Novel Orange-Emitting YPO4:Sm3+/Polymer Nanocomposite Phosphor Films for LED Applications.

A polymer based nanocomposite (NC) material embedded with highly luminescent nanopowders could be promising for replacing traditional luminescent materials from a technological point of view. In this study, we have successfully obtained YPO4: Sm3+ /Polymer nanocomposite phosphor films by embedding YPO4: Sm3+ luminescent nanoparticles (NPs) for orange-light emitting diode (LED) applications. These luminescent NPs were synthesized using the sol gel method in different polymer matrices i.e. polystyrene (PS) and poly (methyl methacrylate) (PMMA) by using direct solution mixing. The structural, morphological, and photoluminescence characteristics of the nano-phosphors and resulting NC films were examined and discussed. The emission spectra of YPO4: Sm3+ (x at.%) nano-phosphors under near-UV excitation at 404 nm were dominated by orange emission attributed to 6H5/2 →   4F7/2 (601 nm) luminescence of Sm3+ ions. The optimum doping concentration of activator Sm3+ in YPO4 matrix was found to be 5 at.%. When the doping concentration of Sm3+ was higher than 5 at.%, concentration quenching occurred. The incorporation of YPO4: Sm3+ NPs into polymer matrices indicated that the NCs retained the original luminescence properties of the luminescent NPs, although a decrease in their emission intensity was observed for the NC films, attributable to a polymer matrix effect, which dominated in PS matrix. The fluorescence decay times of NPs in the NC films were measured and compared to those of proper YPO4: Sm3+ nano-phosphors. A decrease in decay time in NC film was observed due the effective refractive index effect. Temperature-dependent photoluminescence (TDPL) of PMMA NC film was studied in 100-400 K range, investigating the thermal stability of the film. Additionally, CIE coordinates confirmed the red-orange light emission of the prepared phosphors and NC films. The obtained results indicate that the synthesized polymer-nanophosphor NC films are promising candidates for orange-LED applications.

Standalone Highly Efficient Graphene Oxide as an Emerging Visible Light-Driven Photocatalyst and Recyclable Adsorbent for the Sustainable Removal of Organic Pollutants.

Carbon-based nanostructures are promising eco-friendly multifunctional nanomaterials because of their tunable surface and optoelectronic properties for a variety of energy and environmental applications. The present study focuses on the synthesis of graphene oxide (GO) with particular emphasis on engineering its surface and optical properties for making it an excellent adsorbent as well as a visible light-active photocatalyst. It was achieved by modifying the improved Hummers method through optimizing the synthesis parameters involved in the oxidation process. This controlled synthesis allows for systematic tailoring of structural, optical, and surface functionality, leading to improved adsorption and photocatalytic properties for the sustainable removal of organic pollutants in water treatment. Several spectroscopic and microscopic characterization techniques, such as XRD, SEM, Raman, UV-visible, FTIR, TEM, XPS, BET, etc. were employed to analyze the degree of oxidation, surface chemistry/functionalization, morphological, optical, and structural properties of the synthesized GO nanostructures. The analyses showed excellent surface functionality with surface active sites for better adsorptive removal and a tunable band gap from 2.51 to 2.76 eV exhibiting excellent natural sunlight activity (>99%) for photocatalytic removal of the organic pollutant. Various adsorption isotherms have been studied with excellent adsorption capability (Qmax = 454.54 mg/g) as compared to the literature. The study introduces GO both as a proficient stand-alone (sole) nanoadsorbent as well as a nanophotocatalyst for the efficient removal of organic dye pollutants in water treatment. Additionally, the article highlights the sustainable solar light-induced green chemistry aspects of GO as an excellent recyclable adsorbent as a result of its self-cleaning ability under natural sunlight, demonstrating its potential in real eco-friendly environmental and practical applications.

The role of thickness on the structural and luminescence properties of Y2O3:Ho3+, Yb3+ upconversion films.

