Intense Green Luminescence Research Articles

Analysis of the reasons for the enhanced green luminescence of Mg2+-doped Zn2SiO4:Mn2+ phosphor

In the present work, the role of the optically inactive co-dopant magnesium in increasing the emission intensity of Zn2SiO4:Mn2+ has been established. It is shown that the dominant reasons for the increase in green luminescence intensity are the enhancement in the prohibition of the 4T2(4G) → 6A1(6S) transition and the decrease in non-radiative dissipation of absorbed excitation energy upon the introduction of Mg2+ ions.

Effect of surfactants on the luminescence, bonding, and catalytic properties of CaWO4 spheres

BackgroundThis work focuses on improving the luminescence and catalytic properties of CaWO4 spheres by manipulating their electron density distribution. The goal is to enhance their suitability for optoelectronic applications and to increase their efficiency in degrading the industrial dye methylene blue (MB). The study utilizes a co-precipitation technique and the addition of three surfactants to synthesize phase-pure CaWO4 with a tetragonal crystal structure. MethodsThe synthesis involved a co-precipitation technique with simultaneous addition of three surfactants. Extensive characterization employed various analytical and spectroscopic methods to assess structural, morphological, luminescent, and catalytic properties. Particularly, the use of cetyltrimethylammonium bromide (CTAB) surfactant induced intense green emission around 500 nm attributed to luminescent center WO42−. Solar irradiation evaluated catalytic performance, with CaWO4: CTAB degrading methylene blue remarkably in just 40 min under natural sunlight. Significant FindingsThe research yielded a CaWO4 material, particularly when assisted by the CTAB surfactant, exhibiting intense green luminescence, making it promising for optoelectronic applications. Furthermore, this material demonstrated remarkable catalytic performance in degrading methylene blue under solar irradiation, suggesting its potential in environmental remediation. The study also delved into electron density distribution by examining differences in bond lengths and mid-bond electron density within a single unit cell, shedding light on the material's underlying properties.

Crystal Growth of Quaternary AkRE2Si2S8 (Ak = Ca and Sr; RE = La-Tb) Thiosilicates Using Flux-Assisted Boron Chalcogen Mixture Method: Exploring X-ray Scintillation, Luminescence, and Magnetic Properties.

We report on the detailed structural analysis of a series of 11 new quaternary rare earths containing thiosilicates, AkRE2Si2S8 (Ak = Ca and Sr; RE = La, Ce, Pr, Nd, Sm, Gd, and Tb), synthesized using the flux-assisted boron chalcogen mixture method. High quality crystals were grown and used to determine their crystal structures by single crystal X-ray diffraction. All members of the AkRE2Si2S8 series crystallize in the trigonal crystal system with space group R3̅c (space group no. 167). Polycrystalline powders were used for physical property measurements, including magnetic susceptibility, diffuse reflectance in the UV-visible range, and scintillation. Magnetic measurements indicated that CaRE2Si2S8 (RE = Nd and Tb) exhibits paramagnetic behavior with a slightly negative Weiss constant. The band gaps of the materials were determined from diffuse reflectance data, and optical band gaps were estimated to be 2.5(1) and 2.9(1) eV for CaCe2Si2S8 and CaGd2Si2S8, respectively. CaCe2Si2S8, CaTb2Si2S8, and SrCe2Si2S8 exhibited intense green luminescence upon irradiation with 375 nm ultraviolet light and, furthermore, scintillated when exposed to X-rays. Radioluminescence measurements of CaCe2Si2S8 powder revealed green emission with an intensity approximately 14% of that emitted by bismuth germanium oxide powder.

Cation Occupation Engineering Realizes Valence Modulation of Manganese-Activated ZnGa2O4.

