Absorption Bands Research Articles

Optical spectra in pure-silica-core single mode optical fibers after high-fluence reactor irradiation

The paper describes the study of radiation-induced attenuation (RIA) spectra in reactor-irradiated single mode optical fibers (OFs) with differente high-temperature coatings (polyimyde, aluminum and copper). The OFs were previously irradiated up to fast neutron fluence 1.8·1020 n/cm2 and gamma dose 2.32 GGy. After three years of annealing at room temperature (RT), the RIA spectra were examined within the range of 650–1700 nm. All RIA mechanisms acting within this spectral range were identified: absorption bands attributed to non-bridging oxygen hole centers, a long-wavelength (LW) band with a maximum at λ > 1800 nm, and unsaturated “grey” loss due to coating microbendings or damage. It was found out that RIA asocciated with the LW band can be significantly annealed at room temperature in polyimide-coated OFs. RIA mechanisms influenced by the coating were found to be more stable than those causing LW-RIA.The LW-RIA arising during reactor and gamma irradiation exhibits a similar shape, approximated by the Kubo-Greenwood formula for alternative conductivity, which describes the absorption of self-trapped holes (STH) and exibits close thermal stability at RT. This suggests a STH-like nature of LW-RIA. The accurate approximation of the RIA spectrum in the near-infrared range requires considering contributions of the unsaturated loss or contributions of an absorption band peaking at an energy of 1.33 eV with a half-width of 0.45 eV.

Manipulating Cellulose-Based Dual-Network Coordination for Enhanced Electromagnetic Wave Absorption in Magnetic Porous Carbon Nanocomposites

A novel dual-network coordination strategy was utilized to prepare carbon based magnetic porous EMW absorption nanocomposites with controllable magnetic particles deposition on carbon matrices. Due to the conversion of carboxymethyl cellulose (CMC) into Prussian blue (PB) through coordination with Fe3+, the deposition of Fe3+ gradually tends to aggregate. Consequently, significant changes occur in the polycrystalline structure of magnetic Fe3O4 particles in the pyrolysis products, including alterations in grain size, orientation, and the overall size of polycrystalline particle. Finally, the obtained Fe3O4 decorated porous carbon nanocomposites showed ultrawide effective absorption band of 6.7 GHz owing to the advantageous impedance matching and the synergistic dielectric and magnetic loss effects. Overall, this study offers valuable insights into the design and comprehension of magnetic porous nanocomposites for efficient EMW absorption through the regulation of polycrystalline structure by controllable coordination deposition.

Investigation of borate glasses reinforced with iron (III) oxide [Fe2O3]: Preparation, physical, UV–Vis properties and γ-ray attenuation efficacy

Five samples of borate glasses reinforced with various ratios of Fe3+ ions with chemical formula (60-X)B2O3–10ZnO–10CdO–5Li2O–15Na2O-XFe2O3: (0.0 (Fe-0.0) ≤ X ≤ 1 (Fe-1.0) mol%) were prepared using the melt-quenching technique. The structure, physical, optical characteristics, and γ-ray attenuation properties of the prepared Fe-X glasses have been investigated. The amorphous state of Fe-X glasses confirmed by XRD observations. Density (ρglass) of the Fe-X glasses increased from 3.21 g cm−3 to 3.91 g cm−3. Molar volume (Vm) gradually reduced from 18.87 cm3/mol to 15.35 cm3/mol with increasing Fe2O3 content in the glass network from 0.0 to 1.0 mol%. The color of Fe-X glasses changed from yellow to brown according to the absorption bands located at around 385–412 nm and 407–429 nm within the visible spectrum. The indirect optical band gap (Eg) decreased from 3.37 eV to 2.78 eV, while the linear refractive index (no) increased from 2.31 to 2.45. Mass- (MAC) and linear- (LAC) attenuation coefficients increased as Fe3+ ions increased in the glass network. The Fe-1.0 sample with highest Fe2O3 content possessed the lowest values of half-value layer (HVL) and mean free path (MFP) shielding parameters. Results revealed that the suggested glass compositions can be applied in optical and radiation protection fields.

Strongly Bound Excitons and Anisotropic Linear Absorption in Monolayer Graphullerene.