The structural, surface, and upconversion (UC) luminescence properties of Y2O3:Ho3+,Yb3+ films grown by pulsed laser deposition, for different numbers of laser pulses, were studied. The crystallinity, surface, and UC luminescence properties of the thin films were found to be highly dependent on the number of laser pulses. The X-ray powder diffraction analysis revealed that Y2O3:Ho3+,Yb3+ films were formed in a cubic structure phase with an Ia 3 ¯ space group. The thicknesses of the films were estimated by using cross-sectional scanning electron microscopy, depth profiles using X-ray photoelectron spectroscopy (XPS), and the Swanepoel method. The high-resolution XPS was used to determine the chemical composition and oxidation states of the prepared films. The UC emissions were observed at 538, 550, 666, and 756 nm, assigned to the 5F4 → 5I8, 5S2 → 5I8, 5F5 → 5I8, and 5S2 → 5I7 transitions of the Ho3+ ions. The power dependence measurements confirmed the involvement of a two-photon process in the UC process. The color purity estimated from the Commission International de I'Eclairage coordinates confirmed strong green UC emission. The results suggested that the Y2O3:Ho3+,Yb3+ UC transparent films are good candidates for various applications, including solar cell applications.

High-contrast multi-surface imaging of latent fingerprints using color-tunable YOF:Tb3+,Eu3+ ultrafine nanophosphors with high quantum yield.

Visualization of latent fingerprints (LFPs) using conventional powders has faced challenges on multicolor surfaces. However, these challenges are addressed by the advent of fluorescent powders in LFP detection, and they have redefined the effectiveness of the powder dusting method. In this study, color-tunable YOF:Tb3+,Eu3+ nanophosphors were examined for LFP recognition and were evaluated for their practicality on different types of surfaces. Under 254 nm UV irradiation, the LFPs developed using these nanophosphors showed clear and distinct ridge patterns with level 1, 2, and 3 details. The ultrafine particles of these nanophosphors adhered to the ridge patterns and replicated the minutiae of the LFPs. Meanwhile, the variation of the Tb3+/Eu3+ ratio demonstrated multicolor fluorescence emission from the nanophosphors, which provided better contrast between the ridge patterns on complex surfaces. Furthermore, the high luminescence quantum yield of the nanophosphors ensured high-resolution fluorescence images of the LFPs with a well-defined pattern that was recognizable even without any microscope or sophisticated instrumentation.

Engineering of Mesoporous Cube-like In2O3 Products as Ethanol Detection Platform at Low Operating Temperature: Effects of Different Transition Metals as Dopant Ions.

Although most semiconductor metal oxides including In2O3 show acceptable sensitivity to volatile organic compounds, it is difficult to detect ethanol effectively at low operating temperatures and detection levels. In this study, pure and Co-, Ni-, and Cu-doped In2O3 products with their doping content maintained at 1 mol % were successfully produced using a hydrothermal approach. Explicit contrast on the structural, microstructural, and textural properties of the synthesized In2O3 products was examined to determine their gas sensing performance. The Cu-doped In2O3 sensor demonstrated improved response of 15.3 to 50 ppm ethanol and has satisfactory selectivity, stability, low detection limit of 0.2, humidity resistance, and decreased working temperature of 80 °C compared to 150 °C of the pure In2O3 sensor. This optimal gas sensing performance is derived from the cube-like morphology assembled with interlinked nanoparticles, which favors trapping more target gas molecules and exposing more active sites, thereby greatly improving its sensing ability. This study showed that the Cu-doped In2O3 sensor with 1 mol % is suitable for monitoring ethanol gas for food safety applications.

Effect of annealing conditions on the luminescence properties and thermometric performance of Sr3Al2O5Cl2:Eu2+ and SrAl2O4:Eu2+ phosphors.

We report on the synthesis, photoluminescence optimization and thermometric properties of Sr3Al2O5Cl2:Eu2+ and SrAl2O4:Eu2+ phosphor powders. The photoluminescence of Sr2.9Al2O5Cl2:0.1Eu2+ phosphors exhibits a blue-shift with an increasing annealing temperature owing to a decrease in the crystal field strength of the host caused by evaporation of Cl from the material. The quenching of the blue band in favour of the red band observed in the luminescence spectra of Sr2.9Al2O5Cl2:0.1Eu2+ with an increased annealing temperature was explained using the mechanism of the Landau-Zener transitions. The quantum yield and the lifetime of the phosphors depend on the annealing temperature. Phosphor samples annealed at 850 °C, 1000 °C, 1200 °C and 1500 °C were found to be potential luminescence thermometers using the luminescence spectral method. For Sr3Al2O5Cl2:Eu2+ annealed at 1000 °C, the temperature-dependent dual-band intensity ratio demonstrated a high-temperature sensitivity of ∼1.47%/°C in the temperature range of 23 °C to 40 °C which is superior to other reported phosphors with a microsecond decay time, suggesting that the material has potential for sensitive thermometry applications at ambient temperatures.

