Dual-mode optical thermometry based on intervalence charge transfer excitations in Tb3+/Pr3+ co-doped CaNb2O6 phosphors

Self-calibrated temperature measurements combined with luminescence intensity ratio (LIR) and luminescence lifetime are more accurate. A dual-mode self-calibration optical thermometer was designed based on CaNb₂O₆: Tb³⁺/Pr³⁺ phosphor. The obtained sample has excellent sensitivity, with the maximum values of absolute sensitivity (S_a) and relative sensitivity (S_r) being 0.69 K^-1 at 612 K and 2.50% K^-1 at 532 K for LIR mode, and 0.0059 K^-1 at 475 K and 2.62% K^-1 at 535 K for luminescence lifetime mode, respectively. These results indicate that CaNb₂O₆: Tb³⁺/Pr³⁺ phosphor has valuable potential application for self-calibration optical temperature measurement.     

Preparation and properties of CdSiO3: Mn2+, Tb3+ phosphor

CdSiO₃: Mn²⁺, Tb³⁺ long-lasting phosphor was prepared by the conventional high temperature solid-state method. Effects of the content of Mn²⁺ and Tb³⁺ on the luminescent properties of phosphor CdSiO₃: Mn²⁺, Tb³⁺ were investigated by means of photoluminescence (PL) spectra, the afterglow intensity decay curves and the thermoluminescence (TL) spectra. It was found that when the Mn²⁺ and Tb³⁺ dopant-concentrations were 0.4 mol% and 0.8 mol% of Cd²⁺ ions in CdSiO₃, respectively, the luminescence of phosphor prepared had better luminescent property and longer afterglow time. Role of Tb³⁺ co-doped into CdSiO₃: Mn²⁺ matrix was discussed in this paper.     

Temperature sensing properties of self-crystalized Ba2LaF7: Tb3+ glass ceramics

Fluorescence intensity ratio (FIR) techniques for temperature sensing based on the thermally-coupled energy levels (TCELs) of two excited states of rare earth ions are widely investigated. However, their performance in lower temperature detection are poor because of thermal decoupling between two emitting levels with relatively large energy gap. On the other hand, most of luminescent thermometer materials so far reported are in powder form, which suffer from severe light scattering and high hygroscopicity. Fortunately, transparent glass ceramics offer an alternative to improve optical property as well as stability of luminescent materials. Hence, herein self-crystallized 20% Tb³⁺ doped transparent Ba₂LaF₇ glass ceramics were synthesized by traditional high-temperature melting method to examine its temperature sensing ability by employing the two low-lying states ⁷F₅ and ⁷F₆ of Tb³⁺, which are thermally coupled even at lower temperature. Under the resonance excitation of ⁷F₅ → ⁵D₄ transition at 543 nm, the emission intensity of ⁵D₄ → ⁷F₆ enhances with the temperature rising from 300 K to 630 K. The maximum relative sensitivity reaches 2.88% K^?1 at 300 K, which is better than the previous results reported. Moreover, the repeatability of the integrated intensity of ⁵D₄ emission of Tb³⁺ under eight consecutive heating-cooling cycles indicates that the sample has a good reliability and reusability. All results suggest that the 20% Tb³⁺ doped transparent Ba₂LaF₇ glass ceramics are one of the excellent candidate materials for optical thermometers.     

Trap engineering in ZnGa2O4:Tb3+ through Bi3+ doping for multi-modal luminescence and advanced anti-counterfeiting strategy

