New Highly Luminescent Hybrid Materials: Terbium Pyridine−Picolinate Covalently Grafted on Kaolinite
journal contributionposted on 27.04.2011, 00:00 by Emerson H. de Faria, Eduardo J. Nassar, Katia J. Ciuffi, Miguel A. Vicente, Raquel Trujillano, Vicente Rives, Paulo S. Calefi
Luminescent hybrid materials derived from kaolinite appear as promising materials for optical applications due to their specific properties. The spectroscopic behavior of terbium picolinate complexes covalently grafted on kaolinite and the influence of the secondary ligand and thermal treatment on luminescence are reported. The resulting materials were characterized by thermal analysis, element analysis, X-ray diffraction, infrared absorption spectroscopy, and photoluminescence. The thermogravimetric curves indicated an enhancement in the thermal stability up to 300 °C for the lanthanide complexes covalently grafted on kaolinite, with respect to the isolated complexes. The increase in the basal spacing observed by X-ray diffraction confirmed the insertion of the organic ligands into the basal space of kaolinite, involving the formation of a bond between Al−OH and the carboxylate groups, as evidenced by infrared spectroscopy. The luminescent hybrid material exhibited a stronger characteristic emission of Tb3+ compared to the isolated complex. The excitation spectra displayed a broad band at 277 nm, assigned to a ligand-to-metal charge transfer, while the emission spectra presented bands related to the electronic transitions characteristic of the Tb3+ ion from the excited state 5D4 to the states 7FJ (J = 5, 4, and 3), with the 4→5 transition having high intensity with green emission.
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state 5 D 4thermogravimetric curvesbasal spaceligandLuminescent Hybrid Materialscarboxylate groupsmaterialelement analysisemission spectrastates 7 FJabsorption spectroscopyexcitation spectra277 nmbasal spacingtransitionterbium picolinate complexes covalentlyspectroscopic behaviorlanthanide complexes covalentlydiffractionTbkaolinite