Emission Spectra Research Articles

Emission spectrum and photon statistics in cavity-QED system under incoherent pumping

The emission spectrum is an important tool for studying the properties and interactions of matter. By comparing analytical and numerical solutions, we validate the applicability and limitations of the low-excitation approximation. Here we show that even with a moderate pumping rate, rich multiple peaks can be observed in the emission spectrum which is the result of excitation of higher dressed rungs. Moreover, we find distinct photon distributions in the steady state under different pumping and coupling conditions and the physical mechanisms behind these phenomena are also illustrated. Additionally, we also show that the interference between the emission channels of the emitter and cavity can result in asymmetry of the emission spectrum of the whole system even if the emitter is resonant with the cavity field. Our findings can help in understanding the nonlinear characteristics and photon statistics in the cavity-QED systems.

Turn-On Fluorescence Probe for Cancer-Related γ-Glutamyltranspeptidase Detection.

The design and development of fluorescent materials for detecting cancer-related enzymes are crucial for cancer diagnosis and treatment. Herein, we present a substituted rhodamine derivative for the chromogenic and fluorogenic detection of the cancer-relevant enzyme γ-glutamyltranspeptidase (GGT). Initially, the probe is non-chromic and non-emissive due to its spirolactam form, which hinders extensive electronic delocalization over broader pathway. However, selective enzymatic cleavage of the side-coupled group triggers spirolactam ring opening, resulting in electronic flow across the rhodamine skeleton, and reduces the band gap for low-energy electronic transitions. This transformation turns the reaction mixture from colorless to intense pink, with prominent UV and fluorescence bands. The sensor's selectivity was tested against various human enzymes, including urease, alkaline phosphatase, acetylcholinesterase, tyrosinase, and cyclooxygenase, and showed no response. Absorption and fluorescence titration analyses of the probe upon incremental addition of GGT into the probe solution revealed a consistent increase in both absorption and emission spectra, along with intensified pink coloration. The cellular toxicity of the receptor was evaluated using the MTT assay, and bioimaging analysis was performed on BHK-21 cells, which produced bright red fluorescence, demonstrating the probe's excellent cell penetration and digestion capabilities for intracellular analytical detection. Molecular docking results supported the fact that probe-4 made stable interactions with the GGT active site residues.

Strain-modulated antiferromagnetic Chern insulator in NiOsCl$_6$ monolayer

Abstract Recently, Chern insulators in an antiferromagnetic (AFM) phase have been suggested theoretically and predicted in a few materials. However, the experimental observation of two-dimensional AFM quantum anomalous Hall effect is still a challenge to date. In this work, we propose that an AFM Chern insulator can be realized in a two-dimensional monolayer of NiOsCl$_6$ modulated by a compressive strain. Strain modulation is accessible experimentally and used widely in predicting and tuning topological nontrivial phases. With first-principles calculations, we have investigated the structural, magnetic and electronic properties of NiOsCl$_6$. Its stability has been confirmed through molecular dynamical simulations, elasticity constant and phonon spectrum. It has a collinear AFM order, with opposite magnetic moments of 1.3 $\mu_B$ on each Ni/Os atom, respectively, and the Néel temperature is estimated to be 93 $K$. In the absence of strain, it functions as an AFM insulator with a direct gap with spin-orbital coupling included. Compressive strain will induce a transition from a normal insulator to a Chern insulator characterized by a Chern number $C = 1$, with a band gap of about 30 meV. This transition is accompanied by a structural distortion. Remarkably, the Chern insulator phase persists within the 3$\%$-10$\%$ compressive strain range, offering an alternative platform for the utilization of AFM materials in spintronic devices.

Enhanced Photodetection Performance of WSe2/V2O5 Nanocomposite on Flexible Substrate: Synergistic Advantages and Improved Efficiency.

