Abstract
Femtosecond stimulated emission pumping in combination with femtosecond photoelectron spectroscopy is used to characterize the potential energy function of the I2−(X̃ 2Σu+) ground state up to vibrational energies within 2% of the dissociation limit. The frequency and anharmonicity of this state are measured at a series of vibrational energies up to 0.993 eV by coherently populating a superposition of ground state vibrational levels using femtosecond stimulated emission pumping, and monitoring the resulting wave packet oscillations with femtosecond photoelectron spectroscopy. The dissociative I2−(Ã′ 2Πg,1/2) state is used for intermediate population transfer, allowing efficient population transfer to all ground state levels. Using the measured frequencies and anharmonicities, the X̃ 2Σu+ state has been fit to a modified Morse potential with the β-parameter expanded in a Taylor series, and the bond length, well depth, and υ=0–1 fundamental frequency set equal to our previously determined Morse potential [J. Chem. Phys. 107, 7613 (1997)]. At high vibrational energies, the modified potential deviates significantly from the previously determined potential.
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