Lanthanide ions luminescent properties

The unique luminescent properties of rare earth metal clathrochelates have been used in the development of luminescent materials (luminophores and laser materials). The luminescence of these clathrochelates in solution makes their application as biological probes and concentrators of the luminescence (i.e., the antenna effect ) promising. These complexes can also serve as efficient molecular devices to convert UV light absorbed by the ligand to lanthanide ion luminescence in the visible region. Even in very dilute (10-5 mol l-i) solutions, the conversion of irradiated photons to luminescent ones has been observed to occur at a rate of approximately 1%. For rare earth metal aqua ions at the same concentration, the efficiency of conversion is equal to 4 x IQ- % [212, 390-392]. 

Luminescent lanthanide ions have numerous practical applications in chemistry and technical devices, some of them involving electrical excitation of the lanthanide ions. Photophysical properties of lanthanide ions as well as perhaps the most important application field, photoluminescence of lanthanide chelates, and lanthanide-containing nanoparticles are treated elsewhere in this volume. 

Until very recently, studies of the use of luminescent lanthanide complexes as biological probes concentrated on the use of terbium and europium complexes. These have emission lines in the visible region of the spectrum, and have long-lived (millisecond timescale) metal-centered emission. The first examples to be studied in detail were complexes of the Lehn cryptand (complexes (20) and (26) in Figure 7),48,50,88 whose luminescence properties have also been applied to bioassay (vide infra). In this case, the europium and terbium ions both have two water molecules... 

Anion concentrations can also be monitored through lanthanide luminescence. Once again, a wide range of pathways can be responsible for luminescence quenching. For instance, complex (60) with a pendant phenanthridinium group exhibits halide ion-dependent luminescence properties as a result of collisional quenching of the phenanthridinium-centered singlet state by halide ions.165... 

Kawa, M., and Frechet, J.M.J. (1998) Self-assembled lanthanide-cored dendrimer complexes enhancement of the luminescence properties of lanthanide ions through site-isolation and antenna effects. Chem. Mater. 10, 286-296. 

Trivalent lanthanide cations have luminescent properties which are used in a number of applications. The luminescence of the lanthanide ions is unique in that it is long-lasting (up to more than a millisecond) and consists of very sharp bands. Lanthanide emission, in contrast to other long-lived emission processes, is not particularly sensitive to quenching by oxygen because the 4f electrons found within the inner electron core... 

During recent years it has become clear that the temperature quenching of lanthanide luminescence is determined by the properties of the c.t. or 4f 5d state. Let us first mention shortly the mechanisms that have been proposed for temperature quenching of lanthanide ion emission. 

The formation of luminescent lanthanide complexes relies on a number of factors. The choice of coordinating ligand and the method by which the antenna chromophore is attached to it, as well as the physical properties of the antenna, are important. In order to fully coordinate a lanthanide ion, either a high-level polydentate ligand such as a cryptate 1 or a number of smaller ligands (such as 1,3-diketones, 2) working in cooperation are required. Both 1 and 2 are two of the simplest coordination complexes possible for lanthanide ions. In both cases there are no antennae present. However, the number of bound solvent molecules is decreased considerably from nine (for lanthanide ions in solution) to one to two for the cryptate and three for the 1,3-diketone complexes. 

Given their favourable luminescence properties and propensity to coordinate oxy-anions, it is perhaps surprising that complexes of lanthanide(III) ions have received comparatively little attention as anion sensors. 

Lanthanides activated luminescent materials are widely used for solid-state lasers, luminescent lamps, flat displays, optical fiber communication systems, and other photonic devices. It is because of the unique solid-state electronic properties that enable lanthanide ions in solids to emit photons efficiently in visible and near IR region. Due to the pioneer work by Dieke, Judd, Wyboume, and others in theoretical and experimental studies of the... 

In the past decade, lanthanide ions doped in nanocrystalline semiconductors have been the subject of numerous investigations. Although quantum size effects are not expected on lanthanide energy level structures, influence of quantum confinement in semiconductor on the luminescence properties of the lanthanides is expected. One of the advantages of lanthanide-doped semiconductor nanocrystals is that the lanthanide luminescence can be efficiently sen-... 

Following the introduction to size-dependent nanophenomena presented in the previous sections, we now focus our attention on the luminescence properties of lanthanide ions at additional sites or distorted structure existing in nanophases. Phenomena of prolonged luminescence lifetime, anomalous thermalization, upconversion luminescence, dynamics of long-range interaction with two-level-systems (TLS), and quantum efficiency are to be discussed. 

Generally, quantum size effects are not expected in lanthanide-doped nanoinsulators such as oxides since the Bohr radius of the exciton in insulating oxides, like Y2O3 and Gd2C>3, is very small. By contrast, the exciton Bohr radius of semiconductors is larger (e.g., 2.5 nm for CdS) resulting in pronounced quantum confinement effects for nanoparticles of about 2.5 nm or smaller (Bol et al., 2002). Therefore, a possible influence of quantum size effects on the luminescence properties of lanthanide ions is expected in semiconductor nanocrystals. 

Apart from Eu3+ and Tb3+, few studies have been reported on optical properties of lanthanide ions doped in ZnS nanociystals. Bol et al. (2002) attempted to incorporate Er3"1" in ZnS nanociystal by ion implantation. They annealed the sample at a temperature up to 800 °C to restore the crystal structure around Er3"1", but no Er3"1" luminescence was observed. Schmidt et al. (1998) employed a new synthesis strategy to incorporate up to 20 at% Er3"1" into ZnS (1.5-2 nm) cluster solutions which were stabilized by (aminopropyl)triethoxysilane (AMEO). Ethanolic AMEO-stabilized Er ZnS clusters in solutions fluoresce 200 times stronger at 1540 nm than that of ethanolic AMEO-Er complexes. This is explained by the very low phonon energies in ZnS QDs, and indicates that Er3+ ions are trapped inside chalcogenide clusters. However the exact position of Er3+ in ZnS clusters remains unknown. Further spectroscopic and structural analyses are required in order to obtain more detailed information. 

It is possible to alter the intrinsic properties of materials by chemical nanocoating, which cannot be achieved by conventional methods. Generally the core-shell nanostructures are divided into two categories (1) lanthanides doped in the core (2) lanthanides doped in the shell. The former are synthesized in order to improve the quantum efficiency of lanthanide ions or design bio-labels, while the latter are meant for the study of surface modifications on the lanthanide luminescence or the synthesis of lanthanide-doped hollow nanospheres. 

---