Herein, a series of Mn-activated ZnGa2O4 (ZGO) phosphors have been developed for multifunctional applications. The characteristic green and red emission at 503 and 668 nm of Mn-activated ZGO phosphors can be observed under excitation of 247 and 375 nm, respectively, attributed to the partial oxidation of Mn2+ ions resulting in the coexistence of Mn2+ and Mn4+ ions in the host lattice. The valence modulation of Mn content not only realizes the adjustment of red and green luminescence intensity but also achieves the management of persistent luminescence time and thermo-luminescence time. Further, the codoping of Mg2+ could transform the position occupancy preference of Mn and effectively facilitate the conversion of Mn2+ to Mn4+, leading to the regulation of the valence state of manganese ions. Surprisingly, the existence of Mg2+ ions broadens the emission band of Mn4+ and enhances the photoluminescence intensity to 3.8 times, which can be ascribed to the weakened crystal field leading to the downward shift of the 4T2 energy level and the increase of Mn4+ concentration. For this valence modulation behavior, two different hypotheses about the occupancy of Mg2+ have been proposed to explain the corresponding phenomenon. Finally, the potential applications of the synthesized phosphors have been explored in advanced anticounterfeiting strategies, information storage, and plant lighting field.

Significantly enhanced upconversion luminescence intensity and tailorable chromaticity of Sn4+-doped NaYF4:Yb3+/Er3+

The internal modification with rare earth ion doping proved to be a very effective strategy for improving the luminescent properties of NaYF4-based upconversion materials. However, greatly enhancing the luminescence efficiency of NaYF4:Yb3+/Er3+ remains a major challenge. Herein, the effects of Sn4+ doping on the structure and luminescent performance of such material were explored. The hydrothermal molten-salt method was applied to synthesize the Sn4+-doped NaYF4:Yb3+/Er3+ upconversion materials, and their crystal structures, morphologies, surface chemical composition and element states, and luminescence performance were characterized. It was found that Sn4+ doping can significantly enhance the luminescence intensity and tailor the chromaticity of NaYF4:Yb3+/Er3+. In particular, the green (G) and red (R) luminescence intensity levels of the 30 mol% Sn4+ doped material were increased by factors of 26.97 and 38.91, respectively. The R/G ratio was incremented from 0.34 for the undoped material to 0.83 for the 40 mol% Sn4+ doped counterpart. The Sn4+ doping led to the change of lattice distortion and crystal growth pattern of NaYF4:Yb3+/Er3+. The mechanism for Sn4+ doping to affect the luminescence properties of the prepared upconversion material was also explored. The changes in luminescence intensity levels and R/G ratios could be attributed to the highly asymmetric distorted lattice and crystal field resulting from Sn4+ doping.

Extremely intense pure green upconversion luminescence in Ho3+/Yb3+ co-doped BiTa7O19 phosphors under 980 nm laser excitation

Extremely intense pure green upconversion luminescence in Ho3+/Yb3+ co-doped BiTa7O19 phosphors under 980 nm laser excitation

Versatile luminescence thermometry via intense green defect emission from an infrared-pumped fluorosilicate optical fiber

An all-glass optical fiber capable of two distinct methods of optical thermometry is described. Specifically, a silica-clad, barium fluorosilicate glass core fiber, when pumped in the infrared, exhibits visibly intense green defect luminescence whose intensity and upper-state lifetime are strong functions of temperature. Intensity-based optical thermometry over the range from 25°C to 130°C is demonstrated, while a lifetime-based temperature sensitivity is shown from 25°C to 100°C. Time-domain measurements yield a relative sensitivity of 2.85%K−1 at 373 K (100°C). A proof-of-concept distributed sensor system using a commercial digital single-lens reflex camera is presented, resulting in a measured maximum relative sensitivity of 1.13%K−1 at 368 K (95°C). The sensing system described herein stands as a new blueprint for defect-based luminescence thermometry that takes advantage of pre-existing and relatively inexpensive optical components, and allows for the use of standard cameras or simply direct human observation.

