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    Yuxin Tan, Yaling Wang, Chang Luo, Daofu Yuan, Xiaoguo Zhou, Xingan Wang, Xueming Yang. Photodissociation Dynamics of H2S+ via A2A1 (0, 11, 0) State†[J]. Chinese Journal of Chemical Physics , 2024, 37(6): 840-850. DOI: 10.1063/1674-0068/cjcp2410140
    Citation: Yuxin Tan, Yaling Wang, Chang Luo, Daofu Yuan, Xiaoguo Zhou, Xingan Wang, Xueming Yang. Photodissociation Dynamics of H2S+ via A2A1 (0, 11, 0) State†[J]. Chinese Journal of Chemical Physics , 2024, 37(6): 840-850. DOI: 10.1063/1674-0068/cjcp2410140

    Photodissociation Dynamics of H2S+ via A2A1 (0, 11, 0) State

    • Time-sliced velocity map ion imaging (VMI) experiments were performed to investigate the photodissociation of H2S+ X2B1 via the excitation to the A2A1 (0, 11, 0) state. Experimental images of the S+ (4Su) products were recorded near 349.60 nm for the K = 1 band, and near 344.30 nm for the K = 2 band. The derived product total kinetic energy release (TKER) spectra exhibit partially rotationally resolved structures corresponding to the H2 (X1\Sigma_\mathrmg^+) co-products. The observed product state and angular distributions both exhibit sensitive dependence on the photolysis wavelength at near 349.60 nm and 344.30 nm. These phenomena indicate the underlying rich dynamic details and the role of the rotational excitation of H2S+.
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