The hydrothermal synthesis and structural characterization of the lanthanide silicate system [Na6Ln2Si12O30x H2O] (Ln=La3+, Sm3+, Eu3+, Gd3+, and Tb3+), named AV-21, has been reported. Structural elucidation of the Sm3+ analogue (isomorphous with the Eu3+, Gd3+, and Tb3+ frameworks) using single-crystal synchrotron X-ray diffraction and solid-state NMR spectroscopy reveal disorder in the Si(1) second coordination sphere. La-AV-21 presents a distinct framework. These materials combine microporosity and interesting photoluminescence features with structural flexibility that allows the introduction of a second or third type of lanthanide center. Room-temperature lifetime decay dynamics have been used to estimate the Ln3+Ln3+ distances and the maximum distance over which energy transfer is active. Though the majority of Ln3+ centers occupy regular framework positions, the Ln(2) defect centers are disordered over the Na(1) sites in the pores and greatly influence the energy-transfer process, providing a unique opportunity for studying the relationship between structural disorder and photoluminescence properties in framework solids.
Rosario Scopelliti, Kay Severin, Farzaneh Fadaei Tirani, Paul Varava, Wolfram Feuerstein
David Lyndon Emsley, Andrea Bertarello