Optical information encryption based on luminescence materials have received much attention recently. However, the single luminescence mode of the luminescence materials greatly limits its anti-counterfeiting application with high safety level. Here, a series of luminescence materials of Tb³⁺ and Bi³⁺ co-doped ZnGa₂O₄ phosphors with great correspondence in photoluminescence (PL), persistent luminescence (PersL), and thermoluminescence (TL) modes was synthesized by the conventional solid-phase method for the application in multi-modal anti-counterfeiting fields. Under the excitation of 254 nm, ZnGa_1.99O₄:0.01 Tb³⁺, yBi³⁺ (y = 0.001,0.002) sample exhibited a broad blue emission band (the transition from [GaO₆]) at 440 nm and the characteristic emission peaks of Tb³⁺ at 495 nm, 550 nm, 591 nm and 625 nm, corresponding to the transitions of ⁵D₄-⁷F_n (n = 6, 5, 4, 3), respectively. Interestingly, the co-doping of Bi³⁺ ions improve the crystallinity and particle size of the phosphor, subsequently enhanced the PL intensity of Tb³⁺ to 6 times that of Tb³⁺ singly doped ZnGa₂O₄ phosphor. Further, the flexible films with multi-modal luminescence properties have been fabricated through the unique TL and PersL characteristics of ZnGa₂O₄: Tb³⁺, Bi³⁺ phosphors, including “Optical information storage film”, “snowflake and characters” and “QR code”. Moreover, a set of optical information encryption is obtained by combining ZnGa₂O₄:Tb³⁺, Bi³⁺ phosphor and red emitting phosphor. The results indicate that ZnGa₂O₄:Tb³⁺, Bi³⁺ phosphor with multi-modal stimulus response can be expected to be potentially used in the applications of optical information storage and anti-counterfeiting fields.     

Mn2+/Pr3+/Tb3+ single-doped Mg4Ga4Ge3O16 persistent luminescence materials for optical information storage application

Persistent luminescence (PersL) phosphors are considered as promising candidates for the next generation of information storage medium. Mg₄Ga₄Ge₃O₁₆ (MGG) is an electron trapping material which exhibits defect luminescence, and the luminescent properties are easily tuned via doping various activated ions. In this work, undoped and Mn²⁺/Pr³⁺/Tb³⁺ single-doped MGG phosphors were synthesized via high temperature solid phase reactions. X-ray diffraction and scanning electron microscope results confirm that the activated ions tend to occupy Mg²⁺ sites. Excited at 265 nm, the MGG host exhibits a defect emission band peaked at 450 nm. Red, pink and green emissions are observed in the Mn²⁺/Pr³⁺/Tb³⁺ single-doped MGG samples, which are ascribed to the Mn²⁺: ⁴T₁(G) → ⁶A₁(S), Pr³⁺: ¹D₂ → ³H₄ and Tb³⁺: ⁵D₄ → ⁷F₅ transitions, respectively. All the samples exhibit bright PersL for minutes after the cessation of excitation. The energy transfer, concentration quenching, luminescence decay and afterglow mechanisms are also discussed in detail. The phosphors exhibit efficient thermal and optical stimuli response, showing great potentials in the optical information storage.     

Photoluminescence and temperature sensing of lanthanide Eu3+ and transition metal Mn4+ dual-doped antimoniate phosphor through site-beneficial occupation

For a long time, rare-earth ion-doped phosphors have been widely used in temperature sensing because of their excellent light-emitting properties. However, most of the rare earth elements are relatively rare and expensive, so the transition group elements that are economical and easy to obtain have been favored by researchers. This paper presents a new type of phosphor doped with rare earth ion and transition metal for optical temperature measurement. In recent years, Mn⁴⁺-doped phosphors have attracted wide attention because of their strong deep red light-emitting properties. La₂LiSbO₆ provides a good host environment for Mn⁴⁺ and Eu³⁺ due to its unique crystal structure. In this paper, a series of La₂LiSbO₆ phosphors singly doped with Mn⁴⁺ and Eu³⁺, and co-doped with Eu³⁺/Mn⁴⁺ were synthesized. The crystal phases and optical properties of these materials were characterized and analyzed in detail. We specifically studied the temperature dependence of the fluorescence intensity of the optimized La₂LiSbO₆: Eu³⁺, Mn⁴⁺ phosphors at 303K–523K. The experimental results prove that the thermal responses of Mn⁴⁺ and Eu³⁺ are different. With increasing temperature, the thermal quenching of the Mn⁴⁺ fluorescence intensity is much faster than that of Eu³⁺, so the temperature characteristics can be explored by the fluorescence intensity ratio (FIR) of Eu³⁺ to Mn⁴⁺. At 523 K, its maximum relative sensitivity and maximum absolute sensitivity can reach 0.891% K⁻¹ and 0.000264 K^-1, respectively. Our experimental analysis shows that La₂LiSbO₆:Eu³⁺/Mn⁴⁺ phosphors have relatively high temperature sensitivity and have potential application prospects in the field of high temperature sensing.     