High Quantum Yield Shortwave Infrared Luminescent Tracers for Improved Sorting of Plastic Waste.

More complete recycling of plastic waste is possible only if new technologies that go beyond state-of-the-art near-infrared (NIR) sorting are developed. For example, tracer-based sorting is a new technology that explores the upconversion or down-shift luminescence of special tracers based on inorganic materials codoped with lanthanide ions. Specifically, down-shift tracers emit in the shortwave infrared (SWIR) spectral range and can be detected using a SWIR camera preinstalled in a state-of-the-art sorting machine for NIR sorting. In this study, we synthesized a very efficient SWIR tracer by codoping Li3Ba2Gd3 (MoO4)8 with Yb3+ and Er3+, where Yb3+ is a synthesizer ion (excited near 976 nm) and Er3+ emits near 1550 nm. Fine-tuning of the doping concentration resulted in a tracer (Li3Ba2Gd(3-x-y)(MoO4)8:xYb3+, yEr3+, where x = 0.2 and y = 0.4) with a high photoluminescence quantum yield for 1550 nm emission of 70% (using 976 nm excitation). This tracer was used to mark plastic objects. When the object was illuminated by a halogen lamp and a 976 nm laser, the three parts could be easily distinguished based on reflectance and luminescence spectra in the SWIR range: a plastic bottle made of polyethylene terephthalate, a bottle cap made of high-density polyethylene, and a label made of the tracer Li3Ba2Gd3(MoO4)8:Yb3+, Er3+. Importantly, the use of the tracer in sorting may require only the installation of a 976 nm laser in a state-of-the-art NIR sorting system.

Boltzmann relation reliability in optical temperature sensing based on upconversion studies of Er3+ /Yb3+ co-doped PZT ceramics.

The fluorescence intensity ratio (FIR) of two thermally coupled levels with temperature follows the Boltzmann equation and shows an exponential nature to the temperature that is purely dependent on the energy difference between the levels. Despite the identical energy difference between the thermally coupled levels, researchers have observed varying sensitivities for various samples. In this article, the FIR and sensitivities were calculated using the Boltzmann equation by changing various parameters such as energy difference (ΔE) and the value of the constant C. The results were compared with various reports for Er3+ /Yb3+ ions. After analysis, a new polynomial fit equation was used to determine the temperature sensitivities for the Er3+ /Yb3+ co-doped PbZrTiO3 phosphor in lieu of the conventional Boltzmann equation. The polynomial fit equation eliminated the dependency of the sensitivity on the inverse of the FIR factor and a flat sensitivity curve was obtained with temperature.

Persistent luminescent nanophosphors for applications in cancer theranostics, biomedical, imaging and security.

The extraordinary and unique properties of persistent luminescent (PerLum) nanostructures like storage of charge carriers, extended afterglow, and some other fascinating characteristics like no need for in-situ excitation, and rechargeable luminescence make such materials a primary candidate in the fields of bio-imaging and therapeutics. Apart from this, due to their extraordinary properties they have also found their place in the fields of anti-counterfeiting, latent fingerprinting (LPF), luminescent markings, photocatalysis, solid-state lighting devices, glow-in-dark toys, etc. Over the past few years, persistent luminescent nanoparticles (PLNPs) have been extensively used for targeted drug delivery, bio-imaging guided photodynamic and photo-thermal therapy, biosensing for cancer detection and subsequent treatment, latent fingerprinting, and anti-counterfeiting owing to their enhanced charge storage ability, in-vitro excitation, increased duration of time between excitation and emission, low tissue absorption, high signal-to-noise ratio, etc. In this review, we have focused on most of the key aspects related to PLNPs, including the different mechanisms leading to such phenomena, key fabrication techniques, properties of hosts and different activators, emission, and excitation characteristics, and important properties of trap states. This review article focuses on recent advances in cancer theranostics with the help of PLNPs. Recent advances in using PLNPs for anti-counterfeiting and latent fingerprinting are also discussed in this review.

