1)B1 diabatic state is presented. Signatures of the oscillatory motion on the ([Formula: see text])(1)B1/(Ã)(1)A2 lower adiabatic surface responsible for the Clements band structure were observed. The recorded spectra also indicate that a component of the excited state wavepacket undergoes intersystem crossing from the Clements manifold to the underlying triplet states on a sub-picosecond time scale. Photoelectron signal growth time constants have been predominantly associated with intersystem crossing to the ([Formula: see text])(3)B2 state and were measured to vary between 750 and 150 fs over the implemented pump photon energy range. Additionally, pump beam intensity studies were performed. These experiments highlighted parallel relaxation processes that occurred at the one- and two-pump-photon levels of excitation on similar time scales, obscuring the Clements band dynamics when high pump beam intensities were implemented. Hence, the Clements band dynamics may be difficult to disentangle from higher order processes when ultrashort laser pulses and less-differential probe techniques are implemented.},
	number = {20},
	urldate = {2014-06-04},
	journal = {The Journal of chemical physics},
	author = {Wilkinson, Iain and Boguslavskiy, Andrey E and Mikosch, Jochen and Bertrand, Julien B and Wörner, Hans Jakob and Villeneuve, David M and Spanner, Michael and Patchkovskii, Serguei and Stolow, Albert},
	month = may,
	year = {2014},
	pmid = {24880274},
	keywords = {\#nosource},
	pages = {204301},
}

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