Absorption Bands Research Articles

Surface and Atmospheric Heating Responses to Spectrally Resolved Albedo of Frozen and Liquid Water Surfaces

AbstractMultiple Earth system models (ESMs) discretize surface albedo into two semi‐broadbands comprising the UV/visible and near‐infrared (NIR) wavelengths. Here, we use an offline single‐column radiative transfer model to investigate the radiative effects of spectrally resolving the surface albedo. We use the Snow, Ice, and Aerosol Radiative model, extended to simulate liquid water, to calculate snow, ice, and liquid water albedo. We flux‐weight the hyperspectral albedo into the coarser spectral bands used by the atmospheric shortwave radiative transfer model. We establish representative atmospheric profiles for the three surface types and compare their shortwave fluxes and atmospheric warming rates with the spectrally resolved albedo to those calculated with the semi‐broadband approximation. Spectrally resolved surface albedo over snow and ice reduces atmospheric warming by darkening the albedo of NIR bands, correcting the too‐strong surface absorption in visible bands, and too‐weak surface absorption in shortwave infrared bands caused by the semi‐broadband approximation. We explore the effects on surface and atmospheric warming rates of varying solar zenith angle, cloud cover, relative humidity, and snow grain/air bubble radii. The semi‐broadband albedo biases can exceed 10% and 2% for the surface and atmospheric net flux respectively, being particularly strong under conditions which alter the distributions of surface insolation (i.e., cloud cover or increased atmospheric water vapor). These results show that transmitting a higher resolution spectral radiation field between the atmosphere and surface reduces biases in surface absorption and atmospheric heating present in ESMs that currently use the semi‐broadband approximation.

Manganese 11 Complexes of Salycilhydroxamix Acid with Aniline and Ammonia with Its Properties the Effect on Microorganism

The salicylichyroxamic acid (SHA) its complex of Mn (II) along with their mixed ligand complexes of ammonia and aniline were prepared in high yields. Both the ligands and complexes were both soluble in methanol, DMSO but are insoluble in chloroform and distilled water. Their melting point were high and falls between 1910C - 400 0C. The IR spectra of the synthesized compound showed the coordination of the ligand through the oxygen of the phenolic NOH and C=O functional groups to the metals. The electronic spectra of the complexes in methanol showed some observable absorption bands of the following transitions; for Mn(SHA) complex transition is at 6A1g(s)→ 4T2g, that of Ammonia mixed complex 6A1g(s)→ 4T2g and that of Aniline mixed complex 6A1g(s)→ 4T2g. All the transitions were in the range of those observed for octahedral complexes. The antimicrobial activity of the ligand SHA (C7H7NO3), the complexes and reference drug was study against two bacterial species staphylococcus auerus and Escherichia coli, and one fungi species candida albicans. This was done using agar disc diffusion method measuring the diameter of inhibitions zone for each compound. The Mn (II) complexes produced in this study showed significant activity against the used micro-organisms. Therefore, they have potential application as anti-microbial agent.

Distyryl Carboxylic Acid Substituted BODIPY and BODIPY‐C60 Systems for Generation of Singlet Oxygen

AbstractBODIPY based molecules functionalized with water soluble moieties have been developed and recognized as liable triplet photosensitizers for phototherapeutic applications. In this work, we have prepared BODIPY analogues with dicarboxylic acid groups and bearing iodine or fullerene moieties for efficient intersystem crossing which display far‐red absorption band and high singlet oxygen production both in organic and aqueous media. In this perspective by using similar design the effect of the halogenation of the dyes versus spin converter on the skeleton were compared. The structures of the synthesized BODIPYs and BODIPY‐C60 (6–10) were elucidated by mass, 1H and 13C NMR spectroscopic techniques. Photophysical and photochemical properties of the compounds were examined using UV‐Vis. absorption and fluorescence emission spectrophotometers. The absorption intensities of the trap molecules (DPBF and ADBA) reduced because of singlet oxygen generation in the media. This study may provide useful infrastructure to elucidate the relationship between the use of fullerene (9) or iodine (10) where singlet oxygen quantum yield of 9 and 10 are determined as 0.87 and 0.97 respectively.

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.

Near-Infrared Absorbing BODIPY-Xanthene Hybrids for Multiplexed Photoacoustic Imaging.

