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- W2029334002 abstract "In this paper, we report the first comparison study between ${mathrm{N}}_{2}$ and ${mathrm{O}}_{2}$ on their triple-ionization-induced dissociation channels using near-IR 800-nm ultrashort laser pulses. Our experiment shows that the ${mathrm{O}}^{2+}+{mathrm{O}}^{+}$ channel is predominately formed nonvertically through the intermediate ${mathrm{O}}^{+}+{mathrm{O}}^{+}$ channel, while the ${mathrm{N}}^{2+}+{mathrm{N}}^{+}$ channel appears to be formed vertically at the lower intensity range but nonvertically at higher intensities. Interestingly, ${mathrm{N}}^{2+}+{mathrm{N}}^{+}$ appears to be in the electronically excited state when it is reached vertically in the lower intensity range. The different triple ionization and dissociation behaviors between ${mathrm{N}}_{2}$ and ${mathrm{O}}_{2}$ can be understood by considering the ionization dynamics of the two molecules in our ultrashort laser pulses." @default.
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- W2029334002 date "2006-05-19" @default.
- W2029334002 modified "2023-09-27" @default.
- W2029334002 title "Dynamics of triple-ionization-induced dissociation in diatomic molecules in strong fields" @default.
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- W2029334002 doi "https://doi.org/10.1103/physreva.73.051402" @default.
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