Realization of sensible peak shift thermometry from multiple site occupied Eu3+ ions in magnetically frustrated SrGd2O4

Magnetically frustrated lattices even at low temperatures are well-known for not minimizing interaction energies. In a magnetically frustrated structure like strontium gadolinium oxide (SrGd 2 O 4 ), there exists more than one suitable site for rare-earth doping due to availability of two low Gd 3+...

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Veröffentlicht in:Journal of materials science 2022-05, Vol.57 (18), p.8530-8543
Hauptverfasser: Pavani, K., Jamalaiah, B. C., Neves, A. J., Soares, M. J., Shim, J., Nagajyothi, P. C., J.B.Pinto, Ricardo, Graça, M. P. F., Jakka, S. K.
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Sprache:eng
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Zusammenfassung:Magnetically frustrated lattices even at low temperatures are well-known for not minimizing interaction energies. In a magnetically frustrated structure like strontium gadolinium oxide (SrGd 2 O 4 ), there exists more than one suitable site for rare-earth doping due to availability of two low Gd 3+ site symmetries. In the present work SrGd 2 O 4 doped with Eu 3+ ions were prepared by solid-state reaction method. Structural characterization confirms the nature of structure and bonding. Existence of different sites in the host lattice for the doped Eu 3+ ions were observed via excitation spectra. Photoluminescence studies with varying temperature (15–300 K) have been extensively used with high-resolution to distinguish different sites in this structure. Studies confirm that apart of the Gd 3+ sites, Sr 2+ could also accommodate the Eu 3+ ions. Variation of temperature that leads to shift in emission spectral peak positions has been thoroughly examined for line shift temperature sensing applicability. Low temperature uncovers emission peaks from 5 D 1 level that are unprovable at room temperature. Maximum relative sensitivity of 5 D 0  →  7 F 0 peak intensity to one of the multiple sites in SrGd 2 O 4 :Eu 3+ has been found to be 12.08 × 10 –3 % K −1 while using McCumber-Sturge equation to quantify line shift. Graphical abstract
ISSN:0022-2461
1573-4803
DOI:10.1007/s10853-022-07034-w