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- W2056829232 abstract "Ab initio potential energy surfaces and the corresponding analytical energy functions of the ground 1A' and excited 2A' states for the Li(2(2)P) plus H(2) reaction are constructed. Quasiclassical trajectory calculations on the fitted energy functions are performed to characterize the reactions of Li(2(2)P) with H(2)(v = 0, j = 1) and H(2)(v = 1, j = 1) as well as the reaction when the vibrational energy is replaced by collision energy. For simplicity, the transition probability is assumed to be unity when the trajectories go through the crossing seam region and change to the lower surface. The calculated rotational distributions of LiH(v = 0) for both H(2)(v = 0, j = 1) and H(2)(v = 1, j = 1) reactions are single-peaked with the maximum population at j' = 7, consistent with the previous observation. The vibrational excitation of H(2)(v = 1) may enhance the reaction cross section of LiH(v' = 0) by about 200 times, as compared to a result of 93-107 reported in the experimental measurements. In contrast, the enhancement is 3.1, if the same amount of energy is deposited in the translational states. This endothermic reaction can be considered as an analog of late barrier. According to the trajectory analysis, the vibrational excitation enlarges the H-H distance in the entrance channel to facilitate the reaction, but the excess energy may not open up additional reaction configuration." @default.
- W2056829232 created "2016-06-24" @default.
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- W2056829232 date "2011-01-21" @default.
- W2056829232 modified "2023-10-16" @default.
- W2056829232 title "Quasiclassical trajectory calculations for Li(2<sup>2</sup>P<sub>J</sub>) + H<sub>2</sub> → LiH(X<sup>1</sup>Σ<sup>+</sup>) + H: Influence by vibrational excitation and translational energy" @default.
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- W2056829232 doi "https://doi.org/10.1063/1.3519801" @default.
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