Keywords:Zircon Xenotime Monazite Titanite Laser-induced REE photoluminescence Raman artefact Laser-induced photoluminescence of trivalent rare-earth elements (REEs), which is obtained as analytical artefacts in Raman spectra of selected accessory minerals, was studied. Spectra of natural titanite, monazite-(Ce), xenotime-(Y), and zircon samples from various geological environments were compared with emission spectra of synthetic, flux-grown analogues doped with REEs. The latter is of great importance to identify potentially mistakable bands as either Raman or PL signal, and to assign them to certain REE centres. In the samples investigated, various REE centres are excited selectively using 473, 514, 532, 633, and 785 nm laser excitation. Their assignment was verified by photoluminescence-excitation experiments. Luminescence spectral patterns of zircon and titanite vary in dependence of trace-REE concentrations, hence reflecting geochemical growth conditions. "REE artefacts" in Raman spectra of accessory minerals may be used as fingerprint tool for mineral phaseidentification. The distribution of REE emission-intensities, revealed by hyperspectral mapping, opens up the opportunity to visualise mineral textures, complementary to cathodoluminescence imaging-techniques.
Even in good quality undoped GaN samples, as assessed by the intense excitonic emission, the yellow band is present. This band has been attributed either to a shallow donor to deep double donor pair recombination [1], to a deep donor to a shallow acceptor [2] or to a shallow donor and a deep state [3]. However, its origin is not yet clear. We present data on time resolved spectroscopy compared with steady state results. These results indicate that there is no difference in band shape between steady state and time resolved spectra at all temperatures. However, in some samples there is an increase in intensity of the yellow band. It is concluded that besides a fast emission, due to prompt excitation of the centre, an indirect path from a trap 13.7 meV below the shallow donor is responsible for the long component of the decay and the intensity increase. An emission with a lifetime of ca. 300 ms is also present with a maximum at 2.35 eV.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.