The density functional theory-based hybrid method B3LYP was used to study the interaction of the dioxymethylene species with the copper (111) surface. This species has been proposed experimentally as one possible intermediate in the oxidation of methanol catalysed by metal surfaces. The H2CO2 species is very unstable, and this makes the experimental study too difficult. As far as we know, there are no direct theoretical or experimental studies of H2CO2 adsorption on metal surfaces in the literature. The experimental knowledge is limited to the IR frequencies obtained for adsorption on metal oxides.In this study, two different clusters and two different adsorption sites have been studied. A two-layer Cu7 cluster was used to model the H2CO2 and [H2CO2]2− adsorption on a small copper island, and a large three-layer Cu30 cluster was used to model the H2CO2 adsorption on a copper (111) surface. These clusters were used to extract information concerning the energetics, geometry and IR frequencies for the dioxymethylene adsorption. When compared with a similar species, formate, dioxymethylene is stabilized more efficiently on the cross-bridge site than on the aligned-bridge site, which is the preferred orientation for formate. However, the oxygen-to-surface distances are similar, and the same is observed for the bonding type, which is mainly ionic. A bridge-bonded conformation is predicted for adsorption on the two sites considered. The comparison of the adsorption energy of the dioxymethylene species and the adsorption energy of atomic oxygen and free formaldehyde yields an interesting result: H2CO2(ads) is energetically more stable than adsorbed O(ads) and H2CO(g). The IR frequencies are in good agreement with experimental data obtained for dioxymethylene adsorption on several oxide surfaces.