Absorption spectra, defect site distribution and upconversion excitation spectra of CaF2/SrF2/BaF2:Yb3+:Er3+ nanoparticles

Abstract

We report studies of the Yb$^{3+}$ site distribution in Er$^{3+}$ co-doped upconverting alkaline earth fluoride nanoparticles using high-resolution absorption measurements. Similar to bulk crystals, Yb$^{3+}$ single ion cubic (O$_h$), and preferentially formed clusters are the dominant centres for moderate dopant concentrations. At higher concentrations, and for larger particle sizes, a minority C$_{4v}$(F$^-$) centre is also observed. Furthermore, the behaviour of Yb$^{3+}$ cluster centres, whose primary absorption band is located around 10205 cm$^{-1}$ (in near resonance with 980 nm laser diodes) was studied by tuning the metal cation in the host lattice from Ca$^{2+}{\rightarrow}$Sr$^{2+}{\rightarrow}$Ba$^{2+}$. For co-doped materials, with heterogeneous cluster centres, Er$^{3+}$ upconversion fluorescence was observed upon selective excitation of Yb$^{3+}$, resulting in strong visible emission from $^4$H$_{11/2}$, $^4$S$_{3/2}$ and $^4$F$_{9/2}$ multiplets. By monitoring the Er$^{3+}$ $^4$S$_{3/2}{\rightarrow}^4$I$_{15/2}$ (540 nm) fluorescence, whilst scanning a laser through the wavelength dependent Yb3+ absorption, we obtain an excitation spectrum for these heterogeneous cluster centres. It is demonstrated that the group of Yb$^{3+}$ ions residing near an Er$^{3+}$ ion represent a small subset of the overall Yb$^{3+}$ ensemble and therefore a linear absorption measurement is not necessarily a good indication of the optimum laser pump wavelength.