We report a series of ethenylene-bridged D-π-A BODIPY-xanthene hybrid dyes with precisely regulated absorption bands ranging from the far-red to the near-infrared region (NIR, 700-1000 nm) through rational molecular design. These dyes have excellent photoacoustic properties, and their biocompatibility can be significantly improved by facilely introducing water-soluble groups. In vivo two-channel multiplexed photoacoustic imaging demonstrated their high-resolution imaging capabilities, making them promising candidates for future NIR bioimaging applications.

Conformational analysis and spectroscopic properties of antichagasic nifurtimox

Considering the health relevance of Chagas' disease, recent research efforts have focused on developing more efficient drug delivery systems containing nifurtimox (NFX). This paper comprehensively investigates NFX through conformational analysis and spectroscopic characterization. Using a conformer-rotamer ensemble sampling tool (CREST-xtb), five distinct conformers of NFX were sampled within a 3.0 kcal mol−1 relative energy window. Subsequently, such structures were used as inputs for geometry optimization by density functional theory (DFT) at B3LYP-def2-TZVP level of theory. Notably, harmonic vibrational frequencies were calculated to establish an in-depth comparison with experimental results and existing literature for the NFX or similar molecules and functional groups, thereby achieving a widely reasoned assignment of the mid-infrared band absorptions for the first time. Moreover, UV–VIS spectra of NFX were obtained in several solvents, enabling the determination of the molar absorptivity coefficient for the two electronic transitions observed for NFX. Among the aprotic solvents, a bathochromic effect was observed in the function of the dielectric constants. Furthermore, a hypochromic effect was observed when the drug was dissolved in protic solvents. These findings offer crucial support for new drug delivery systems containing NFX while demonstrating the potential of spectrophotometric studies in establishing quality control assays for NFX drug products.

Phase and Morphology of Water-ice Grains Formed in a Cryogenic Laboratory Plasma

Grains of ice are formed spontaneously when water vapor is injected into a weakly ionized laboratory plasma in which the background gas has been cooled to cryogenic temperatures comparable to those of deep space. These ice grains are levitated indefinitely within the plasma so that their time evolution can be observed under free-floating conditions. Using microscope imaging, ice grains are shown to have a spindle-like fractal structure and grow over time. Both crystalline and amorphous phases of ice are observed using Fourier transform infrared spectroscopy. A mix of crystalline and amorphous grains coexists under certain thermal conditions, and a linear mixing model is used on the ice absorption band surrounding 3.2 μm to examine the ice phase composition and its temporal stability. The extinction spectrum is also affected by inelastic scattering as grains grow, and characteristic grain radii are obtained from Mie scattering theory and compared to size measurements from direct imaging. Observations are used to compare possible ice nucleation mechanisms, and it is concluded that nucleation is likely catalyzed by ions, as ice does not nucleate in the absence of plasma and impurities are not detected. Ice grain properties and infrared extinction spectra show similarity to observations of some astrophysical ices observed in protoplanetary disks, implying that the fractal morphology of the ice and observed processes of homogeneous ice nucleation could occur as well in such astrophysical environments with weakly ionized conditions.

Optical and photoluminescence properties of trivalent rare earth ions doped LiMgPO4

Trivalent rare-earth-activated luminescent materials have attracted a lot of attention due to their fascinating optical properties and broad range of applications. In this study, polycrystalline Sm and Eu-doped LiMgPO4 luminescent materials were synthesized using a solid-state reaction technique. The crystalline structures, morphological features, and optical characteristics of the synthesized materials were thoroughly investigated using x-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Field-Emission Scanning Electron Microscopy (FE-SEM) and UV–vis spectroscopy. The Rietveld refinement analysis confirmed the phase purity of synthesized phosphors. In addition, the strain induced owing to the incorporation of trivalent rare-earth ions and crystallite sizes of each synthesized material was estimated using the Williamsons-Hall (W-H) and modified Debye-Sherrer equations. The estimated results of the microstrain were reported to be 0.0010, 0.0023 and 0.0020. Subsequently, as a consequence of distinct peak profile options, the projected average crystallite size by both approaches was distinct. The UV–vis spectroscopy analysis reveals that Sm and Eu doped materials exhibit absorption bands around 402 nm and 396 nm and depicts the declining band gap values. The Photoluminescence (PL) spectra at 402 nm and 395 nm excitation wavelengths exhibited the distinctive emissions of both Sm3+ (4G5/2 → 6H7/2) and Eu3+ (5D0 → 7F2) ions emanating due to the intra-configurational f - f and 4 f − 4 f transitions. Finally, the CIE diagram explicitly demonstrates that the Sm and Eu-modified materials reveal their exceptional color purity. McCamy’s approach was used to determine various parameters of trivalent rare-earth doped materials. The correlated color temperature ( TCCT ) and their coordinates TCCT (ζ, β) was found to be 2287 K, 1900 K, 0.281, 0.632, and 0.302, 0.681 respectively. Temperature-dependent emission spectra exhibit excellent color and thermal stability at high temperatures. The obtained results in this study indicate that the synthesized luminescent materials can potentially be used in white light-emitting diode applications.

