Thermoluminescence as a Research Tool to Investigate Luminescence Mechanisms.

Thermally stimulated luminescence (TSL) is known as a technique used in radiation dosimetry and dating. However, since the luminescence is very sensitive to the defects in a solid, it can also be used in material research. In this review, it is shown how TSL can be used as a research tool to investigate luminescent characteristics and underlying luminescent mechanisms. First, some basic characteristics and a theoretical background of the phenomenon are given. Next, methods and difficulties in extracting trapping parameters are addressed. Then, the instrumentation needed to measure the luminescence, both as a function of temperature and wavelength, is described. Finally, a series of very diverse examples is given to illustrate how TSL has been used in the determination of energy levels of defects, in the research of persistent luminescence phosphors, and in phenomena like band gap engineering, tunnelling, photosynthesis, and thermal quenching. It is concluded that in the field of luminescence spectroscopy, thermally stimulated luminescence has proven to be an experimental technique with unique properties to study defects in solids.

Charge Carrier Trapping Processes in RE2O2S (RE = La, Gd, Y, and Lu).

Two different charge carrier trapping processes have been investigated in RE2O2S:Ln3+ (RE = La, Gd, Y, and Lu; Ln = Ce, Pr, and Tb) and RE2O2S:M (M = Ti4+ and Eu3+). Cerium, praseodymium and terbium act as recombination centers and hole trapping centers while host intrinsic defects provide the electron trap. The captured electrons released from the intrinsic defects recombine at Ce4+, Pr4+, or Tb4+ via the conduction band. On the other hand, Ti4+ and Eu3+ act as recombination centers and electron trapping centers while host intrinsic defects act as hole trapping centers. For these codopants we find evidence that recombination is by means of hole release instead of electron release. The released holes recombine with the trapped electrons on Ti3+ or Eu2+ and yield broad Ti4+ yellow-red charge transfer (CT) emission or characteristic Eu3+ 4f-4f emission. We will conclude that the afterglow in Y2O2S:Ti4+, Eu3+ is due to hole release instead of more common electron release.

Low-temperature VUV photoluminescence and thermoluminescence of UV excited afterglow phosphor Sr3AlxSi1-xO5:Ce(3+),Ln(3+) (Ln = Er, Nd, Sm, Dy and Tm).

Low-temperature (10 K) photoluminescence excitation and emission spectra of undoped Sr3SiO5 as well as Ce(3+) and Eu(3+) single doped Sr3SiO5 have been investigated. They show the host exciton band and the O(2-) to Eu(3+) charge transfer band at 5.98 eV (207 nm) and 3.87 eV (320 nm) respectively. Low-temperature thermoluminescence measurements are reported for Ce(3+) and lanthanide (Er, Nd, Sm, Dy, Er and Tm) co-doped Sr3AlxSi1-xO5. The results show that Ce(3+) is the recombination centre and Nd, Sm, Dy and Tm work as electron traps with trap depths of 0.95 eV, 1.89 eV, 1.02 eV, and 1.19 eV, respectively. Thermoluminescence excitation spectra of Sr2.98Al0.02Si0.98O5:0.01Ce(3+),0.01Dy(3+) show that the traps can be charged by 260 nm UV excitation.

The in vivo activation of persistent nanophosphors for optical imaging of vascularization, tumours and grafted cells.

Optical imaging for biological applications requires more sensitive tools. Near-infrared persistent luminescence nanoparticles enable highly sensitive in vivo optical detection and complete avoidance of tissue autofluorescence. However, the actual generation of persistent luminescence nanoparticles necessitates ex vivo activation before systemic administration, which prevents long-term imaging in living animals. Here, we introduce a new generation of optical nanoprobes, based on chromium-doped zinc gallate, whose persistent luminescence can be activated in vivo through living tissues using highly penetrating low-energy red photons. Surface functionalization of this photonic probe can be adjusted to favour multiple biomedical applications such as tumour targeting. Notably, we show that cells can endocytose these nanoparticles in vitro and that, after intravenous injection, we can track labelled cells in vivo and follow their biodistribution by a simple whole animal optical detection, opening new perspectives for cell therapy research and for a variety of diagnosis applications.

Electron transfer process between Ce3+ donor and Yb3+ acceptor levels in the bandgap of Y3Al5O12 (YAG).

Thermoluminescence (TL) properties of Ce(3+) and Yb(3+) co-doped in Y(3)Al(5)O(12) (YAG) were studied with the aim of determining the location of energy levels of Ce(3+) and Yb(2+) relative to the bottom of the conduction band (CB) and the top of the valence band (VB) of YAG. The TL glow peak at about 180 °C when heating rate ß = 1°C s(-1) was assigned to electron release from Yb(2+), indicating that Yb(3+) acts as an electron trap. The trap depth, which is the depth of the ground-state level of Yb(2+) below the bottom of the CB, was derived from the temperatures of the maximum of the TL glow peak at different heating rates. The value is, within the experimental and theoretical uncertainties, in good agreement with that derived from the O(2-) --> Yb(3+) charge transfer energy. Thermoluminescence excitation spectroscopy (TLES) was used to establish the location of energy levels of Ce(3+). From the derived data the energy level diagram of YAG:Ce(3+), Yb(3+) is constructed and possible electron transfer processes are discussed.

