Absorption Bands Research Articles

Passivation Effect of Rock-Salt Nitride Materials on a Planar p-Si Photocathode for Solar Water Reduction.

Photoelectrochemical water splitting, which uses sunlight to produce clean hydrogen fuel, is gaining traction with rising concerns about fossil fuels and pollution. Silicon (Si) photocathodes are promising for this process due to their light absorption and favorable band alignment for hydrogen production. However, limitations such as reflectance, low photovoltage, and rapid photocorrosion hinder their overall performance and stability. An interfacial insulating layer such as SiOx ensures superior durability to p-Si photocathodes. However, the inherent heterogeneity and intrinsic defects pose challenges to effective surface passivation. This study investigates the challenges of photocorrosion and utilization of a thin titanium nitride (TiN) passivation layer deposited using direct-current magnetron sputtering to protect the native silicon oxide (SiOx) layer. Additionally, a molybdenum oxynitride (Mo(O,N)x) bifunctional layer is employed to enhance both the electrocatalytic activity and durability of the photocathode. The presence of oxygen and nitrogen within this cocatalyst layer modifies the surface chemistry of the p-Si photocathode, promoting favorable interfacial interactions with electrolyte species during PEC reactions. This modification facilitates efficient charge transfer processes and accelerates reaction kinetics, ultimately optimizing the performance and operational lifetime of the photocathode. The resulting Mo(O,N)x/TiN/p-Si photocathode exhibited a remarkable onset potential of +0.46 VRHE in harsh acidic conditions under simulated sunlight (AM 1.5G illumination, 100 mW·cm-2). Notably, the photocathode demonstrated exceptional long-term stability exceeding 140 h, highlighting the combined TiN passivation and Mo(O,N)x cocatalyst as a protection strategy.

Highly Elastic Full Hydrocarbon Ultralong RTP Polymers with Visible Light Excitable S0→T1 Population

AbstractHighly elastic ultralong organic room temperature phosphorescence (RTP) polymers are highly desired in wearable optoelectronic fields, but they are hardly realized in rubbers since chain segment motions deactivate triplet excitons. In the current work, it is revealed that polystyrene (PS) can inhibit triplet thermal deactivation of coronene (Cor), and it is the serious oxygen diffusion and quenching that disables RTP emission of Cor/polymers. In view of oxygen barrier function of rubbers, PS−polyisoprene−PS tri‐block elastomers (SIS) are used as Cor's doping matrices. The results show that Cor/SIS sheets show bright and ultralong afterglow with RTP lifetime up to 3.64 s in air after brief 365 nm light excitation. More impressively, Cor/SIS and its red fluorescent dye doped sheets all exhibit ultralong room temperature afterglow under large dynamic elastic deformation. Further, all these sheets exhibit long‐wave blue light excited afterglow despite Cor/SIS having no visible light absorption band, and the unique photoexcitation and emission mechanism is verified. This work not only provides the development strategy of the latest elastic RTP materials, but also will evoke a fresh understanding on organic doped RTP polymers.

Nanotube formation and coating of hydroxyapatite-polyvinyl alcohol-collagen composite on Ti-6Al-4V metal alloy

Abstract Ti-6Al-4V metal is widely used as an implantable material due to its biocompatibility and corrosion resistance; however, it has low bioactive properties. The formation of nanotubes and a hydroxyapatite-polyvinyl alcohol-collagen composite coating on Ti-6Al-4V metal aims to enhance its biocompatibility and bioactivity. The nanotube oxide layer Ti-6Al-4V was formed by the anodization method. The composite’s infrared spectrum showed characteristic absorption bands from Hydroxyapatite (HAp), polyvinyl alcohol, and collagen. The composite-coated Ti-6Al-4V metal, both non-nanotube, and nanotube, showed a typical diffraction pattern of HAp and titanium element. The electron microscope image showed the uniform granular form of HAp. The corrosion test results showed that composite-coated nanotube Ti-6Al-4V metal could not improve corrosion resistance. It is also relevant to the in vitro test in a lactate ringer solution that showed the higher Ca2+ ion of nanotube Ti-6Al-4V metal than that of non-nanotube Ti-6Al-4V metal.

Synthesis of 2-Amino-4-arylazulenes from 8-Aryl-2H-cyclohepta[b]furan-2-ones and Transformation into 6-Aryl-7H-naphth[3,2,1-cd]azulen-7-ones.

2-Amino-4-arylazulene derivatives were prepared from 8-aryl-2H-cyclohepta[b]furan-2-ones, which were converted into 6-aryl-7H-naphth[3,2,1-cd]azulen-7-ones through a several step process. The reaction of 8-aryl-2H-cyclohepta[b]furan-2-ones bearing an ester group at the 3-position with malononitrile in the presence of triethylamine afforded 2-amino-4-arylazulenes. The prepared 2-amino-4-arylazulenes were converted to the corresponding 2-chloro derivatives by the Sandmeyer reaction, which were subsequently transformed into 2,4-diarylazulenes by Suzuki-Miyaura coupling with various aryl boronic acids. 2,4-Diarylazulenes underwent intramolecular cyclization between aryl and cyano groups by Brønsted acid to give 6-aryl-7H-naphth[3,2,1-cd]azulen-7-ones. UV/vis spectral analysis revealed that 6-aryl-7H-naphth[3,2,1-cd]azulen-7-one with a N,N-dimethylaminophenyl group at the 6-position exhibited a broad and strong absorption band in the visible region due to intramolecular charge transfer. Furthermore, 6-aryl-7H-naphth[3,2,1-cd]azulen-7-ones exhibited halochromism in 30% CF3CO2H/CH2Cl2. Although fluorescence was not observed in solution, 8-aryl-2H-cyclohepta[b]furan-2-ones with an ester function were found to fluoresce in the solid state. 6-Aryl-7H-naphth[3,2,1-cd]azulen-7-ones also displayed spectral changes with good reversibility under the electrochemical redox conditions.

