Excellent Photoluminescence Research Articles

Robust Sandwich‐Structured Thermally Activated Delayed Fluorescence Molecules Utilizing 11,12‐Dihydroindolo[2,3‐a]carbazole as Bridge

AbstractConstructing folded molecular structures is emerging as a promising strategy to develop efficient thermally activated delayed fluorescence (TADF) materials. Most folded TADF materials have V‐shaped configurations formed by donors and acceptors linked on carbazole or fluorene bridges. In this work, a facile molecular design strategy is proposed for exploring sandwich‐structured molecules, and a series of novel and robust TADF materials with regular U‐shaped sandwich conformations are constructed by using 11,12‐dihydroindolo[2,3‐a]carbazole as bridge, xanthone as acceptor, and dibenzothiophene, dibenzofuran, 9‐phenylcarbazole and indolo[3,2,1‐JK]carbazole as donors. They hold outstanding thermal stability with ultrahigh decomposition temperatures (556–563 °C), and exhibit fast delayed fluorescence and excellent photoluminescence quantum efficiencies (86 %–97 %). The regular and close stacking of acceptor and donors results in rigidified molecular structures with efficient through‐space interaction, which are conducive to suppressing intramolecular motion and reducing reorganized excited‐state energy. The organic light‐emitting diodes (OLEDs) using them as emitters exhibit excellent electroluminescence performances, with maximum external quantum efficiencies of up to 30.6 %, which is a leading value for the OLEDs based on folded TADF emitters. These results demonstrate the proposed strategy of employing 11,12‐dihydroindolo[2,3‐a]carbazole as bridge for planar donors and acceptors to construct efficient folded TADF materials is applicable.

Perylene Based Twisted Emissive Curved Nanographene Synthesis through Scholl Reaction

A twisted chiral nanographene (NG) surrounded by eight bulky tert‐butyl groups fused with emissive chromophore perylene was synthesized by highly regioselective cyclodehydrogenation strategy in which a double [6]helicene was formed simultaneously. The twisted 4‐meso was unambiguously confirmed by single crystal X‐ray analysis. The NG showed an excellent photoluminescence quantum yield (φf) of 55%, indicating its great potential for chiral optoelectronics.

Realizing Near-Unity Photoluminescence Efficiency in Antimony-Doped Indium-Based Halides Induced by Strong Electron-Phonon Coupling.

Exploring a zero-dimensional (0D) hybrid halide with a large Stokes shift and efficient broad-band emission is highly desirable due to its enormous potential for solid-state lighting (SSL) application. However, it is still challenging to develop a highly emissive 0D hybrid halide with low toxicity and remarkable stability. Herein, we developed a novel indium-based metal halide A5In2Cl16·4H2O (A = doubly protonated 1,4-diaminobutane) whose inorganic octahedrons are completely isolated by the organic cations to form the 0D structure. Experimental and theoretical studies confirmed that Sb-doped A5In2Cl16·4H2O exhibits broad yellow emission with a photoluminescence quantum yield (PLQY) of up to 98%. The intense yellow emission can be attributed to the radiative recombination of triplet self-trapped excitons (STEs) in [SbCl6]3- octahedrons caused by the strong electron-phonon coupling. Benefiting from the excellent stability and photoluminescence performance, A5In2Cl16·4H2O:15%Sb was used as the yellow phosphor to prepare a white-light-emitting diode (WLED) device with a color rendering index of 87.8 and a luminous efficiency of up to 36.18 lm/W, demonstrating its potential in SSL applications. This work provides a guidance for developing environmentally friendly, efficient, and stable ultraviolet (UV)-excited broad-band emission materials.

Efficient Blue Emission in Organic–Inorganic Metal Halide (TEA)2InCl5 Triggered by Bi3+‐Doping

AbstractLead‐free 0D In‐based organic–inorganic metal halides (OIMHs) have attracted tremendous attention because of their nontoxicity, environmental stability, and excellent photoluminescence properties. However, it remains controversial and unclear whether the luminous division exists in ns2 doping In‐based materials, as the majority of In‐based materials are considered non‐luminous. Herein, a series of Bi3+‐doped (TEA)2InCl5 (TEA = tetraethylammonium) crystals are synthesized and it is determined that the blue emission stemmed from Bi ions. Remarkably, the photoluminescence quantum yield (PLQY) of the blue emission at 469 nm reached 69.69% under 371 nm excitation, exceeding those of previously reported Bi3+‐doped OIMHs. In addition, pristine and Bi3+‐doped compounds exhibited excellent structure and optical stability under humid conditions. This study provides new insights into the photoluminescence properties of In‐based OIMHs, especially regarding the high‐efficiency emission of Bi3+‐doped materials.