The two-dimensional (2D) chalcogenide WSe2/V2O5 composite nanostructures were synthesized using the hydrothermal method and extensively characterized with various spectroscopic techniques. X-ray diffraction analysis confirmed the hexagonal crystal structure exhibiting space symmetry of P63/mmc. Scanning electron microscopy images provided insights into the irregular and nonuniform morphology. Optical spectrum analysis indicated a band gap value of 2.01 eV for 15% WSe2/V2O5 nanostructures, as determined by the Wood and Tauc equation. Photoluminescence (PL) excitation spectra at emission wavelengths of 550 and 750 nm exhibited broad emission attributed to self-trapped excitons for V2O5 and WSe2 nanostructures. Under excitation at λexc = 365 nm, PL emission spectra displayed distinct peaks at 550 and 750 nm, demonstrating the ability to emit vivid red light. A device optimized for photoresponsivity (R) of approximately 7.80 × 10-1 A W-1 and detectivity (D) of around 8.65 × 1011 Jones, and quantum efficiency of approximately 3.42 × 10-2 A W-1 were achieved at a wavelength of 390 nm while using a lamination sheet as a substrate. These findings underscore the capability of devices for efficient photoconversion at specified wavelengths, indicating potential applications in sensing, imaging, and optical communication. The photoresponsivity of the device remained stable at 3.38 × 10-3 A W-1 at 0° and 3.09 × 10-3 A W-1 at 55° bending angle. This indicates the resilience of device to mechanical strain, making it ideal for flexible and wearable sensor applications. The structural, morphological, and optical characterizations confirm the suitability of luminescent WSe2/V2O5 chalcogenide for practical optoelectronic applications, especially in display technologies.

Genetic analyses in a cohort of pediatric patients with congenital hypothyroidism based on congenital hypothyroidism consensus guideline.

Pathogenic variants in the genes involved in the formation of thyroid tissue and thyroid hormone secretion have been reported to cause congenital hypothyroidism (CH) in some cases. This study aimed to evaluate the clinical and genetic findings of CH cases thought to be due to genetic variants. The study included cases whose genetic analysis was performed in accordance with the Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update Guidelines recommendations criteria and analyzed them using the next-generation sequencing panel. 61 Turkish patients from 45 families were included in the study. The overall frequency of variant detection was 37.7% (Out of 45 families, 17 had a positive mutation). Segregation was carried out for all families with positive variants. Variants in the TPO gene are the most frequently encountered, and this situation was identified in 10 families. Variants followed this in the TSHR gene in 7 families, variants in the DUOX2 gene in 5 families, and two variants in the TG and NKX2-1 genes in 2 families each, which are six novel variants. Furthermore, among the NKX2-1 cases, one had thyroid involvement only, while the other had chorea only. We did not find differences between cases with detected mutations and mutation-negative cases regarding gender, neonatal/perinatal parameters, initial thyroid function values, and thyroid morphology. In the current investigation, rare new variations in genes known to be related to CH were discovered, adding to the molecular genetic spectrum. When we compare the overall variant detection frequency, the selection criterion for genetic analysis based on the current guidelines is quite rational, considering the benefits and costs, on the other hand, present in new genes awaiting discovery. Also, TSHR mutations are likely to be common and may account for more than 5% of thyroid dysgenesis cases if we include non-familial thyroid dysgenesis.

Inferring the dust emission at submillimeter and millimeter wavelengths using neural networks