Photocatalytic Decomposition of an Azo Dye Using Transition-Metal-Doped Tungsten and Molybdenum Carbides.

The preparation, characterization, and photocatalytic application of tungsten or molybdenum carbides (Ni-WC, 1, Co-WC, 2, Ni-MoC, 3, Co-MoC, 4, NiCo-WC, 5, NiCo-MoC, 6, NiFe-WC, 7, and NiFe-MoC, 8) doped with transition metals (Fe, Co, and Ni) are reported. These transition-metal carbide (TMC) particles show that the submicrometer globular particles agglomerated to form larger particles, with smaller crystallites present on the surface of the large particles. These crystallite sizes range between 4 and 34 nm (as calculated from X-ray diffraction data) depending on the metal dopant and type of carbide. Oxidation of the metal carbides is evident from the two sets of photoelectron lines present in the X-ray photoelectron spectroscopy (XPS) of the W 4f area. The Mo 3d spectra reveal four sets of photoelectron lines associated with oxidized MoO2 and MoO3 as well as Mo2+ and Mo3+ associated with MoC1-x . The XPS of the dopant metals Ni, Co, and Fe also show partial oxidation. The photocatalytic decomposition of Congo red (an azo dye) is used as a model reaction to determine the photocatalytic activities of the transition-metal carbides, which is related to the TMCs' optical band gap energies.

Crystal phase modified blue upconversion on Tm3+/Yb3+:BCZT ceramic phosphor benefits multifunctionality in white-light applications.

Rare earth (RE) doped perovskite oxide hosts especially titanates, are promising phosphor materials in terms of white-light emission owing to their extraordinary properties such as an exceptional hosting environment for RE-ions and a switchable crystal phase near the phase boundary. Here, we report a new strategy of crystal phase modification to enhance the blue upconversion (UC) efficiency to such an extent that the combinational mixing of blue and green/red-emitting phosphor gives intense white emission. The Lead free (Ba0.85Ca0.15)(Zr,Ti)O3 ceramics were synthesised at different sintering temperatures by incorporation of Tm3+/Yb3+ ions as dopants. The UC quantum efficiency of the Tm3+/Yb3+:BCZT sample sintered at 1300 °C was recorded at different excitation power densities. It was observed that the crystal phase transformation from tetragonal to rhombohedral symmetry in the sample near the phase boundary plays a cruicial role in improving the quantum efficiency. White-light emission applications were demonstrated by preparing biphasic samples with powder mixing of a BCZT:Tm3+/Yb3+ (blue-emitting) + BCZT:Er3+/Yb3+ (green/red-emitting) phosphor, and their composition were optimised at a mixed ratio. Thereafter, photometric characterization (CIE chromaticity, colour purity and corelated colour temperatures) was performed, and it indicated the suitability of the current biphasic samples in direct white-light (cooler) applications on an industrial scale. Crystal phase modified blue emission efficiency enhancement is a key feature of this work, which helps to generate approximately pure white-light with ideal chromacity (∼0.333, 0.343) emission when Tm3+/Yb3+:BCZT is mixed with a green emitting BCZT:Er3+/Yb3+ phosphor.

Erbium energy bridging upconversion mechanism studies on BAKL:Er3+/Yb3+ glass-ceramics and simultaneous enhancement of color purity of the green luminescence.

Borate oxyfluoride glasses are transparent in the infrared, ultraviolet and visible regions and represent an ideal host matrix for optically active dopants. Due to their lower phonon energies compared to a silicate glass matrix, non-radiative transitions are suppressed and high luminescence efficiency is expected. This work reports on a complete upconversion (UC) luminescence study of the optically active B2O3-Al2O3-KF-LiO (BAKL) glass-ceramics incorporated with Er3+/Yb3+ ions. The triclinic BAKL:Er3+/Yb3+ glass-ceramic (GC) phosphor was synthesized using the conventional melt-quenching technique and the subsequent heat treatment of the precursor glass. The successful synthesis of BAKL:Er3+/Yb3+ GCs was confirmed by X-ray diffraction, Fourier transform infra-red and differential thermal analysis measurements. The glasses were crystallized under controlled conditions, and the influence of phase composition (glass-to-crystalline phase ratio) on the wavelength and UC luminescence was thoroughly studied under 980 nm excitation. Interesting color tuning properties (white to intense green emission) of the sample were observed with laser pump power increment. The color tuning properties were explained using a new strategy i.e. the energy bridging mechanism between Er3+ ion clusters through an intermediate Yb3+ level. Moreover, their high color purity is well retained by varying the NIR excitation pump power densities and photometric characterization indicated the suitability in light emitting diodes and Er3+ doped fiber amplifier applications.