Lithography‐Free Method to Synthesize Quasiperiodic Silicon Inverted‐Pyramid Arrays: A Broadband Light Trapper for High‐Efficiency Thin Silicon Solar Cells

Thin silicon solar cells can be a low‐cost effective photo‐conversion device, if the device can efficiently absorb the solar spectrum. Herein, a new lithography‐free technique is developed for the fabrication of quasiperiodic silicon inverted‐pyramids arrays (SiIPAs), which show a high‐light‐trapping phenomenon in the ultraviolet–visible—near‐infrared (300–2000 nm). Fabricated SiIPA samples show a significant reduction of reflectance (3%) in the silicon absorption band (300–1000 nm). A unique additional absorption of 33–44% compared to the planar silicon is observed in the sub‐bandgap region of silicon (1100–2000 nm) for these samples. Photocurrent response measurement confirms the generation of additional electron–hole pairs in the sub‐bandgap region of silicon for the SiIPA samples in comparison with planar sample. In these results, the effect of field confinement and the creation of optical resonance modes within these structures, qualitatively supported by numerical simulation, are signified. The estimated short‐circuit current density using the experimental absorption spectrum of SiIPAs is 55.46 mA cm−2, which is far higher than the Lambertian limit of ≈43 mA cm−2. The theoretical efficiency of the solar cell can be achieved up to 35.22%, which surpasses the Shockley–Queisser limit of 33.7%.

Novel assaying method for the accurate and rapid analysis of antioxidant total capacity based on hexachloroiridate(IV)

We introduce a novel method, namely IrRAC, for assessing total antioxidant capacity utilizing the single electron oxidant hexachloroiridate(IV). This method leverages the 488 nm absorption band of [IrCl6]2− largely reducing interferences from antioxidants and their oxidation products. [IrCl6]2− is stable 6 h in phosphate-buffered saline (PBS) ensuring consistent and reproducible absorbance readings and rendering spectrophotometric determinations under physiological neutrality. Individual assessments of 23 antioxidants reveal a linear correlation between decreasing absorbance and increasing antioxidant concentration. When the IrRAC assay was compared with several established water-based methods, strong correlations were found. Importantly, [IrCl6]2− shows a minimal oxidation of non-antioxidative substances. Moreover, IrRAC performs well with synthetic antioxidant mixtures and real samples, highlighting that the nature of antioxidants dominates the assay without much disturbance. Commercial availability of K2[IrCl6] eliminates the need of pretreatment of the oxidant. Undoubtedly, the new method confers a compelling and cost-effective alternative to the existing electron transfer-based methodologies.

Wavelength and polarisation dependence of pump-induced loss in Ti:sapphire

We use pump beam wavelength and polarisation to demonstrate that the phenomenon of pump-induced loss in Ti:sapphire is linked to simultaneous excitation of two separate absorption bands: the Ti3+ pump band and the parasitic 400 nm residual absorption. We find that the degree of pump-induced loss is linked to the relative absorption strengths of the residual absorption band and the Ti3+ pump band at the wavelength(s) of excitation.

9-Borafluoren-9-yl and diphenylboron tetracoordinate complexes of 8-quinolinolato ligands with heavy-atoms substituents: Synthesis, fluorescence and application in OLED devices