A single‐phase full‐color emitting phosphor Na3Sc2(PO4)3:Eu2+/Tb3+/Mn2+ with near‐zero thermal quenching and high quantum yield for near‐UV converted warm w‐LEDs

A single‐phase full‐color emitting phosphor Na₃Sc₂(PO₄)₃:Eu²⁺/Tb³⁺/Mn²⁺ has been synthesized by high‐temperature solid‐state method. The crystal structure is measured by X‐ray diffraction. The emission can be tuned from blue to green/red/white through reasonable adjustment of doping ratio among Eu²⁺/Tb³⁺/Mn²⁺ ions. The photoluminescence, energy‐transfer efficiency and concentration quenching mechanisms in Eu²⁺‐Tb³⁺/Eu²⁺‐Mn²⁺ co‐doped samples were studied in detail. All as‐obtained samples show high quantum yield and robust resistance to thermal quenching at evaluated temperature from 30 to 200°C. Notably, the wide‐gamut emission covering the full visible range of Na₃Sc₂(PO₄)₃:Eu²⁺/Tb³⁺/Mn²⁺ gives an outstanding thermal quenching behavior near‐zero thermal quenching at 150°C/less than 20% emission intensity loss at 200°C, and high quantum yield‐66.0% at 150°C/56.9% at 200°C. Moreover, the chromaticity coordinates of Na₃Sc₂(PO₄)₃:Eu²⁺/Tb³⁺/Mn²⁺ keep stable through the whole evaluated temperature range. Finally, near‐UV w‐LED devices were fabricated, the white LED device (CCT = 4740.4 K, Ra = 80.9) indicates that Na₃Sc₂(PO₄)₃:Eu²⁺/Tb³⁺/Mn²⁺ may be a promising candidate for phosphor‐converted near‐UV w‐LEDs.     

Color tunable Ba3Lu(PO4)3:Tb3+,Mn2+ phosphor via Tb3+→Mn2+ energy transfer for white LEDs

Series of UV excited Ba₃Lu(PO₄)₃:Tb³⁺,Mn²⁺ phosphors with tunable green to red emissions had been prepared using solid state reactions. Powder X-ray diffraction and Rietveld structure refinement were used to investigate the phase purity and crystal structure of the prepared samples. Under UV excitation, the Ba₃Lu(PO₄)₃:Tb³⁺,Mn²⁺ samples exhibited not only the typical Tb³⁺ emission peaks but also the broad emission band of Mn²⁺ ions due to the efficient Tb³⁺→Mn²⁺ energy transfer which had been verified by luminescence spectra and decay curves. Utilizing the Inokuti-Hirayama model, the Tb³⁺→Mn²⁺ energy transfer mechanism was determined to be the electronic dipole–quadrupole interaction. Moreover, the emission spectra of Ba₃Lu(PO₄)₃:0.80Tb³⁺,0.015Mn²⁺ sample at different temperatures manifested that our prepared phosphors possessed good thermal stability. The luminescence properties investigation results revealed the potential value of Ba₃Lu(PO₄)₃F:Tb³⁺,Mn²⁺ in application for UV excited phosphor converted white light emitting diodes.     