Review on recent progress in metal-organic framework-based materials for fabricating electrochemical glucose sensors.

Diabetes is a type of disease that threatens human health, which can be diagnosed based on the level of glucose in the blood. Recently, various MOF-based materials have been developed as efficient electrochemical glucose sensors because of their tunable pore channels, large specific surface area well dispersed metallic active sites, etc. In this review, the significance of glucose detection and the advantages of MOF-based materials for this application are primarily discussed. Then, the application of MOF-based materials can be categorized into two types of glucose sensors: enzymatic biosensors and non-enzymatic sensors. Finally, insights into the current research challenges and future breakthrough possibilities regarding electrochemical glucose sensors are considered.

Entanglement-Enhanced Water Dissociation in Bipolar Membranes with 3D Electrospun Junction and Polymeric Catalyst.

With the use of bipolar membranes (BPMs) in an expanding range of applications, there is an urgent need to understand and improve the catalytic performance of BPMs for water dissociation, as well as to increase their physical and chemical stability. In this regard, electrospinning BPMs with 2D and 3D junction structures have been suggested as a promising route to produce high-performance BPMs. In this work, we investigate the effect of entangling anion and cation exchange nanofibers at the junction of bipolar membranes on the water dissociation rate. In particular, we compare the performance of different tailor-made BPMs with a laminated 2D junction and a 3D electrospun entangled junction, while using the same type of anion and cation exchange polymers in a single/dual continuous electrospinning manufacturing method. The bipolar membrane with a 3D entangled junction shows an enhanced water dissociation rate as compared to the bipolar membrane with laminated 2D junction, as measured by the decreased bipolar membrane potential. Moreover, we investigate the use of a third polymer, that is, poly(4-vinylpyrrolidine) (P4VP), as a catalyst for water dissociation. This polymer confirmed that a 3D entangled junction BPM (with incorporated P4VP) gives a higher water dissociation rate than does a 2D laminated junction BPM with P4VP as the water dissociation catalyst. This work demonstrates that the entanglement of the anion exchange polymer with P4VP as the water dissociation catalyst in a 3D junction is promising to develop bipolar membranes with enhanced performance as compared to the conventionally laminated membranes.

Synthesis of biocompatible chitosan functionalized Ag decorated biocomposite for effective antibacterial and anticancer activity.

The transition-metal dichalcogenides (TMDCs) like MoS2 and WS2 are a new and interesting class of materials and show considerable promise for use in a wide variety of fields, including nanomedicine for cancer. The eco-friendly, biodegradability, toxicity, and antimicrobial activity remain an open issue. Herein, we focused on the current demands of two dimensional (2D) TMDCs and produced high-quality, few-layered MoS2 nanosheets. Noble metal Ag incorporated into the 2D-CS/MoS2 NC by the liquid exfoliated process. The manufactured CS/MoS2/Ag hybrid NC showed excellent antibacterial activity against two microorganisms such as Gram-positive (21, 27, and 33 mm) and Gram-negative bacteria (23, 30, and 39 mm). The CS/MoS2/Ag hybrid NC was designed to have significant antibacterial activity against E.coli bacteria than S.aureus. Furthermore, the hybrid NC has a 74.18% cell inhibition against MCF-7 cancer cells. According to the literature relevant, it is the first extensive experimental analysis on the nano-bio interaction of 2D TMDCs nanomaterials in MCF-7 breast cancer cells.

Luminescent MoS2 Quantum Dots with Tunable Operating Potential for Energy-Enhanced Aqueous Supercapacitors.