Reversible Interconversion between Ag2 and Ag6 Clusters and Their Responsive Optical Properties.

The exploration of structural interconversion in clusters triggered by external stimuli has attracted significant interest due to its potential to elucidate structure-property relationships of metal clusters. In this study, two types of silver clusters, Ag2 and Ag6, are synthesized. Interestingly, the clusters exhibit reversible transformations in response to changes in the solvent conditions. The structures and optical properties of these clusters are thoroughly characterized using techniques such as mass spectrometry, single-crystal X-ray diffraction, photoluminescence, and radioluminescence spectroscopy. While both Ag2 and Ag6 display excellent photoluminescence properties, Ag2 demonstrates superior performance in X-ray radioluminescence compared to Ag6. Flexible scintillator films fabricated from Ag2 clusters exhibit outstanding X-ray imaging capabilities, achieving a spatial resolution of 15.0 lp/mm and an impressive detection limit for an X-ray dose of 0.58 μGy s-1. This detection limit is nearly 10 times lower than the typical dose rate used in X-ray diagnostics (5.5 μGy s-1). This work introduces a novel approach for designing thiol-free silver clusters capable of solvent-dependent reversible interconversion, offering new insights into the development of silver clusters for advanced X-ray imaging applications.

Combining SSVD and subsequent heat treatment processes to fabricate high-quality CsPbBr3 perovskite films

Perovskites, known for their excellent photoluminescence efficiency and color purity, have seen widespread application in flat panel displays and lighting in recent years. Here, we present a process for fabricating CsPbBr3 perovskite film (PeFilm) with high luminescent properties and remarkable weather resistance. By combining single-source vapor deposition (SSVD) with subsequent heat treatment, the quality of PeFilms has been significantly improved. We enhanced the quality of PeFilms by using a thermal annealing process to remove PbBr2 from CsPb2Br5. During annealing, PbBr2 evaporates from PeFilms, changing the crystal phase to CsPbBr3. The heat treatment rearranges atoms between grains, promoting grain growth and fusion, producing larger crystals and reducing defects. The research results demonstrate that the integration of SSVD and appropriate heat treatment enables the fabrication of the CsPbBr3 PeFilm with an emission wavelength of 533 nm, CIE coordinates of (0.1842, 0.7797), and a photoluminescence quantum yield (PLQY) of 52.1%, and even after storing it in atmospheric conditions for 100 days, the PLQY of the CsPbBr3 PeFilm remains above 52%, demonstrating excellent stability.

Efficient and tunable emission of Na5Lu(WO4)4:Tb3+,Eu3+ phosphors for warm white LEDs with high color rendering index

Phosphors with high luminescence efficiency, tunable emission and high color rendering index (CRI) are vital importance for the quality of white light emitting diodes (w-LEDs) in real application. In this work, a new single phase color-tunable Na5Lu(WO4)4:Tb3+,Eu3+ phosphor with outstanding luminescent properties was designed and synthesized. Its crystal structure, electronic structure, and luminescence features were studied in detail. The band gap of the host was calculated to be at about 4.68 eV. The differential charge distribution after Tb, Eu doping through density functional theory simulation theoretically proved the electron redistribution in the W-O bond upon substitution of Tb3+/Eu3+. The energy transfer of Tb3+→Eu3+ enabled tunable emission of luminescent colors from green to orange-red due to the quadrupole-quadrupole interaction. The optimal Na5Lu(WO4)4:60%Tb3+,20%Eu3+ phosphor exhibited excellent photoluminescence quantum yield of 84.19% and good luminescent thermal stability (I423K/298K = 75.90%) with an activation energy of 0.1976 eV. Finally, a white LED device with color coordinates of (0.3371, 0.3636), color rendering index of 89.4 and correlated color temperature of 5334 K was fabricated. These findings demonstrated that Na5Lu(WO4)4:60%Tb3+,20%Eu3+ phosphor could be a potential orange-red-emitting color converter for white LEDs. This work not only assisted in the understanding of experimental observations but also provided a theoretical basis for the rational design of phosphors.

