Unraveling the electronic structure of transition metal dimers using resonant four-wave mixing

The potential of two-color resonant and degenerate four-wave mixing spectroscopy for investigations of the complex spectra of transition metal dimers is explored. Two-color resonant and degenerate four-wave mixing spectroscopy scans of the well-known A-X and B-X transitions in Cu2 are reported and compared with previous experimental data obtained from standard single-resonance techniques. The selectivity of the method is shown to enable the measurement of isotopologue pure spectra without the need for isotopically enriched metal targets. Specific subsets of the rovibronic structure are separated in a congested spectral region of overlapping transitions. The sensitivity of the method compares satisfactorily with linear spectroscopic methods such as laser-induced fluorescence and cavity ring-down. A new laser vaporization source for the production of transition metal dimers and clusters has been constructed. The new design aims for a high number density and maximum possible shot-to-shot stability. The possibilities of further applications of non-linear four-wave mixing spectroscopy to Cu2 and other transition metal dimers are discussed. Copyright © 2015 John Wiley & Sons, Ltd.