Emission Peak Research Articles

Infall Motions in the Hot Core Associated with the Hypercompact H ii Region G345.0061+01.794 B

We report high angular resolution observations, made with the Atacama Large Millimeter Array in band 6, of high excitation molecular lines of CH3CN and SO2 and of the H29α radio recombination line toward the G345.0061+01.794 B HC H ii region in order to investigate the physical and kinematical characteristics of its surroundings. Emission was detected in all observed components of the J = 14 →13 rotational ladder of CH3CN and in the 304,26–303,27, and 324,28–323,29 lines of SO2. The peak of the velocity-integrated molecular emission is located ∼0.″4 northwest of the peak of the continuum emission. The first-order moment images and channel maps show a velocity gradient of 1.1 km s−1 arcsec−1 across the source and a distinctive spot of blueshifted emission toward the peak of the zero-order moment. The rotational temperature is found to decrease from 252±24 K at the peak position to 166±16 K at its edge, indicating that our molecular observations are probing a hot molecular core that is internally excited. The emission in the H29α line arises from a region of 0.″65 in size, where its peak coincides with that of the dust continuum. We model the kinematical characteristics of the “central blue spot” feature as due to infalling motions, suggesting a central mass of 172.8±8.8 M ⊙. Our observations indicate that this HC H ii region is surrounded by a compact structure of hot molecular gas, which is rotating and infalling toward a central mass, that is most likely confining the ionized region. The observed scenario is reminiscent of a “butterfly pattern” with an approximately edge-on torus and ionized gas roughly parallel to its rotation axis.

Ultra-broadband near-infrared emission of Cr3+-containing oxy-fluoride glass-ceramics

Broadband near-infrared (NIR) light sources cover unique optical wavelengths and are valuable in the fields of bioimaging and photodynamic therapy, night vision lighting and security monitoring. NIR phosphor converted light-emitting diode (NIR pc-LED) devices have attractive features such as tunable emission peak, low cost of production, compact in sizes and high luminous efficiency. However, heat accumulation during operation due to poor thermal conductivity of the organic resin used in packaging often causes serious reduction in luminous efficiency and accelerated degradation of the device. In present work, we developed a Cr3+-doped transparent CaF2-based oxy-fluoride glass-ceramic (GC) that showed a broadband emission of 700∼1400 nm under 470 nm excitation. The emission peaked at ∼880 nm, the full-width at half maximum was about ∼297 nm, and the photoluminescence quantum yield reached ∼31.19 %. The emission was derived from the electronic transition of Cr3+ ions from the 4T2(F) to 4A2(F). Through structural analysis and numerical simulation, we showed that during the heat treatment process, Cr3+ ions were enriched into the CaF2 crystal phase and replaced the Ca2+ in the GC host with occupied the center position of the polyhedrons, which provided a weak crystal field and led to NIR emission. We built NIR pc-LED devices using optimized GC and commercial blue LED chips, and we demonstrated the application of this NIR pc-LED in night-vision lighting. Our approaches to prepare simple and stable inorganic NIR luminous materials sealed in bulk in a transparent CaF2-based oxy-fluoride GC and to construct pc-LED devices could provide new concept to the field and have practical implications to applications in related fields.

Synthesis and Investigation of Electrochemical Studies on Thulium Tellurite (TmTeO3) for Supercapacitor Electrode Application