Strategic engineering of cationic systems for spatial & temporal anti-counterfeiting applications in zero-dimensional Mn(II) halides

While spatial and time-resolved anti-counterfeiting technologies have gained increasing attention owing to their excellent tunable photoluminescence, achieving high-security-level anti-counterfeiting remains a challenge. Herein, we developed a spatial-time-dual-resolved anti-counterfeiting system using zero-dimensional (0D) organic–inorganic Mn(II) metal halides: (EMMZ)2MnBr4 (named M−1, EMMZ=1-Ethyl-3-Methylimidazolium Bromide) and (EDMMZ)2MnBr4 (named M−2, EDMMZ=1-Ethyl-2,3-Dimethylimidazolium Bromide). M−1 shows a bright green emission with a quantum yield of 78 %. It undergoes a phase transformation from the crystalline to molten state with phosphorescence quenching at 350 K. Reversible phase and luminescent conversion was observed after cooling down for 15 s. Notably, M−2 exhibits green light emission similar to M−1 but undergoes phase conversion and phosphorescence quenching at 390 K, with reversible conversion observed after cooling down for 5 s. The photoluminescence switching mode of on(green)-off–on(green) can be achieved by temperature control, demonstrating excellent performance with short response times and ultra-high cyclic reversibility. By leveraging the different quenching temperatures and reversible PL conversion times of M−1 and M−2, we propose a spatial-time-dual-resolved photoluminescence (PL) switching system that combines M−1 and M−2. This system enables multi-fold tuning of the PL switch for encryption and decryption through cationic engineering strategies by modulating temperature and cooling time. This work presents a novel and feasible design strategy for advanced-level anti-counterfeiting technology based on a spatial-time-dual-resolved system.

Suppression of efficiency roll-off in solution-processed OLEDs using pyrimidine-based iridium complexes modified with sterically hindered groups

Three bis-cyclometalated iridium complexes Ir1-Ir3 were successfully synthesized through mild reaction conditions. All complexes exhibit emission peaks at 507-509 nm, with excellent photoluminescence quantum efficiencies (PLQY) ranging from 69% to 97%. Self-quenching is significantly reduced because the steric spacers lead to minimum bimolecular interactions. Accordingly, the electroluminescence device based on complex Ir3 exhibits a maximum luminous efficiency of 39.6 cd A−1, a high EQE of 13.1% with an efficiency roll-off of 4.2% at 1000 cd m−2, which is much smaller than that (10.8%) of the Ir1-based device. Moreover, its devices exhibit excellent stability even at elevated doping concentrations, suggesting a notable reduction in intermolecular interactions caused by the steric pinene spacer.

Robust Sandwich-Structured Thermally Activated Delayed Fluorescence Molecules Utilizing 11,12-Dihydroindolo[2,3-a]carbazole as Bridge.

Constructing folded molecular structures is emerging as a promising strategy to develop efficient thermally activated delayed fluorescence (TADF) materials. Most folded TADF materials have V-shaped configurations formed by donors and acceptors linked on carbazole or fluorene bridges. In this work, a facile molecular design strategy is proposed for exploring sandwich-structured molecules, and a series of novel and robust TADF materials with regular U-shaped sandwich conformations are constructed by using 11,12-dihydroindolo[2,3-a]carbazole as bridge, xanthone as acceptor, and dibenzothiophene, dibenzofuran, 9-phenylcarbazole and indolo[3,2,1-JK]carbazole as donors. They hold outstanding thermal stability with ultrahigh decomposition temperatures (556-563 oC), and exhibit fast delayed fluorescence and excellent photoluminescence quantum efficiencies (86%-97%). The regular and close stacking of acceptor and donors results in rigidified molecular structures with efficient through-space interaction, which are conducive to suppressing intramolecular motion and reducing reorganized excited-state energy. The organic light-emitting diodes (OLEDs) using them as emitters exhibit excellent electroluminescence performances, with maximum external quantum efficiencies of up to 30.6%, which is a leading value for the OLEDs based on folded TADF emitters. These results demonstrate the proposed strategy of employing 11,12-dihydroindolo[2,3-a]carbazole as bridge for planar donors and acceptors to construct efficient folded TADF materials is applicable.

Long-Range Self-Hybridized Exciton-Polaritons in Two-Dimensional Ruddlesden-Popper Perovskites.

