CO2 activation by copper oxide clusters: size, composition, and charge state dependence.

The interaction of CO2 with copper oxide clusters of different size, composition, and charge is investigated via infrared multiple-photon dissociation (IR-MPD) spectroscopy and density functional theory (DFT) calculations. Laser ablation of a copper target in the presence of an O2/He mixture leads to the preferred formation of oxygen-rich copper oxide cluster cations, CuxOy+ (y > x; x ≤ 8), while the anionic cluster distribution is dominated by stoichiometric (x = y) and oxygen-deficient (y < x; x ≤ 8) species. Subsequent reaction of the clusters with CO2 in a flow tube reactor results in the preferred formation of near-stoichiometric CuxOy(CO2)+/- complexes. IR-MPD spectroscopy of the formed complexes reveals the non-activated binding of CO2 to all cations while CO2 is activated by all anions. The great resemblance of spectra for all sizes investigated demonstrates that CO2 activation is largely independent of cluster size and Cu/O ratio but mainly determined by the cluster charge state. Comparison of the IR-MPD spectra with DFT calculations of the model systems Cu2O4(CO2)- and Cu3O4(CO2)- shows that CO2 activation exclusively results in the formation of a CO3 unit. Subsequent CO2 dissociation to CO appears to be unfavorable due to the instability of CO on the copper oxide clusters indicating that potential hydrogenation reactions will most likely proceed via formate or bicarbonate intermediates.