Thulium tellurite ([Formula: see text]) is synthesized by hydrothermal method. It exhibits nearly cuboid-shaped particles along with triangular particles. [Formula: see text] is found to be monoclinic. The energy gap is 5.87[Formula: see text]eV, the Urbach energy value is 0.287[Formula: see text]eV and the refractive index is 1.881. The size of the particle is determined as 107[Formula: see text]nm. Optical transitions between energy levels assign absorption and emission peaks. Tm, was found in the oxide matrix as Tellurite. Magnetic susceptibility between 20[Formula: see text]K and 300[Formula: see text]K decreases with temperature, reaches saturation and aligns all Thulium spins. M–H curve confirms paramagnetic nature at 300[Formula: see text]K and feeble ferromagnetic nature at 77[Formula: see text]K. Cyclic voltammogram and chronopotentiometry analysis exhibit pseudo-capacitive behavior. The potential window is 0.82. Specific capacitance is found to be 87[Formula: see text]F/g. Chronopotentiometry analysis shows 55[Formula: see text]F/g specific capacitance. Impedance analysis shows a pseudo-capacitive nature. [Formula: see text] symmetrical supercapacitor device is fabricated with potential window of 1.52[Formula: see text]V. A specific capacitance of 37.75[Formula: see text]F/g at 1 A/g, energy density 6.055[Formula: see text]Wh kg[Formula: see text] and power density 760.99[Formula: see text]W kg[Formula: see text] was achieved. Impedance analysis shows low series resistance of 2.567[Formula: see text][Formula: see text] and charge transfer resistance of 0.473[Formula: see text][Formula: see text]. Cyclic performance with 80% specific capacitance retention is observed after 5000 cycles. The [Formula: see text] symmetric supercapacitor electrodes possess good electrochemical properties due to wider potential window, long cycle stability and notable energy density.

Enhancing luminescence performance via adjusting the doping concentration and boron aluminum ratio in Dy3+ -activated barium-boroaluminosilicate glasses for laser and W-LED applications

A series of barium-boroaluminosilicate [30SiO2-11Al2O3-44B2O3-5BaO-(10-x)K2O-xDy2O3 (with x = 0.25, 0.5, 0.75, 1.0, 1.25, 1.5 mol%)] glasses doped with Dy3+ ions were prepared by the high temperature (melt quenching) method. In the glass matrix, the relationship among structure, luminescence properties, and B/Al ratio was analyzed; also studied are the physical properties of glass and influence of Dy3+ concentration on the luminescence properties. Differential Scanning Calorimeter (DSC) results have shown the glass matrix exhibiting good thermal stability and high resistance to crystallization. FTIR and Raman spectra have confirmed the presence of stretching and bending vibrations of [BO3], [AlO4] and [SiO4] structural units in the prepared glass. The observed UV–Vis–NIR spectra have indicated that the existence of thirteen bands corresponding to the transition Dy3+ ions from 6H15/2 level to different excited levels; the transmittance curves obtained have shown the transmittance up to 91 %. Increase in Dy3+ concentration is found to decrease the optical band gap; the calculated Judd-Oflet parameter is found to follow the trend Ω2＞Ω4＞Ω6. Photoluminescence studies have shown three emission peaks which could be associated to the transitions: 4F9/2 → 6H15/2 (blue light), 4F9/2 → 6H13/2 (yellow light), and 4F9/2 → 6H11/2 (red light); the maximum intensity obtained for the glass with x = 0.75 mol%, with spacing between Dy3+ ions being 1.9137 Å; and the decay curve could be fitted with double exponential function. The CIE results have revealed that the chromaticity coordinates are closer to that of standard white light, and the color temperature located in the region of cold white light.

Characteristics, preservation mechanisms, and significance of aragonite in lacustrine shale: A case study from the Jiyang Depression, Bohai Bay Basin

Aragonite is a metastable mineral, which is easily transformed into calcite, and generally difficult to preserve in the stratum. However, large amounts of aragonites were found in the Paleogene shale of the Jiyang Depression. The characteristics and preservation mechanisms of these aragonites were analyzed through a series of analytical methods, including cathodoluminescence, field-emission scanning electron microscopy (FESEM), laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), micro-area carbon and oxygen isotopes, Sr isotopes, and dissolution simulation experiments under high temperature and high pressure. The research results show that: ①Aragonite in the Paleogene shale of the Jiyang Depression is related to algal microbial fossils, primarily composed of coccoliths and characterized by two emission peaks at 420 nm and 480 nm in cathodoluminescence; ②The primary factor allowing biological aragonite to be preserved is the immaturity of the organic matter and the deficiency of abundant organic acids necessary for its dissolution or transformation, which is confirmed by the evidence of organic matter maturity and simulation experiments of organic acid dissolution on aragonite under high-temperature and high-pressure conditions. Additional factors that may aid in the preservation of aragonite are the ideal sedimentation conditions, the defense of organic coating, and the enclosed environment with tiny pores, low porosity, and low permeability; ③These aragonite-rich shales, characterized by coccolithophores, provide a solid evidence for seawater intrusion into terrestrial lake basin, and have a significant implication for the source and storage of shale oil.

