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Two-photon photodissociation dynamics of carbon disulfide (CS2) were studied by means of the sliced velocity map ion imaging technique. The S(1S) + CS(X1Σ+) channel was directly observed from the measured images of S(1S) products in the wavelength range of 290.10-336.88 nm. The translational energy distributions and angular distributions of fragments have been derived. Rovibrational states of the CS(X1Σ+) co-products were partially resolved in the translational energy spectra and can be populated up to the energy limit of the available energy. Experimental results also show that the product anisotropy parameters are β2 > 0 and β4 ∼ 0. The latter indicates that the intermediate state reached by the first one photon excitation has a quite long lifetime, while the former suggests the molecules undergo a parallel transition from the intermediate state to the final state upon the second photon excitation and then experience a fast dissociation process. Combined with previous studies, we propose a possible dissociation mechanism: after absorbing two photons in the range of 290.10-336.88 nm, the CS2 molecule may undergo a sequential transition 1A1(1Σg+) ← 11B2(1Δu)/1A2(1Δu) ← X1Σg+, then directly dissociate or couple to other electronic states and dissociate.
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http://dx.doi.org/10.1063/5.0283135 | DOI Listing |
J Chem Phys
July 2025
State Key Laboratory of Chemical Reaction Dynamics and Dalian Coherent Light Source, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning 116023, China.
Two-photon photodissociation dynamics of carbon disulfide (CS2) were studied by means of the sliced velocity map ion imaging technique. The S(1S) + CS(X1Σ+) channel was directly observed from the measured images of S(1S) products in the wavelength range of 290.10-336.
View Article and Find Full Text PDFJ Phys Chem A
February 2025
Institut für Optik und Atomare Physik, Technische Universität Berlin, Hardenbergstraße 36, 10623 Berlin, Germany.
Silicates and silica are the major components of interstellar silicon-based dust grains and mainly composed of silicon and oxygen. Information about their geometric, electronic, optical, and photochemical properties is crucial for developing astrochemical models describing dust grain formation. To this end, we characterize herein the optical spectrum of mass-selected SiO cations in the 295-709 nm range using electronic photodissociation (EPD).
View Article and Find Full Text PDFJ Chem Phys
February 2025
Anhui Province Key Laboratory for Control and Applications of Optoelectronic Information Materials, Department of Physics, Anhui Normal University, Wuhu, Anhui 241002, China.
The photodissociation and photoionization of O2 and the subsequent photodissociation of O2+ in the wavelength region of 200 to 240 nm are reported using resonance enhanced multiphoton ionization (REMPI) and velocity map imaging detection. A series of two-photon allowed Rydberg states with principle quantum number n = 3-11 converging to the ground electronic state of O2+X2Πg are used as doorway states to reach the region of superexcited states of O2 in the three-photon energy range of 15.8-18.
View Article and Find Full Text PDFPhys Chem Chem Phys
December 2024
Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Collaborative Innovation Centre of Chemistry for Energy Materials (iChEM), Fudan University, Shanghai, 200438, China.
SiO is a widespread molecule found in interstellar space, and its dissociation requires a substantial input of energy due to its high bond energy of 8.34 eV. The present study initially demonstrated across a broad range of ultraviolet (UV) wavelengths (243-288 nm) the one-photon and two-photon dissociation of SiO molecules, which were generated from the laser ablation of a Si rod colliding with an oxygen molecular beam.
View Article and Find Full Text PDFJ Chem Phys
December 2024
State Key Laboratory of Precision Spectroscopy, and School of Physics and Electronic Science, East China Normal University, Shanghai 200241, China.
The direct photodetachment and two-photon photodissociation-photodetachment processes of a series of PtIn- (n = 2-5) anions were systematically studied using cryogenic anion photoelectron spectroscopy and first-principles electronic structure calculations. The adiabatic/vertical detachment energies (ADEs/VDEs) of these anions were determined from their 193 nm photoelectron (PE) spectra, i.e.
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