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A radioluminescent (RL) dosimetric system, based on a SiO2 optical fiber with the core doped by Ce3+ ions as luminescent activators has been investigated. Structural and optical properties of the luminescent fiber have been studied by Raman, refractive index, RL and scintillation time decay measurements, and compared to those obtained on bulk material. The RL response of a composite fiber made of a short portion of active Ce-doped fiber coupled to a long commercial one has been investigated by x-ray irradiation. A linear RL intensity response has been found in the dose rate interval 6×10−3–40mGy∕s together with a good radiation hardness, suggesting possible application in low-dose monitoring.

We present the effect of a rapid thermal treatment (RTT) at high temperature (1800 °C) on the radio-luminescence properties of Ce-doped SiO2 glasses prepared by the sol–gel method and previously densified at 1050 °C. Cerium concentrations ranging from 0.05 up to 1 mol % were considered. We found that, for all concentrations, the RTT induces a strong increase of the Ce3+ radio-luminescence efficiency; the x-ray-induced luminescence intensity of the SiO2:0.1% Ce is about twice that of Bi3Ge4O12. The decay time of the scintillation response, evaluated as ≈50 ns, is not affected by RTT. Infrared absorption measurements indicate that the luminescence increase cannot be related to significant release of OH groups during RTT. The conversion of Ce4+ ions into Ce3+ ions can also be ruled out since an increase of about 20% of the intensity of the 4.8 eV optical absorption band related to Ce4+ was observed after RTT. The occurrence of dissolution of rare-earth aggregates is suggested.

Photo- and radioluminescence, decay kinetics, and thermoluminescence are reported for a set of Ce3+-doped phosphate glasses. The presence of Gd3+ ions in the glass host matrix at concentrations above 20% enhances the energy transfer towards the Ce3+ emission centers, which results in a remarkable enhancement of the radioluminescence light output.