Tuning of photoluminescence properties: Impact of Pr-doping in SrTiO3 crystallites

Materials having deep blue emission characteristics with a CIEy chromaticity value less than 0.1 are highly desired. Here we incorporated Pr3+ into the Sr2+ site of the Sr1-x PrxTiO3 (x=0.05, 0.075, 0.10, 0.125, 0.15, 0.20) to quench the typical red photoluminescence (PL) emission in Pr-doped compounds and tune it to a blue-emitting system. XRD analysis and structural refinement demonstrate transition from cubic to tetragonal symmetry at Pr concentrations of, x≥0.1. The contribution of oxygen vacancies in emission mechanism was investigated through XPS analysis. High-resolution FE-SEM analysis of morphological features revealed the creation of tiny grains with the appearance of micro pebbles. Under 380 nm UV illumination a narrow-band blue emission peak FWHM of 19.3 nm was obtained at 428 nm for x=0.05. CIE plots were used to examine the quality of emission peaks and samples show CIEy less than 0.1. This blue emission is crucial for lighting and display applications.

Electrical, optical and nonlinear optical process in spray pyrolyzed Zn:CuO nanostructures for optoelectronic device applications

Nanostructured pure and Zn doped CuO thin films were deposited on a glass substrate at 400 °C using the chemical spray pyrolysis method. The fabricated thin films were characterized to study the compositional, structural, morphological, optical and electrical properties. X-ray diffraction spectra show the polycrystalline nature of the sample and confirm the monoclinic phase of copper oxide. Raman analysis further confirms the absence of cuprous oxide phases and impurities. High absorbance in the visible region was observed for the films with bandgap values ranging from 1.7–2.0 eV. A near-band edge emission peak in the red region is recorded in the photoluminescence spectra. Uniformly distributed nanoparticles are observed in SEM images. Hall effect measurements indicate p-type conductivity and 5% Zn doped copper oxide showed the highest conductivity and carrier concentration. The non-linear absorption coefficient (β eff) of the samples was obtained with the help of z-scan method with a Helium-Neon laser under the CW regime. Zn doping results in an increase in nonlinear absorption, supporting the use of Zn:CuO for optoelectronic devices.

Designing Green Synthesis-Based Silver Nanoparticles for Antimicrobial Theranostics and Cancer Invasion Prevention.

Researchers are increasingly favouring the use of biological resources in the synthesis of metallic nanoparticles. This synthesis process is quick and affordable. The current study examined the antibacterial and anticancer effects of silver nanoparticles (AgNPs) derived from the Neurada procumbens plant. Biomolecules derived from natural sources can be used to coat AgNPs to make them biocompatible. UV-Vis spectroscopy was used to verify the synthesis of AgNPs from Neurada procumbens plant extract, while transmission electron microscopy (TEM), photoluminescence (PL) spectroscopy, dynamic light scattering (DLS), and Fourier transform infrared spectroscopy (FTIR) were used to characterize their morphology, crystalline structure, stability, and coating. UV-visible spectrum of AgNPs shows an absorption peak at 422 nm, indicating the isotropic nature of these nanoparticles. As a result of the emergence of a transmission peak at 804.53 and 615.95 cm-1 in the spectrum of the infrared light emitted by atoms in a sample, FTIR spectroscopy demonstrated that the Ag stretching vibration mode is metal-oxygen (M-O). Electron dispersive X-ray (EDX) spectral analysis shows that elementary silver has a peak at 3 keV. Irradiating the silver surface with electrons, photons, or laser beams triggers the illumination. The emission peak locations have been found between 300 and 550 nm. As a result of DLS analysis, suspended particles showed a bimodal size distribution, with their Z-average particle size being 93.38 nm. The findings showed that the antibacterial action of AgNPs was substantially (p≤0.05) more evident against Gramme-positive strains (S. aureus and B. cereus) than E. coli. The biosynthesis of AgNPs is an environmentally friendly method for making nanostructures that have antimicrobial and anticancer properties.