Graphullerene is a novel two-dimensional carbon allotrope with unique optoelectronic properties. Despite significant experimental characterization and prior density functional theory calculations, unanswered questions remain as to the nature, energy, and intensity of the electronic and optical excitations. Here, we present first-principles calculations of the quasiparticle band structure, neutral excitations, and absorption spectra of monolayer graphullerene and bulk graphullerite, employing the GW-Bethe-Salpeter equation (GW-BSE) approach. We show that strongly bound excitons dominate the absorption spectrum of monolayer graphullerene with binding energies up to 0.8 eV, while graphullerite exhibits less pronounced excitonic effects. Our calculations also reveal a strong linear polarization anisotropy, reflecting the in-plane structural anisotropy from intermolecular coupling between neighboring C60 units. We further show that the presence of Mg atoms, crucial to the synthesis process, induces structural modifications and polarizability effects, resulting in a ∼1 eV quasiparticle gap renormalization and a reduction in the exciton binding energy to ∼0.6 eV.

A series of triphenylamine-derived fluorophores attached to a Cu-based MOF for gaseous CO optical sensing: synthesis, performance, and mechanism.

A series of triphenylamine-derived fluorescent dyes were attached to a Cu2+-containing MOF (metal-organic framework), denoted as Pm@CuMOF. The molecular structures of these dyes were discussed by the single crystal structures. Their major absorption bands peaked at 410-450 nm, showing emission bands ranging from 556 to 586 nm with emission quantum yields ranging from 8.0 to 15.1%. It was found that the [-N(C2H5)2] group generally improved sensing performance, and the -OH group in the dyes helped the Cu2+ quenching effect. Pm@CuMOF was observed by SEM as nanorods with a width of ~100 nm and a length of 300 nm. Their XRD patterns and N2 adsorption/desorption isotherms were recorded to confirm their porous structure. A low probe loading level of ~4% was determined by TGA result. The CO sensing mechanism was revealed as a Cu2+/Cu+-involved sensing mechanism based on the result of NMR titration, IR, XPS, and EPR. The fluorescence of these triphenylamine-derived dyes was firstly quenched by CuMOF. In contact with CO, Cu2+ was reduced to Cu+, accompanied by the release and fluorescence recovery of the fluorescent dyes, showing emission turn-on effect towards CO gas. Pm@CuMOF showed increased emission intensity at CO level of 0.005% (versus N2), with response times ranging from 123 s to 280 s (depending on various temperatures). Good selectivity was observed over competing alkane gases, with stable emission for at least 5 days, but no linear calibration plots were observed.

Effect of annealing temperature on physical properties and photoelectrochemical behavior of electrodeposited nanostructured NiO thin films for optoelectronic applications

Our paper used a low-cost electrodeposition technique to grow Nickel Oxide (NiO) thin films on fluorine-doped tin oxide (FTO) substrate. As-deposited films were annealed at different temperatures (350, 400, 450, and 500 °C). X-ray diffraction (XRD), Raman spectroscopy (RAM), scanning electron microscopy (SEM), UV–vis spectrophotometer, photoluminescence (PL), Cyclic voltammetry (CV), photocurrent (PC), electrochemical impedance spectroscopy (EIS), and Mott-Schottky analysis (MS) were used to study and investigate the effect of annealing temperatures on the structural, morphological, electrical, and optical properties of prepared thin films. XRD patterns proved the cubic phase of all NiO samples with the preferential orientation in (111) direction. SEM results showed that the grain size increased with increasing annealing temperature. The optical transmission was studied by a UV–vis spectrophotometer, where high transmittance for NiO thin films was found to vary in the range of 73–84 % in the visible wavelength region, depending on the annealing temperatures. At the same time, UV–visible measurements indicate an absorption band edge at 311 nm, mainly recognized as a characteristic direct band gap for prepared NiO. The optical gap calculated from the Tauc relation showed a decreasing trend from 3.97 to 3.86 eV with increasing annealing temperature from 300 °C to 500 °C. PL spectra of synthesized samples revealed two distinct emission peaks at around 400 nm and 490 nm. RAM analysis confirmed the presence of three characteristic peaks related to the vibration of Ni–O bonds. The NiO film annealed at 500 °C displays the highest specific capacitance value by CV analysis. The P-type conductivity of manufactured arrays and enhanced electrical properties were confirmed by PC, EIS, and MS analysis. The highest carrier concentration values (9.19 × 1018 cm−3) and flat band potential (0.82 V) were obtained for samples annealed at 500 °C. Our outcomes proved that NiO-500 °C thin films are ideal candidates for optoelectronic applications.