Some developments in neutron and charged particle dosimetry.

There is an increasing need for dosimetry of neutrons and charged particles. Increasing exposure levels are reported in the nuclear industry, deriving from more frequent in-service entries at commercial nuclear power plants, and from increased plant decommissioning and refurbishment activities. Another need stems from the compliance with requirements of the regulations and standards. The European Council directive 96/29 requires dosimetric precautions if the effective dose exceeds 1 mSv a(-1). On average, aircrew members exceed this value. Further, there is a trend of increasing use of charged particles in radiotherapy. The present situation is that we have reasonably good photon dosemeters, but neutron and charged particle dosemeters are still in need of improvements. This work highlights some of the developments in this field. It is mainly concentrated on some developments in passive dosimetry, in particular thermally and optically stimulated luminescent detectors, indicating the direction of ongoing research. It shows that passive dosemeters are still a very active field. Active dosemeters will not be discussed with the exception of new developments in microdosimetric measurements [new types of tissue equivalent proportional counters (TEPCs)]. The TEPC is unique in its ability to provide a simultaneous determination of neutron / charged particle / gamma ray doses, or dose equivalents using a single detector.

Broad-beam transmission data for new brachytherapy sources, Tm-170 and Yb-169.

The characteristics of the radionuclides (170)Tm and (169)Yb are highly interesting for their use as high dose-rate brachytherapy sources. The introduction of brachytherapy equipment containing these sources will lead to smaller required thicknesses of the materials used in radiation protection barriers compared with the use of conventional sources such as (192)Ir and (137)Cs. The purpose of this study is to determine the required thicknesses of protection material for the design of the protecting walls. Using the Monte Carlo method, transmission data were derived for broad-beam geometries through lead and concrete barriers, from which the first half value layer and tenth value layer are obtained. In addition, the dose reduction in a simulated patient was studied to determine whether transmission in the patient is a relevant factor in radiation protection calculations.

Passive detectors for neutron personal dosimetry: state of the art.

Passive, solid-state detectors still dominate the field of neutron personal dosimetry, mainly thanks to their low cost, high reliability and elevated throughput. However, the recent appearance in the market of several electronic personal dosemeters for neutrons presents a challenge to the exclusive use of passive systems for primary or official dosimetry. This scenario drives research and development activities on passive dosemeters towards systems offering greater accuracy of response and lower detection limits. In addition, further applications and properties of the passive detectors, which are not met by the electronic devices, are also being explored. In particular, extensive investigations are in progress on the use of solid-state detectors for aviation and space dosimetry, where high-energy neutron fields are encountered. The present situation is also stimulating an acceleration in the development of international standards on performance and test requirements for passive dosimetry systems, which can expedite significantly the implementation of techniques in commercial personal dosimetry services. Upcoming standards will cover thermoluminescence albedo dosemeters, etched-track detectors, superheated emulsions and direct ion storage chambers, attesting to the level of maturity reached by these techniques. This work reviews the developments in the field of passive neutron dosimetry emerged since the previous Neutron Dosimetry Symposium, reporting on the current status of the subject and indicating the direction of ongoing research.

The radial depth-dose distribution of a 188W/188Re beta line source measured with novel, ultra-thin TLDs in a PMMA phantom: comparison with Monte Carlo simulations.

The radial depth-dose distribution of a prototype 188W/188Re beta particle line source of known activity has been measured in a PMMA phantom, using a novel, ultra-thin type of LiF:Mg,Cu,P thermoluminescent detector (TLD). The measured radial dose function of this intravascular brachytherapy source agrees well with MCNP4C Monte Carlo simulations, which indicate that 188Re accounts for > or = 99% of the dose between 1 mm and 5 mm radial distance from the source axis. The TLDs were calibrated using a 90Sr/90Y beta secondary standard. Several correction factors are calculated using analytical and Monte Carlo methods. An analysis of the measurement uncertainty is made. Since it is partly determined by components of uncertainty arising from random effects, repeated measurements yield a lower uncertainty. The expanded uncertainty in the absolute dose at 2 mm radial distance equals 11%, 10%, 9% and 8% for 1, 2, 3 and 5 measurements, respectively. After a correction for source non-uniformity, the measured dose rate per unit source activity at 2 mm radial distance equals (1.53 +/- 0.16) Gy min(-1) GBq(-1) (2sigma), in agreement with the value of (1.45 +/- 0.01) Gy min(-1) GBq(-1) (2sigma) predicted by the MCNP4C simulations.