Investigation on spontaneous recombination mechanisms in GaN based laser diodes under low injection current

This study works on the spontaneous recombination mechanisms of GaN-based laser diodes (LDs) under low injection current by examining their power–current (P–I) curves and electroluminescence spectra. Our investigation focuses on the behavior of differential efficiency in LDs under low injection current, revealing that a competition between impurity-related yellow emissions and band-edge blue emissions leads to a change in total luminescence efficiency. Using both experimental and simulating methods, the yellow emission peak is primarily attributed to carrier recombination in deep-level defects located on the LD's p-side. A detailed explanation to the differential efficiency changing mechanism is beneficial to improve the GaN-based LD performance in future fabrication.

Photoluminescence-based biosensor for the detection of antibodies against SARS-CoV-2 virus proteins by ZnO tetrapod structure integrated within microfluidic system

This paper reports on development of an optical biosensor for the detection of antibodies against SARS-CoV-2 virus proteins in blood serum. ZnO nanotetrapods with high surface area and stable room temperature photoluminescence (PL) were selected as transducers. Structure and optical properties of the ZnO tetrapods have been studied by XRD, SEM and Raman spectroscopy. Crystallinity, dimensions and emission peaks of the ZnO tetrapods were determined. The ZnO tetrapods were fixed on glass chip. Silanization of ZnO tetrapods surface resulted in forming of functional surface groups suitable for the immobilization of bioselective layer. Two types of recombinant proteins (rS and rN) have been used to form bioselective layer on the surface of the ZnO tetrapods. Flow through microfluidic system, integrated with optical system, has been used for the determination of antibodies against SARS-CoV-2 virus proteins present in blood samples. The SARS-CoV-2 probes, prepared in PBS solution, have been injected into the measurement chamber with a constant pumping speed. Steady-state photoluminescence spectra and photoluminescence kinetics have been studied before and after injection of the probes. The biosensor signal has been tested to anti-SARS-CoV-2 antibodies in the range of 0.001 nM–1 nM. Control measurements have been performed with blood serum of healthy person. ZnO-SARS-CoV-2-rS and ZnO-SARS-CoV-2-rN biosensors showed high stability and sensitivity to anti-SARS-CoV-2 antibodies in the range of 0.025–0.5 nM (LOD 0.01 nM) and 0.3–1 nM (LOD 0.3 nM), respectively. Gibbs free energy of interaction between ZnO/SARS-CoV-2-rS and ZnO/SARS-CoV-2-rN bioselective layers with anti-SARS-CoV-2 antibodies showed −35.5 and −21.4 kJ/mol, respectively. Average detection time of biosensor integrated within microfluidic system was 15–20 min. The detection time and pumping speed (50 μL/min) were optimized to make detection faster. The developed system and ZnO-SARS-CoV-2-rS nanostructures have good potential for detection of anti-SARS-CoV-2 antibodies from patient's probes.

Demystification of luminescence properties and the near imperceptible thermal quenching of Sm3+-doped tungstate phosphors.

Ultra-high thermally stable Ca2MgWO6:xSm3+ (x = 0.5, 0.75, 1, 1.25, and 1.5mol%) double perovskite phosphors were synthesized through solid-state reaction method. Product formation was confirmed by comparing the X-ray diffraction (XRD) patterns of the phosphors with the standard reference file. The structural, morphological, thermal, and optical properties of the prepared phosphor were examined in detail using XRD, Fourier transform infrared spectra, scanning electron microscopy, diffused reflectance spectra, thermogravimetric analysis (TGA), photoluminescence emission, and temperature-dependent PLE (TDPL). It was seen that the phosphor exhibited emission in the reddish region for the near-ultraviolet excitation with moderate Colour Rendering Index values and high colour purity. The optimized phosphor (x = 1.25mol%) was found to possess a direct optical band gap of 3.31 eV. TGA studies showed the astonishing thermal stability of the optimized phosphor. Additionally, near-zero thermal quenching was seen in TDPL due to elevated phonon-assisted radiative transition. Furthermore, the anti-Stokes and Stokes emission peaks were found to be sensitive toward the temperature change and followed a Boltzmann-type distribution. All these marked properties will make the prepared phosphors a suitable candidate for multifield applications and a fascinating material for further development.

