Yuxin Tan, Yaling Wang, Chang Luo, Zhiwen Luan, Jie Li, Daofu Yuan, Xiaoguo Zhou, Xingan Wang, Xueming Yang
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引用次数: 0
Abstract
The photodissociation dynamics of the hydrogen sulfide cation (H2S+) (X2B1) were investigated using the time-sliced velocity map ion imaging technique. S+ (4Su) product images were measured at four photolysis wavelengths around 393.70 nm, corresponding to the excitation of the H2S+ (X2B1) cation to the A2A1 (0, 8, 0) state. The raw images and the derived total kinetic energy releases (TKERs) spectra exhibited partial rotational resolution for the H2 products. A sensitive dependence on the photolysis wavelength was observed in the TKER spectra and anisotropy parameters. Within a narrow excitation energy range of ∼12 cm-1, the H2 products showed two distinct rotational excitations. Furthermore, clear differences in anisotropy parameters were observed. These phenomena indicate that the rotational excitation of the H2S+ ions plays a role in the non-adiabatic photodissociation dynamics.
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The Journal of Chemical Physics publishes quantitative and rigorous science of long-lasting value in methods and applications of chemical physics. The Journal also publishes brief Communications of significant new findings, Perspectives on the latest advances in the field, and Special Topic issues. The Journal focuses on innovative research in experimental and theoretical areas of chemical physics, including spectroscopy, dynamics, kinetics, statistical mechanics, and quantum mechanics. In addition, topical areas such as polymers, soft matter, materials, surfaces/interfaces, and systems of biological relevance are of increasing importance.
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