Multiphonon assisted upconversion thermal enhancement for optical temperature sensing and high penetration depth

Thermal quenching that the upconversion (UC) luminescence intensities decrease with increasing temperature limits the application of UC luminescence materials in the field of optical temperature sensing. Herein, we report that Tm³⁺/Yb³⁺ doped Gd₂O₃ phosphors achieve thermal enhancement of UC luminescence with the multiphonon assisted process. Significantly, a possible mechanism of Yb³⁺ ions in thermal enhancement and multiphonon assisted UC luminescence process is proposed. Based on the luminescence intensity ratio technique of non-thermally coupled energy levels, research shows that thermal enhancement can effectively improve the optical temperature sensing absolute sensitivity. Owing to the near-infrared excitation and strong near-infrared emission, the UC luminescence of the Gd₂O₃: Tm³⁺/Yb³⁺ phosphors can penetrate 12 mm pork tissue and achieve UC thermal enhancement in 287-314 K after penetrating 6 mm pork tissue, which shows its potential in vivo application. The results not only provide a pathway to realize the thermal enhancement of UC luminescence and the improvement of the temperature sensing sensitivity, but also promote the understanding and utilization of the UC luminescence thermal enhancement.     

High-temperature persistent luminescence and visual dual-emitting optical temperature sensing in self-activated CaNb2O6: Tb3+ phosphor

The long persistent luminescence (PersL) and color adjustable properties in high-temperature environment are of great significance for luminescent materials in the fields of multiple anti-counterfeiting, biological imaging, and optical temperature sensing (OTS). In this work, a series of self-activated CaNb₂O₆ (CNO): Tb³⁺ phosphors have been successfully synthesized by solid-state reaction route, the OTS, and temperature-dependent PersL of these phosphors is carried out and investigated in detail. Relying on the energy transfer from host to the activator Tb³⁺ ion, the visual color-tunable emissions from blue to green were detected with the increase of temperature and the maximum absolute and relative sensitivities reach 0.955% K^-1 and 1.243% K^-1. Moreover, the temperature-dependent PersL characteristics were investigated systematically, and the initial brightness and the lasting time all reach a maximum value at 323 K in the representative CNO: 1%Tb³⁺ sample. All the results show that the high-temperature persistent phosphor has potential applications in OTS and anti-counterfeiting field.     

Highly sensitive optical thermometer of Sm3+, Mn4+ activated LaGaO3 phosphor for the regulated thermal behavior

Sm³⁺, Mn⁴⁺ co-activated LaGaO₃ phosphors, giving the characteristic emissions of orange and red emission simultaneously, were prepared by a solid-state reaction. Their luminescence properties, energy transfer behavior, thermal stability, and ratiometric temperature sensing performance were investigated. Thanks to the inhibition of energy transfer between Sm³⁺ and Mn⁴⁺ ions at high temperature and the reconstruction of the traps, the distinct optical behavior of the involved activators dependent on the ambient temperature was evaluated. Anti-thermal quenching performance of Sm³⁺ ions along with the emission declination of Mn⁴⁺ ions was observed. Hence, the optical thermometry characteristics of the resultant phosphor based on the fluorescent intensity ratio (orange/red) realize a recorded temperature sensitivity of 4.19% K⁻¹ and 2.09% K⁻¹. Moreover, the as-explored film combined with the LaGaO₃: Sm³⁺, Mn⁴⁺ phosphor is demonstrated to be a promising multi-color optical thermometer.     

Ultra-sensitive low-temperature thermometer regulated by the crystal field strength

Developing novel optical thermometry with ultrahigh relative sensitivity and temperature resolution has become a cutting-edge topic. For this purpose, under obeying Boltzmann distribution, a series of Li₂Zn_0.9992-xA_xGe_3-yB_yO₈:0.08% Cr³⁺ (B= Sc³⁺, In³⁺, A = Si⁴⁺) phosphors were studied, which the luminescence intensity ratio between the transition of ⁴T_2g→⁴A_2g emission and the R line based on thermally coupled energy levels constitutes a temperature sensing work with a relative sensitivity of 9.46% K^?1, 9.73% K^?1, and 10.38% K^?1, respectively. It is worth mentioning that the luminescence intensity of the R line (peak 1) increases significantly with the increase of temperature, while the transition of ⁴T_2g→⁴A_2g (peak 2) with high intensity at low temperature gradually quenching, and this opposite trend is an important advantage for the design of excellent thermometers. Compared the best relative sensitivity of Li₂Zn_0.9992-xA_xGe_3-yB_yO₈:0.08%Cr³⁺ (B= Sc³⁺, In³⁺, A = Si⁴⁺) with the crystal field Dq/B, it can be concluded that relative sensitivity increasing gradually with decreasing the intensity of crystal field. Finally, by testing the stability of the sample at 50 K, a thermal resolution of 0.082 K, 0.080 K and 0.077 K was obtained, respectively, which is one of the best thermal resolutions so far, while the repeatability of the sample stability at 50 K and 300 K cycles was higher than 99%. Our work is expected to provide guiding insights for optimizing the sensitivity of Cr³⁺-based luminescence intensity ratio thermometers.     