Wide band gap luminescent MoS2 quantum dots (QDs) and MoS2 nanocrystals (NCs) have been synthesized by using laser-assisted chemical vapour deposition and used as an electrode material in supercapacitors. Size-dependent properties of the MoS2 QDs and NCs were examined by UV-vis absorption, photoluminescence, and Raman spectroscopy. The morphological evolution of the NCs and QDs were characterized by using field emission scanning electron microscopy, high-resolution transmission electron microscopy, and atomic force microscopy. The as-synthesized uniform QDs with a size of ∼2 nm exhibited an extended electrochemical potential window of 0.9 V with a specific capacitance value of 255 F/g, while the NCs values were 205 F/g and 0.8 V and the pristine MoS2 with values of 105 F/g and 0.6 V at a scan rate of 1 mV s-1. A shorter conductive pathway and 3D quantum confinement of MoS2 QDs that exhibited a higher number of active sites ensure that the efficient charge storage kinetics along with the intercalation processes at the available edge sites enable significant widening of operating potential window and enhance the capacitance. The symmetric device constructed with the QDs showed a remarkable device capacitance of 50 F/g at a scan rate of 1 mV s-1 with an energy density of ∼5.7 W h kg-1 and achieved an excellent cycle stability of 10,000 consecutive cycles with ∼95% capacitance retention.

Power-dependent upconversion luminescence properties of self-sensitized Er2WO6 phosphor.

A Yb3+ free self-sensitized Er2WO6 phosphor has been synthesized via a solid-state reaction method. The phosphor material, Er2WO6, has a monoclinic crystal structure with space group P2/c (13). The deconvoluted high-resolution X-ray photoelectron spectra of all the core elements in the Er2WO6 phosphor material were explored. The highly resolved absorption peaks in the ultra-violet, visible and near-infra-red (NIR) regions of the diffuse reflectance spectrum were due to the Stark-splitting of the 4f energy levels of the Er3+ ions. Under 980 nm NIR laser excitation, the Er2WO6 phosphor showed an intense up-converted red emission at 677 nm due to the 4F9/2→4I15/2 transitions of the Er3+ ions. The cross-relaxation and resonance energy transfer process involved in the key intermediate 4F3/2 and 4F5/2 levels of the Er3+ and their role in generating red emissions were investigated. The laser pump power versus upconversion intensity plot showed a slope with an n value <1 and the possible reasons behind this behavior were investigated. The photoluminescence properties of the Er2WO6 phosphor in the visible and NIR region were further analyzed. The potential application of the phosphor as a marker in latent fingerprint detection was also evaluated.

Electronic and Simple Oscillatory Conduction in Ferrite Gas Sensors: Gas-Sensing Mechanisms, Long-Term Gas Monitoring, Heat Transfer, and Other Anomalies.

The early detection and warning of the presence of hazardous gases have been well studied. We present a study that focuses on some fundamental properties of gas sensors for liquefied petroleum gas (LPG) using spinel nanoferrites, namely, CoSm0.1Fe1.9O4, CoCe0.1Fe1.9O4, MgCe0.1Fe1.9O4, and MgFe2O4. A highly sensitive and selective response of 846.34 at 225 °C toward 10,000 ppm concentration of LPG was recorded. Other flammable gases tested were hydrogen, methane, propane, and butane. Electronic conduction of LPG sensors near saturation showed simple electrical oscillations that can be attributed to the self-dissociation of water molecules physically adsorbed on the surface of the chemisorbed oxygen species due to proton transfer. The oscillatory behaviors follow fluctuations in the operating temperature attributed to heat transfer between the physisorbed water molecules and the hot sensor surface. This depends on the LPG concentration because higher LPG concentration gives rise to greater heat transfer from the sensors. The adsorption and desorption of these water molecule multilayers take a few hundreds of seconds at low concentrations, while the adsorption formation process takes longer at higher concentrations. Other parameters such as LPG exposure time, bias voltage, relative humidity, ambient conditions, operating temperatures, and temperature of the gas not only affect electrical oscillations and thermal fluctuations but also switch the dominant charge carriers from p- to n-type or vice versa. The type of sensor surface, either p- or n-type, did not appear to affect the oscillatory behavior, while the exposure time, short or long, determined the appearance and further behavior of the oscillations. The long-time exposure to 10,000 ppm concentration resulted in the resistance gradually decreasing due to the lack of oxygen supply, while at 5000 ppm, this was constant, stable, and oscillated indefinitely. Changing the dry air to argon gas as a carrier and for dilution of the hazardous gas prevented the electrical oscillations and thermal fluctuations and significantly lowered the response values. Both the inert ambient (argon gas) and changing operating temperature flipped the dominant charge carriers of these sensors. The concentration of these chemisorbed oxygen species governs the charge space and depletion layers. In addition, the spinel nanoferrites used contained higher oxygen vacancies than the lattice oxygen and chemisorbed oxygen. When using dry air, the oscillations were observed at 3000 ppm concentration, while using argon gas, they were observed at 7000 ppm concentration. The room-temperature LPG responses were about 35 and 80 under 45% relative humidity using dry air and argon gas, respectively. These room-temperature measurements showed electrical oscillations but did not show any thermal fluctuations or heat transfer phenomena. This study presents a deeper insight into the fundamentals of gas-sensing mechanisms and energy costs involved.

