Abstract

We successfully demonstrate new heavy metal-gallium-doped oxide glass media, which are capable of accommodating a significant level of Er3+ doping, while avoiding the deleterious effects of concentration quenching. We examine the effects of composition and microstructure of the glass networks on optical properties. Near-infrared and visible emission demonstrate the absence of concentration quenching and Er3+ clustering. Both Raman spectroscopy and X-ray absorption fine structure spectroscopy confirm that gallium enters the glass as a tetrahedral network former. The incorporation of gallium into the glass modifies the energy landscape and creates two distinct crystal field environments, which promote Er3+ radiative transitions.

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