Highly Tuning of Sunlight-Photocatalytic Properties of SnO2 Nanocatalysts: Function of Gd/Fe Dopants

Gd/Fe-SnO2 nanopowders as novel photocatalysts for the active removal of Rose Bengal dye and methyl parathion pesticide were synthesized with a low-cost coprecipitation route. The X-ray diffraction analysis of SnO2, Sn0.96Gd0.02Fe0.02O2 and Sn0.94Gd0.02Fe0.04O2 nanopowders proved the formation of a tetragonal phase of tin oxide with average crystallite sizes in the range of 13–18 nm. The Fourier transform infrared (FTIR) spectra of all samples displayed the characteristic absorption bands of SnO2. The nanopowder of the pure SnO2 sample, as seen in its transmission electron microscope (TEM) image, contains spherical-like particles of variable sizes. The TEM images of the Sn0.96Gd0.02Fe0.02O2 and Sn0.94Gd0.02Fe0.04O2 powders revealed the synthesis of fine spherical nanoparticles. Based on the TEM images, the average particle size of the pure, (Gd, 2 wt% Fe) and (Gd, 4 wt% Fe) codoped SnO2 nanopowders was estimated to be 14, 10 and 12 nm, respectively. After the addition of (Gd, 2 wt% Fe) and (Gd, 4 wt% Fe) to the SnO2 structure, the band gap energy of SnO2 was reduced from 3.4 eV to 2.88 and 2.82 eV, respectively. Significantly, the Sn0.96Gd0.02Fe0.02O2 nanocatalyst exhibited a high removal efficiency of 98 and 96% for Rose Bengal dye and methyl parathion pesticide after activation by sunlight for 35 and 48 min, respectively. Furthermore, this catalyst has shown perfect mineralization as well as high stability properties for the treatment of Rose Bengal dye and methyl parathion pesticide. These results suggest the suitability of the Sn0.96Gd0.02Fe0.02O2 nanocatalyst for the treatment of agriculture and industrial effluent under sunlight light energy.

The Polysaccharides from Pinellia ternata and Their Derivatives: Preparation, Structure Characteristics, and Activities inVitro.

Three polysaccharides, PTC, PTH, and PTB, were extracted from Pinellia ternata using three different extraction conditions: room temperature water, hot water, and 2% Na2CO3 solution. PTC and PTH were composed of rhamnose, glucose, galactose, mannose, glucuronic acid, galacturonic acid, and arabinose, which combine to form complex structures. PTB was composed solely of glucose and rhamnose. Further analysis indicated that PTC and PTB exhibited triple-helix structures. PTC showed the highest scavenging capacity against DPPH, superoxide anion, and hydroxyl radicals, with half maximal inhibitory concentrations (IC50) of 1004.1, 1584.1, and 1584.1 μg/mL, respectively. Additionally, PTC, PTH, and PTB were subjected to sulfation, phosphorylation, and selenization, resulting in the production of nine derivates. The distinctive absorptive bands of these derivates were determined through infrared spectroscopy. Selenized and sulfated derivates have shown significant antitumor and immunoenhancing properties. Our findings revealed that at 400 μg/mL, the inhibition rate of selenated PTB on HeLa cells was 54.2% and that on HepG2 cells was 43.1%. Additionally, selenized PTC displayed significant immunoenhancing activity, with a proliferation rate of 63.7% at 400 μg/mL in RAW264.7 cells. These results provide valuable evidence supporting the consideration of polysaccharides from Pinellia ternata as a potential candidate for the development of antineoplastic drugs.

Coordination of bioactive phytochemicals from Aloe vera extracts to metal ions; investigation of the metal complexes and bioactive compound formed.

The bioactive compounds contained within many plants account for their pharmacological values. Aloe vera has a wide range of organic and inorganic components, including carbohydrate polymers, glucomannans, and a variety of other natural and synthetic materials. The study aims to take a look into the characteristics of some metal complexes produced from Aloe vera extracts. The extracts from Aloe vera were derived by means of acetone, distilled water and ethanol. The solubility of the metal complexes with the ligand at varying temperatures was established. FT-IR was used to carry out the infra-red examination of the ligand. The results revealed that alcoholic extract of Aloe vera leaf was not soluble in Cu, Fe, or Zn but only soluble in Fe, the extract by distilled water was soluble in Cu, Fe and Zn. However, the Aloe vera in acetone as well as in the Zn (II) and Cu (II) composites displayed a bending that was found at 1430.97cm-1, 1500.01cm-1 and 1615.90cm-1.every functional groups are assigned to be coordinating sites as a result of increase or decrease in the wave number, and absorption band. Findings from the investigation reveal that the complexion of the metal salts with diverse donor sites in the extract is indicated by an increase in the absorption peak of the functional groups in the metal composites of the extracts.