Up-conversion luminescent properties of CaGdAl3O7: Er3+, Yb3+, Lu3+ as a ratio optical thermometer

Rare earth doped up-conversion luminescent materials have been extensively studied for ratio optical thermometry. Compared with commonly used fluorides, oxides have low up-conversion luminous efficiencies but good thermal stability and are more suitable for high temperature environments. In this paper, a series of CaGdAl3O7: x% Er3+, y% Yb3+, z% Lu3+ phosphors were successfully prepared by high temperature solid-state reaction. Upon 980 nm laser excitation, the optimal CaGdAl3O7: 5 % Er3+, 35 % Yb3+, 1.5 % Lu3+ shows bright characteristic emission peaks of Er3+. CaGdAl3O7: 5 % Er3+, 35 % Yb3+, 1.5 % Lu3+ shows good temperature sensing performance from 303 K to 503 K. The absolute sensitivity reaches the maximum value at 428 K (Sa = 0.292 % K−1). The maximum relative sensitivity is 0.917 % K−1 at 303 K. Moreover, CaGdAl3O7: 5 % Er3+, 35 % Yb3+, 1.5 % Lu3+ shows superior repeatability and reversibility. The results suggest that it is potential candidates as temperature sensors.

Novel CeF3:Tm3+, Er3+ nanoparticles: NIR up-down conversion luminescence properties based on energy transfer of Tm3+ and Ce3+

A novel CeF3:Tm3+, Er3+ NIR up-down conversion luminescent nanoparticles with highly efficient visible and near-infrared second window (NIR-II) emission were synthesized by direct precipitation and hydrothermal methods. The two different emission modes of visible-NIR II light of Er3+were realized through the energy transfer of Tm3+ and Ce3+at the excitation wavelength of 808 nm. Which successfully combined the narrow emission peaks of visible light and the deep tissue penetration advantage of NIR-II. First, the effects of preparation conditions on the structure, morphology, stability and luminescence properties of CeF3:Tm3+, Er3+ nanoparticles were analyzed by XRD, SEM, TEM and PL. The results showed that the crystallinity, morphology and luminescence intensity of CeF3:Tm3+,Er3+ nanoparticles produced by hydrothermal method (reaction time of 10 h) were optimal compared with that of direct precipitation method. CeF3: Tm3+,Er3+ nanoparticles has better thermal stability, and fluorescence lifetime of 5D0→7F2 (525 nm), 4I15/2→4I11/2 (1066 nm) and 4I15/2→4I13/2 (1386 nm) for Er3+ are 15.51 ns, 48.78 us and 57.06 us, separately. At the same time, the surface of CeF3:Tm3+, Er3+ nanoparticles was modified by PEG and Lys. And then the effects of the surface modification on the hydration size, zeta potential and up-down conversion luminescent properties (visible and NIR-II light emission) were investigated. The results show that the modification of PEG effectively slows down the agglomeration of CeF3:Tm3+, Er3+ nanoparticles and improves their stability and dispersion under the same conditions. More importantly, the modification of PEG effectively increases the up-conversion luminescence intensity of CeF3:Tm3+, Er3+ nanoparticles under 808 nm excitation. Moreover, the CeF3:Tm3+, Er3+-PEG nanoparticles with 20–40 nm showed stronger NIR up-down conversion emission intensity in aqueous solutions (pH = 5,6,7) and better thermal stability. Furthermore, the CeF3:Tm3+, Er3+-PEG nanoparticles has low cytotoxicity and good biocompatibility. This study provides a theoretical basis for the development of high-performance rare-earth NIR up-down conversion luminescence materials.