This work describes the synthesis and characterisation of new tetrahedral boron complexes, incorporating bromine- or iodine-substituted 8-quinolinolato chelate chromophores connected to 9-borafluoren-9-yl or diphenylboron orthogonal fragments. The molecular features and photophysical properties of these complexes are analysed in both solution and solid state. Steady-state photophysical studies reveal photoluminescence quantum yields (Φf) ranging from 0.02 to 0.15 and prompt fluorescence (PF) lifetimes (τf) between 2 and 16 ns. Time-resolved photophysical experiments show the presence of delayed fluorescence (DF) and phosphorescence at both 77 K and room temperature. The DF intensity increases with a rise in temperature. This variation is ascribed to an enhancement in the intersystem crossing (ISC) process promoted by the bromine or iodine heavy-atom effect. Investigations into the dependence of DF intensity relative to the excitation dose indicate emissions stemming either from Triplet-Triplet Annihilation (TTA), Thermally Activated Delayed Fluorescence (TADF), or a combination of these competing mechanisms. The effect is related to the size and number of heavy-atom substituents in each boron complex. A study of the DF emission intensity as a function of the excitation dose reveals that diiodo-substituted 8-quinolinolato boron complexes, whether rigid or flexible, display TADF emission. Rigid 5,7-dibromo- and 5-chloro-7-iodo-substituted 8-quinolinolato complexes exhibit a combined TADF-TTA mechanism, whereas the other complexes predominantly demonstrate pure TTA emission. DFT and TDDFT calculations showed that the ground state structures reproduced the experimental geometries and only small increases in bond lengths were observed in the excited state geometries. The low energy absorption bands displayed mainly intra-ligand π→π* (8-quinolinato) character. The fluorescence emission energies were well reproduced, while the singlet-triplet energy gaps were relatively high and spin-orbit coupling was relevant for complexes with heavy-atoms. Ultimately, organic light-emitting diodes (OLEDs) are fabricated using the most luminescent boron complexes. The best OLED is obtained when using complex 3a, which displays green electroluminescence (EL) (λEL = 502 nm) with maximum external quantum efficiency (EQEmax) of 2.5% and maximum luminance (Lmax) of 2200 cd m−2.

A Halogen Bonding [2]Rotaxane Shuttle for Chloride-Selective Optical Sensing.

The first example of a [2]rotaxane shuttle capable of selective optical sensing of chloride anions over other halides is reported. The rotaxane was synthesised via a chloride ion template-directed cyclisation of an isophthalamide macrocycle around a multi-station axle containing peripheral naphthalene diimide (NDI) stations and a halogen bonding (XB) bis(iodotriazole) based station. Proton NMR studies indicate the macrocycle resides preferentially at the NDI stations in the free rotaxane, where it is stabilised by aromatic donor-acceptor charge transfer interactions between the axle NDI and macrocycle hydroquinone moieties. Addition of chloride ions in an aqueous-acetone solvent mixture induces macrocycle translocation to the XB anion binding station to facilitate the formation of convergent XB⋅⋅⋅Cl- and hydrogen bonding HB⋅⋅⋅Cl- interactions, which is accompanied by a reduction of the charge-transfer absorption band. Importantly, little to no optical response was induced by addition of bromide or iodide to the rotaxane, indicative of the size discriminative steric inaccessibility of the interlocked cavity to the larger halides, demonstrating the potential of using the mechanical bond effect as a potent strategy and tool in chloride-selective chemo-sensing applications in aqueous containing solvent environments.

Effect of doping TiO2 with Fe on the loading of a natural extract

This study explores the relationship between Fe doping in TiO2 nanoparticles and their capacity to load a natural citrus extract. Synthesized TiO2 (T) and TiO2-Fe (TF) nanoparticles were characterized using XRD patterns, N2 physisorption, UV–Vis and FTIR spectroscopy, and electron microscopy. Fe doping induced shifts in X-ray diffraction patterns and broadened absorption bands in UV–Vis spectra, reflecting changes in crystal structure and electronic transitions. BET analysis revealed increased surface area with Fe doping. Loading of the natural citrus extract was confirmed by FTIR. SEM and TEM images displayed slight morphological changes and a reduced nanoparticle size after Fe doping. Finally, Fe doped TiO2 demonstrated an improvement in loading ability with loading values up to 82.4%.

POLYIMIDE FILMS IMPLANTED BY MANGANESE IONS

The optical and strength properties of Kapton polyimide films implanted with manganese ions with an energy of 40 keV and a dose of 5·1016 – 1·1017 cm–2 at a current density in the ion beam of 4 μA/cm2 have been studied. It has been experimentally established that during the process of ion implantation, modification of a thin nearsurface layer of polyimide occurs not only on the implanted side, but also on the reverse side of the film. Radiationstimulated modification of the back surface of the polyimide film leads to the formation of a surface layer up to 5 μm thick with increased microhardness. This may be due to the restructuring of metastable defects formed during the film manufacturing process and the simultaneous relaxation of elastic stresses in the surface layer. During the implantation process, a decrease in the intensity of absorption bands with maxima at ~ 2870 and ~ 2750 nm is observed, due to the evaporation of residual water under high vacuum conditions and reactions of residual solvent molecules, as well as radiation-induced processes on by-products of polyimide synthesis.