The Planck mission provided all-sky dust emission maps in the submillimeter (submm) to millimeter (mm) range at an angular resolution of 5$^ prime $. In addition, some specific sources can be observed at long wavelengths and higher resolution using ground-based telescopes. These observations are limited to small scales and are sometimes not delivered to the community. These ground-based observations require extensive data processing before they become available for scientific analysis, and suffer from extended emission filtering. At present, we are still unable to fully understand the emissivity variations observed in different astrophysical environments at long (submm and mm) wavelengths. Several models have been developed to reproduce the diffuse Galactic medium, and each distinct environment requires an adjustment of the models. It is therefore challenging to estimate any dust emission in the submm-mm at a better resolution than the 5$^ prime $ from Planck . In this analysis, based on supervised deep learning algorithms, we produced dust emission predictions in the two Planck bands centered at 850 mic (353 GHz) and 1.38 mm (217 GHz) at the Herschel resolution (37$^ prime $). Prediction or forecasting is a frequently used term in machine learning or neural network research that refers to the output of an algorithm that has been trained on a given dataset and that is being used for modeling purposes. Herschel data of Galactic environments, ranging from 160 mic to 500 mic and smoothed to an angular resolution of 5$^ prime $, were used to train the neural network. This training aimed to provide the most accurate model for reproducing Planck maps of dust emission at 850 mic and 1.38 mm. Then, using Herschel data only, the model was applied to predict dust emission maps at 37$^ prime The neural network is capable of reproducing dust emission maps of various Galactic environments with a difference of only a few percent at the Planck resolution. Remarkably, it also performs well for nearby extragalactic environments. This could indicate that large dust grains, probed by submm or mm observations, have similar properties in both our Galaxy and nearby galaxies, or at least that their spectral behaviors are comparable in Galactic and extragalactic environments. For the first time, we provide to the community dust emission prediction maps at 850 mic and 1.38 mm at the 37$^ prime $ of several surveys: Hi-GAL, Gould Belt, Cold Cores, HERITAGE, Helga, HerM33es, KINGFISH, and Very Nearby Galaxies. The ratio of these two wavelength brightness bands reveals a derived emissivity spectral index statistically close to 1 for all the surveys, which favors the hypothesis of a flattened dust emission spectrum for wavelengths larger than 850 mic . Neural networks appear to be powerful algorithms that are highly efficient at learning from large datasets and achieving accurate reproductions with a deviation of only a few percent. However, to fully recover the input data during the training, it is essential to sample a sufficiently large range of datasets and physical conditions.

Photoluminescence and photocatalytic activity of sol gel synthesized Mg doped TiO2 nanoparticles

The influence of magnesium doping on the optical properties, structural characteristics, and photocatalytic performance of TiO2 nanoparticles was investigated. Pure and Mg-doped TiO2 nanoparticles with varying weight percentages of magnesium were synthesized via the sol–gel method, followed by calcination at 100 °C for 12 h and annealing at 400 °C for 2 h to promote crystallization. X-ray diffraction (XRD) analyses confirmed the formation of crystalline mixed phases of anatase and rutile TiO2 nanoparticles, exhibiting their crystalline nature upon synthesis. Scanning electron microscopy (SEM) images were employed to study the morphological features of the samples, while energy dispersive spectroscopy (EDS) provided insights into their elemental composition. Photoluminescence (PL) emission spectra revealed ultraviolet (UV) to visible region emission for both pure and doped TiO2 samples. The photocatalytic activity was evaluated by monitoring the degradation of methyl orange under natural sunlight irradiation, elucidating the impact of visible light exposure. Furthermore, investigations were conducted to assess the influence of catalyst loading, initial dye concentration, and pH of the dye solution on the methyl orange removal efficiency. The 3 wt% Mg doped TiO2 exhibited 95 % of decolorization of Methyl Orange. X-ray photoelectron spectroscopy measurements was performed to verify the elemental composition and chemical valence states of each element. The scavenger test in photodegradation mechanism revealed that the main reactive species was superoxide species. The electron species resonance (ESR) measurement demonstrate that the synthesized sample shows the low spin state of Mg2+ in TiO2. The correlation between Mg doping on photocatalytic activity and crystal structure were studied. Theoretical calculations were performed to gain insights into the potential mechanism underlying the tuning of luminescent and photocatalytic properties of Mg-doped TiO2 nanoparticles, enabling a comprehensive discussion.

Spectral and timing properties of the accreting millisecond X-ray pulsar IGR J17498-2921 during its 2023 outburst

We present a comprehensive study of the spectral properties of the accreting millisecond X-ray pulsar IGR J17498$-$2921 during its 2023 outburst. Similar to other accreting millisecond X-ray pulsars, the broadband spectral emission observed quasi-simultaneously by NICER and NuSTAR is well described by an absorbed Comptonized emission with an electron temperature of sim 17 keV plus a disk reflection component. The broadening of the disk reflection spectral features, such as a prominent iron emission line at 6.4--6.7 keV, is consistent with the relativistic motion of matter in a disk truncated at sim $21 \ R_g $ from the source, near the Keplerian corotation radius. From the high-cadence monitoring data obtained with NICER, we observed that the evolution of the photon index and the temperature of seed photons tracks variations in the X-ray flux. This is particularly evident close to a sudden sim -0.25 cycle jump in the pulse phase, which occurs immediately following an X-ray flux flare and a drop in the pulse amplitude below the $3 detection threshold. We also report on the non-detection of optical pulsations with TNG/SiFAP2 from the highly absorbed optical counterpart.

