High Luminescence Intensity Research Articles

Indexes for evaluation of dynamic characteristics of pressure-sensitive paint based on pressure sensitivity and frequency response

Two evaluation indexes were proposed to select the optimal PSP for unsteady pressure measurement from various PSPs with different pressure sensitivity and frequency response. An effective sensitivity coefficient calculated by pressure sensitivity and gain attenuation due to the response delay was proposed. Furthermore, an effective amount of intensity change was recommended, which takes into account the emission intensity and the effective sensitivity coefficient, because the magnitude of the intensity of a PSP is also important for unsteady-pressure measurement with high-speed sampling. A total of five types of PC-PSPs developed in previous studies were compared: two types of fast-response PC-PSPs using Pt(II) meso-tetra (pentafluorophenyl) porphine (PtTFPP) with poly(isobutyl methacrylate) (poly(IBM)) and ruthenium complex with RTV silicone, respectively, and three types of PC-PSPs using PtTFPP with poly[1-trimethylsilyl)-1-propyne] (poly(TMSP)). A comparison was made using the proposed evaluation indexes under various pressure ranges. The results shows that poly(TMSP)-based PC-PSP has a high effective sensitivity coefficient at pressures less than 20 kPa. On the other hand, poly(IBM)-based PC-PSP has the highest effective sensitivity coefficient at a pressure of 100 kPa. The effective amount of intensity change of poly(TMSP)-based PC-PSP is the highest at 2 kPa, but that of poly(IBM)-based PC-PSP is the highest at a pressure higher than 5 kPa among the evaluated PC-PSPs due to its high luminescence intensity. A PSP with high emission intensity will provide high performance in terms of fluctuation of emission intensity detected by the photodetector when the excitation intensity and the exposure time are limited due to limitations of optical equipment or high-speed sampling.

Effect of Sintering Time and Cl Doping Concentrations on Structural, Optical, and Luminescence Properties of ZnO Nanoparticles

Zinc oxide (ZnO) nanoparticles were synthesized hydrothermally using zinc acetate dihydrate and sodium thiosulfate pentahydrate precursors. The synthesized powders were sintered in air at 600 °C for different durations with a Cl-doping concentration of 25 mg/g. The optimal sintering time was found to be 5 h, resulting in the successful formation of the ZnO phase with small particle sizes of around 90 nm, nominal atomic fractions of Zn and O (~50%, ~50%), and increased luminescence intensity. The ideal concentration of Cl was discovered to be 25 mg/g of ZnO, which resulted in the highest luminescence intensity. The ZnO luminescence characteristics were observed in emission bands peaking at approximately 503 nm attributed to the transition from oxygen vacancies. A considerable improvement in the emission intensity was observed with increased Cl doping concentration, up to eight orders of magnitude, compared to pristine ZnO nanoparticles. However, the luminescence intensity decreased in samples with higher concentrations of Cl doping due to concentration quenching. These preliminary outcomes suggest that Cl-doped ZnO nanoparticles could be used for radiation detector development for radon monitoring and other related applications.

Shear Stress‐Triggered Theranostic Nanoparticles for Piezoelectric‐Fenton‐Photodynamic Thrombolysis and Endogenous Thrombus Imaging

AbstractThrombus therapy is challenged by potential bleeding risk of thrombolytic agents, and external irradiation is usually needed in thrombus imaging. Herein, highly efficient theranostic platforms are designed for piezoelectric‐Fenton‐photodynamic thrombolysis and endogenous thrombus imaging in response to the elevated shear stress at the thrombus site. Piezoelectric tetragonal barium titanate (tBT) nanoparticles (NPs) are coated with Fe3+‐coordinated metal‐organic frameworks (MOFs), followed by inoculation of chlorin e6‐luminol conjugates and heparin absorption to obtain theranostic tBT@MOFCL/Hep NPs. Shear stress‐induced piezopotential on NPs accelerates Fe3+/Fe2+ transformation to deplete MOF layers, activates Fenton reaction and produces reactive oxidative species (ROS) for non‐pharmacological thrombolysis. In the meantime, the site‐specific ROS generation oxidizes luminol and the chemiluminescent resonance energy transfer with chlorin e6 generates red fluorescence for thrombus imaging without using external light irradiation. After intravenous injection into a carotid artery thrombosis model, the heparin‐mediated thrombus targeting yields 6.5‐fold higher luminescent intensity at the thrombus site. Thrombi in the carotid arteries are almost completely dissolved with integration of piezoelectric dynamic therapy, piezopotential‐enhanced Fenton reaction, and chemiluminescence‐excited photodynamic therapy, while causing no haematologic and histopathologic abnormality. This study demonstrates a concise strategy to generate shear stress‐responsive built‐in piezoelectric potentials, site‐specific non‐pharmacological thrombolysis, self‐illuminating, and stenosis degree‐adaptable thrombus imaging.

