Mode specific photodissociation of CS2+via the A2Πu state: a time-sliced velocity map imaging study
Cuimei Zhang, Jialin Li, Qun Zhang, Yang Chen, Cunshun Huang, Xueming Yang
Abstract
Cuimei Zhang, Jialin Li, Qun Zhang, Yang Chen, Cunshun Huang, Xueming Yang
Abstract
The vibrationally mediated photodissociation of CS(2)(+) cations via the A(2)Π(u)(ν(1),ν(2),0) state has been studied by means of the velocity map ion imaging technique. The measurements were made with a double resonance strategy. The CS(2)(+) cations were prepared by a (3 + 1) resonance enhanced multiphoton ionization method. The photo-fragment excitation spectrum of S(+) was recorded by scanning the photolysis laser via the A(2)Π(u)(ν(1),ν(2),0) state. By fixing the photolysis laser wavelength at the specific vibrational state, the (1 + 1) photodissociation images of S(+) photofragments from numerous vibrationally mediated states have been accumulated. The translational energy release spectra derived from the resulting images imply that the co-fragments, CS radicals, are both vibrationally and rotationally excited. The one-photon photodissociation without the vibrational state selection has also been performed. Comparing the vibrationally mediated photodissociation with one-photon photodissociation observations, clear evidence of vibrational state control of the photodissociation process is observed.
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The vibrationally mediated photodissociation of CS(2)(+) cations via the A(2)Π(u)(ν(1),ν(2),0) state has been studied by means of the velocity map ion imaging technique. The measurements were made with a double resonance strategy. The CS(2)(+) cations were prepared by a (3 + 1) resonance enhanced multiphoton ionization method. The photo-fragment excitation spectrum of S(+) was recorded by scanning the photolysis laser via the A(2)Π(u)(ν(1),ν(2),0) state. By fixing the photolysis laser wavelength at the specific vibrational state, the (1 + 1) photodissociation images of S(+) photofragments from numerous vibrationally mediated states have been accumulated. The translational energy release spectra derived from the resulting images imply that the co-fragments, CS radicals, are both vibrationally and rotationally excited. The one-photon photodissociation without the vibrational state selection has also been performed. Comparing the vibrationally mediated photodissociation with one-photon photodissociation observations, clear evidence of vibrational state control of the photodissociation process is observed.
Key concepts: Photodissociation, Excited state, Resonance-enhanced multiphoton ionization, Chemistry, Atomic physics, Ionization, Resonance (particle physics), Excitation