Synthesis and Properties of Eu and Ni Co-Doped ZnS Nanoparticles for the Detection of Ammonia Gas

Zinc sulfide nanoparticles were synthesized successfully via chemical co-precipitation, both in undoped form and co-doped with Europium (Eu) and Nickel (Ni). All prepared samples exhibited cubic zinc blende structure as confirmed by X-ray diffraction (XRD). The average particle size ranged from 3 to 6 nm for both pure and (Eu, Ni) co-doped ZnS, with no alteration in the crystal structure due to Eu and Ni co-doping. However, increasing the Ni dopant concentration (0, 2, 4, & 6 at%) while maintaining a constant Eu concentration (4 at%) led to an enhancement in the crystallite size. This was further validated by transmission electron microscopy (TEM), which showed particle sizes consistent with the XRD findings (3–5 nm). Microscopic analysis via scanning electron microscopy and TEM revealed spherical agglomerated morphology for the (Eu, Ni) co-doped nanoparticles. Energy-dispersive X-ray spectroscopy spectra confirmed the stoichiometric chemical composition of ZnS: Eu, Ni. Photoluminescence studies demonstrated an increased intensity of green luminescence at 6 at% Ni co-dopant concentration. Moreover, the synthesized samples exhibited promising gas sensing properties, particularly towards ammonia gas, with good selectivity. Notably, both pure and (Eu, Ni) co-doped ZnS nanoparticles showed rapid response and recovery times at room temperature, suggesting their potential applicability in gas sensing applications.

Highly Emissive and Robust Cd-Based MOF with an Unprecedented Topology for Tetracycline Sensing.

Herein, an unprecedented cadmium-based metal-organic framework (JNU-106) fabricated by utilizing pyrazole-functionalized tetraphenylethylene ligands (Py-TPE) and rod-shaped secondary building units is reported, possessing a new (3,3,3,6,6,8)-connected topological network. Thanks to the ingeniously designed intramolecular charge transfer behavior, which originates from the congruent coplanarity between Py and TPE, JNU-106 exhibits intense green luminescence with a quantum yield increased by 1.5 times. The phenomenon of remarkable fluorescence quenching of JNU-106 reveals that it possesses extremely high anti-interference performance, superior sensitivity, and dedicated selectivity toward tetracycline antibiotics (TCAs) in aqueous solutions, which are comparable to those of the state-of-the-art porous sensing compounds. Taking the theoretical calculations and experimental results into account, the luminescence quenching is mainly attributed to the internal filtration effect and the static quenching effect. Considering the portable and rapid performance of JNU-106-based testing strips for sensing TCAs, the fabricated JNU-106 provides an alternative for ecological monitoring and environmental governance.

High quenching concentration of the CaLuAlO4:Er3+ upconversion phosphor with short-range energy migration

Low activator concentration in upconversion phosphors has been a hindrance in improving luminescence performance. Herein, we report an Er3+ doping concentration as high as 30 at. % in the CaLuAlO4 upconversion host. The CaLuAlO4:Er3+ phosphors were prepared by the traditional high-temperature solid-state method. Under the excitation of a 980 nm laser, the optimal concentration of Er3+ approaches 30% according to the total integrated intensity of red and green upconversion luminescence. This quenching concentration is one order of magnitude higher than that in the traditional Er3+ doped upconversion polycrystals. The results obtained from first-principles calculations suggest that there are no in-plane or chain rare-earth ions in the cell. This increases the difficulty of propagating excitation energy to quench centers and is advantageous for high doping concentration. Our work can spark people's interest in the research and application of highly doped upconversion phosphors.

Dual-drive acoustic micromixer for rapid nucleation and ultrafast growth of perovskite nanoparticles.