Lead halide perovskites have emerged as platforms for exciton-polaritonic studies at room temperature, thanks to their excellent photoluminescence efficiency and synthetic versatility. In this work, we find proof of strong exciton-photon coupling in cavities formed by the layered crystals themselves, a phenomenon known as the self-hybridization effect. We use multilayers of high-quality Ruddlesden-Popper perovskites in their 2D crystalline form, benefiting from their quantum-well excitonic resonances and the strong Fabry-Pérot cavity modes resulting from the total internal reflection at their smooth surfaces. Optical spectroscopy reveals bending of the cavity modes typical for exciton-polariton formation, and absorption and photoluminescence spectroscopy shows splitting of the excitonic resonance and thickness-dependent peak positions. Strikingly, local optical excitation with energy below the excitonic resonance of the flakes in photoluminescence measurements unveils the coupling of light to in-plane polaritonic modes with directed propagation. These exciton-polaritons exhibit high coupling efficiencies and extremely low loss propagation mechanisms, which are confirmed by finite difference time domain simulations. Thus, we prove that mesoscopic 2D Ruddlesden-Popper perovskite flakes represent an effective but simple system to study the rich physics of exciton-polaritons at room temperature.

Facile Light-Driven Synthesis of Highly Luminous Sulfur Quantum Dots for Fluorescence Sensing and Cell Imaging.

Sulfur quantum dots (SQDs) are emerging fluorescent nanomaterials, whereas most of the methods for synthesizing SQDs are limited to thermal synthesis. In this study, we report the first case of a light-driven strategy for facile synthesis of SQDs and further applied the SQDs for fluorescence cell imaging. The light-driven synthesis strategy only utilized Na2S as the sulfur source and nano-TiO2 as the photosensitizer. Under ultraviolet illumination, the nano-TiO2 photosensitizer generated a large number of •O2- and •OH to oxidize S2- to Sx2- and further to elemental sulfur, which could be obtained as monodispersed SQDs after etching by H2O2. The prepared SQDs exhibit excellent tunable photoluminescence properties, superior stability, and a uniform small size, with particle diameters in the range of 0.5-4 nm, and the fluorescence absolute quantum yield is as high as 27.8%. Meanwhile, the prepared SQDs also exhibited extreme biocompatibility and stability, and we further applied it for intracellular imaging and Hg2+ sensing with satisfactory results. In comparison to the widely reported thermal synthesis, the light-driven synthesis method is greener and simpler, opening a new way for the preparation of biocompatible SQDs.

Coal derived highly fluorescent N-Doped graphene quantum dots with graphitic and chemisorbed nitrogen

Graphene quantum dots (GQDs) constitute a novel category of quantum dots distinguished by their distinctive properties. The introduction of nitrogen heteroatom in GQD is an effective strategy for tuning its intrinsic properties and band gap toward its optoelectronic application. This work explores the synthesis and characterization of nitrogen-doped graphene quantum dots (N-GQDs) derived from low-cost precursor coal. The synthesized N-GQD contains both graphitic and chemisorbed nitrogen states along with pyrollic and pyridinic nitrogen states which is the key responsible factor for excellent photoluminescence properties. The excitation dependent photoluminescence of the synthesized N-GQD exhibited excellent emission at 520 nm in neutral and basic pH due to the additional conjugation provided by the doped nitrogen on the surface and functional groups as well. The pH dependent photophysical properties support the existence of doped graphitic and chemisorbed nitrogen states which is also well supported by the high resolution N1s XPS peaks at 402 eV (graphitic N) and 406 eV (chemisorbed N/N2). DFT calculations further showed the decrease in fermi energy level by introducing chemisorbed-N. TEM analysis evident the formation of quantum dots with an average diameter of 3 - 7 nm with d-spacing of 0.20 - 0.34 nm. Additionally, the cyclic voltammetry analysis of the synthesized N-GQDs sheds light on the participation of doped nitrogen in redox reactions.

Achieving Ultrahigh Thermal Stability in Cr3+-Activated Garnet Phosphors through Electron Migration between Thermally Coupled Levels.