HF-free molten salt route for synthesis of highly efficient and water-resistant K2SiF6:Mn4+ for warm white LED

It has been one of the hot issues to prepare the red-emitting Mn⁴⁺-doped fluoride phosphors with highly efficient and waterproofness for warm white-light-emitting diodes (WLEDs) by the green and environmentally friendly method. Herein, we design a novel green molten salt route to synthesize K₂SiF₆:Mn⁴⁺ red powder using molten NH₄HF₂ salt instead of HF liquor as the reaction medium. The results show that KMnO₄ and MnF₂ could produce Mn⁴⁺ in NH₄HF₂ molten salt through a reduction reaction, and the resulting Mn⁴⁺-doped K₂SiF₆ exhibited a bright red emission peaked at 632 nm under blue light excitation. The luminescence intensity of the as-obtained product after immersing into water for 24 hours maintain nearly 100% of that before soaking and emission peak shape remains unchanged. The thermal stability of the sample was evaluated by temperature-dependent luminescence spectral intensity during heating and cooling. Furthermore, a warm white-light-emitting diodes (WLEDs) with an excellent color rendering index (Ra = 87.1), lower correlated color temperature (CCT = 3536K), and high luminous efficacy (116.99 lm·W⁻¹) was fabricated based on blue chip and K₂SiF₆:Mn⁴⁺ and commercial yellow phosphor (Y₃Al₅O₁₂:Ce³⁺).     

Tunable emission color of Li2SrSiO4:Tb3+ due to cross‐relaxation process and optical thermometry investigation

A series of Li₂SrSiO₄:xTb³⁺ (0.2%, 0.4%, 0.6%, 0.8%, 2%, 4%, and 6%) phosphors were prepared by conventional solid‐state reaction. It was found that this silicate phosphor has a wide excitation band at near‐ultraviolet region (230‐300 nm) due to spin‐allowed 4f ⁸→4f⁷5d¹ transitions of Tb³⁺ ions, with the exact position dependent on the crystal field of the lattice. The cross‐relaxation process originating from ⁵D₃→⁵D₄ and ⁷F₆→⁷F₀ happened between different Tb³⁺ ions. It leads to the luminescence color of Li₂SrSiO₄: xTb³⁺ tuning from blue to green just by controlling Tb³⁺ concentrations. Furthermore, concentration quenching mechanism, energy migration type, cross‐relaxation rate and efficiency, are discussed in detail. Finally, optical thermometry properties were investigated via temperature‐dependent emission spectra. The results show that low‐concentration‐doped sample (Li₂SrSiO₄:0.4%Tb³⁺) shows remarkable optical thermometry based on fluorescence intensity ratio (FIR) between the blue and green emission of Tb³⁺ ions, whereas the high‐concentration‐doped sample (Li₂SrSiO₄:4%Tb³⁺) demonstrates small emission intensity loss. It illustrates that terbium‐doped silicate phosphor is a multifunctional material with potential application for display field and optical thermometry .     

