Structure and photoluminescence of di-amidosil nanohybrids incorporating europi...

• Author(s): Nunes, Sílvia ; Zea Bermudez, V. de ; Cybinska, J. ; Ferreira, R. A. Sá ; Carlos, Luís ; Legedziewicz, J. ; Silva, Maria Manuela ; Smith, Michael John ; Ostrovskii, David
• Date: 2008
• Persistent ID: http://hdl.handle.net/1822/7747
• Origin: RepositóriUM - Universidade do Minho
• Subject(s): Alkyl/siloxane hybrids; Amide crosslinks; Europium triflate; Photoluminescence
• Document Type: Article
• Language: English

Description

The sol–gel process was used to prepare amorphous di-amide cross-linked alkyl/siloxane hybrid materials (di-amidosils) incorporating europium triflate (Eu(CF3SO3)3). Samples with 200 ≤ n ≤ 8 (where n is the molar ratio of carbonyl oxygen atoms per Eu3+ ion) were studied. The conformations of the alkyl chains of the host matrix in the doped di-amidosils (essentially gauche) are not affected by the presence of the salt. The Eu3+ ions bond to the C=O groups of the amide cross-links in the whole range of salt concentration examined. “Free” and weakly coordinated triflate ions were detected in all the samples analyzed. At n = 8 an ionic aggregate of unknown nature is formed. The hybrids introduced are room temperature white light emitters due to the convolution of the hybrid host emitting centers (amide cross-linkages and siliceous nanodomais) and the Eu3+ intra-4f6 5D0 → 7F0–4 transitions. Photoluminescence data suggest that in the dilute di-amidosil with n = 100 the Eu3+ ions occupy the same type of chemical local environment.