New europium(III) methoxycinnamates complex: synthesis, thermal and luminescence properties

A method was proposed for the preparative synthesis of mixed-ligand Eu(III) compounds with para -methoxycinnamic acid, ligands from the sodium salt of para -methoxycinnamic acid. It was found that europium(III) methoxycinnamate with hexamethylphosphotriamide has the highest luminescence intensity. Luminescent polymer materials with synthesized europium(III) methoxycinnamates were obtained.

Fabrication and spectral performance of Ndx:(La0.05Lu0.05Gd0.05Y0.05)Ca0.8-xF2.2+x High-entropy transparent fluoride ceramics

In this study, Ndx:(La0.05Lu0.05Gd0.05Y0.05)Ca0.8-xF2.2+x (x = 0.0–0.012) high-entropy transparent ceramics were prepared by the vacuum hot pressing method. The crystal structure, microstructure, elemental distribution and spectral properties of Ndx:(La0.05Lu0.05Gd0.05Y0.05)Ca0.8-xF2.2+x, as well as the impact of Nd3+ content on these properties was systematically examined. The material demonstrates high optical transparency, achieving a maximum on-line transmittance of nearly 90 % at 1200 nm, which is very close to the theoretical CaF2 transmittance (92%–94 %). Porosity and grain size are identified as the primary scattering factors. The EDX analysis revealed that the prepared transparent ceramics exhibited a high level of density and uniform distribution of elements. The highest luminescence intensity is observed at a Nd3+ concentration of 1 at.%, the fluorescence lifetime decays relatively slowly with increasing concentration of doped Nd3+ ions.

Surface motifs regulated aggregation induced emission in AuAg nanoclusters combined with Ce(III)/Ce(IV) catalytic cyclic amplification strategy for sensitive bioanalysis

Achieving high luminescence intensity in electrochemiluminescence biosensors is a challenge for metal nanoclusters (MNCs) due to their non-radiative relaxation-mediated self-quenching tendency. Here, the surface motifs [M(I)-SR] of MNCs were regulated based on aggregation-induced emission (AIE) strategy was proposed to mitigate non-radiative relaxation vibrations, and an efficient luminescent AuAg NCs was designed via host-guest assembly as a signal probe. The Au(I)-SR of AuAg NCs used glutathione (GSH) as a template and reducing agent, and the introduction of Ag(I) made the Au(I)-SR of AuAg NCs cross-linked and interlocked, resulting in AuAg NCs with denser surface patterns. The aggregation of surface motifs limited the ligand movement to reduce the non-radiative energy dissipation. Furthermore, the spontaneous catalytic cycle amplification strategy of Ce(III)/Ce(IV) redox pairs in the matrix material of Ce-MOF promoted the reaction of more co-reactants triethylamine (TEA), obtaining potent reducing radicals TEA* for further improving the ECL efficiency of AuAg NCs. Using cardiac troponin I (cTnI) as the analytical model, the biosensor exhibited a wide linear relationship range (50 fg·mL−1 - 500 ng·mL−1) and a low detection limit (4.77 fg·mL−1). The breakthrough in surface motifs regulation of MNCs guides a new way to design high luminiferous MNCs, and further expands the application potential of MNCs.

Efficient broadband yellow-emitting Mg2.5Lu1.5Al1.5Si2.5O12:Ce3+ garnet phosphors for blue-light-pumped white light-emitting diodes