Suppression of the hole trap for high-quality amino-phosphine based InP quantum dots

InP quantum dots (QDs) have emerged as promising nanomaterials in various fields due to their exceptional optical properties. However, its wide emission linewidth limits further application. In this study, we synthesized high-quality InP/ZnSe/ZnS QDs by suppressing hole defects. The unreacted In precursors during nucleation easily enter ZnSe in the subsequent shelling process, forming a hole trapping center that adversely affects the photo-excitons radiative recombination. Our results demonstrate that the presence of In ions in ZnSe shell enhances exciton-phonon coupling, broadens the fluorescence emission spectrum, and weakens exciton binding energy. The optimized InP QDs exhibit a line width of 44 nm and 90% PLQY at 630 nm. Furthermore, our investigation into the interaction between shell hole defects and core exciton function provides valuable insights for designing and preparing another high-performance core-shell heterojunction QDs.

A Low-Cost, Portable, Multi-Cancer Screening Device Based on a Ratio Fluorometry and Signal Correlation Technique.

The autofluorescence of erythrocyte porphyrins has emerged as a potential method for multi-cancer early detection (MCED). With this method's dependence on research-grade spectrofluorometers, significant improvements in instrumentation are necessary to translate its potential into clinical practice, as with any promising medical technology. To fill this gap, in this paper, we present an automated ratio porphyrin analyzer for cancer screening (ARPA-CS), a low-cost, portable, and automated instrument for MCED via the ratio fluorometry of porphyrins. The ARPA-CS aims to facilitate cancer screening in an inexpensive, rapid, non-invasive, and reasonably accurate manner for use in primary clinics or at point of care. To accomplish this, the ARPA-CS uses an ultraviolet-excited optical apparatus for ratio fluorometry that features two photodetectors for detection at 590 and 630 nm. Additionally, it incorporates a synchronous detector for the precision measurement of signals based on the Walsh-ordered Walsh-Hadamard transform (WHT)w and circular shift. To estimate its single-photodetector capability, we established a linear calibration curve for the ARBA-CS exceeding four orders of magnitude with a linearity of up to 0.992 and a low detection limit of 0.296 µg/mL for riboflavin. The ARPA-CS also exhibited excellent repeatability (0.21%) and stability (0.60%). Moreover, the ratio fluorometry of three serially diluted standard solutions of riboflavin yielded a ratio of 0.4, which agrees with that expected based on the known emission spectra of riboflavin. Additionally, the ratio fluorometry of the porphyrin solution yielded a ratio of 49.82, which was ascribed to the predominant concentration of protoporphyrin IX in the brown eggshells, as confirmed in several studies. This study validates this instrument for the ratio fluorometry of porphyrins as a biomarker for MCED. Nevertheless, large and well-designed clinical trials are necessary to further elaborate more on this matter.

The Influence of Thickness and Spectral Properties of Green Color-Emitting Polymer Thin Films on Their Implementation in Wearable PLED Applications.

A systematic investigation of optical, electrochemical, photophysical, and electrooptical properties of printable green color-emitting polymer (poly(9,9-dioctylfluorene-alt-bithiophene)) (F8T2) and spiro-copolymer (SPG-01T) was conducted to explore their potentiality as an emissive layer for wearable polymer light-emitting diode (PLED) applications. We compared the two photoactive polymers in terms of their spectral characteristics and color purity, as these are the most critical factors for wearable lighting sources and optical sensors. Low-cost, solution-based methods and facile architecture were applied to produce rigid and flexible light-emitting devices with high luminance efficiencies. Emission bandwidths, color coordinates, operational characteristics, and luminance were also derived to evaluate the device's stability. The tuning of emission's spectral features by layer thickness variation was realized and was correlated with the interplay between H-aggregates and J-aggregates formations for both conjugated polymers. Finally, we applied the functional green light-emitting PLED devices based on the two studied materials for the detection of Rhodamine 6G. It was determined that the optical detection of the R6G photoluminescence is heavily influenced by the emission spectrum characteristics of the PLED and changes in the thickness of the active layer.

