Exit-channel recoil resonances by imaging the photodissociation of single quantum-state-selected OCS molecules

Autor: J. Suárez, Johan A. Schmidt, Dimitris Sofikitis, T. Peter Rakitzis, Maurice H. M. Janssen, Stavros C. Farantos
Přispěvatelé: AIMMS, Physical Chemistry, Photo Conversion Materials, LaserLaB - Analytical Chemistry and Spectroscopy
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Zdroj: Physical Review A, 98(3):033417, 1-11. American Physical Society
Sofikitis, D, Suarez, J, Schmidt, J A, Rakitzis, T P, Farantos, S C & Janssen, M H M 2018, ' Exit-channel recoil resonances by imaging the photodissociation of single quantum-state-selected OCS molecules ', Physical Review A, vol. 98, no. 3, 033417, pp. 1-11 . https://doi.org/10.1103/PhysRevA.98.033417
ISSN: 2469-9934
2469-9926
0031-9007
Popis: In a recent letter [Phys. Rev. Lett. 118, 253001 (2017)PRLTAO0031-900710.1103/PhysRevLett.118.253001] we have described how studies of the recoil velocity distribution in the photodissociation of OCS in the energy interval 42 600-42 900 cm-1 revealed an unexpected behavior: the recoil velocity distribution of only the lowest-kinetic-energy photofragments exhibited rapid, resonantlike variations with energy and caused complete inversion of the recoil direction. Periodic orbit analysis and quantum nonadiabatic calculations unveiled the existence of a resonance state localized at large bending angles towards the exit of the dissociation channel. In this article, we present an extensive theoretical study and we show how the fingerprints of these resonances are identified by the analysis of the nonadiabatic transitions and the stereodynamics of photofragments trajectories. Additionally, the experimental study is extended to a second photolysis energy region, 43 300-43 650 cm-1, where a similar rapid variation of the recoil direction is detected. The energy separation between this second resonance region and the one previously reported is ∼800cm-1, which is twice the calculated period of the localized resonant state, offering a second point of convergence between the experiment and the theory.
Databáze: OpenAIRE