Band Gap Modulation in Zn2TiO4 Spinels for Efficient UV-A Persistent Luminescence

Spinels are important materials for an application in bioimaging. The key advantage with spinel-type hosts is the presence of antisite defects, which act as charge reservoirs for trapping electrons and holes at complementary defect sites. This makes them a host system similar to a molecular system. Herein, we present a systematic approach to modulating the band gap of an inverse Zn2TiO4 spinel. With a change in ZnO concentration, the absorption band at 375 nm diminishes and disappears at a ZnO:TiO2 concentration of 1.40:1.00. The band gap of the material is modified from 3.30 to 4.40 eV. The crystal structure of the sample does not change drastically as determined using X-ray diffraction and Rietveld refinement. The Zn2TiO4 emits in the UV-A region with a lifetime in the time domain of `ns’. The sample also shows persistent luminescence of at least 15 min upon excitation with 254 nm with prominent emission in the UV-A region (300–390 nm). The present results open a new avenue for the synthesis of spinel hosts where the band gap can be modified with ease. The UV emission thus observed is expected to find usage in interesting applications like photocatalysis, anti-counterfeiting, water disinfecting, etc.

Facile Recycling of Waste Biomass for Preparation of Hierarchical Porous Carbon with High-Performance Electromagnetic Wave Absorption

Hierarchical-porous-structured materials have been widely used in the field of electromagnetic wave (EMW) absorption, playing a critical role in minimizing EMW interference and pollution. High-quality EMW absorbers, characterized by a lower thickness, lighter weight, wider absorption band, and stronger absorption capacity, have been instrumental in reducing damage and preventing malfunctions in the automotive and aviation industries. The utilization of discarded nut shells through recycling can not only alleviate environmental problems but relieve resource constraints. Herein, a facile method for the preparation of hierarchical porous biomass carbon derived from abandoned Xanthoceras Sorbifolium Bunge Shell (XSS) biomass was developed for high-performance EMW absorption. The porous structures of XSS biochar were studied by using different levels of the K2CO3 activator and simple carbonization. The effect of K2CO3 on the EMW parameters, including the complex permittivity, complex permeability, polarization relaxation, and impedance matching, was analyzed. The best EMW absorption performance of the XSS biochar was observed at a mass ratio of activator-to-biomass of 2:1. A minimum reflection loss (RLmin) of −38.9 dB was achieved at 9.12 GHz, and a maximum effective absorption bandwidth (EABmax) of up to 3.28 GHz (14.72~18.0 GHz) could be obtained at a 1.8 mm thickness. These results demonstrated that hierarchical porous XSS carbon was prepared successfully. Simultaneously, the prepared XSS biochar was confirmed as a potential and powerfully attractive EMW-absorbing material. The proposal also provided a simple strategy for the development of a green, low-cost, and sustainable biochar as a lightweight high-performance absorbing material.

Chemical Synthesis of Bimetallic Ag/Co Nanoparticles for Colorimetric Detection of Cr3+ and Fe3+ and Its Catalytic Performance

Precious metal nanoparticles, especially Ag-based nanoparticles due to their strong surface plasma effect and excellent catalytic performance, have been widely applied in environmental remediation and detection of heavy metal ions in aqueous solution. In this study, first, bimetallic Ag/Co nanoparticles (Ag/Co NPs) modified by sodium citrate were synthesized by chemical reduction method. Second, bimetallic Ag/Co NPs were used as colorimetric probe for detecting [Formula: see text] and [Formula: see text] in aqueous solution simultaneously for the first time. The results showed that the probe had high specificity towards [Formula: see text] and [Formula: see text] among the tested metal ions. When [Formula: see text] was mixed with Ag/Co NPs, the solution quickly changed from yellow to pink, meanwhile, the UV–Vis absorption intensity declined at 400[Formula: see text]nm and a new prominent absorption band was formed at 530[Formula: see text]nm. While [Formula: see text] was mixed with Ag/Co NPs, the solution quickly changed from yellow to nearly colorless. The linear relationship between absorbance of bimetallic Ag/Co NPs at 400[Formula: see text]nm and −log of [Formula: see text] concentration is 1[Formula: see text]nM to 10[Formula: see text][Formula: see text]M, which [Formula: see text] and [Formula: see text]. The limit of detection (LOD) for this study was 1.14[Formula: see text]nM. Similar to [Formula: see text], the LOD for [Formula: see text] was calculated 16.3[Formula: see text][Formula: see text]M. In addition, the catalytic performance of bimetallic Ag/Co NPs was evaluated by methylene blue (MB) in the presence of H2O2. The catalytic degradation efficiency of bimetallic Ag/Co NPs was about 4.8 times greater than monometallic Ag NPs, confirming Ag and Co NPs had obviously synergistic effect. Therefore, this result made bimetallic Ag/Co NPs had potential application in the field of environmental remediation.

