Photodissociation of Noble Metal-Doped Carbon Clusters

Abstract

Noble metal carbide cluster cations (MC(n)(+), M = Cu, Au) are produced by laser vaporization in a pulsed molecular beam and detected with time-of-flight mass spectrometry. Copper favors the formation of carbides with an odd number of carbon atoms, while gold shows marked drops in ion intensity after clusters with 3, 6, 9, and 12 carbons. These clusters are mass selected and photodissociated at 355 nm. Copper carbides with an odd number of carbons fragment by eliminating the metal from the cluster; for the small species it is eliminated as Cu(+) and for the larger species it is lost as neutral Cu. Copper carbides with an even number of carbons also lose the metal, but in addition to this they eliminate neutral C(3). This even-odd alternation, with the even clusters having mixed fragments, holds true for clusters as large as CuC(30)(+). No loss of C(2) is observed for even the largest clusters studied, indicating that fullerene formation does not occur. The gold carbide photodissociation data closely parallel that of copper, with even clusters losing primarily C(3) and odd ones losing gold. Comparisons to known carbon cluster ionization potentials give some insight into the structures of carbon photofragments. DFT calculations performed on CuC(3-11)(+) allow comparisons of the energetics of isomers likely present in our experiment, and metal-carbon dissociation energies help explain the even-odd alternation in the fragmentation channels. The simplest picture of these metal-doped carbides consistent with all the data is that the small species have linear chain structures with the metal attached at the end, whereas the larger species have cyclic structures with the metal attached externally to a single carbon.