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Physical Review B

Optical activity of Er3+ ions in Si/Si:Er nanolayers grown by sublimation MBE method

N. Q. Vinh, Salvatore Minissale, Henk Vrielinck, T. Gregorkiewicz

Published Jan 1, 2007• 1 citation
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The obtention of quantum-grade rare-earth doped oxide thin films that can be integrated with optical cavities and microwave resonators is of great interest for the development of scalable quantum devices. Among the different growth methods, Chemical Vapour Deposition (CVD) offers high flexibility and has demonstrated the ability to produce oxide films hosting rare-earth ions with narrow linewidths. However, growing epitaxial films directly on silicon is challenging by CVD due to a native amorphous oxide layer formation at the interface. In this manuscript, we investigate the CVD growth of erbium-doped yttrium oxide (Er:Y2O3) thin films on different substrates, including silicon, sapphire, quartz or yttria stabilized zirconia (YSZ). Alternatively, growth was also attempted on an epitaxial Y2O3 template layer on Si (111) prepared by molecular beam epitaxy (MBE) in order to circumvent the issue of the amorphous interlayer. We found that the substrate impacts the film morphology and the crystalline orientations, with different textures observed for the CVD film on the MBE-oxide/Si template (111) and epitaxial growth on YSZ (001). In terms of optical properties, Er3+ ions exhibit visible and IR emission features that are comparable for all samples, indicating a high-quality local crystalline environment regardless of the substrate. Our approach opens interesting prospects to integrate such films into scalable devices for optical quantum technologies.

arXiv:2411.10196•Nov 15, 2024•1 citation
Yb:Er: codoped CaF2 monocrystalline films have been grown by molecular beam epitaxy (MBE) using YbF3, ErF3, and CaF2 evaporation on CaF2 substrates. Luminescence and excitation of luminescence at 25 K are measured in order to investigate the role of Yb3+ codoping and the effect of the growth conditions during the MBE process on the incorporation of active rare-earth species in CaF2. It is found, from a comparison with earlier work on singly doped thin films, that the energies of the levels of Er3+ ions are not modified by the double doping, whereas mixed complex centers are formed. Growth conditions are found to be important controlling factors for the incorporation of Yb3+ as a sensitizer, and, consequently, for the transfer efficiency. From excitation and absorption spectra it is shown that the lowest component of the Er:4I11/2 manifold has an energy higher than that of Yb:2F5/2 and the consequences are discussed.
The obtention of quantum-grade rare-earth doped oxide thin films that can be integrated with optical cavities and microwave resonators is of great interest for the development of scalable quantum devices. Among the different growth methods, Chemical Vapour Deposition (CVD) offers high flexibility and has demonstrated the ability to produce oxide films hosting rare-earth ions with narrow linewidths. However, growing epitaxial films directly on silicon is challenging by CVD due to a native amorphous oxide layer formation at the interface. In this manuscript, we investigate the CVD growth of erbium-doped yttrium oxide (Er:Y2O3) thin films on different substrates, including silicon, sapphire, quartz or yttria stabilized zirconia (YSZ). Alternatively, growth was also attempted on an epitaxial Y2O3 template layer on Si (111) prepared by molecular beam epitaxy (MBE) in order to circumvent the issue of the amorphous interlayer. We found that the substrate impacts the film morphology and the crystalline orientations, with different textures observed for the CVD film on the MBE-oxide/Si template (111) and epitaxial growth on YSZ (001). In terms of optical properties, Er3+ ions exhibit visible and IR emission features that are comparable for all samples, indicating a high-quality local crystalline environment regardless of the substrate. Our approach opens interesting prospects to integrate such films into scalable devices for optical quantum technologies.