ELECTRON IRRADIATED PI2610 POLYIMIDE FILMS ON MONOCRYSTALLINE SILICON

The optical and strength properties of electron-irradiated films of a polyimide composition (polyimide PI2610) deposited on the surface of single-crystalline silicon wafers of the KDB-10 grade by centrifugation were studied. Irradiation with electrons with an energy of 5 MeV was carried out on a linear accelerator U-003 in the dose range 1·1014 – 2·1015 cm–2. It has been experimentally established that at an irradiation dose of Ф = 1∙1014 cm–2, relaxation of elastic stress fields in the polyimide film is observed, which is expressed in modification of the shape of bands with maxima at 1349 and 1700 cm–1, caused by vibrations of the C–N–Cst bond and the C=O double bond imide ring. Polyimide PI-2610 films on silicon are quite stable when irradiated with electrons. A noticeable transformation of the ATR spectrum at a dose of 2∙1015 cm–2 was observed only in the region of stretching vibrations of C–H and O–H bonds, which is due to radiation-induced processes on by-products of polyimide synthesis and residual solvents. No noticeable decrease in the intensity of absorption bands caused by vibrations of the skeleton of the aromatic ring, imide ring, single and double C–C and C–O bonds, and imide C=O bonds was observed.

Superparamagnetic nanocubes of Co and Cu co-doped Mn-based ferrites as microwave absorbing material

The requirement in resolving electromagnetic (EM) problems in stealth warhead technologies are excellent absorption ability, lightweight, and thin dimensions. In this direction, this study provides a straightforward hydrothermal one-pot method to synthesize superparamagnetic Mn-based ferrite co-doped with Co and Cu (MCCF), and the article presents its microwave absorption properties. Using cutting-edge techniques, the MCCF nanocomposite phase structure, morphological, superparamagnetic, and microwave absorption properties were measured and analyzed. MCCF-822 ferrite shows superparamagnetic properties simultaneously with a high Ms value 71.4 emu/g. Vector network analysis of MCCF-822 with 70 wt% loading demonstrates an effective absorption bandwidth (EAB) of 5.2 GHz with a maximum reflection loss (RLmax) of −19.2 dB at 2 mm thickness, and it spans almost 92.77 % frequency region (3.3–18 GHz range with RL < −10 dB) by varying thickness 1.7 mm–6 mm. At 60 wt% loading, it covers the whole X & Ku band with a thickness range from 2 to 9 mm with a good EAB of 4.3 GHz at 2.5 mm thickness with RLmax of −16 dB. The dual absorption bands are also present in MCCF-613, which increases the EAB with RLmax −52.99 dB at 9 mm, fulfilling the superparamagnetic properties. Thus, MCCF-822 is proposed as a cost-effective superior ferrite nanocomposite for microwave absorption applications.

Substituent effect on the electronic and optical properties of newly designed pyrrole derivatives using density functional theory

Abstract This work explores six newly designed compounds obtained by several substitutions in 2,5-di(2-thienyl) pyrrole molecule. For this series of compounds, the electronic and optical properties were investigated using density functional theory and time-dependent density functional theory (TD-DFT). The new compounds were characterized by calculating the chemical parameters that correlated with their optical and electrical properties. The lowest unoccupied molecular orbital (LUMO) and the highest occupied molecular orbital (HOMO) energies are calculated using the B3LYP functional with the 6-311G (d, p) basis set. The most low-lying energy level of the LUMO was found for Perr-NO2, indicating its effective electron injection capabilities and oxidation resistance. The HOMO and LUMO distributions of Perr-Cl and Perr-NO2 displayed a remarkable complementarity throughout each component of the two compounds, indicating an effective intermolecular charge transfer. The molecular electrostatic potential analysis demonstrated that the proposed compounds have a broad distribution of electrophilic and nucleophilic sites, which predict a high degree of chemical reactivity. The electron density analysis at the bonding and anti-bonding sites of the title compounds was performed using the electron localization function and local orbital locator techniques. Non-covalent interaction analysis using the reduced density gradient approach classified all types of interaction: repulsive, weak, and attractive interactions within compound fragments. All compounds exhibited a robust repulsive interaction, as proved by the red spikes at 0.038 a.u. The ultraviolet/visible (UV/vis) spectrum was obtained by TD-DFT using CAM-B3LYP models in conjunction with 6-311G (d, p) basis set and methanol as a solvent, the absorption bands were found within the UV range, and the maximum wavelength showed red-shifted increases. These compounds could serve as a base material for developing selective gas sensors with considerable UV/vis absorption (180–400 nm). According to the research results, the designed compounds are good candidates for use as precursors in polymer designs for optoelectronic and sensor applications due to their high electrical conductivity and photochemical properties.