All-inorganic cesium lead halide perovskites have garnered significant attention owing to their favorable optical properties. Microfluidics-based acoustic mixers are capable of achieving rapid nucleation and ultrafast growth kinetics. Nevertheless, conventional acoustic mixers rely on the response of microstructures to the acoustic field for mixing fluids, the majority of these disturbances occur in the central region of the channel, with minimal impact on the fluid within the side walls. This paper proposes a novel acoustic mixer that combines the effects of sharp corners and bubbles in response to the acoustic field, thereby producing effective disturbance of the fluid throughout the channel. The combined effect enables the micromixer to achieve complete mixing at different inlet flow ratios with mixing times as low as 5 ms. The superiority of acoustic mixers in controlling the nanocrystal formation stage was further validated through the synthesis of chalcogenide nanocrystals using the LARP method. The millisecond mixing time facilitated the rapid formation of nanocrystals and their subsequent rapid growth. The results demonstrate that the green luminescence intensity at 520 nm of the samples synthesized using the acoustic micromixer is 118% higher than that of the samples synthesized using an intermittent reactor. The novel micromixer broadens the range of applications and offers a promising avenue for the large-scale continuous synthesis of high-quality lead-halide perovskite nanocrystals (NCs).

Low-dose X-ray stimulated NO-releasing nanocomposites for closed-loop dual-mode cancer therapy.

X-ray-excited photodynamic therapy (X-PDT) employs X-rays as an energy source, overcoming the light penetration limitations of traditional photodynamic therapy (PDT) but is constrained by high-energy radiation and the hypoxic tumor microenvironment. Low-dose X-ray-excited photodynamic therapy and reduction of mitochondrial oxygen consumption can serve as significant breakthroughs in overcoming these barriers. In this study, NaLuF4:Tb/Gd (15%/5%)@NaYF4 (ScNP) nanoparticles adsorbing the photosensitizer MC540 and loaded with α-(nitrate ester) acid (NEAA) were prepared as low X-ray dose triggered nano-scintillators. The final product obtained was NaLuF4:Tb/Gd (15%/5%)@NaYF4@mSiO2@MC540@NEAA (ScNP-MS@MC540@NEAA) nanocomposites, which exhibited intense green luminescence. X-PDT generates cytotoxic reactive oxygen species (ROS) with minimal ionizing radiation damage. Simultaneously, NEAA reacts with glutathione (GSH) to generate nitric oxide (NO) for gaseous treatment of the damaged mitochondrial respiratory chain to reduce oxygen consumption and alleviate hypoxia, enhancing the X-PDT efficacy and realizing a closed-loop treatment. The superoxide ions (˙O2-) can rapidly react with NO produced to form the highly cytotoxic reactive nitrogen species (RNS) peroxynitrite anion (ONOO-), which exhibits higher cytotoxicity compared to ROS. Furthermore, GSH scavenges toxic ROS and maintains the physiological function of tumor cells. It can induce cancer cell overoxidation and nitrosative stress. This work describes a low-dose X-ray-triggered X-PDT system with total radiation of 50 mGy, which involves GSH consumption, self-supplied NO, mitochondrial damage alleviation, and hypoxia relief to generate ROS and RNS, forming a closed-loop anti-hypoxia dual-mode system with synergistically enhanced anti-tumor effects, without significant biological side effects. It provides a promising platform for deep-seated tumor X-PDT with considerable application prospects.

UP-CONVERSION LUMINESCENCE IN TbAl3(BO3)4:Yb3+ SYNTESIZED BY SOLUTION COMBUSTION METHOD

Phase pure Tb1-xYbxAl3(BO3)4 (x=0-1) crystalline powders were prepared by the combustion synthesis method. Down-conversion experiments under UV excitation of 375 nm revealed optimal concentration of Yb x=0.5 providing intensive green luminescence with 24% of quantum efficiency. Also up-conversion luminescence via energy transfer from Yb3+ to Tb3+ using a low power IR diode laser operating at 980 nm was achieved. Here the most powerful green emission was obtained with x=0.1.