The discovery of yellow-emitting phosphors with higher luminescence intensity and wider bandwidth than the commercial Y3Al5O12:Ce3+ (YAG:Ce3+) phosphor upon blue light excitation remains one of the significant challenges for establishing human-centered warm white light-emitting diode towards high-performance illumination. Herein, we innovatively synthesized a novel Ce3+-activated broadband yellow-emitting garnet phosphor of Mg2.5Lu1.5Al1.5Si2.5O12:Ce3+ (MLASO:Ce3+) via conventional high-temperature solid-state reaction method. The as-prepared MLASO:10%Ce3+ garnet sample possesses a cubic structure with Ia3‾d space group and lattice parameters of a = b = c = 11.85098 Å and V = 1664.421(0.044) Å3. Luminescence spectroscopy tests indicates that the optimal MLASO:10%Ce3+ yellow-emitting phosphor features 1.2 times higher relative integral luminescence intensity and an impressive full width at half maximum (FWHM) of up to 145 nm with respect to the most extensively available commercial YAG:Ce3+ phosphor (FWHM = 122 nm) under the identical blue light irradiation, which can provide more red-components for improving color rendering index. Additionally, the CIE color coordinates and a satisfactory internal quantum efficiency are determined to be (0.4751,0.5028) and 74%, respectively. More importantly, the representative optimal sample can preserve 77% luminescence emission intensity at a 423 K high temperature thermal treatment environment compared to the ambient temperature. As a result, this study sheds light on newly discovered broadband yellow-emitting MLASO:10%Ce3+ garnet phosphor containing more of the red chromatic spectrum can sever as one of the promising color-conversion-materials in high-performance white LEDs with high color rendering index for healthy solid-state lighting.

A mechanoluminescent material, ZnS:Mn,Li, with enhanced brightness for visualizing dental occlusion.

Mechanoluminescent materials are characterized by high luminescence intensity, high repeatability, no external voltage activation, and a good linear relationship between stress and mechanoluminescence intensity within a certain range. Therefore, mechanoluminescent materials have attracted increasing attention from researchers in the fields of stress sensing, encryption and anti-counterfeiting, structural health monitoring, energy-saving lighting, intelligent wearable devices, and other fields. In this study, ZnS:Mn powders with different Mn2+ ratios and different ion doping were synthesized by a high-temperature solid-phase reaction, and the synthesis of various materials was characterized. Then, the optimal mechanoluminescence effect of the ZnS:1%Mn,1%Li materialwas obtained. The photoluminescence intensity of ZnS:1%Mn,1%Li was 16.7 times higher than that of the sample without doping with Li+, and the mechanoluminescence intensity was 1.64 times higher. Finally, polyethylene terephthalate (PET) film was combined with ZnS:Mn,Li mechanoluminescent powders to prepare flexible three-layer composite film. Based on this, a feasible strategy for the detection of temporomandibular disorders was proposed. The composite film is easy to use, economical, and safe, and has good mechanoluminescent performance, which has potential application value in the field of occlusal force detection and visualization.

Internalization of Pegylated Er:Y2O3 Nanoparticles inside HCT-116 Cancer Cells: Implications for Imaging and Drug Delivery.

Lanthanide-doped nanoparticles, featuring sharp emission peaks with narrow bandwidth, exhibit high downconversion luminescence intensity, making them highly valuable in the fields of bioimaging and drug delivery. High-crystallinity Y2O3 nanoparticles (NPs) doped with Er3+ ions were functionalized by using a pegylation procedure to confer water solubility and biocompatibility. The NPs were thoroughly characterized using transmission electron microscopy (TEM), inductively coupled plasma mass spectrometry (ICP-MS), and photoluminescence measurements. The pegylated nanoparticles were studied both from a toxicological perspective and to demonstrate their internalization within HCT-116 cancer cells. Cell viability tests allowed for the identification of the "optimal" concentration, which yields a detectable fluorescence signal without being toxic to the cells. The internalization process was investigated using a combined approach involving confocal microscopy and ICP-MS. The obtained data clearly indicate the efficient internalization of NPs into the cells with emission intensity showing a strong correlation with the concentrations of nanoparticles delivered to the cells. Overall, this research contributes significantly to the fields of nanotechnology and biomedical research, with noteworthy implications for imaging and drug delivery applications.

ZnGa2O4 : Cr3+@Calcium Phosphate Nanocomposite with Near‐Infrared Persistent Luminescence and High Stability

AbstractPersistent luminescence (PersL) is an optical phenomenon which allows for materials to emit luminescence after ceasing excitation. The long‐lasting luminescence is ascribed to the presence of trap states, which can be exploited through the introduction of various dopants and post‐synthesis treatment. In this study, ZnGa2O4 : Cr3+ (CZGO), one of the most widely investigated near‐infrared‐emitting PersL materials, is synthesized in the form of nanoparticles, and incorporated into amorphous calcium phosphate (ACP) to form a luminescent nanocomposite with drug attachment potential. The effects of annealing CZGO in the composite are comparatively studied alongside the composite that contains unannealed CZGO. We find that ACP with annealed CZGO exhibits much higher luminescence intensity and longer PersL duration. The formation of the nanocomposite also results in the redistribution of Zn, and its influence on the composite luminescence intensity and the long‐term chemical stability are investigated.

