The phenanthroline adduct of the tris(2 -thenoyltrifluoroaceto-O,O')europium(III) complex, Eu(TTA)(3)phen, was doped into organically modified silicate (ORMOSIL) matrixes via the sol-gel process, and the luminescence properties of the resultant ORMOSIL composite phosphors (ORMOSIL:Eu(TTA)(3)phen) were characterized. The emission intensity of the composite phosphors maximized at similar to 50% vs the commercially available lamp phosphor Y(P,V)O-4:Eu, and transparent ORMOSIL:Eu(TTA)(3)phen composite phosphor disks (45 mm in diameter by 1.5 mm) were obtained under appropriate complex concentration and matrix composition. Moreover, the emission intensity of the composite phosphors was found to be maintained at the same level even after standing for up to 180 days in air, but lowered after heat treatments (100-300 degrees C), possibly due to the transformation of the beta-diketonate ligand fl om the photoactive pi electron-conjugated enolate to the corresponding nonphotoactive ketone form. In particular, the ORMOSIL:Eu(TTA)(3)phen composite phosphor powders treated with (CH3)(3)SiNHSi(CH3)(3) (hexamethyldisilazane, HMDS) showed a remarkable increase in emission intensity, owing to the improved water repellency resulting from the implantation of the -OSi(CH3)(3) (trimethylsilyl substituent: TMS) in the ORMOSIL composites and the favorable reconversion of the ligand from the nonconjugated beta-diketone to the photoactive conjugated enolate form as induced by the NH3 evolved during the TMS modification process. A composite phosphor with high emission intensity (similar to 70% vs Y(P,V)O-4:Eu) was obtained after the modification.