Organoboron Polymorphs with Different Molecular Packing Modes for Optical Waveguides.

Organoboron compounds offer a new strategy to design optoelectronic materials with high fluorescence efficiency. In this paper, the organoboron compound B-BNBP with double B←N bridged bipyridine bearing four fluorine atoms as core unit is facilely synthesized and exhibits a narrowband emission spectrum and a high photoluminescence quantum yield (PLQY) of 86.53 % in solution. Its polymorphic crystals were controllable prepared by different solution self-assembly methods. Two microcrystals possess different molecular packing modes, one-dimensional microstrips (1D-MSs) for H-aggregation and two-dimensional microdisks (2D-MDs) for J-aggregation, owing to abundant intermolecular interactions of four fluorine atoms sticking out conjugated plane. Their structure-property relationships were investigated by crystallographic analysis and theoretical calculation. Strong emission spectra with the full width at half maximum (FWHM) of less than 30 nm can also be observed in thin film and 2D-MDs. 1D-MSs possess thermally activated delayed fluorescence (TADF) property and exhibit superior optical waveguide performance with an optical loss of 0.061 dB/μm. This work enriches the diversity of polymorphic microcrystals and further reveals the structure-property relationship in organoboron micro/nano-crystals.

Role of Dark States and Stokes Shift Simulations for Tetraphenylpyrazine Compared to Other Donor-Acceptor Photosensitizers.

An excellent agreement for simulated and measured absorption and emission spectra is found for four donor-acceptor aromatic molecules (tetraphenylpyrazine, tetraphenylethene, distirylanthracene and hexaphenylsilole) whose derivatives serve as solid state photosensitizers. After comparing several hybrid TDDFT functionals, EOM-CCSD, and experiments, the best agreement was found with TD-B3LYP and double zeta basis sets (6-31G** and def2-SVP) for one molecule in gas phase. A full characterisation of twelve to twenty electronic excited states was performed in every system. Symmetry-forbidden bands are found in the absorption spectra by sampling fifty to hundred geometries from a Wigner distribution. The density of states in the region 2-6 eV was also analysed, showing a very packed region of excited states and suggesting that dark electronic states may play a role in the dynamics of some of the photoexcited systems. Further calculations were done with QM/xTB at geometries extracted from previously published X-ray data to evaluate the influence of the environment on the excitations of the four aggregated molecular crystals.

Preparation, characterization and emission of Na3-3xLnxFe2(PO4)3 (Ln = Eu, Tb; 0 ≤ x ≤ 0.1 mol %) and photocatalytic activity of Na3Fe2(PO4)3

Rare earth doped compositions Na3-3xLnxFe2(PO4)3 (x = 0, 0.025, 0.05, 0.075 and 0.1) were prepared by ion-exchange method using Na3Fe2(PO4)3 and LnCl3 (Ln = Eu and Tb). Pristine Na3Fe2(PO4)3 was obtained by ethylene glycol assisted gel burning procedure. The phase characterization was performed by powder X-ray diffraction (XRD). All the compositions were well crystalized in monoclinic lattice. The FE-SEM images and elemental mapping were obtained. The infrared and Raman profiles of all-compounds were dominated by the bands owing to the (PO4) units. Investigation on photoluminescence emission and excitation spectra of Ln3+ (Ln = Eu, Tb) were carried out. The excitation spectra of Na3-3xLnxFe2(PO4)3 (Ln = Eu and Tb) gave intensive band at 256 (370) nm for Eu (Tb) doped phosphors. The photoluminescence emission spectra of Ln3+ (Ln = Eu, Tb) were carried out. The emission spectra of these composition were characterized by f -f transitions corresponding to 613 (5D0→7F2) for Eu and 543 (5D4→7F5) for Tb doped compositions. The maximum emission intensity for Eu (Tb) doped phosphors was found at x = 0.075 (0.05). The analysis of CIE and CCT values of all prepared phosphors were also carried out. Decay curves were analyzed in detail. The visible-light photo-catalytic activity of parent Na3Fe2(PO4)3 was examined against decomposition of methylene blue and methyl orange dyes. Parent Na3Fe2(PO4)3 exhibits good efficiency against MB (≈94.5 %) and moderate efficiency against MO (≈64 %) in 180 min of visible light irradiation. Scavengers’ experiments were carried to identify the active species during photodegradation.

