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Mn5+-activated Ca6Ba(PO4)4O near-infrared phosphor and its application in luminescence thermometry

  • Miroslav D. Dramićanin*
  • , Łukasz Marciniak
  • , Sanja Kuzman
  • , Wojciech Piotrowski
  • , Zoran Ristić
  • , Jovana Periša
  • , Ivana Evans
  • , Jelena Mitrić
  • , Vesna Đorđević
  • , Nebojša Romčević
  • , Mikhail G. Brik
  • , Chong Geng Ma*
  • *Corresponding author for this work
  • Chongqing University of Posts and Telecommunications
  • University of Belgrade
  • Polish Academy of Sciences
  • Durham University
  • University of Tartu
  • Jan Dlugosz University in Czestochowa
  • Academy of Romanian Scientists

Research output: Contribution to journalArticlepeer-review

88 Citations (Scopus)

Abstract

The near-infrared luminescence of Ca6Ba(PO4)4O:Mn5+ is demonstrated and explained. When excited into the broad and strong absorption band that spans the 500–1000 nm spectral range, this phosphor provides an ultranarrow (FWHM = 5 nm) emission centered at 1140 nm that originates from a spin-forbidden 1E → 3A2 transition with a 37.5% internal quantum efficiency and an excited-state lifetime of about 350 μs. We derived the crystal field and Racah parameters and calculated the appropriate Tanabe–Sugano diagram for this phosphor. We found that 1E emission quenches due to the thermally-assisted cross-over with the 3T2 state and that the relatively high Debye temperature of 783 K of Ca6Ba(PO4)4O facilitates efficient emission. Since Ca6Ba(PO4)4O also provides efficient yellow emission of the Eu2+ dopant, we calculated and explained its electronic band structure, the partial and total density of states, effective Mulliken charges of all ions, elastic constants, Debye temperature, and vibrational spectra. Finally, we demonstrated the application of phosphor in a luminescence intensity ratio thermometry and obtained a relative sensitivity of 1.92%K−1 and a temperature resolution of 0.2 K in the range of physiological temperatures.

Original languageEnglish
Article number279
JournalLight: Science and Applications
Volume11
Issue number1
DOIs
Publication statusPublished - Dec 2022
Externally publishedYes

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