A thiazole-based colorimetric and photoluminescent chemosensors for As3+ ions detection: Density functional theory, test strips, real samples, and bioimaging applications

A Schiff-base Ethyl (E)-2-(3-((2-carbamothioylhydrazono)methyl)-4-hydroxyphenyl)-4-methylthiazole-5-carboxylate (TZTS) dual functional colorimetric and photoluminescent chemosensor which includes thiazole and thiosemicarbazide has been synthesized to detect arsenic (As3+) ions selectively in DMSO: H2O (7:3, v/v) solvent system. The molecular structure of the probe was characterized via FT-IR, 1H, and 13C NMR & HRMS analysis. Interestingly, the probe exhibits a remarkable and specific colorimetric and photoluminescence response to As3+ ions when exposed to various metal cations. The absorption spectral changes of TZTS were observed upon the addition of As3+ ions, with a naked eye detectable color change from colorless to yellow color. Additionally, the chemosensor (TZTS) exhibited a new absorption band at 412 nm and emission enhancements in photoluminescence at 528 nm after adding As3+ ions. The limit of detection (LOD) for As3+ ions was calculated to be 16.5 and 7.19 × 10−9 M by the UV–visible and photoluminescent titration methods, respectively. The underlying mechanism and experimental observations have been comprehensively elucidated through techniques such as Job’s plot, Benesi-Hildebrand studies, and density functional theory (DFT) calculations. For practical application, the efficient determination of As3+ ions were accomplished using a spike and recovery approach applied to real water samples. In addition, the developed probe was successfully employed in test strip applications, allowing for the naked-eye detection of arsenic ions. Moreover, fluorescence imaging experiments of As3+ ions in the breast cancer cell line (MCF-7) demonstrated their practical applications in biological systems. Consequently, these findings highlight the significant potential of the TZTS sensor for detecting As3+ ions in environmental analysis systems.

Hollow Fe3O4/Fe@C nanocubes for broadband microwave absorption spanning low- and high-frequency bands

Rationally constructing hollow structures with heterogeneous interface is usually an effective strategy to regulate the electromagnetic response behavior for lightweight and strong absorption, but achieving low-frequency and broadband absorption is a major challenge. This work adopts a novel Fe(II)/Fe(III) ions regulation strategy to design and synthesize hollow Fe(OH)X (x = 2, 3) nanocubes, which addresses the disadvantages of time-consuming or using etchant. Subsequently, a unique hollow Fe3O4/Fe@C nanoboxes with adjustable magnetic composition and uniformly coated shell have been successfully synthesized by in-situ carbonization with the assistance of phenolic resin and hydrogen thermal reduction. Notably, the different magnetic components induce the magnetic coupling assembly and play a crucial role in determining its electromagnetic parameters, whereas Fe3O4 contributes to more dipole polarization and stronger low-frequency response characteristics. For Fe3O4@C hollow nanoboxes, the minimum reflection loss (RLmin) is as low as –119.9 dB at 2.3 mm, and extremely wide effective absorption bandwidth (EAB) of 11.4 GHz is achieved spanning low-frequency band of 2.8 ∼ 7.2 GHz and high-frequency band of 11.0 ∼ 18 GHz at 5.0 mm. Surprisingly, the Fe3O4@C also has satisfactory EAB20 (RL＜ –20 dB) reaching 7.1 GHz (14.9 ∼ 18 GHz) at a thin thickness of 1.8 mm. The RLmin of other hollow nanoboxes is also below –30 dB, and the EAB is greater than 9 GHz. This study provides a competitive candidate for efficient microwave absorption in complex frequency bands, especially low-frequency bands.