Thermally assisted OSL: A potent tool for improvement in minimum detectable dose and extension of dose range of Al2O3:C

The influence of electron-phonon interaction on the shape of the optically stimulated luminescence decay curve of Al2O3:C has been studied using thermally assisted optically stimulated luminescence (TA-OSL). The minimum detectable dose (MDD) of a phosphor depends on the standard deviation of the background signal which affects the signal-to-noise ratio. The standard deviation of the background signal reduces at lower stimulation light intensity while the readout time increases. Further, measurement at higher temperature enhances the OSL signal with faster decay due to the temperature dependence of photo-ionization cross-section. To achieve the same decay constant and more signal, the temperature of measurement was raised. As a result of lowering the stimulation in-tensity at higher temperature (85°C) the overall MDD of α-Al2O3:C was found to improve by 1.8 times. For extension of dose linearity in higher range, deeper traps were studied by simultaneous application of CW-OSL and thermal stimulation up to 400°C, using a linear heating rate of 4K/s. By using this method, two well defined peaks at 121°C and 232°C were observed. These TA-OSL peaks have been correlated with two deeper defects which can be thermally bleached at 650°C and 900°C respectively. These deeper defects are stable up to 500°C, so they can store absorbed dose information even if the sample is inadvertently exposed to light or heat. The dose vs. TA-OSL response from deep traps of α-Al2O3:C was found to be linear up to 10 kGy, thus extending its application for high dose dosimetry.

Fabrication and Characterization of Silica Opals

We present the details of the sol-gel processing used to realize inverse silica opal, where the silica was activated with 0.3 mol% of Er3+ ions. The template (direct opal) was obtained assembling polystyrene spheres of the dimensions of 260 nm by means of a vertical deposition technique. The Er3+-activated silica inverse opal was obtained infiltrating, into the void of the template, the silica sol doped with Er3+ ions and subsequently removing the polystyrene spheres by means of calcinations. Scanning electron microscope showed that the inverse opals possess an fcc structure with a air hollow of about 210 nm. A photonic band gap in the visible range was observed from reflectance measurements. Spectroscopic properties of Er3+activated silica inverse opal were investigated by photoluminescence spectroscopy. A bandwidth of 21 nm was measured for the 4I13/2 → 4I15/2 transition of Er3+ ions upon excitation at 514.5 nm. The luminescence decay curve of the 4I13/2 metastable state of the Er3+ ions presents a lifetime τ = 16.8 ± 0.1 ms giving a very high quantum efficiency of the fabricated system. Core-shell Er3+-activated silica spheres, where the core is the silica sphere and the shell is an Er2O3-SiO2 coating is proposed as a possible route for opal fabrication. For core-shell system a quantum efficiency of about 70% was estimated.

One-Step Synthesis and Luminescent Properties of Nanocrystalline YVO4:Eu3+ Powders

In this paper, nanocrystalline YVO4:Eu3+ powders have been successfully synthesized via high-temperature solution-phase synthesis process. The nanocrystalline YVO4:Eu3+ particles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), UV/Vis absorption spectra and luminescence spectra, luminescence decay curve and Fourier transform infrared (FT-IR), X-ray photoelectron spectra (XPS) respectively. The as-prepared nanocrystalline YVO4:Eu3+ particles are well crystallized with ellipsoidal morphology. The emission of YVO4:Eu3+ particles show emission originating from the 5D0 level, with 5D0–7F2 at 616 nm as the most prominent group. The excitation spectrumfits basically with the absorption spectrumfromthe vanadate ions. FT-IR and XPS spectra indicate that the surface ligands of nanocrystalline particles were oleic acid and oleylamine. The lifetime for the luminescence of Eu3+ in the as-prepared YVO4:Eu3+ samples are shorter than that of the bulk material due to the absorption of organic ligands on the nanoparticle surface.

Kinetics of the Back Reaction of Photosystem II as Derived from Delayed Light Emission in the Presence of DCMU and the Conformational State of the Thylakoid Membrane

It is shown that the kinetics of the back reaction of photosystem II in the seconds time range as derived from the luminescence decay curve in the presence of DCMU is controlled by the internal pH of the thylakoids. Modifications of the conformational state of the photosynthetic membrane while leaving the internal pH unchanged, however, reaction.