Fabrication and Scintillation Performance of Nonstoichiometric LuAG:Ce Ceramics

Nonstoichiometric LuAG:Ce Ceramics ([Lu_(1–x)Ce_x]₃Al₅O₁₂, x = 0.005) with different excess of Lu³⁺ were designed on the basis of Lu₂O₃‐Al₂O₃ phase diagram and fabricated by a solid‐state reaction method. Without using any traditional sintering aids, pure phase and good optical performance were obtained in such a Lu‐rich LuAG:Ce ceramics. In addition, scintillation efficiency and light yield of 1% excess of Lu³⁺ ceramic sample were found 16 times and 1.82 times higher than that of commercial Bi₄Ge₃O₁₂ (BGO) single crystals, respectively. Such values are comparable or even better than those in most of LuAG:Ce single crystals. However, antisite defects were also induced by excess of Lu doping, whose luminescence was found at 350–410 nm in Lu‐rich LuAG:Ce ceramics. The relationship of excess content of Lu and the microstructure, optical quality, and scintillation performance were clarified and discussed. Furthermore, by utilizing X‐ray absorption near edge spectroscopy technique, the charge state stability of cerium in Lu‐rich LuAG:Ce ceramics was examined. It appears that the excess of isovalence Lu³⁺ doping has a negligible effect on the cerium valence instability and creation of stable Ce⁴⁺ center.     

Energy transfer,tunable emission and optical thermometry in Tb3+/Eu3+ co-doped transparent NaCaPO4 glass ceramics

Tb³⁺/Eu³⁺ co-doped glass ceramics containing NaCaPO₄ nanocrystals were successfully synthesized via traditional melt-quenching route with further heat-treatment and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence spectroscopy. The energy transfer process of Tb³⁺→Eu³⁺ was confirmed by excitation and emission spectra and luminescence decay curves, and the energy transfer efficiency was also estimated. The results indicated that the efficient emission of Eu³⁺ was sensitized by Tb³⁺ under the excitation of 378 nm, realizing tunable emission in the transparent bulk glass ceramics containing NaCaPO₄ nanocrystals. Furthermore, optical thermometry was achieved by the fluorescence intensity ratio between Tb³⁺:⁵D₄→⁷F₅ (~542 nm) and Eu³⁺:⁵D₀→⁷F₂ (~612 nm). The maximum absolute sensitivity of 4.55% K⁻¹ at 293 K and the maximal relative sensitivity of 0.66% K⁻¹ at T=573 K for Tb³⁺/Eu³⁺ co-doped transparent NaCaPO₄ glass ceramic are obtained. It is expected that the investigated transparent NaCaPO₄ glass ceramics doped with Tb³⁺/Eu³⁺ have prospective applications in display technology and optical thermometry.     

Visible Quantum Cutting and Energy Transfer in Tb3+‐Doped KSr(Gd,Y)(PO4)2 Under VUV–UV Excitation

KSr(Gd,Y)(PO₄)₂: Tb³⁺ phosphors were synthesized using the high‐temperature solid‐state reaction method. The VUV–UV spectroscopic properties of these phosphors were studied. The results show that efficient energy transfer (ET) from Gd³⁺ to Tb³⁺ occurs in this system, and the ET efficiency increases with increasing of Tb³⁺ doping concentrations, which is evidenced that both the emission intensity and decay time of Gd³⁺ decreases with increasing Tb³⁺ doping concentrations. Visible quantum cutting via cross relaxation between the neighboring Tb³⁺ ions was observed in the high Tb³⁺ concentration doped sample. In addition, the emission color of KSr(Gd,Y)(PO₄)₂: Tb³⁺ phosphors can be tuned from blue to yellowish‐green by varying the doping concentration of Tb³⁺. Under 147 nm excitation, the sample KSrGd_0.5(PO₄)₂: 0.5Tb³⁺ exhibits the strongest emission, which is about 70% of the commercial green‐emitting phosphor Zn₂SiO₄: Mn²⁺ indicating the potential application of this phosphor for plasma display panels, Hg‐free lamps, and three‐dimensional displays.     