Highly Luminescent Rb-Doped Cs4PbBr6 Nanocrystals in Borogermanate Glass

For the first time, the synthesis, luminescent and structural properties of stable perovskite-type (Cs1−xRbx)4PbBr6 (R = Cs, Rb) nanocrystals are shown. In the absence of rubidium, Cs4PbBr6 and CsPbBr3 perovskite crystals precipitate in the ZnO–Na2O–B2O3–GeO2 glass matrix. With ascending rubidium content, the precipitation of (Cs,Rb)4PbBr6 nanocrystals is replaced by the Rb4PbBr6 nanocrystals nucleation. Nucleated nanocrystals exhibit an intense green luminescence. With an increase of the rubidium content, the luminescence maximum shifts to the blue region, the luminescence quantum yield increases from 28 to 51%, and the average decay time increases from 2 to 8 ns. Several assumptions have been made about the nature of the green luminescence of perovskite-like Cs4PbBr6 and (Cs,Rb)4PbBr6 crystals in glasses. It is concluded that the most probable cause is the impurity inclusions of CsPbBr3 and (Cs,Rb)PbBr3 crystals.

Green emission characteristics of Er3+ -doped TeO2-WO3-GeO2 glasses through up and down conversion processes

Different concentrations of Er3+ions doped TeO2-WO3-GeO2 transparent oxyfluoride glassy materials were fabricated by conventional melt quench method and analyzed through X-ray diffraction, Fourier Transform infrared, scanning electron microscope and energy dispersive X-ray, photoluminescence-excitation, visible emission and luminescence decay studies. Various physical, structural, spectroscopic and laser characteristic parameters were evaluated following the Judd-Ofelt theory. The studied glasses were capable of emitting intense green luminescence through (2H11/2,4S3/2) → 4I15/2 transitions. The emission of green luminescence was studied through down-conversion process at 377 nm excitation and up-conversion process at 980 nm excitation. The color coordinates were found to fall in the green region of chromaticity diagram and close to the European Broadcosting Union green illuminant. The evaluated branching ratio, stimulated emission cross-section, gain linewidth, figure of merit and the quantum efficiency corresponding to 4S3/2 → 4I15/2 transition suggests that the studied glasses find wide suitability to design green emitting solid state lighting devices.

Energy Transfer in Dy3+ and Tb3+ Double-Doped Barium Borate Glass

In this work, single- and double-doped Dy3+ and Tb3+ barium borate glasses are investigated for their potential as light converters. The density and the absorption coefficient show linearly increasing trends with an increasing lanthanide content. The external quantum efficiency of the double-doped samples is a combination of the respective single-doped samples. The strong energy transfer from Dy3+ to Tb3+ results in an intense Tb3+-related emission, i.e., an intense green luminescence. Thus, excitation at a Dy3+-related wavelength of 452 nm enables a Tb3+-related emission, at which a single-doped Tb3+ sample barely shows any luminescence. Lifetime measurements show that there is not only an energy transfer from Dy3+ to Tb3+, but also vice versa.

Experimental optimization design synthesis and up-conversion luminescence properties of YNbO4:Ho3+/Yb3+

In order to obtain the maximum green up-conversion luminescence intensity of Ho3+/Yb3+ co-doped YNbO4, a uniform design and a quadratic general rotation combination design were applied to optimize the doping concentration. The concentration of the rare earth corresponding to the strongest green luminescence intensity was determined to be 10% Ho3+/34.9% Yb3+. Maximum luminous intensity of green light tested under 980 nm excitation was 157373.266, which was close to the theoretical calculated integral intensity value of 157290.825. The variation of the up-conversion luminescence spectra at different power density of the 980 nm laser was characterized. According to the formula fitting, the up-conversion luminescence process is a two-photon process. Meanwhile, the temperature sensing characteristic of the samples has been discussed. Finally, the CIE coordinates were analyzed and calculated to be (0.297, 0.692).