Visible-Light-Responsive Novel Ru(II)-Metallo-Antibiotics with Potential Antibiofilm and Antibacterial Activity.

Growing challenges with antibiotic resistance pose immense challenges in combating microbial infections and biofilm prevention on medical devices. Lately, antibacterial photodynamic therapy (aPDT) is now emerging as an alternative therapy to overcome this problem. Herein, we synthesized and characterized four Ru(II)-complexes, viz., [Ru(ph-tpy)(bpy)Cl]PF6 (Ru1), [Ru(ph-tpy)(dpq)Cl]PF6 (Ru2), [Ru(ph-tpy)(dppz)Cl]PF6 (Ru3), and [Ru(ph-tpy)(dppn)Cl]PF6 (Ru4) (where 4'-phenyl-2,2':6',2″-terpyridine = ph-tpy; 2,2'-bipyridine = bpy; dipyrido[3,2-f:2',3'-h]quinoxaline = dpq; dipyrido[3,2-a:2',3'-c]phenazine = dppz; and Benzo[I]dipyrido[3,2-a:2',3'-c]phenazine = dppn), among which Ru2-Ru4 are novel. Octahedral geometry of the complexes with a RuN5Cl core was evident from the crystal structure of Ru2. Ru1-Ru4 showed an MLCT absorption band in the 450-600 nm region, useful for aPDT performances. Further, optimum triplet excited state energy and excellent photostability of Ru1-Ru4 made them good photosensitizers for aPDT. Ru1-Ru4 demonstrated enhanced antimicrobial activity on visible-light exposure (400-700 nm, 10 J cm-2), confirmed using different antibacterial assays. Mechanistic studies revealed that inhibition of bacterial growth was due to the generation of oxidative stress (via NADH oxidation and ROS generation) upon treatment with Ru2-Ru4, resulting in destruction of the bacterial wall. Ru2 performed best killing performance against both Gram-negative (Escherichia coli) and Gram-positive (Bacillus subtilis) bacteria when exposed to light. Ru2-Ru4, when coated on a polydimethylsiloxane (PDMS) disk, showed long-term reusability and durable antibiofilm properties. Molecular docking confirmed the efficient interaction of Ru2-Ru4 with FabH (regulates fatty acid biosynthesis of E. coli) and PgaB (gives structural stability and helps biofilm formation of E. coli), resulting in probable downregulation. In vivo studies with healthy Wistar rats confirmed the biocompatibility of Ru2. This study shows that these lead complexes (Ru2-Ru4) can be used as potent alternative antimicrobial agents in low concentrations toward bacterial eradication with photodynamic therapy (PDT).

Polymer-integrated acoustic graphene plasmon resonator for sensitive detection of CO2 gas

