Structure and spectroscopic properties of Er3+ doped LiNbO3 thin film grown by e-beam evaporation
Er3+ doped LiNbO3 (Er: LN) single crystal films with varied doping levels of Er3+ were grown on z-cut LiTaO3 bulk single crystals by using e-beam evaporation method. The crystallographic orientation, fluorescence properties, ions valence states, Er3+ concentration and Li2O content of films were stud...
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Veröffentlicht in: | Materials today communications 2023-08, Vol.36, p.106522, Article 106522 |
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Sprache: | eng |
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Zusammenfassung: | Er3+ doped LiNbO3 (Er: LN) single crystal films with varied doping levels of Er3+ were grown on z-cut LiTaO3 bulk single crystals by using e-beam evaporation method. The crystallographic orientation, fluorescence properties, ions valence states, Er3+ concentration and Li2O content of films were studied. The main phase of the obtained films is determined to be LN from X-ray diffraction and Raman scattering studies, and the films are found to be orienting along (006). Enhancement in the visible and near-infrared luminescence is observed as the doping concentration of Er3+ is increased. The Li2O content of films is determined using the optical birefringence method and found to be at a constant value of 48.8 mol%, which is consistent with the Raman results. XPS results show that the Er concentration in the films is lower than that in the polycrystalline powder since e-beam evaporation has a low efficiency for heavier Er3+. Fluorescence intensity ratios estimated at different measurement temperatures suggest that the Er: LN films have excellent temperature sensitivity, which shows the potential of the films for optical thermometry applications.
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•The Er3 + doped LiNbO3 single crystal thin films were grown by the e-beam evaporation method.•The fluorescence properties enhance remarkably with a rise in Er-doping concentration.•The accurate Li2O content have been evaluated by the birefringence method.•Based on the FIR results, the films have an excellent sensitivity of temperature. |
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ISSN: | 2352-4928 2352-4928 |
DOI: | 10.1016/j.mtcomm.2023.106522 |