Antioxidant, antibacterial, enzyme inhibition and fluorescence characteristics of unsymmetrical thiourea derivatives

A series of six unsymmetrical thiourea derivatives, namely 1-cyclohexyl-3-(pyridin-2-yl) thiourea (1), 1-cyclohexyl-3-(3-methylpyridin-2-yl)thiourea (2), 1-cyclohexyl-3-(2,4-dimethylphenyl) thiourea (3), 1-(4-chlorophenyl)-3-cyclohexylthiourea (4), 1-(3-methylpyridin-2-yl)-3-phenylthiourea (5), and 1-(3-chlorophenyl)-3-phenylthiourea (6), were successfully synthesized via reaction between different amines with isothiocyanates under a non-catalytic environment. Structural elucidation of compounds (1–6) was performed using FT-IR and NMR (1H and 13C) spectroscopy. The infrared spectra displayed characteristic stretching vibrations, while the 13C NMR chemical shifts of the thiourea moiety (CS) were observed in the range of 179.1–181.4 ppm. The antioxidative and antimicrobial properties of the compounds were assessed, as well as their inhibitory effects on acetylcholinesterase and butyrylcholinesterase were evaluated. In order to analyze the fluorescence characteristics of each compound (1–6), the excitation (λex) and emission (λem) wavelengths were scanned within the range of 250–750 nm, with the solvent blank serving as a standard. It was observed that when dissolved in acetone, toluene, tetrahydrofuran, and ethyl acetate, these compounds exhibited emission peaks ranging from 367 to 581 nm and absorption peaks ranging from 275 to 432 nm.

Crystal structures and photoluminescence properties of undoped and Fe3+ doped Li2Ba3(P2O7)2 pyrophosphate nanopowders

Undoped and Fe3+ doped Li2Ba3(P2O7)2 pyrophosphate nanopowders were produced by a solid-state reaction process. The prepared samples underwent characterizations using XRD, SEM with EDS, HR-TEM with SAED, FTIR, Raman, UV-Vis, EPR and PL techniques. The XRD analysis confirms the orthorhombic crystal structure of the prepared samples and unit cell parameters were evaluated. The samples exhibited stone-like structures with low aggregation based on the micrographs obtained from SEM and HR-TEM images. Additionally, the grain and particle sizes of the powder samples were evaluated. The elements Li, O, P, Ba and Fe were confirmed to be present in the produced samples by EDS spectra. FT-IR and Raman spectral investigation revealed the fundamental vibrational and bending modes of various phosphate groups. The energy bands, identified as characteristic bands of Fe3+ ions, were produced in the UV–visible region of the optical absorption spectrum for the doped sample. The crystal field and inter-electronic parameters (Dq = 915, B = 700 and C = 2715 cm−1) were also evaluated. Furthermore, the refractive index and metallization criteria properties were calculated using energy bandgap values of 4.46 and 4.38 eV of the produced samples. The doping of Fe3+ ions led to a reduction in the bandgap energy, resulting in a red-shift. A resonance signal was observed in the EPR spectrum at g = 2.05, which can be ascribed to iron ions entering the host lattice at a distorted octahedral symmetry sites and this was also supported by optical absorption studies. The produced sample showed emission peaks at 354, 440 and 530 nm in the ultraviolet, blue and green regions of its photoluminescence spectrum. Photometric parameters, such as CCT, CRI and CIE chromatic coordinates, reveal that the prepared samples could bee used in LEDs applications. This work offers novel visions into diphosphate compounds doped with transition metal ions.