Photoluminescence properties of Mn2+-activated red-emitting phosphors with superior thermal stability for backlighting display applications

The red-emitting phosphors, Na2Mg1-x(PO3)4:xMn2+ with concentrations ranging from 0.01 to 0.11, have been successfully synthesized using a simple solid-state method. The as-synthesized phosphors are crystallized in an orthorhombic structure. The luminescence mechanism of Mn2+ ions in Na2Mg(PO3)4 lattice has been deeply explained using the Tanabe-Sugano (T-S) energy level diagram for the d5 electron configuration. The typical photoluminescent emission (PL) and photoluminescent excitation (PLE) spectra were measured. Several excitation peaks in the spectral range of 250–550 nm on the PLE spectrum and a strong emission peak at 613 nm indicate that the as-synthesized phosphors can be effectively excited using ultraviolet (UV) and near-UV LED chips. Several photometric characteristics were measured, such as the Commission International de'LEclarirage (CIE) chromaticity coordinate (x, y), color purity (CP), and correlated color temperature (CCT), corresponding to the concentration-dependent PL spectra. Furthermore, the thermal stability of the Na2Mg1-x(PO3)4:xMn2+ phosphors was investigated through temperature-dependent PL spectra and decay curves from 10 to 500 K. All results confirm that the as-synthesized red-emitting phosphors exhibit excellent thermal stability, which are attractive characteristics for white light emitting diodes (W-LEDs) applications.

Exploring the activation potential of heme for 2,4-dichlorophenol, 2,4,6-trichlorophenol, and pentachlorophenol

The presence of chlorophenols in water poses a significant threat to human health and the environment. In response to this issue, a study was undertaken to evaluate the catalytic capabilities of chlorinated Heme towards common chlorophenols present in water, such as 2,4-dichlorophenol, 2,4,6-trichlorophenol, and pentachlorophenol. The study employed the B3LYP method, a sophisticated computational technique within density functional theory, to investigate the molecular interactions and transformations involved. It scrutinized structural parameters, Wiberg Bond Indices, which offer insights into the strength and nature of chemical bonds, along with spectroscopic data including infrared vibrational spectra, ultraviolet-visible absorption spectra, and molecular fluorescence spectra. Furthermore, the research analyzed molecular binding energies and orbital energy levels before and after the formation of complexes between Heme and the targeted chlorophenols. The findings indicate that Heme displays a notable activation characteristic towards these chlorophenols. This suggests that Heme could act as an effective catalyst in the degradation of chlorophenols in water, presenting a novel approach to water purification. The theoretical insights derived from this study are invaluable, potentially guiding the development of more efficient catalytic systems for treating chlorophenol-contaminated water, thereby reducing the environmental and health risks associated with these hazardous compounds.

Correction to: Determination of Heat and Mass Emission Coefficients in a Hybrid Cooling Tower with Transversely Finned Radiator Pipes

Correction to: Determination of Heat and Mass Emission Coefficients in a Hybrid Cooling Tower with Transversely Finned Radiator Pipes

Facile preparation of NiFe2O4 decorated chitosan-graphene oxide for efficient remediation of Co(II) and adsorption mechanism