Luminescent properties of Mg1.99SnO4:0.01Mn2+ phosphors doped with Zn2+

In this work, a series of ZnxMg1.99-xSnO4:0.01Mn2+ (x = 0, 0.01, 0.02, 0.03, 0.04) green long afterglow phosphors are prepared by high-temperature solid-phase reaction. The photoluminescence and long afterglow performance of host material doped with Zn2+ are investigated. The results show that the emission peak of Mn2+ is red-shifted by 5 nm with increasing Zn2+ concentration. Zn0.03Mg1.96SnO4:0.01Mn2+ phosphor has the strongest green luminescence intensity with the chromaticity coordinates of (0.085 7, 0.608 3) under 270 nm, and Zn0.01Mg1.98SnO4:0.01Mn2+ phosphor has superior long afterglow performance with average lifetime of 102.41s. The afterglow decay and thermoluminescence curve of phosphor are used to explain the mechanism of long afterglow luminescence. Meanwhile, the afterglow intensity distribution of each pixel in Zn0.01Mg1.98SnO4:0.01Mn2+ coating samples is carried out by hyperspectral imaging, and the optimal luminescence intensity and uniformity of the sample are obtained at a phosphor/epoxy mass ratio of 0.002 5. Therefore, Zn0.01Mg1.98SnO4:0.01Mn2+ can be a potential candidate of novel long afterglow phosphors, and hyperspectral imaging also provides new research approaches for the rational proportioning of luminescent materials.

Two phosphorescent iridium(III) complexes containing simple l-alanine ligands as efficient sensors for Cu2+ ions

Two neutral iridium complexes Ir1 and Ir2 were synthesized using 2-(4-(trifluoromethyl)phenyl)pyridine (tfmppy) and 1-(4-(trifluoromethyl)phenyl)isoquinoline (tfmpiq) as cyclometalated ligands and l-alanine as ancillary ligand. The emission peaks of Ir1 and Ir2 are located at 518 nm and 610 nm and they exhibit intense green and red luminescence in acetonitrile solution with quantum efficiencies of 0.51 and 0.20. The effect of the modification of cyclometalated ligands on the spectral properties of the complexes was discussed in detail by theoretical calculation. After the addition of Cu2+ ions, the luminescence intensities of Ir1 and Ir2 were quenched by 90 % and 89 % respectively due to the paramagnetic effect formed by the combination of iridium complexes and Cu2+ ions. According to the titration experiment, a good linear relationship was found between the intensity at the emission peak and Cu2+ ions concentrations in the range of 0 μM to 15 μM, and the calculated detection limits were 0.54 μM and 0.59 μM. Moreover, the recognition of Cu2+ ions by Ir1 and Ir2 exhibits high interference and good reversibility. Therefore, complexes Ir1 and Ir2 containing simple amino acid as ancillary ligands can be used as “turn-off” phosphorescence sensors toward Cu2+ ions.

Cool white light and tunable multicolor emission from Tb3+/Dy3+ co-activated glasses under different excitations for WLEDs

A set of co-doped (Tb3+/Dy3+) lithium zinc borate (LZB) glasses were developed by melt quenching. The structural evaluation was performed for synthesized glassy matrices. The Dy3+ and Tb3+ individually doped glasses exhibit intense yellow and green luminescence bands at 575 nm (4F9/2 → 6H13/2) and 543 nm (5D4→7F5), respectively. The sensitization effect of Dy3+ on Tb3+ was analyzed by increasing the Tb3+ content with respect to the optimum Dy3+ content (0.5 mol%) in Dy3+/Tb3+. The spectral overlay of Dy3+ luminescence and Tb3+ absorption profiles, Dy3+/Tb3+ PL spectra under different excitations 352, 362, 376, and 385 nm, shortening decay lifetimes of Dy3+ in Dy3+/Tb3+ co-activated glasses, energy transfer (ET) parameters, chromaticity coordinates and their corresponding correlated temperatures all help to explain ET from Dy3+ to Tb3+. At 385 nm of Dy3+ excitation, the optimized co-activated (0.5Dy3++1.0Tb3+):LZB glass displays cool white light emission. The non-radiative ET from Dy3+ to Tb3+ is dominated by electric dipole–dipole interaction and its ET efficiency was calculated to be 63%. At the same time, reverse ET from Tb3+ to Dy3+ was also analyzed. The shift in color coordinates from dominant yellow to greenish-yellow, green and white light emission suggests that Dy3+/Tb3+ co-activated LZB glasses can be a potential candidate for UV converted multicolor and white light emitting devices.