alexa Molecular adsorption and metal-support interaction for transition-metal clusters in zeolites: NO adsorption on Pd(n) (n=1-6) clusters in mordenite.
Chemical Engineering

Chemical Engineering

Journal of Advanced Chemical Engineering

Author(s): Grybos R, Benco L, Bucko T, Hafner J

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Abstract The adsorption of NO molecules on Pd(n) clusters of varying size (n=1-6) located in the main channel of mordenite and the interaction of the metallic clusters with the zeolitic framework were investigated using ab initio density-functional calculations under periodic boundary conditions. The supported clusters are created by binding Pd(n) (2+) cations to the inner cavity of a deprotonated Al-exchanged zeolite with an Al/Si ratio of 1/11, such that a charge-neutral system is created. Compared to the highly symmetric structures of the gas-phase clusters, the clusters bound to the zeolitic framework undergo appreciable geometric distortions lowering their symmetry. The distortions are induced by strong interactions with "activated" framework oxygens located close to the charge-compensating Al/Si substitution sites, but the cluster forms also weaker bonds to "nonactivated" oxygen atoms. The interaction with the framework also affects the electronic and magnetic properties of the clusters. While in the gas phase all clusters (except the isolated Pd atom with a closed d(10) ground state) have a paramagnetic moment of 2mu(B), in the zeolite clusters with two to four atoms have zero magnetic moment, while the Pd(5) cluster has a magnetic moment of 2mu(B) and for the Pd(6) cluster, it is even enhanced to 4 mu(B) (but the magnetic energy differences relative to low-spin configurations are modest). Analysis of the magnetization densities shows that in all clusters with zero total moment (singlet ground state), there are sites with excess spin densities of opposite sign. The influence of the cluster-support interaction on the chemical properties of the clusters has been tested by the adsorption of NO molecules. The results demonstrate the interplay between the molecule-cluster and cluster-framework interactions, which can lead to an increase or decrease in the adsorption energy compared to NO on a gas-phase cluster. While on the gas-phase cluster adsorption in low-coordination sites (vertex or bridge) is preferred, for the cluster in the zeolite adsorption in threefold coordinated hollow or twofold bridge sites is preferred. The magnetic properties of the clusters and of the paramagnetic NO molecule play an important role. For the supported clusters with zero magnetic moment, upon adsorption the spin of the molecule is transferred to the cluster (and induces also a modest polarization of the framework). For magnetic clusters, spin pairing induces a reduced magnetic moment of the NO-Pd(n) complex. The redshift of the NO stretching frequencies is reduced compared to the free clusters by the cluster-support interaction for the smaller clusters, while it remains essentially unchanged for the larger clusters. A detailed electronic analysis of the cluster-support interactions and of the adsorption properties is presented. This article was published in J Chem Phys and referenced in Journal of Advanced Chemical Engineering

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