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Upconversion luminescence and temperature sensing in novel CaLa2ZnO5:Ho3+/Yb3+ phosphors

  • Irfan Ayoub
  • , Umer Mushtaq
  • , M. Y.A. Yagoub
  • , R. E. Kroon
  • , Yogendra Kumar Mishra
  • , Hendrik C. Swart
  • , Vijay Kumar*
  • *Kontaktforfatter
  • National Institute of Technology Srinagar
  • University of the Free State

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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Abstract

Phosphors of the ternary metal oxide CaLa2ZnO5 host co-activated with Ho3+/Yb3+ were synthesized using the solution combustion method. X-ray powder diffraction carried out the phase confirmation for different doping concentrations. Surface morphology and elemental composition were assessed through field emission scanning electron microscope images and an energy-dispersive X-ray spectrum. Using a 980 nm laser for excitation, the up-conversion (UC) emission spectra were recorded at 500–800 nm. Photoluminescence measurements for emission between 1100 and 1300 nm were also made for the same excitation. The UC emission spectra recorded between 500 and 800 nm consisted of green, red, and near-infrared emission peaks characteristic of Ho3+ ions. It was found that the variation in Yb3+ concentration significantly affected the UC emission through energy transfer. Power-dependent UC measurements were also carried out for the recorded emission spectra. The temperature sensing capability of the synthesized phosphors was investigated for the non-thermally coupled levels 5F4,5S2 → 5I8 and 5F5 → 5I8, using the fluorescence intensity ratio technique. The maximum values corresponding to the absolute and relative sensitivity were estimated to be 0.19 and 1.78 K−1, respectively. The synthesized phosphor was found to have good thermal stability up to 473 K with an activation energy of 0.73 eV. The synthesized phosphor can, therefore, be efficiently used as a probe for temperature sensing, especially at high temperatures.

OriginalsprogEngelsk
Artikelnummer112681
TidsskriftInorganic Chemistry Communications
Vol/bind166
Antal sider11
ISSN1387-7003
DOI
StatusUdgivet - aug. 2024

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