The phenanthroline adduct of the tris(2-thenoyltrifluoroaceto-O,O‘)europium(III) complex,
Eu(TTA)3phen, 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)3phen) were characterized. The emission intensity of the
composite phosphors maximized at ∼50% vs the commercially available lamp phosphor
Y(P,V)O4:Eu, and transparent ORMOSIL:Eu(TTA)3phen 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 °C), possibly due to the transformation of the β-diketonate
ligand from the photoactive π electron-conjugated enolate to the corresponding nonphotoactive
ketone form. In particular, the ORMOSIL:Eu(TTA)3phen composite phosphor powders treated
with (CH3)3SiNHSi(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 β-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 (∼70% vs Y(P,V)O4:Eu) was obtained
after the modification.