Abstract
© 2016 Optical Society of America. We report on the highly efficient generation of stable Sm 2+ in nanocrystalline BaFCl:Sm 3+ by exposure in the deep UV (UV-C) below 250 nm. The generated Sm 2+ can be read out via its distinct fluorescence signature which is efficiently excited around 425 nm by the relatively strong f-d transitions with ε ≈400 (l mol -1 cm -1 ). The generation of Sm 2+ can also be reversed, erasing the fluorescence signal via two-photon ionization by increasing the power at 425 nm from ≤ 1 mW/cm 2 to ~100 mW/cm 2 . It follows that the switching mechanism is based on oxygen impurities that are in close proximity to the Sm 3+ ions. The photoionization kinetics indicate that the average Sm 3+ - oxide impurity separation is a few interionic spacings. The level of Sm 3+ - Sm 2+ conversion in BaFCl is shown to be tunable over a large dynamic range, and therefore could serve as a platform for rewritable ultra-high density multi-level optical data storage. The present study also sheds light on BaFCl:Sm 3+ as a photoluminescent X-ray storage phosphor.
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CITATION STYLE
Riesen, H., Badek, K., Monro, T. M., & Riesen, N. (2016). Highly efficient valence state switching of samarium in BaFCl:Sm nanocrystals in the deep UV for multilevel optical data storage. Optical Materials Express, 6(10), 3097. https://doi.org/10.1364/ome.6.003097
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