Acoustic graphene plasmons (GPs) exhibit an exceptional density of electromagnetic states within the mid-infrared (MIR) and terahertz frequency ranges, leading to a pronounced near-field amplification and localization at the nanometer scale. This characteristic renders them highly promising for the development of ultra-sensitive plasmon-enhanced MIR sensing and spectroscopic applications. However, the tight spatial confinement inherent to acoustic GPs results in a significant momentum mismatch, which in turn leads to poor coupling efficiency with light in free space. To overcome this limitation, we leverage numerical simulations to show that GPs can act as an intermediary to facilitate efficient excitation of acoustic GPs by incident MIR radiation, achieving an extinction spectrum peak value of approximately 0.9. The proposed gas sensor based on the acoustic GP resonator is composed of pristine, large-area graphene, an array of periodic metal nanocubes, and a slender polyethylenimine (PEI) layer that adsorbs CO2, situated between the nanocubes and the graphene sheet. The sensing performance of the proposed sensor is numerically investigated. It is demonstrated that by incorporating a CO2-absorbing material into the acoustic GPs, we can perform highly sensitive assessments of the absorption bands within the PEI layer upon CO2 adsorption. The observed behavior of the acoustic GPs indicates a weakening and broadening with increasing CO2 concentrations, a phenomenon attributed to the alteration in the permittivity of the PEI in the interstitial layer due to CO2 adsorption. Numerical simulation results indicate that the sensitivity of the proposed hybrid gas sensor can reach up to 0.0183% ppm−1, which offers a remarkable 95-fold enhancement over the gas sensor based on graphene nanoribbons. Our findings underscore the potential of acoustic GP nanoresonators as a transformative platform for ultrasensitive plasmon-enhanced sensing applications, particularly when integrated with various gas adsorption layers or molecular agents.

Down-film as a new non-frame porous material for sound absorption

Down-polyethylene film material has been introduced for the first time as an excellent non-frame sound absorber, showing a distinctively outstanding performance. It contains down fiber adjacent to each other without firm connection in between, forming a structure of elastic fiber network. The unique structure has broadband response to sound wave, showing non-synchronous vibration in low and middle frequency and synchronous vibration in middle and high frequency. The broadband resonance in middle and high frequency allows the structure to achieve complete sound absorption in resonance frequency band. Moreover, down-polyethylene film material possesses forced vibration, corresponding sound absorption coefficient has been obtained based on vibration theory. The down-film sound absorption material has the characteristics of light weight, soft, environment-friendly, and has excellent broadband sound absorption performance.

Frequency selective rasorber based on cross bend resonators for wideband transmission and absorption

Abstract The wideband absorption and transmission of frequency-selective rasorber (FSR) remain a persistent challenge in the application of radar devices. In this article, a novel high performance wideband FSR design based on cross bend resonators (CBR) was proposed. The FSR consists of an upper absorption lossy layer, which offers broad absorption and transmission bands, and a lower bandpass frequency-selective surface (FSS) that enables a highly selective transmission of incident electromagnetic wave. Full wave simulation results showed that this novel design achieves an absorption bandwidth of 83.7% with more than 90% absorptivity in the frequency range of 5.2-12.7 GHz. Furthermore, the passband's fractional bandwidth (FBW) for the insertion loss (IL) less than -3 dB is 33.9%, ranging from 14.9 to 21 GHz, with the minimum IL recorded at 0.69 dB at 17.7 GHz. To further verify the proposed method, a prototype FSR with 10×10 units of 120 mm×120 mm was fabricated and the performance of the FSR was tested. The experiment results were in good agreement with the simulated results, and it showed a significant monostatic radar cross-section (RCS) reduction in the frequency range of 5.3 GHz to 18.3 GHz compared with a metallic plane of the same size.

Multicolor Inks of Black Phosphorus for Midwave-Infrared Optoelectronics.

Black phosphorus (bP) based ink with a bulk bandgap of 0.33eV (λ = 3.7µm) has recently been shown to be promising for large-area, high performance mid-wave infrared (MWIR) optoelectronics. However, the development of multicolor bP inks expanding across the MWIR wavelength range has been challenging. Here we demonstrate a multicolor ink process based on bP with spectral emission tuned from 0.28eV (λ ∼ 4.4µm) to 0.8eV (λ ∼ 1.5µm). Specifically, through the reduction of bP particle size distribution (i.e., lateral dimension and thickness), the optical bandgap systematically blue-shifts, reaching up to 0.8eV. Conversely, alloying bP with arsenic (bP1- xAsx) induces a red-shift in the bandgap to 0.28eV. The ink processed films are passivated with an infrared-transparent epoxy for stable infrared emission in ambient air. Utilizing these multicolor bP-based inks as an infrared light source, a gas sensing system is demonstrated that selectively detects gases such as CO2 and CH4 whose absorption band varies around 4.3µm and 3.3µm, respectively. The presented ink formulation sets the stage for the advancement of multiplex MWIR optoelectronics, including spectrometers and spectral imaging using a low-cost material processing platform. This article is protected by copyright. All rights reserved.

