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- W2012197800 abstract "Mesoporous silica materials derivatized with propyl-sulfonic groups (SBA-15) with a monovalent cation-exchange capacity of ∼1 meq/g were exchanged with Ce(III) ions to ∼0.5 meq/g to form Ce(III)SBA material displaying high-intensity purple photoluminescence. XPS and NIR-DRS analysis suggests the Ce(III) ion is bound to two proximal propyl-sulfonate groups and capped with a hydroxyl in a complex [≡Si−(CH2)3SO3]2Ce(III)OH·xH2O (x > 4), where the coordinated water can be almost completely removed by anoxic dehydration at 350 C to x < 0.2. The white hydrated (x ≥ 4) CeSBA and the brown-colored dehydrated (x < 0.2) CeSBA exhibit fluorescence with comparable integrated intensities at 368 and 394 nm, respectively. The Ce(III) 4f electron is located by XPS above the top of the Si 3p O 2p valence band, thus identifying the Ce(III) 4f orbital as the HOMO. Photoluminescence emission and excitation spectra of the 5d → 4f transition display Stokes shifts and structure sensitivity consistent with a direct transition process not involving, in these SBA materials, a multistep energy transfer previously invoked for oxide cerium-containing phosphors. A quantitative assessment of the relaxation was made on the basis of calculation of vibrational frequencies in DFT-optimized structures of a disulfonate−La−OH species with and without additional coordinated water." @default.
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- W2012197800 date "2008-01-04" @default.
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- W2012197800 title "Luminescence of Intraporous Cerium(III) Complexes in Alkyl Sulfonic Mesoporous Silica" @default.
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- W2012197800 doi "https://doi.org/10.1021/cm071754g" @default.
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