Recently, Cr3+-activated near-infrared (NIR) phosphors have received much more attention due to their excellent photoluminescence (PL) properties. However, most of them suffer from poor thermal stability which limits further application. Herein, a novel Lu2CaGa4SnO12:Cr3+ phosphor with broadband NIR emission (λem = 750 nm) is synthesized successfully. Despite the good luminescence property, its PL intensity decreases obviously with temperature (I425K = 79%). To improve the thermal stability, a series of Lu2+xCa1-xGa4+xSn1-xO12:Cr3+ (x = 0-1.0) solid solutions with tunable thermal quenching performance have been designed. It is found that the fluorescence intensity ratio (FIR) of 4T2 → 4A2 to 2E → 4A2 [I(4T2)/I(2E)] transitions (i.e. electron occupation) decreases monotonously with increasing [Lu3+-Ga3+] co-substitution, resulting from a strengthened crystal field strength and increased energy difference between 4T2 and 2E energy levels. Benefiting from the various thermal population and energy difference Δ', the PL thermal quenching behavior of Lu2+xCa1-xGa4+xSn1-xO12:Cr3+ can be adjusted easily, and the corresponding mechanism is explored in detail. Most notably, the emission intensity of Lu2+xCa1-xGa4+xSn1-xO12:Cr3+ at 425 K can reach up to 142% compared with that at 300 K, which may be the best for Cr3+-activated NIR phosphors. This work may provide an alternative path for the development of thermally stable broadband NIR phosphors.

Recent Excellent Optoelectronic Applications Based on Two-Dimensional WS2 Nanomaterials: A Review.

Tungsten disulfide (WS2) is a promising material with excellent electrical, magnetic, optical, and mechanical properties. It is regarded as a key candidate for the development of optoelectronic devices due to its high carrier mobility, high absorption coefficient, large exciton binding energy, polarized light emission, high surface-to-volume ratio, and tunable band gap. These properties contribute to its excellent photoluminescence and high anisotropy. These characteristics render WS2 an advantageous material for applications in light-emitting devices, memristors, and numerous other devices. This article primarily reviews the most recent advancements in the field of optoelectronic devices based on two-dimensional (2D) nano-WS2. A variety of advanced devices have been considered, including light-emitting diodes (LEDs), sensors, field-effect transistors (FETs), photodetectors, field emission devices, and non-volatile memory. This review provides a guide for improving the application of 2D WS2 through improved methods, such as introducing defects and doping processes. Moreover, it is of great significance for the development of transition-metal oxides in optoelectronic applications.

Isolation and chemical immobilization of E. coli‐specific bacteriophage with NH2‐MIL‐101(Fe) MOF, a high photoluminescence rod‐shaped microcrystals for low‐level bacteria detection

As concern raised by the World Health Organization (WHO) of antibiotic‐resistant and bio‐defensive bacteria, a metal–organic framework (MOF) based optical biosensor came into consideration for precise, quick, and sensitive detection of Escherichia coli (E. coli) (ATCC 10799) using bacteriophage as a bio‐recognition element. In the present study, amine‐functionalized Fe‐based MOF, i.e., NH2‐MIL‐101(Fe), was synthesized by the solvothermal method (approx. 531–1106 nm in size and 20 mV zeta potentials by DLS) and further characterized by SEM, XRD, ATR‐FTIR, UV–VIS, and photoluminescent (PL) spectroscopy. The lytic bacteriophage was isolated from a sewage sample, purified, and concentrated using the ultra‐centrifugation method and achieved a high titer of 7.3 × 1012 PFU/ml. The concentration, stability, and accessible receptor binding domains (RBDs) of the biorecognition element for binding with their analytes play an important role in developing sensitive and specific biosensor systems. To fulfill the mentioned criteria, optimized glutaraldehyde concentration was estimated at 0.25%, at 30 °C for conjugating maximum bacteriophage titer of 8.6 × 105 PFU/ml for each 1 mg amine functionalized iron‐based MOF. The synthesized detection probe has shown excellent photoluminescence and antibacterial activity and achieved a detection limit of 652 CFU/ml over a bacterial detection concentration range from 5.78 × 101 to 5.78 × 106 CFU/ml for E. coli with 10–12 min of response time, high specificity, and long‐term stability even at room temperature. Therefore, it can be inferred that this MOF‐based strategy can be helpful in the specific and sensitive detection of various bacterial pathogens using bacteriophage as a bio‐recognition element.

Synthesis of Carbon Dots via Microwave-Assisted Process: Specific Sensing of Fe(III) and Antibacterial Activity.

