The photodissociation dynamics of UV excited CS2 are investigated using time-resolved Auger-Meitner (AM) spectroscopy. AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes an electron from the S(2p) orbital leading to secondary emission of a high energy electron through AM decay. We monitor the electron kinetic energy of the AM emission as a function of pump-probe delay and observe time-dependent changes in the spectrum that correlate with the formation of bound, excited-state CS2 molecules at early times, and CS + S fragments on the picosecond timescale. The results are analysed based on a simplified kinetic scheme that provides a time constant for dissociation of approximately 1.2 ps, in agreement with previous time-resolved x-ray photoelectron spectroscopy measurements.
Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS2 / H.J. Thompson, O. Plekan, M. Bonanomi, N. Pal, F. Allum, A.D. Brynes, M. Coreno, S. Coriani, M.B. Danailov, P. Decleva, A. Demidovich, M. Devetta, D. Faccialà, R. Feifel, R. Forbes, C. Grazioli, D.M.P. Holland, P. Piseri, K.C. Prince, D. Rolles, M.S. Schuurman, A. Simoncig, R.J. Squibb, B.N.C. Tenorio, C. Vozzi, M. Zangrando, C. Callegari, R.S. Minns, M. Di Fraia. - In: JOURNAL OF PHYSICS. B, ATOMIC MOLECULAR AND OPTICAL PHYSICS. - ISSN 0953-4075. - 57:21(2024 Nov 14), pp. 215602.1-215602.10. [10.1088/1361-6455/ad7e89]
Time-resolved Auger–Meitner spectroscopy of the photodissociation dynamics of CS2
P. Piseri;
2024
Abstract
The photodissociation dynamics of UV excited CS2 are investigated using time-resolved Auger-Meitner (AM) spectroscopy. AM decay is initiated by inner-shell ionisation with a femtosecond duration x-ray (179.9 eV) probe generated by the FERMI free electron laser. The time-delayed x-ray probe removes an electron from the S(2p) orbital leading to secondary emission of a high energy electron through AM decay. We monitor the electron kinetic energy of the AM emission as a function of pump-probe delay and observe time-dependent changes in the spectrum that correlate with the formation of bound, excited-state CS2 molecules at early times, and CS + S fragments on the picosecond timescale. The results are analysed based on a simplified kinetic scheme that provides a time constant for dissociation of approximately 1.2 ps, in agreement with previous time-resolved x-ray photoelectron spectroscopy measurements.File | Dimensione | Formato | |
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