PHire: A Novel Red Intracellular pH Sensor

Maintaining pH is critical for proper cellular and organ function. To measure intracellular pH, we made a novel genetically encoded protein, pHire, that increases red fluorescence with increasing pH. Thus, pHire allows for the coupling of multiple fluorescent tags without spectral overlap. We have expressed pHire in mammalian epithelial cells, Drosophila, and mice. In this study, our goal was to characterize pHire’s spectral properties by expression in human cells (HEK293) and in E.coli. To biophysically characterize pHire, we made a maltose binding protein (MBP)-pHire fusion protein to purify from E.coli. Pelleting individual colony growths revealed pink bacterial pellets which fluoresced with mCherry filters. Rather than purifying the MBP-pHire protein, equal volumes of bacteria were permeabilized with nigericin and high K+ solution for pH 5 to 9. These aliquots were then used to gather the fluorescence excitation and emission spectra of pHire, allowing us to determine the excitation and emission peaks of pHire as a function of pH. Our results showed peaks at Ex579 nm and Em611 nm, or roughly mCherry. Pelleted bacteria could also be fixed in perfusion chambers, revealing the same calibration curve as in mammalian cells and flies. Next, stable HEK293-pHire cells were selected to assay acid-base transport using NH4Cl or CO2/HCO3− in perfusion experiments. These HEK-pHire cells have less fluorescence than MBP-pHire bacteria but show the same Ex/Em peaks. However, an in-frame ATG 5’ to pHire in a mouse (adding 23 amino acids), removed pHire pH-dependence and decreased bacterial fluorescent output. Together these results indicate that pHire is biophysically similar in cells tested but that unstructured N-terminal additions block pH-responses. Funding: R25-DK101405, R21-DK129897. This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.

The Mantis Network

Context. Using emission lines from metals, we investigate the three-dimensional distribution of temperature and chemistry in ultra-hot Jupiters. Aims. Existing observations of WASP-121 b have suggested an underabundance of titanium and titanium oxide in its terminator region. In this study, we aim to determine whether this depletion is global by investigating the dayside emission spectrum. Methods. We analyzed eight epochs of high-resolution spectra obtained with the ESPRESSO spectrograph, targeting orbital phases when the dayside is in view. We used a cross-correlation method to search for various atoms, TiO, and VO, and compare the results to models. We constrained the velocities and phase function of the emission signal using a Bayesian framework. Results. We report significant detections of Ca I, V I, Cr I, Mn I, Fe I, Co I, and Ni I, but not Ti or TiO. Models containing titanium are unable to reproduce the data. The detected signals are consistent with the known orbital and systemic velocities and with peak emission originating from the substellar point. Conclusions. We find that titanium is depleted from regions of the atmosphere where transmission and emission spectroscopy are sensitive. Supported by recent HST observations of the nightside, we interpret this as evidence for the nightside condensation of titanium, which prevents it from being mixed back into the upper layers of the atmosphere elsewhere on the planet. Species with lower condensation temperatures are unaffected, implying that sharp chemical transitions exist between ultra-hot Jupiters that have slight differences in temperature or dynamical properties. As TiO can act as a strong source of stratospheric heating, cold-trapping creates a coupling between the thermal structures on the dayside and nightside, and thus condensation chemistry needs to be included in global circulation models. Observed elemental abundances in hot Jupiters will not reliably be representative of bulk abundances unless nightside condensation is robustly accounted for or the planet is hot enough to avoid nightside cold traps entirely. Secondary eclipse observations by JWST/NIRISS have the potential to confirm an absence of TiO bands at red-optical wavelengths. We also find that the abundance ratios of metal oxides to their atomic metals (e.g., TiO/Ti) depend strongly on the atmospheric C/O ratio, and that planetary rotation may significantly lower the apparent orbital velocity of the emission signal.

Microwave-assisted solvothermal synthesis of Eu3+-doped CsY2F7 and RbY2F7 phosphorescent nanoparticles

We synthesized Eu3+-doped CsY2F7 and RbY2F7 nanoparticles (orthorhombic crystal structure, Pnna space group, No. 52) by the microwave-assisted solvothermal technique and investigated the influence of reaction temperature and fluoride ion concentration on the particles’ phase and crystal structure. Fluoride ions were added in excess of the stoichiometric amount to achieve the orthorhombic phase for CsY2F7 and to convert the cubic RbY3F10 to the orthorhombic RbY2F7. Mild synthesis conditions yielded nanoparticles with crystallites ranging in size from 19 to 37 nm and a combination of spherical, rod-like, and hexagonal shapes. Nanoparticles emit a strong orange and red light when excited into the Eu3+5L6 level, which is centered around 390 nm. The strongest emission peak is around 612 nm, which comes from the 5D0→7F2 electronic transitions. Emission intensity dependence on Eu3+ concentration revealed that nanoparticles can be heavily doped with Eu3+, up to 25 % with respect to Y3+. Emission decay measurements provided values of excited state lifetimes of 6.2 ms for the Cs(Y0.75Eu0.25)2F7 and 6.0 ms for the Rb(Y0.75Eu0.25)2F7.

