Abstract
Abstract
Luminescent materials enable warm white LEDs, molecular tagging, enhanced optoelectronics and can improve energy harvesting. With the recent development of multi-step processes like down- and upconversion and the difficulty in sensitizing these, it is clear that optimizing all properties simultaneously is not possible within a single material class. In this work, we have utilized the layer-by-layer approach of atomic layer deposition to combine broad absorption from an aromatic molecule with the high emission yields of crystalline multi-layer lanthanide fluorides in a single-step nanocomposite process. This approach results in complete energy transfer from the organic molecule while providing inorganic fluoride-like lanthanide luminescence. Sm3+ is easily quenched by organic sensitizers, but in our case we obtain strong fluoride-like Sm3+ emission sensitized by strong UV absorption of terephthalic acid. This design allows combinations of otherwise incompatible species, both with respect to normally incompatible synthesis requirements and in controlling energy transfer and quenching routes.
Publisher
Springer Science and Business Media LLC
Subject
Materials Chemistry,Biochemistry,Environmental Chemistry,General Chemistry
Reference46 articles.
1. Feldmann, C., Jüstel, T., Ronda, C. R. & Schmidt, P. J. Inorganic luminescent materials: 100 years of research and application. Adv. Funct. Mater. 13, 511–516 (2003).
2. Bünzli, J.-C. & Eliseeva, S. in Lanthanide Luminescence, Volume 7, Springer Series on Fluorescence (eds Hänninen, P. & Härmä, H.) Ch. 3 (Springer, Berlin, 2011).
3. George, N. C., Denault, K. A. & Seshadri, R. Phosphors for solid-state white lighting. Annu. Rev. Mater. Res. 43, 481–501 (2013).
4. Weber, M. J. in Lanthanide and Actinide Chemistry and Spectroscopy, Volume 131, ACS Symposium Series Ch. 14 (American Chemical Society, 1980).
5. Kenyon, A. J. Recent developments in rare-earth doped materials for optoelectronics. Prog. Quantum Electron. 26, 225–284 (2002).
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