New tunable-color luminescent materials are getting a lot of attention. Double-doped activated ions are an important research method. Here, CaSrNb2O7:R3+ (R3+ = Sm3+, Bi3+, and Sm3+/Bi3+) are synthesized by solid state method in the air. Phase purity and successful synthesis of samples are confirmed by X-ray diffractometer (XRD) patterns and energy disperse spectroscopy (EDS) diagram. The luminescence properties of samples are studied. CaSrNb2O7:Sm3+ has an excitation spectrum due to the O2- - Sm3+ charge transfer band (CTB) and the 6H5/2 → 4H9/2, 4D3/2, 4D1/2, 4F7/2, and 4I11/2 transitions of Sm3+ ion. The red-orange emission of CaSrNb2O7:Sm3+ is observed because of the 4G5/2 → 6H5/2, 6H7/2, 6H9/2, and 6H11/2 transitions of Sm3+ ion. PLE spectrum of CaSrNb2O7:Bi3+ comes from the metal-to-metal charge- transfer (MMCT) Bi3+ - Nb5+ and the 1S0 → 1P1 and 3P1 transitions of Bi3+ ion. CaSrNb2O7:Bi3+ shows blue emission due to the 3P1 → 1S0 transition of Bi3+ ion. The excitation spectrum of CaSrNb2O7:Sm3+, Bi3+ contains that of CaSrNb2O7:Bi3+ and CaSrNb2O7:Sm3+. CaSrNb2O7:Sm3+, Bi3+ with excitation at 314, 363, and 406 nm glows orange and red-orange, and red emission, respectively. We observe the energy transfer from Bi3+ to Sm3+ ions and the effect of Bi3+ on luminescence properties of Sm3+ ion by their spectra. The optimal Sm3+ and Bi3+ concentrations are confirmed by the concentration dependent spectra. The energy level diagrams of Sm3+ and Bi3+ are used to analyze the luminous mechanism. The results are conducive to the development of new Sm3+ and Bi3+ co-doped luminescent materials. 

Energy transfer and tunable-color luminescence properties of a single-phase CaSrNb2O7:Sm3+, Bi3+

Near-infrared (NIR) mechanoluminescence (ML) materials have been of great interest within biological tissues due to their biocompatibility and suitability for biostress imaging. However, the reported NIR MLs have predominantly been featured with narrowband ML emissions, which may limit their further applications. In this work, a novel broadband NIR ML material of Lu3Ga4.88O12:0.12Cr3+ (FWHM > 120 nm) is reported. By substituting Al3+ for Ga3+, the local crystal field strength and the defect concentration are reasonably regulated, which further improves the NIR ML (650–1000 nm) intensity of Cr3+ ion by 475 %. In addition, by compounding polydimethylsiloxane with this phosphor, the obtained Cr3+ NIR ML film can penetrate 10 mm pork tissues quite well, indicating potential applications for stress distribution optical imaging within living organisms. Expectingly, broadband NIR ML from Cr3+ ions can be obtained by further solid-solution multiple lattice sites substitution, which may provide a new approach to improve the performance of NIR ML materials towards expanded biological applications. 

Cr3+-Activated Broadband Near-Infrared Mechanoluminescence in Garnet Compound

To settle the low sensitivity of luminescent manometers, the Mn2+ -activated NaY9 (SiO4 )6 O2 red-emitting phosphors with splendid pressure sensing performances are developed. Excited by 408 nm, the resulting products emit bright red emission originating from 4 T1 (4 G) → 6 A1 transition of Mn2+ , in which the optimal concentration of the activator ion is ≈1 mol%. Moreover, the admirable thermal stability of the developed phosphors is studied and confirmed by the temperature-dependent emission spectra, based on which the activation energy is derived to be 0.275 eV. By analyzing the pressure-dependent Raman spectra, the structural stability of the synthesized compounds at extreme conditions is verified. Furthermore, the designed phosphors exhibit remarkable spectral red-shift at elevated pressure. Especially, as pressure increases from 0.75 to 7.16 GPa, the emission band centroid shifts from 617.2 to 663.4 nm, resulting in a high sensitivity (dλ/dP) of 7.00 nm GPa-1 , whereas the full width at half maximum (FWHM) increases from 83.0 to 110.6 nm, leading to the ultra-high sensitivity (dFWHM/dP) of 10.13 nm GPa-1 . These achievements manifest that the designed red-emitting phosphors are appropriate for ultrasensitive optical manometry. More importantly, the developed manometer is a current global leader in sensitivity, when operating in the band-width mode, that is, FWHM.

Pressure-Induced Remarkable Spectral Red-Shift in Mn2+ -Activated NaY9 (SiO4 )6 O2 Red-Emitting Phosphors for High-Sensitive Optical Manometry.