Study on preparation, optical properties and mechanism of Zn2SnO4:Cr3+ with high NIR luminescence intensity

In this work, Zn2SnO4:xCr3+ with high near-infrared luminescence intensity (broad emission centered at 800 nm and sharp emission at 703 nm) were successfully prepared by high temperature solid state method. Measurements indicated that the samples exhibited obvious photoluminescence as well as persistent luminescence properties. The results of X-ray diffraction indicated that high temperature facilitated the entry of Cr3+ into the Zn2SnO4 crystal lattice and formed replacement doping and promoted the luminescence efficiency of the samples. And, under the condition of 1450 °C and 0.002 at% Cr3+ concentration, sample with optimum NIR fluorescence properties was prepared. In the high-temperature sintering process, many defects of Zn2SnO4 were generated, which effectively promoted the formation of vacancies. The energy levels of these lattice defects (trap energy levels) facilitated the sub-stable trapping of electrons and produce afterglow properties. Analysis of luminescence mechanism reveals that the broad emission band centered at 800 nm and the sharp emission peak at 703 nm were derived from the energy level transitions of 4T2(4F)→4A2 and 2E→4A2 of Cr3+, respectively. Though, the long afterglow luminescence duration of Zn2SnO4:Cr3+ needs to be further improved compared with gallate-based NIR phosphors, Zn2SnO4:Cr3+ do have a promising application in bio-imaging due to its special NIR emission range.

Study on the structure and luminescence properties of a novel Li3Sc2(PO4)3: Eu3+ orange-red emission phosphor for wLEDs

The manufacture of high-efficiency and stable red phosphor is the key to solve the matter of high color temperature and poor color rendering of commercial white light-emitting diodes (wLEDs). In this work, a series of Li3Sc2-x(PO4)3: xEu3+ (x = 0–0.4) phosphor samples were prepared by conventional solid-phase reaction. The structure and optical properties of Li3Sc2(PO4)3: Eu3+ are investigated. When the doping amount of Eu3+ is 0.3 mol, phosphors have the highest luminescence intensity. The temperature-dependent characteristics of the prepared phosphors are studied. The combined emission intensity at 423K is 77.4% of that at 298K, showing significant thermal stability. Finally, the prepared Li3Sc2(PO4)3 phosphor package is tested in the LED device. The results of the color temperature of 5423K, as well as color rendering index (CRI) (Ra = 81.6) and color coordinate CIE (0.3343, 0.3471), are satisfactory, suggesting that this red phosphor has potential for wLEDs applications.

Light Inorganic Scintillation Materials for Neutron and Charge Particle Detection

The technological aspects of the light inorganic crystalline compounds suitable to create scintillation materials to detect charged particles and neutrons in a wide energy range have been examined. Among them, Li2CaSiO4:Eu was found to be a prospective candidate to control the valent state of the Rare Earth (RE) and to provide a high intensity of luminescence. It was demonstrated that the material has room for future improvement; however, this requires precise engineering of its composition—an experimental search of compositions or additives that will provide the maximum Eu2+/Eu3+ ratio to achieve a high scintillation light yield. The benefits of light inorganic materials are disclosed through the modeling of the linear density of nonequilibrium carriers along secondary particle tracks created in scintillators utilized for neutron detection. It is shown that oxide matrices have a larger linear density in comparison with halide crystalline compounds under alpha-particles and tritons, whereas light oxides can provide smaller numbers under protons.

Fluorescence signal from carbon quantum dots synthesized from natural resources

The present work deals with synthesis of carbon quantum dots (CQDs) from some easily available organic resources as urea and citric acid. The heating of these precursors leads to formation of strong photoluminescent carbon quantum dots (CQDs). The characteristics of prepared CQDs have been analyzed by UV–Vis absorption, fluorescence and FTIR spectroscopy. The average size of synthesized CQDs obtained was 6.8 nm which was further verified with FESEM image analysis. The band gap of 3.15 eV have been estimated for the synthesized CQDs from absorption data. The appearance of high intense luminescence emission validates CQDs’ strong candidature as promising sensors for today’s optoelectronic and biomedical industries.