Ultra-sensitive and selective p-xylene gas sensor at low operating temperature utilizing Zn doped CuO nanoplatelets: Insignificant vestiges of oxygen vacancies.

p-xylene is a harmful volatile organic compound that needs to be tested for indoor air quality detection. We report on the sensing characteristics of CuO and Zn doped CuO nanoplatelets of various concentrations that were prepared by hydrothermal synthesis, against nine different gases. These CuO and Zn based nanoplatelets were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, photoluminescence emission and vibrating sample magnetometer measurements. CuO and 0.1 at. % Zn doped CuO samples were most sensitive and selective to p-xylene gas with relatively high responses (Ra/Rg ratio) of about 42 and 53 at an operating temperature of 150 °C, respectively. These responses were about six times higher compared to the other 8 tested interfering gases. All these samples further exhibited a paramagnetic behaviour at room temperature, due to small traces of point defects, such as oxygen vacancies. Both these sensor materials did not show green luminescence at room temperature that is normally associated with oxygen vacancies. However, temperature dependent photoluminescence (PL) measurements for the 0.1 at. % Zn doped CuO showed broad visible emission, including green luminescence, which increased with temperature up to 150 °C and coincided with the gas sensing temperature. The pure CuO, however, showed a rapid quenching in PL emission with an increase in the temperature up to 150 °C. Nevertheless, both pure CuO and 0.1 at. % Zn doped CuO based sensors were highly sensitive to the p-xylene gas. The mechanism associated to the xylene superior sensing was considered in terms of point defects and surface area as active sites for adsorption of gas molecules.

Multiple Substitution Strategies toward Tunable Luminescence in Lu2MgAl4SiO12:Eu2+ Phosphors.

The equivalent or heterovalent substitution strategy is an efficient way to stimulate photoluminescence tuning or to optimize the luminescence performances of phosphor materials. Garnet-type compounds receive much attention as phosphor hosts because of their flexible structural frameworks. Herein, a garnet-type Lu2MgAl4SiO12:Eu2+ phosphor with broad-band blue-green emission is first explored with two-site occupation by varying the Eu2+ content. Two host-substitution approaches to controlling the luminescence behavior of Lu2MgAl4SiO12:Eu2+ phosphor are implemented. The cation substitution strategy of Ca2+ for Mg2+ achieves tunable emission from 463 to 503 nm together with broadening emission bands in Lu2Mg1-yCayAl4SiO12:Eu2+ phosphors. Moreover, chemical unit cosubstitution of [Ca2+-Ge4+] replacing [Lu3+-Al3+] results in Lu2-zCazMgAl4-zGezSiO12:Eu2+ phosphors, which induce a red shift of the emission peak of about 60 nm and a broadening in the emission spectra with increasing Ca2+ and Ge4+ concentrations. The possible photoluminescence tuning mechanism is ascribed to the coordination sphere variation in the EuO8 polyhedron depending on the changing neighboring cations. The proposed approaches on equivalent or heterovalent substitution can contribute to the development of Eu2+-activated garnet-type phosphors with regulation of the luminescence performance and further initiate research discovering new phosphors for white-light-emitting diodes.