Luminescence probes that facilitate multimodal non-contact measurements of temperature are of particular interest due to the possibility of cross-referencing results across different readout techniques.
Two series of nanocrystalline powders of PrCo1 − xFexO3 (x = 0.1, 0.3, 0.5, 0.7 and 0.9) of high purity were obtained by sol-gel citrate method at 700 and 800 °C. The formation of continuous solid solution with an orthorhombic perovskite structure (sp. group Pbnm) was observed. A peculiarity of the PrCo1 − xFexO3 solid solution is the lattice parameter crossovers, which occurred at certain compositions and revealed in the pseudo-tetragonal or pseudo-cubic metric. An average crystallite size of the PrCo1 − xFexO3 samples estimated from the analysis of the angular dependence of the X-ray diffraction (XRD) line broadening varies between 30 and 155 nm, depending on the composition and synthesis temperature.
In this study, we
carried out a detailed investigation of the photoluminescence
of Mn4+ in Ga2O3–Al2O3 solid solutions as a function of the chemical composition,
temperature, and hydrostatic pressure. For this purpose, a series
of (Al1–x
Ga
x
)2O3:Mn4+,Mg phosphors (x = 0, ..., 0.1.0) were synthesized and characterized for
the first time. A detailed crystal structure analysis of the obtained
materials was done by the powder X-ray diffraction technique. The
results of the crystal structure and luminescence studies evidence
the transformation of the ambient-pressure-synthesized material from
the rhombohedral (α-type) to monoclinic (β-type) phase
as the Ga content exceeds 15%. Spectroscopic features of the Mn4+ deep-red emission, including the temperature-dependent emission
efficiency and decay time, as well as the possibility of their tuning
through chemical pressure in each of these two phases were examined.
Additionally, it has been shown that the application of hydrostatic
pressure of ≥19 GPa allows one to obtain a corundum-like α-Ga2O3:Mn4+ phase. The luminescence properties
of this material were compared with β-Ga2O3:Mn4+, which is normally synthesized at ambient pressure.
Finally, we evaluated the possibility of application of the studied
phosphor materials for low-temperature luminescence thermometry.
Micro- and nanocrystalline lanthanum-samarium ferrites La1−xSmxFeO3 with orthorhombic perovskite structure were obtained by using both solid state reactions (x = 0.2, 0.4, 0.6 and 0.8) and sol-gel synthesis (x = 0.5) techniques. Obtained structural parameters of both series of La1−xSmxFeO3 are in excellent agreement with the “pure” LaFeO3 and SmFeO3 compounds, thus proving formation of continuous solid solution in the LaFeO3–SmFeO3 system. Peculiarity of La1−xSmxFeO3 solid solution is divergence behaviour of unit cell dimensions with increasing x: systematic decrease of the a and c lattice parameters is accompanied with increasing b parameter. Such behaviour of the unit cell dimensions in La1−xSmxFeO3 series led to crossover of the a and c perovskite lattice parameters and formation of dimensionally tetragonal structure near x = 0.04. Linear decrease of the unit cell volume of La1−xSmxFeO3 with decreasing x according with the Vegard’s rule indicate absence of short-range ordering of R-cations in the LaFeO3–SmFeO3 system.
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