The structure, IR absorption, luminescence, and luminescence excitation spectra of La0.99xYxEu0.01BO3 orthoborates (0 ≤ x ≤ 0.25) synthesized at 970°С were studied at 0 ≤ x ≤ 0.99. An increase in х leads to a sequential change of the structural state of these compounds. At 0 ≤ x ≤ 0.1, the samples are single-phase and have the aragonite structure. Within the range of 0.1 < x ≤ 0.8, the samples are two-phase: the vaterite phase is observed along with the aragonite structure. At 0.8 < x ≤ 0.99, the samples are single-phase and have the vaterite structure. Correspondence between the structure and spectral characteristics of these compounds was established. It is demonstrated that with an increase in the Y3+ concentration, the vaterite phase is formed first in the bulk of microcrystals having the aragonite structure and then in the entire sample. It is shown for the first time that a band with the maximum of 469 nm is observed in the luminescence excitation spectrum (LES) of samples having the vaterite structure and is absent in samples having the aragonite structure. It is revealed that a band in the luminescence spectrum, corresponding to the 5D0→7F0 electron transition, as well as 469-nm-band in the LES, can be an indicator of the structural state of the sample.
The structure, IR, luminescence, and luminescence excitation spectra of Ce3+, Tb3+, and Eu3+ ions in Lu1−2xCexEuхBO3 and Lu0.91−2xCexTb0.09EuхBO3 solid solutions were studied. The minimum "threshold" distance between Ce3+ and Eu3+ ions was estimated, at which there is no charge transfer between these ions, leading to the quenching of Ce3+ and Eu3+ luminescence. It is shown that in Lu0.91−2xCexTb0.09EuхBO3 compounds, the range of Ce and Eu concentrations of 0.2 – 0.25 at. % is optimal for obtaining the maximum luminous intensity of this compound.
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