ИССЛЕДОВАНИЕ ВОЗМОЖНОСТИ ИЗМЕРЕНИЯ ГЛИКИРОВАННОГО ГЕМОГЛОБИНА МЕТОДОМ СКАНИРУЮЩЕЙ ПРОТОЧНОЙ ЦИТОМЕТРИИ

The article explores the possibility of measuring glycated hemoglobin in single erythrocytes using scanning flow cytometry. Calculations of the intensity of scattered radiation from an erythrocyte in a wide angular range (light scattering indicatrix) were carried out for wavelengths at the maximum of the absorption band of glycated hemoglobin. The maximum sensitivity for the concentration of glycated hemoglobin was set at a wavelength of 415 nm. As a result, it is possible to reliably separate the concentrations of glycated hemoglobin in donors and patients with diagnosed diabetes with a difference in HbA1c concentrations of more than 5% on the existing practical implementation of a scanning flow cytometer, which includes lasers: 405 nm (30 mW, Radius, Coherent Inc., Santa Clara, USA) and 660 nm (LM–660–20–S, 40 mW). A theoretical calculation for a wavelength of 415 nm showed that a noticeable difference in the value of the scattering intensity (more than 10%) is observed only in the case of a difference in the concentrations of glycated hemoglobin of at least 3%. Thus, if a laser with a wavelength of 415 nm is installed on the existing practical implementation of the device, then the determination of glycated hemoglobin will become possible with an accuracy of no more than 3%.

Copper nanoparticle and point defect formation in Cu+-Na+ ion-exchanged glass using protons of 2 MeV energy.

There are several applications for irradiating materials with protons that could provide alternative methodologies to synthesize and induce the formation of new compounds of different size scales. In this study, we explored the effects of proton irradiation oncommercial glass silicate that was previously subjected to a Cu+-Na+ ion exchange (IE) treatment at 600 °C for a duration of 60 min. The ion-exchanged glass samples were irradiated with protons (p+) of 2 MeV energy at doses in the range of thousands of grays (3.3 × 103, 7.9 × 103 Gy) and hundreds of thousands of grays (3.6 × 105 Gy). Significant changes in the optical and structural properties were observed post the radiation treatment. The UV-Visible absorption spectra of the irradiated samples revealed the appearance of overlapping absorption bands, which could be deconvoluted into three Gaussian-shaped bands peaking at 566, 620 and 680 nm. These three bands could be attributed to the surface plasmon resonance (SPR) of copper nanoparticles, non-bridging oxygen hole centers (NBOHCs) and self-trapped hole (STH) defects, respectively. Prominent photoluminescence (PL) was observed in the Cu-exchanged and irradiated samples, mainly induced by the presence of both Cu+ and Cu2O. Increasing the irradiation dose led to an increase in the PL intensity due to the conversion of Cu2+ ions into Cu+. This result was confirmed by electron paramagnetic resonance (EPR) spectroscopy that shows a decrease in the Cu2+ signal when increasing the dose of proton exposure. Transmission electron microscopy (TEM) and high-resolution TEM (TEM and HRTEM) observations confirmed the presence of copper nanoparticles (CuNPs) in the doped and p+ irradiated Cu-exchanged glass silicate samples. These CuNPs were found to be crystalline with an average size of 12.39 nm.

Theoretical prediction of broadband ambient light optogenetic vision restoration with ChRmine and its mutants

Vision restoration is one of the most promising applications of optogenetics. However, it is limited due to the poor-sensitivity, slow-kinetics and narrow band absorption spectra of opsins. Here, a detailed theoretical study of retinal ganglion neurons (RGNs) expressed with ChRmine, ReaChR, CoChR, CatCh and their mutants, with near monochromatic LEDs, and broadband sunlight, halogen lamp, RGB LED light, and pure white light sources has been presented. All the opsins exhibit improved light sensitivity and larger photocurrent on illuminating with broadband light sources compared to narrow band LEDs. ChRmine allows firing at ambient sunlight (1.5 nW/mm2) and pure white light (1.2 nW/mm2), which is lowest among the opsins considered. The broadband activation spectrum of ChRmine and its mutants is also useful to restore color sensitivity. Although ChRmine exhibits slower turn-off kinetics with broadband light, high-fidelity spikes can be evoked upto 50 Hz. This limit extends upto 80 Hz with the improved hsChRmine mutant although it requires double the irradiance compared to ChRmine. The present study shows that ChRmine and its mutants allow activation of RGNs with ambient light which is useful for goggle-free white light optogenetic retinal prostheses with improved quality of restored vision.