Influence of the DEA Concentration on Structural and Optical Properties of Nanodot PbS Thin Films Growth by Chemical Solution Deposition: Unveiling Dual Optical Absorption Edges

The present paper presents a straightforward method for producing thin film layers of sulfide quantum dots (PbS-QDs) on a glass substrate using chemical solution deposition (CSD) assisted by dipcoating technique. The deposited PbS-QDs films were subjected to a comprehensive analysis using atomic force microscopy (AFM), energy dispersive X-ray (EDX) scanning electron microscopy (SEM), X-ray diffraction (XRD), UV–vis–IR absorption, and photoluminescence spectroscopic (PL) techniques to investigate the effects of varying concentrations of diethanol amine (DEA) on their morphology, crystal structure, elemental composition, light absorption, and emission characteristics. The spherical shape of the PbS-QDs was confirmed by AFM and SEM images with average sizes around 100 and 50 nm, respectively. The energy dispersive X-ray (EDX) analysis provides evidence the existence of Pb and S elements within the PbS matrix. X-ray diffraction (XRD) results validate that the deposited films exhibit high crystallinity, with a preferential orientation along the (111) plane and a face-centered cubic lattice structure of PbS. The crystallite size of PbS is measured to be 46.6 nm. Based on the optical absorption measurements, we have determined the size range of PbS nanocrystals to be between 4.3 and 11.5 nm. The optical studies reveal the presence of two optical absorption edges within the visible and infrared spectrum, two direct band gap energy, two cut-off wavelengths, two confinement energy, two Urbach energy tail, and dual emission peaks of PbS-QDs at room temperature. The analysis reveals the presence of two distinct band gap energies, one in the visible range (1.3–2.28 eV) and the other in the infrared range (0.65–0.88 eV), which can be attributed to the formation of two distinct sizes of quantum dots situated in two different layers. The first layer, deposited directly on the glass substrate, comprises quantum dots with an average size of approximately 5.2 nm, while the second layer contains quantum dots with an average size of about 9.5 nm. This ability to tune the band gap of PbS in the visible range up to the IR band (0.65–2.28 eV) is a critical feature that holds the potential for the development of innovative optoelectronic devices.

J-Aggregate Promoting NIR-II Emission for Fluorescence/ Photoacoustic Imaging-Guided Phototherapy.

J-aggregate is a promising strategy to enhance second near-infrared window (NIR-II) emission, while the controlled synthesis of J-aggregated NIR-II dyes is a huge challenge because of the lack of molecular design principle. Herein, bulk spiro[fluorene-9,9'-xanthene] functionalized benzobisthiadiazole-based NIR-II dyes (named BSFX-BBT and OSFX-BBT) were synthesized with different alkyl chains. The weak repulsion interaction between the donor and acceptor units and the S…N secondary interactions make the dyes to adopt a co-planar molecular conformation and display a peak absorption > 880nm in solution. Importantly, BSFX-BBT can form a desiring J-aggregate in the condensed state, and femtosecond transient absorption spectra reveal that the excited states of J-aggregate are the radiative states, and J-aggregate can facilitate stimulated emission. Consequently, the J-aggregated nanoparticles (NPs) display a peak emission at 1124nm with a high relative quantum yield of 0.81%. The efficient NIR-II emission, good photothermal effect and biocompatibility make the J-aggregated NPs demonstrate efficient antitumor efficacy via fluorescence/photoacoustic imaging-guided phototherapy. The paradigm illustrates that tuning the aggregate states of NIR-II dye via spiro-functionalized strategy is an effective approach to enhance photo-theranostic performance. This article is protected by copyright. All rights reserved.