Microwave-assisted synthesis of GdOF: Eu3+/Tb3+ ultrafine phosphor powders suitable for advanced forensic and security ink applications

The rare-earth-doped inorganic ultrafine oxyfluoride host matrices in forensic science, especially in latent fingerprint detection and anti‐counterfeiting applications, were still unexplored and may replace the existing technology owing to its high sensitivity. Herein, GdOF: Eu3+/Tb3+ ultrafine red and green phosphors were synthesized via a rapid, green microwave-assisted hydrothermal method at 150 °C. The phosphors synthesized by this novel method possess good luminescent intensity for the hypersensitive 5D0→7F2 transition of Eu3+ and 5D4→7F5 transition of Tb3+ ions as compared to the phosphors prepared via other conventional methods such as co-precipitation synthesis, sol–gel synthesis, and microwave-assisted co-precipitation synthesis. Further, an enhancement in the luminescent intensity of the ultrafine phosphor was noticed when the microwave parameters and pH values were tuned. The optimized red and green phosphors having high luminescence intensity, good color purity, and high quantum yields of 89.3%, and 71.2%, respectively, were used for the visualization of latent fingerprints on various substrates. These promising phosphors exhibited excellent visualization regardless of the background interference and limit the risk of duplication and are highly reliable. The security inks developed using these phosphors are highly efficient for anti-counterfeiting applications. These multifunctional properties of investigated phosphors can be explored for security applications.

Highly stable multi-encapsulated red-emitting cesium lead halide nanocrystals for efficient copper ion detection and imaging in live cells

Recently, cesium lead halide (CsPbX3: X = Cl, Br, I) perovskite nanocrystals (NCs) have shown potentiality in the detection of different heavy metal ions and bioimaging applications for their smaller particle size, tunable emission spectra, high luminescent intensity, narrow emission spectra, multiphoton absorption property, etc. CsPbBr3 NCs are explored extensively in bioimaging applications for their comparatively higher stability in water. A longer wavelength excitation light source is recommended due to less scattering of light results in deeper penetration in living cells. However, imaging in live cells with red-emitting perovskite NCs is not suitable because of their poor structural stability, low emission intensity, and complex synthesis process. To tackle these issues, we introduce a specific halide exchange to the NCs and then multi-encapsulation shelling techniques that eventually improve the structural and environmental stability of the red-emitting NCs. Here, we synthesized Zn-doped CsPbBr3 NCs via the ligand-assisted reprecipitation (LARP) synthesis method in an open atmosphere. Then the highly luminescent red emitting CsPbBrxI3−x NCs with Zn doping were grown via the exchange of halide ions from pre-synthesized Zn-doped CsPbBr3 NCs to maintain the stable perovskite crystal structure in the nanoscale regime. Such NCs were further encapsulated with different shelling materials and then compared their photophysical properties. Among them, n-isopropyl acrylamide passivated Zn-doped CsPbBrxI3−x/SiO2/polyvinylpyrrolidone core/shell/shell NCs showed the highest stability against water and UV-irradiation. These NCs efficiently detect Cu2+-ions in water and achieved a detection limit of around 9.68 µM. The NCs were also tested for their compatibility as a fluorescent probe for live cell imaging using mammalian Chinese Hamster Ovary cells. As a proof-of-principle, we demonstrate both the efficient uptake and biocompatibility of the perovskite NCs. This work provides insight for expanding research activities on red-emitting perovskite NCs by developing a new strategy to improve the stability of the NCs, which is beneficial for both cost-effective bioimaging applications and heavy metal ion detection in water.

Growth phase diagram and X-ray excited luminescence properties of NaLuF4:Tb3+ nanoparticles

