Abstract

The local dopant coordination environment and its effect on the photoluminescent (PL) spectral features of erbium-doped yttrium oxide nanotubes (NTs) were probed by synchrotron-based x-ray diffraction (XRD), x-ray absorption near-edge spectroscopy (XANES), and extended x-ray absorption fine structure (EXAFS). XRD, XANES, and EXAFS data demonstrate that single phase solid solutions of Y(2−x)ErxO3 were formed at 0≤x<0.4 and 1.2<x≤2, and the valence state of Er ions in the Y2O3 NTs is +3. The x-ray spectroscopic data clearly show that the erbium dopants largely reside in two types of sites in the Y2O3 host material, both of which possess a well-defined intermediate-range structure, and that the doping of erbium into Y2O3 does not cause a loss in intermediate-range order and crystallinity in the Er3+:Y2O3 NTs. This well-defined distribution of erbium doping inside the Y2O3 matrix correlates well with the observed sharp and well-resolved PL behavior of these Er3+:Y2O3 NTs at around 1.535 μm.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call