In the background of severe water pollution, adsorption is a charming technique for heavy metal remediation. In this work, NiFe2O4 decorated chitosan-graphene oxide (NFCG) was prepared by simple hydrothermal method for Co(II) remediation application. Adsorption mechanism was elaborately elucidated based on multiple evidences extracted from adsorption fitting (isotherms, thermodynamics and kinetics), spectroscopic test (XPS, UV–Vis absorption, fluorescent emission and Raman spectra) and the hard-soft acid-base (HSAB) theory inspection. Result shows, for Co(II) with initial concentration 200 mg·L−1, NFCG with dosage 500 mg·L−1 reaches adsorption equilibrium in 24 min, rendering removal percentage and adsorption amount 96.87 % and 387.48 mg·g−1, respectively. Owing to the efficient recovery enabled by paramagnetism, NFCG keeps adsorption amount 311.01 mg·g−1 for Co(II) after six consecutive cycles. Moreover, NFCG exhibits selectivity towards Co(II) under the coexistence of common interfering substances. Adsorption fitting suggests chemical adsorption based on heterogeneous affinity. Spectroscopic analysis discloses, CO, CO, -C(=O)NH-, OH and aromatic part contribute to Co(II) adsorption via electron donation, forming CoO bond. This atomic scale adsorption mechanism was substantiated by HSAB theory calculation. In brief, this work provides basic knowledge and technical support for fabricating high efficiency magnetic bio adsorbent.

Experimental study of shooting sound around semi-open shooting ranges

Measurements of shooting sound around semi-open shooting ranges are analyzed. Recorded sound signals show bullet sound and muzzle sound contributions. Time differences between bullet and muzzle sound pulses are explained by calculation of acoustical travel times. In general bullet sound contributions are stronger in forward directions (angles 0 to 90 degrees with respect to the shooting direction) than in backward directions. A representative frequency is defined to characterize the relative importance of bullet sound in the emitted sound spectrum. This is further analyzed by means of silencers on the firearms, as silencers suppress the muzzle sound but not the bullet sound. The effect of acoustical absorption material on the shooting range is also investigated. Differences of the order of 10 dB between different shooting ranges are attributed to acoustical absorption material of the overhead screens (baffles) on the range. For practical applications it would be useful to represent a shooting range by a single point source with a direction-dependent sound emission spectrum. The accuracy of this approximation is investigated.

Ultrasensitive and Adjustable Nanothermometers Based on Er3+-Sensitized Core@Shell Nanoparticles for Use in the First Biological Window.

In recent years, intensive research has focused on lanthanide-doped nanoparticles (NPs) used as noncontact temperature sensors, particularly in nanomedicine. These NPs must be capable of excitation and emission within biological windows, where biological materials usually show better transparency for radiation. In this article, we propose that NPs sensitized with Er3+ ions can be applied as temperature sensors in biological materials. We synthesized the NPs through a reaction in high-boiling solvents and confirmed their crystal structure and the formation of core@shell NPs by using X-ray diffraction, high-resolution transmission electron microscopy, and element distribution mapping within the NPs. NaErF4@NaYF4, NaYF4:12.5% Er3+, 2.5% Tm3+@NaYF4, NaYF4:7.5% Er3+@NaYF4, and NaYF4:12.5% Er3+, 2.5% Ho3+@NaYF4 exhibited intense upconversion (UC) emission under 1532 nm laser excitation detectable also in the whole human blood. We propose that this UC results from energy transfer between Er3+ ions and from Er3+ to Tm3+ or Ho3+ codopants. To determine the mechanism of UC, we measured the dependence of the emission band intensities on the laser power densities. Importantly, we also analyzed the temperature-dependent emission of the NPs within the 295-360 K range. Based on the collected emission spectra, we calculated the luminescence intensity ratios (LIRs) of the emission bands to assess their potential for optical temperature sensing. The temperature-sensing properties varied with the concentration of Er3+ ions and the presence of additional Tm3+ or Ho3+ codopants. Depending on the NP composition and the emission bands used for luminescence ratio calculations, the maximum relative temperature sensitivity ranged from 4.55%·K-1 to 1.12%·K-1, with temperature resolution between 0.05 and 2.53 K at room temperature. Finally, as proof of using NPs as temperature sensors in biomedicine, we successfully measured the temperature-dependent emission of NaYF4:7.5% Er3+@NaYF4 NPs dispersed in whole blood under 1532 nm excitation. We demonstrated that the ratio of Er3+ ion emission bands changes with temperature, indicating that these NPs have potential applications in temperature sensing within biological environments. We also confirmed the properties of NPs as temperature sensors by measuring the temperature reading uncertainty and the repeatability of the LIR readings during heating-cooling cycles, thereby confirming the excellent properties of the studied systems as temperature sensors.