The Journal of Chemical Physics · 1988 · 151 citations · 33 references
EngineeringChemistryElectronic Excited StateSpectroscopic PropertyElectronic StatesJet-cooled Pt2Optical SpectroscopyPhotophysical PropertyMolecular SpectroscopyPhotonicsPhysicsPhotochemistryChemical BondAtomic PhysicsPhysical ChemistryQuantum ChemistryExcited State PropertyNatural SciencesSpectroscopyApplied Physics
The gas phase optical spectrum of jet-cooled Pt2 has been investigated over the range of 11 300 to 26 300 cm−1 using resonant two-photon ionization spectroscopy in combination with time-of-flight mass spectrometry. Numerous vibronic bands are observed. Analysis of the data gives the location of some 26 excited electronic states, which are characterized by the frequencies of their origin bands, vibrational frequencies, and anharmonicities. Variation of the second color in a two-color resonant two-photon ionization scheme has determined the ionization threshold of Pt2 to be 8.68±0.02 eV. The observation of the onset of predissociation, characterized by a sharp drop in excited state lifetime, places the dissociation energy of Pt2 at 3.14±0.02 eV. In combination with the Pt atomic ionization potential of 8.8±0.2 eV, these results give the bond strength of Pt+2 as D0(Pt−Pt+)=3.26±0.24 eV. The strength of the chemical bond in Pt2, as compared to Au2, demonstrates that there are significant 5d contributions to the chemical bonding in Pt2.
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Surface reactions of metal clusters. II. Reactivity surveys with D2, N2, and CO
Michael D. Morse, M. E. Geusic, J. R. Heath et al. · The Journal of Chemical Physics · 1985 · 403 citations
Engineering, Nanocluster, Chemistry +19
David E. Powers, Steven G. Hansen, M. E. Geusic et al. · The Journal of Chemical Physics · 1983 · 273 citations