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In this study, we investigate the effect of water-cluster formation in the supercritical (SC) systems CO2/(H2O)nas a function of water content using DFT-based molecular dynamics simulations. The dependence of the intermolecular and intramolecular structure and dynamic properties upon water concentration in the supercritical CO2/H2O phase at a density of 0.74 g cm−3and temperature of 318.15 K is investigated in detail and compared to previous studies of the pure sc-CO2system, single D2O in sc-CO2, and Monte-Carlo simulations of a single water molecule in sc-CO2phase. Analysis of radial and orientational distribution functions of the intermolecular interactions shows that the presence of water molecules does not disturb the previously established distorted T-shaped orientation of CO2molecules, though there is evidence of perturbation of the second shell structure which enhances the preference for the slipped parallel orientation in this region. There is also evidence of short-lived hydrogen bonds between CO2and water molecules. For higher water concentrations, water clustering is observed, consistent with the low solubility of water in CO2under these conditions of temperature and pressure. Finally, the water–water and water–CO2interactions are discussed and analyzed in terms of the water self-association and thermodynamic quantities derived from the molecular dynamics simulations. [ABSTRACT FROM AUTHOR]