The sensitivity of luminescent Boltzmann thermometers is restricted by the energy difference between the thermally coupled excitement levels of trivalent lanthanides, and their values further decrease with increases in temperature, rendering their use at high temperatures difficult. Here, we demonstrate how to overcome this sensitivity limitation by employing multiparameter and multilevel cascade temperature readings. For this purpose, we synthesized Dy³⁺:Y₂SiO₅, a phosphor whose emission is known to begin quenching at very high temperatures. Its photoluminescence-emission features, later used for thermometry, consisted of two blue emission bands centered around 486 nm and 458 nm, and two bands centered around 430 nm and 398 nm, which were only visible at elevated temperatures. Next, we performed thermometry using the standard luminescence-intensity ratio (LIR) method, which employs the ⁴F_9/2 and ⁴I_15/2 Dy³⁺ levels’ emissions and the multilevel cascade method, which additionally uses the ⁴G_11/2 level and overlapping intensities of ⁴I_13/2, ⁴M_21/2, ⁴K_17/2, and ⁴F_7/2 levels to create two LIRs with a larger energy difference than the standard LIR. This approach yielded a sensitivity that was 3.14 times greater than the standard method. Finally, we simultaneously exploited all the LIRs in the multiparameter temperature readings and found a relative sensitivity that was 30 times greater than that of the standard approach.

We report the procedure for hydrothermal synthesis of ultrasmall Yb³⁺/Tm³⁺ co-doped Sr₂LaF₇ (SLF) upconversion phosphors. These phosphors were synthesized by varying the concentrations of Yb³⁺ (x = 10, 15, 20, and 25 mol%) and Tm³⁺ (y = 0.75, 1, 2, and 3 mol%) with the aim to analyze their emissions in the near IR spectral range. According to the detailed structural analysis, Yb³⁺ and Tm³⁺ occupy the La³⁺ sites in the SLF host. The addition of Yb³⁺/Tm³⁺ ions has a huge impact on the lattice constant, particle size, and PL emission properties of the synthesized SLF nanophosphor. The results show that the optimal dopant concentrations for upconversion luminescence of Yb³⁺/Tm³⁺ co-doped SLF are 20 mol% Yb³⁺ and 1 mol% Tm³⁺ with EDTA as the chelating agent. Under 980 nm light excitation, a strong upconversion emission of Tm³⁺ ions around 800 nm was achieved. In addition, the experimental photoluminescence lifetime of Tm³⁺ emission in the SLF host is reported. This study discovered that efficient near IR emission from ultrasmall Yb³⁺/Tm³⁺ co-doped SLF phosphors may have potential applications in the fields of fluorescent labels in bioimaging and security applications.

The method of measuring temperature using luminescence by analyzing the emission spectra of Pr³⁺-doped YF₃ using principal component analysis is presented. The Pr³⁺-doped YF₃ is synthesized using a solid-state technique, and its single-phase orthorhombic crystal structure is confirmed using X-ray diffraction. The emission spectra measured within the 93–473 K temperature range displays characteristic Pr³⁺ f-f electronic transitions. The red emission from the ³P_0,1→³H₆,³F₂ electronic transition mostly dominates the spectra. However, at low temperatures, the intensity of the green emissions from the ³P_0,1→³H₅, deep-red ³P_0,1→³F₄, and the deep-red emissions from the ³P_0,1→³F₄ transitions are considerably lower compared to the intensity of the red emissions. Temperature variations directly impact the photoluminescent spectra, causing a notable increase in the green and deep-red emissions from the ³P₁ excited state. We utilized the entire spectrum as an input for principal component analysis, considering each temperature as an independent group of data. The first principal component explained 99.3% of the variance in emission spectra caused by temperature and we further used it as a reliable temperature indicator for luminescence thermometry. The approach has a maximum absolute sensitivity of around 0.012 K⁻¹. The average accuracy and precision values are 0.7 K and 0.5 K, respectively.

Powders of Y3NbO7:xDy3+ (x = 0.5, 1, 1.5, 3 and 5 mol%) were produced through a solid-state process. X-ray diffraction investigations confirm the fluorite-type structure (space group 𝐹𝑚3̅𝑚) of powders with crystallite size in the range of 19–60 nm. Both the photoluminescence excitation and emission spectra revealed the presence of defects within the material. With different excitation wavelengths, the emission spectra exhibited distinct emission patterns. At each excitation wavelength, the emission was quenched at Dy3+ concentration higher than 1 mol%. The decay time measurements of the highest intensity emission revealed a progressive decrease from 0.472 milliseconds for x = 0.5 mol% to 0.246 milliseconds for x = 5 mol%. The CIE chromaticity coordinates investigation revealed that the emission color may be altered by varying the excitation wavelength, ranging from blue (excitation at 333 nm) and near-white (excitation at 353 nm and 390 nm) to orange (excitation at 457 nm). The chromaticity of emission under 353 nm and 390 nm excitation validated the material's suitability as an almost-white phosphor.

This study investigates the thermally induced phase transformation of Ni-exchanged LTA zeolite as a dual-purpose method for nickel immobilization and the synthesis of stable ceramic pigments. The process describes a cost-effective and sustainable alternative to conventional pigment production, aligning with circular economy principles. Upon thermal treatment at temperatures ranging between 900 °C and 1300 °C, Ni-exchanged LTA zeolite undergoes a transformation to NiAl₂O₄ spinel, confirmed by XRPD, FTIR, and thermal analysis. Initially, NiO is formed, but as the temperature increases, it dissolves and transforms into NiAl₂O₄. Colorimetric studies revealed intensified blue pigmentation with increasing temperature, correlating with crystallite growth and structural evolution. SEM analysis showed morphological changes from cubic particles to sintered agglomerates, enhancing pigment stability and hardness. The Ni-LTA sample calcined at 1300 °C showed the highest hue angle, which was consistent with the formation of over 99 wt.% of the nickel aluminate crystalline phase at this temperature. The results demonstrate that Ni-LTA zeolite can be effectively transformed into durable greenish-blue pigments suitable for application in porcelain. This transformation is especially evident at 1300 °C, where a spinel phase (NiAlSi₂O₄) forms, with colorimetric values: L = 58.94, a* = –16.08, and b* = –15.90.

Accelerated industrial development, mass production, economic viability, and environmental sustainability impose new requirements on contemporary materials, positioning basalt as a promising, cost-effective, and abundant environmentally benign raw material. This study explores the influence of sintering temperature on the physical properties of ceramics obtained from andesite basalt aggregate. Relative density, shrinkage, and color changes were monitored to optimize the sintering temperature for the serial production of high-density ceramics. Varying the sintering temperature by 10 °C within the 1040–1080 °C range, while maintaining a constant sintering time of 60 min, leads to significant changes in relative density, shrinkage, and color. Beyond visual appearance, color changes can be quantified with coordinates in color spaces, usually in the CIELAB color space, standardized by the Commission Internationale de l’Eclairage (CIE). The best physical properties were achieved at a sintering temperature of 1060 °C for 60 min with a relative density of 99.501%, shrinkage of 12.811%, and color coordinates L*(32.03), a*(9.25), and b*(7.58) according to the CIELAB analysis. The favorable physical properties and distinctive reddish-brown color of sintered andesite basalt ceramics make them promising for floor and wall tile applications.