X-rays are energy sources exhibiting extended penetration depths, and they have attracted increasing attention in industry and for clinical application. With the rapid development of nanomaterials and X-ray excited luminescent nanoparticles (XLNPs), new modalities for bioimaging and cancer therapy have been developed, such as X-ray luminescent computed tomography (XLCT) and X-ray excited photodynamic therapy (X-PDT). To meet the requirements of biomedical applications, XLNPs must exhibit high luminescence intensities, appropriate size distributions (less than100 nm) and negligible cytotoxicity. Due to the optical properties associated with f-electrons, rear earth (RE) elements are highly suitable for creating XLNPs. NaREF4 nanoparticles (NPs) have been shown to be suitable hosts with high luminescence intensities, controllable sizes, and biocompatibility for X-ray-based biomedical applications. Syntheses of NaLuF4 NPs doped with rare earth elements for upconversion applications have been systematically studied. However, for X-ray excited applications, the doping levels of the NPs must be totally different, which greatly affects the morphologies and sizes of the NaLuF4 NPs. Thus, in this paper, nucleation, phase transitions, morphologies and sizes, and luminescence properties of Tb3+-doped NaLuF4 NPs were systematically studied. OA-capped NaLuF4:Tb3+ NPs were synthesized via coprecipitation processes with different reaction temperatures and reaction times to study the nucleation mechanism systematically, and the morphologies, size distributions and crystal phases were characterized with TEM and XRD. The morphologies, size distributions and crystal phases of these NPs were seriously influenced by the reaction temperature and reaction time. At 295 ℃, the NP sizes increased with prolonged reaction time, and the crystalline phase was a mixture of cubic and hexagonal phases. At 300 ℃ and 310 ℃, the pure hexagonal phase was obtained after 20 min and 35 min reaction times, respectively. The luminescence strengths of these NPs were associated with the particle sizes, crystalline phases, and Tb3+ doping levels. Stronger luminescence was achieved with larger particle sizes and purer hexagonal crystal phases. In addition, the 15 % doping level for Tb3+ provided the maximum luminescence intensity. The present work provides insights into the mechanism of NaLuF4:Tb3+ nanocrystal growth.

Surface Modification Strategy Synthesized CsPbX3 Perovskite Quantum Dots with Excellent Stability and Optical Properties in Water

AbstractThe poor stability of CsPbX3 (X = Cl, Br, I) perovskite quantum dots (PQDs) in polar solvents such as water, seriously hinders their practical application. Herein, 5‐Bromovaleric acid (BVA) is used to replace oleic acid (OA), the most common surface ligand in CsPbX3 PQDs synthesis. Under the synergic action of oleylamine (OLA), CsPbX3 PQDs with high water stability can be synthesized directly in water. Because the carboxyl ligands provided by BVA, and the long chain amines provided by OLA formed hydrophobic shells on the surface of CsPbBr3 PQDs, the obtained CsPbBr3 PQDs still has high luminescence intensity and photoluminescence quantum yield after being dispersed in water for several days, and the luminescence peak is always maintained at 518 nm. In contrast, the luminescence intensity of CsPbBr3 PQDs synthesized with OA and OLA is <1% of the initial intensity after only 30 min. CsPbCl3 and CsPbI3 PQDs synthesized directly in water by this method also show high water stability. In this study, for the first time the synthesis method of CsPbX3 PQDs with high water stability using BVA/OLA as surface ligands is proposed, which provides an effective way to explore the synthesis of PQDs that can maintain stability in water.

Fourier-transform infrared photoreflectance spectroscopy of the InSb/InAs/In(Ga,Al)As/GaAs metamorphic heterostructures with a superlattice waveguide

Fourier-transform infrared photoreflectance (PR) spectroscopy was used to study the energy spectrum of InSb/InAs/In(Ga,Al)As/GaAs metamorphic heterostructures with a superlattice waveguide at room temperature (RT). Theoretical calculations in the framework of the eight-band Kane model were performed to obtain a reliable knowledge of the actual energies of the most probable optical transitions. The experimental results were analyzed to determine the influence of the design features and stress balance on the energy spectra of the structures. Photoluminescence studies performed at 11 K and RT, as well as the determination of the internal quantum efficiency of luminescence, enabled us to characterize the emission characteristics of the structures, regardless of their waveguide efficiency. The structure with a 5-nm-thick GaAs insertion within the metamorphic buffer layer exhibited the highest probability of the main optical transition observed in the PR spectra as well as the highest luminescence intensity and quantum efficiency.

Development and Application of Ruthenium(II) and Iridium(III) Based Complexes for Anion Sensing.

Improvements in the design of receptors for the detection and quantification of anions are desirable and ongoing in the field of anion chemistry, and remarkable progress has been made in this direction. In this regard, the development of luminescent chemosensors for sensing anions is an imperative and demanding sub-area in supramolecular chemistry. This decade, in particular, witnessed advancements in chemosensors based on ruthenium and iridium complexes for anion sensing by virtue of their modular synthesis and rich chemical and photophysical properties, such as visible excitation wavelength, high quantum efficiency, high luminescence intensity, long lifetimes of phosphorescence, and large Stokes shifts, etc. Thus, this review aims to summarize the recent advances in the development of ruthenium(II) and iridium(III)-based complexes for their application as luminescent chemosensors for anion sensing. In addition, the focus was devoted to designing aspects of polypyridyl complexes of these two transition metals with different recognition motifs, which upon interacting with different inorganic anions, produces desirable quantifiable outputs.