Double nanocrystalline engineering for effective enhanced photoluminescence of Tb3+ in glass ceramic

Despite possessing good feature for optical thermometry, the rare (RE) ions-based temperature sensing (TS) has innate shortcoming of thermally coupled levels (TCLs) energy gap overlap, which reduces the sensitivity. In this work, a dual-luminous centers TS based on Tb³⁺ doped Cs₄PbBr₆ quantum dots (QDs) glass ceramic is fabricated. By locating in low phonon energy crystal field environment of Cs₂ZnSi₅O₁₂ nanocrystalline (NS) and Cs₄PbBr₆ QDs, the emission intensity of Tb³⁺ can be enhanced by 14 times. The large exciton binding energy (420 meV) indicates that the prepared QDs glass ceramic has a good thermal stability and the PL intensity of Cs₄PbBr₆ QDs and Tb³⁺ can be well-maintained above 70% and 89% after 8 thermal cycles between 323K and 373K. Furthermore, the obtained maximum absolute sensitivity (S_a) and relative sensitivity (S_r) is as high as 0.2541 K^-1 and 2.68% K^?1, respectively. It is expected that the finding of this work can offer a help in exploring novel QDs/RE ions-based TS and further optimize their practical applications.     

Scintillating properties of gallogermanate glass scintillators doped with Tb3+/Eu3+

Compared with single-crystal scintillator, the glass scintillators have the benefits of low cost, big size, straightforward manufacturing method, and adjustable component. In this work, a succession of diaphanous gallogermanate glass scintillators doped with Tb³⁺ or Eu³⁺ were manufactured using melt-quenching technique. The thermal, structural, photoluminescent, and scintillating properties were studied. For photoluminescent properties, 12 mol% Tb³⁺-doped glass sample has high internal quantum efficiency (87.8%) and no obvious concentration quenching phenomenon can be observed. For scintillating properties, the optimal doping concentration of Tb³⁺ and Eu³⁺ are 4 mol% and 8 mol%, respectively. The integral intensity of X-ray excited luminescence of Tb³⁺-doped sample is 73.1% of that of Bi₄Ge₃O₁₂ scintillator, while the ratio of Eu³⁺-doped sample is 26.5%. The radiation damage of 4 mol% Tb³⁺-doped sample resulted by high power X-ray could be repaired through heat-treatment, while 8 mol% Eu³⁺-doped sample exhibits fine stability that the transmittance keeps constant after exposed to high power X-ray. Our research indicates Tb³⁺ or Eu³⁺ doped gallogermanate glass might be candidate for X-ray detection of slow events.     

Multicolor upconversion emission and highly optical temperature sensing based on lanthanide-doped double perovskite Sr2LaNbO6 phosphors

Here we adopt trivalent lanthanide (Ln³⁺ = Er³⁺, Er³⁺/Ho³⁺, and Yb³⁺/Tm³⁺) doped Sr₂LaNbO₆ (SLNO) as novel upconversion luminescence (UCL) materials for achieving UCL and optical temperature sensing under 980 nm excitation. Specifically, Er³⁺ single doped Sr₂LaNbO₆ phosphors present bright high-purity green emission under the 980 nm excitation. While co-doping with the Ho³⁺ ions, the component of red emission from Er³⁺ ions increases significantly and sample show a remarkable enhancement of luminescent intensity relative to SLNO:Er³⁺ sample. The above-mentioned phosphors and Yb³⁺/Tm³⁺ co-doped phosphor (blue emission) successfully achieve high-purity trichromatic UCL and mixed white light output in the same host. Furthermore, the temperature sensing performance of the SLNO:Er³⁺/Ho³⁺ phosphor based on the fluorescence intensity ratio (FIR) is systematically studied for the first time. The temperature sensing based on the non-thermal coupling levels (NTCLs) exhibit higher sensitivity than that based on the thermal coupling levels (TCLs). The maximum absolute and relative sensitivity for ⁴F_9/2/⁴I_9/2 NTCLs reach 0.16803 K^?1 at 427 K and 0.01591 K^?1 at 641 K, respectively. Interestingly, NIR emission of ⁴I_9/2 → ⁴I_15/2 transition presents a thermal enhancement, while visible emissions show thermal quenching. These results indicate that the Ln³⁺ doped Sr₂LaNbO₆ UCL phosphors have potential applications in the fields of non-contact temperature sensors, full-color displays, and anti-counterfeiting.