The near‐infrared (NIR) persistent luminescence (PersL) materials have attracted widespread attention owing to the unique self‐sustained light with good penetrability. Currently, most of the reported NIR PersL materials are activated by Cr3+. Considering the potential toxicity of chromium ions, there is an urgent requirement to explore the Cr3+‐free NIR phosphors. Herein, a novel NIR phosphor Sr2LuSbO6:Fe3+ (SLSO:Fe3+) is prepared and its luminescence properties are systematically studied. The Fe3+‐activated Sr2LuSbO6 exhibits a long‐wavelength NIR emission band centered at 890 nm with a 110 nm full‐width at half maximum (FWHM), and its PersL can last over 18 h. The phosphor shows excellent PersL stability even after being dispersed in solutions of different environments for 7 days. Furthermore, the PersL emitted by the phosphor can penetrate the 2 cm thickness beef, evidencing its good NIR PersL penetration property. This work provides a novel NIR PersL materials based on Fe3+ luminescence for technological applications and also contributes to accelerate the development of new‐generation Fe3+‐doped NIR PersL phosphor toward versatile applications.

A Novel Near‐Infrared Emitting Sr2LuSbO6:Fe3+ Phosphor with Persistent Luminescence Performance

Exploring mechanoluminescence (ML) materials having multi-stimulus-responsive luminescence is conducive to promoting the development of ML field applications. However, integrating the multi-stimulus-responsive luminescence into a single material is challenging, especially when concerning the unclear multi-stimulus-responsive luminescence mechanisms. Herein, we successfully synthesized a Mn2+-activated broadband multi-stimulus-responsive ML material in a non-centrosymmetric piezoelectric host (LiGaO2: Mn2+). Utilizing the defects' homology characteristic between ML and persistent/photo-stimulated luminescence, it is confirmed that one can manage the distribution and depth of defects to determine the internal relationship between the multi-stimulus-responsive luminescence and defects. Meanwhile, the V••o and V'Li defects and distribution play a dominant role in multi-mode luminescence. The dynamic process of multi-stimulus-responsive luminescence that charge carriers trapped in deep defects are supplemented to shallow defects can be proved by experimental and DFT calculation results. Based on the excellent multi-stimulus-responsive luminescence performance, the proof-of-concept multi-mode application prospects are demonstrated. This work will deepen our understandings of the multi-stimulus-responsive luminescence mechanism via regulating the distribution and composition of defects to further promote research on flexible X-ray detectors and anti-counterfeiting fields. 

Defect-management-induced multi-stimulus-responsive mechanoluminescence in Mn2+ doped gallate compound

Single Tb3+ ion doped ratiometric mechanoluminescence for tunable stress visualization

Luminous properties play an essential role in the phosphor-converted white light-emitting diodes for high-quality illumination, where the self-reducing behavior of doped activators and excellent thermal stability have received significant attention....

Self-reduction of NaY9Si6O26:Mn2+ red phosphor with excellent thermal stability for NUV LEDs

An activator's selective occupation of a host is of great significance for designing high-quality white light-emitting diode phosphors, while achieving a full-spectrum single-phase white light emission phosphor is challenging. In this study, a boron phosphate solid-solution Na2Y2(BO3)2-x(PO4)xO:0.005 Bi3+ (NYB2-xPxO:0.005 Bi3+) white phosphor was designed by selectively occupying Bi3+ activators in the mixed anionic groups. The substitutes of the anionic unit (BO3)3- by the (PO4)3- unit are supposed to force part of the Bi3+ ion to enter the Na lattice site, which produces an intense orange-red emission peaked at 590 nm. In parallel, spectral tuning from blue to white light and an internal quantum efficiency of 56.42% was obtained, and the thermal stabile luminescence intensity remains at 94.2% of the initial intensity after four heating-cooling cycles from 30 to 210 °C (luminescent intensity is 83.6% of room temperature (RT) at 150 °C, with excellent thermal stability and recovery performance). Finally, an excellent color rendering index (Ra = 90.8 and R9 = 85) was demonstrated for white light-emitting diode devices using only an NYB1.5P0.5O:0.005 Bi3+ phosphor and a near-ultraviolet (n-UV) 365 nm LED chip. This work delves into the different selective occupancy of Bi3+ ions and explores a new avenue for the design of phosphors for full-spectrum white light emission.

Anionic Regulation toward Bi3+ Selective Occupation for Full-Spectrum White Light Emission.

Mechanoluminescence (ML) materials are featured with the characteristic of "force to light" in response to external stimuli, which have made great progress in artificial intelligence and optical sensing. However, how to effectively enable ML in the material is a daunting challenge. Here, a Lu3 Al2 Ga3 O12 :Cr3+ (LAGO: Cr3+ ) near infrared (NIR) ML material peaked at 706 nm is reported, which successfully realizes the key to unlock ML by the lattice-engineering strategy Ga3+ substitution for Al3+ to "grow" oxygen vacancy (Ov ) defects. Combined with thermoluminescence measurements, the observed ML is due to the formation of defect levels and the ML intensity is proportional to it. It is confirmed by X-ray photoelectron spectroscopy and electron paramagnetic resonance that such a process is dominated by Ov , which plays a crucial role in turning on ML in this compound. In addition, potential ML emissions from 4 T2 and 2 E level transitions are discussed from both experimental and theoretical aspects. This study reveals the mechanism of the change in ML behavior after cation substitution, and it may have important implications for the practical application of Ov defect-regulated turn-on of ML.

Realizing Near Infrared Mechanoluminescence Switch in LAGO:Cr Based on Oxygen Vacancy.

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