期刊
JOURNAL OF MATERIALS CHEMISTRY C
卷 9, 期 19, 页码 6268-6276出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1tc01272j
关键词
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资金
- European Union under the European Regional Development Fund
- European Union Horizon 2020 FET-Open program NanoTBTech [801305]
This study demonstrates the potential of Fe3+ ion as a sensitive luminescence thermometry in aluminate hosts and proposes different modes of luminescence thermometry. By selectively changing the Fe-O bond distances, the relative sensitivity in CaAl4O7:Fe3+,Tb3+ can be modulated to values as high as around 2% K-1, with connected relative temperature uncertainties of around 0.3%.
Luminescence (nano)thermometry is an emerging and promising field for remote temperature sensing and thermal imaging of both the surface and interior of objects. While the field is dominated by trivalent lanthanide ions (Ln(3+)) the transition metal ions have a so far underestimated role in that regard, although their luminescence properties are far more sensitive to changes in the embedding host matrix than in the case of the Ln(3+) ions. In this work, we demonstrate the potential of the abundant Fe3+ ion as a candidate for sensitive luminescence thermometry in the aluminate hosts MAl4O7 (M = Ca, Sr, Ba). Although this ion is usually considered an efficient luminescence quencher, it is shown that a targeted control of its luminescence properties makes this activator an interesting and only scarcely investigated alternative to the Ln(3+) ions. We investigated the possibility for different modes of luminescence thermometry with Fe3+ (eventually co-doped with Tb3+ as internal thermally insensitive intensity reference), which include absolute intensity, ratiometric or lifetime thermometry. By selective changes in the Fe-O bond distances, it is possible to modulate the relative sensitivity towards values as high as around 2% K-1 at room temperature in CaAl4O7:Fe3+,Tb3+ and connected relative temperature uncertainties of around 0.3%.
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