Carbon dots synthesized from a renewable and sustainable source of biomass have greater attention in the nanomaterial research field. In the present study, we adopted a facile and green synthesis of carbon dots from bio waste of pumpkin seeds using a one-pot microwave-assisted carbonization method. The synthesized carbon dots exhibit excellent photoluminescence properties with a bright blue emission peak at 399nm and fluorescence quantum yield was about 9.5%. The optical properties and structure of carbon dots were examined using various spectroscopy techniques and the synthesized carbon practical size was about 4.37nm and possessed good solubility in water. Carbon dots were used for the detection of Ferric ions in the water bodies and the interaction between Fe3+ ions and carbon dots was evaluated by fluorescence spectroscopy techniques. This method is a simple and selective detection of Fe3+ in the aqueous medium. Interestingly carbon dots also show good antibacterial activity at a very low concentration (1mg/L) for effective control of E. coli 93% and Pseudomonas aeruginosa (81%), within 12h.

Graphene Quantum Dots Reduce Hypertrophic Scar by Inducing Myofibroblasts To Be a Quiescent State.

Contrary to the initial belief that myofibroblasts are terminally differentiated cells, myofibroblasts have now been widely recognized as an activation state that is reversible. Therefore, strategies targeting myofibroblast to be a quiescent state may be an effective way for antihypertrophic scar therapy. Graphene quantum dots (GQDs), a novel zero-dimensional and carbon-based nanomaterial, have recently garnered significant interest in nanobiomedicine, owing to their excellent biocompatibility, tunable photoluminescence, and superior physiological stability. Although multiple nanoparticles have been used to alleviate hypertrophic scars, a GQD-based therapy has not been reported. Our in vivo studies showed that GQDs exhibited significant antiscar efficacy, with scar appearance improvement, collagen reduction and rearrangement, and inhibition of myofibroblast overproliferation. Further in vitro experiments revealed that GQDs inhibited α-SMA expression, collagen synthesis, and cell proliferation and migration, inducing myofibroblasts to become quiescent fibroblasts. Mechanistic studies have demonstrated that the effect of GQDs on myofibroblast proliferation blocked cell cycle progression by disrupting the cyclin-CDK-E2F axis. This study suggests that GQDs, which promote myofibroblast-to-fibroblast transition, could be a novel antiscar nanomedicine for the treatment of hypertrophic scars and other types of pathological fibrosis.

Microstructural evolution and luminescence properties of multi-excitable cubic-ZrW2O8:Dy3+ nanorods for white light applications

ZrW2O8 nanorods doped with various concentrations of Dy3+ ions (5 - 15 mol%) showing excellent photoluminescence (PL) properties were synthesized by the facile hydrothermal method for white light applications. The products were comprehensively analyzed using a range of structural, morphological, and optical techniques. The optical studies were conducted by utilizing UV–visible and photoluminescence spectrophotometers. The photoluminescent emission spectra exhibit two prominent peaks at wavelengths of 479 nm and 572 nm, along with a less intense peak at 661 nm when subjected to excitations at wavelengths of 286 nm and 352 nm, and a highly dominating yellow emission with a faint red emission was obtained at 452 nm excitation. The almost constant value Y/B intensity ratios, lifetime values, CIE coordinates, and CCT values suggest that the obtained nanophosphor can be effectively employed in white light-emitting diodes (WLEDs) and various other lighting devices.

Sb3+ and Er3+ co-doped Cs2NaYCl6 double perovskite with ultra-high sensitivity for optical thermometry

Optical thermometry has attracted great attention because it enables accurate temperature measurement in harsh environments due to non-contact temperature measurement. Three-dimensional (3D) lead-free halide perovskites have a great application potential in this field, due to its outstanding luminous properties and stability. In this work, the Sb3+ and Er3+ are introduced in Cs2NaYCl6 double perovskites (DPs). The Sb3+ doping Cs2NaYCl6 DPs exhibits bright blue emission from the Sb3+ activated self-trapped excitons (STEs) and Sb3+,Er3+ co-doped Cs2NaYCl6 has efficient green emission with excellent photoluminescence quantum yields (PLQY) of 81.1% because of the presence of energy transfer from self-trapped excitons to Er3+ ions. Excitingly, the ratio between the fluorescence intensity at 524 nm and 550 nm (FIR(I524 nm/I550 nm)) and the ratio between the fluorescence intensity at 524 and 456 nm (FIR(I524 nm/I456 nm)) both have a high correlation with temperature in the range of 298–473 K. The maximum of relative sensitivity values reach to 1.18%/K (I524 nm/I550 nm) and 1.19%/K (I524 nm/I456 nm) at 298 K, respectively. The outstanding temperature sensitivity suggests that the Sb3+,Er3+ co-doped Cs2NaYCl6 has enormous application potential in ratiometric optical thermometry.