Adsorption of water in Na-LTA zeolites: an ab initio molecular dynamics investigation

Abstract

The very wide range of applications of LTA zeolites, including the storage of tritiated water, implies that a detailed and accurate atomic-scale description of the adsorption processes taking place in their structure is crucial. To unravel with an unprecedented accuracy the mechanisms behind the water filling in NaA, we have conducted a systematic ab initio molecular dynamics investigation. Two LTA structural models, the conventional Z4A and the reduced one ZK4, have been used for static and dynamic ab initio calculations, respectively. After assessing this reduced model with comparative static DFT calculations, we start the filling of the α and β cages by water, molecule by molecule. This allowed us to thoroughly study the interaction of water molecules with the zeolite structure and between water molecules, progressively forming H-bond chains and ring patterns as the cage is being filled. The adsorption energies could then be calculated with an unprecedented accuracy, which showed that the interaction of the molecules with the zeolite weakens as their number increases. By these methods, we have been able to highlight the primary role of Na⁺ cations in the interaction of water with zeolite, and inversely, the role of water in the displacement of cations when it is sufficiently solvated, allowing the passage between the α and β cages. This phenomenon is possible thanks to the inhomogeneous distribution of water molecules on the cationic sites, as shown by our AIMD simulations, which allows the formation of water clusters. These results are important because they help in understanding how the coverage of cationic sites by water will affect the adsorption of other molecules inside the Na-LTA zeolite.