Effect of the electronic properties of the side charges of neutral solvent molecules on the charges of the N and H atoms of the carbazole molecule: IR experiment and DFT calculations

The IR spectral parameters of the absorption band of the valence vibration of the NH bond of the carbazole molecule in several neutral solvents (n-hexane C6H14, carbon tetrachloride CCl4, chloroform CHCl3, benzene C6H6) have been measured. It has been experimentally established that the position of the maximum of the NH vibrational band of the carbazole molecule in solvents undergoes a low-frequency shift relative to the gas phase. This shift increases in the series C6H14, CCl4, CHCl3, C6H6. The change in the magnitude of the linear shift is well described by the Kirkwood-Bauer-Magat KBM ratio in C6H14, CCl4, CHCl3. The presence of a linear shift may indicate that only universal interactions take place. The deviation of this ratio of shift magnitude for carbazole in benzene is interpreted as a manifestation of intermolecular complexation. Quantum-chemical calculations of the position of the absorption band position of the valence vibration of the NH bond of the carbazole molecule in these solvents, carried out by the electron density functional method B3LYP/6-31G using the Gaussian 09W program package, also showed a low-frequency shift relative to the gas phase.It was found that for the carbazole molecule in the condensed phase relative to the gas phase the following effects of changing the magnitude of charges on atoms N13 and H14 take place: 1 – increase in the positive sign of the charge on both atoms; 2 – the change in charge magnitude is larger on the nitrogen atom than on the hydrogen atom for both solvents (whose molecules have a dipole moment ∼0: C6H14, CCl4); 3 – the chlorine containing environment has a greater effect on the charge change in the carbazole molecule than the proton containing environment (whose molecules have a dipole moment ∼0: C6H14, CCl4).The correlation between the change of charges on atoms N13 and H14 with the value of electronegativity ξ of the side solvent atoms was established.Thus, it is shown that the charges on the 13N and 14H atoms of the carbazole molecule undergo changes in the presence of universal interactions, and the magnitude of the charge change depends on the electronic properties of the side atoms of the nearest solvent molecules. A hypothesis is proposed to explain the different frequency shift of the NH vibrational frequency of the molecule for chlorine-containing and hydrogen-containing side atoms of neutral solvent molecules, which takes into account different values of ξ for nitrogen and hydrogen atoms.

Capping agent-free aqueous gold nanoparticles generated by an environmentally friendly plasma-liquid method

This study investigates a simple approach for synthesizing gold nanoparticles (Au NPs) using atmospheric pressure plasma without the need for reducing agents, additives, or capping agents. The size, morphology, optical properties, and aggregation stability of the synthesized Au NPs were characterized using scanning electron microscopy, UV-vis spectroscopy, and zeta potential analysis. The UV-vis absorption spectra of the gold nanoparticles, obtained at various Au3+ concentrations and treatment durations with anode plasma discharge, were analyzed. The UV-vis spectra revealed a surface plasmon resonance absorption band between 530–600 nm, indicative of Au NP formation. Results demonstrated that the size of Au NPs can be tuned within the range of 30–75 nm by adjusting the gold salt precursor concentration from 0.3 to 2.5 mmol/L. It was found that plasma treatment for 3–10 minutes, at different Au3+ concentrations, resulted in the formation of Au NPs with varying sizes and morphologies. The study showed that particles with different shapes – spherical, hexagonal, and triangular – were formed depending on the initial concentration of Au3+. The plasma-chemically synthesized nanoparticles at an Au3+ concentration of 0.06 mmol/L were predominantly spherical and exhibited the highest stability (lasting 12–24 hours), with a zeta potential of –20 to –22 mV, compared to samples with Au3+ concentrations ranging from 0.3 to 2.5 mmol/L.

The A2Π–X2Σ+ Band System of ScO for M-type Star Spectral Analysis

M-type stars are the most abundant stars in our Galaxy. Their visible spectra are characterized by strong TiO and VO absorption bands with occasional ScO bands near 6000–6100 Å. This region corresponds to the A2Π–X2Σ+ band system and can be used to measure the abundance of ScO. In this work, a new Doppler-limited resolution spectrum of ScO obtained in a hollow-cathode experiment is presented. The A2Π–X2Σ+ electronic transition is analyzed with special care dedicated to fitting the A′2Δ(v+2) ∼ A2Π(v) perturbation. Spectroscopic constants of the A2Π(v) states are reported for v ≤ 9, and a partial fit of spectroscopic constants is made for the A′2Δ(v) states 2 ≤ v ≤ 6. The modeled interaction of the two states reproduces the experimental data remarkably well. New equilibrium constants are extracted from the fit. Band strengths are calculated with the help of a scaled transition dipole moment function, previously calculated with ab initio methods. Finally, a line list of the A2Π–X2Σ+ band system is provided, including Einstein A coefficients and oscillator strengths. Using this line list, the spectrum of ScO can be simulated for different temperature and pressure conditions in stellar atmospheres.

Self-Assembly of Metallo-Supramolecular Amphiphiles Based on Azadipyrromethenes: Consecutive Pathways to Nanodiscs and Nanosheets.

A new class of metallo-supramolecular amphiphilic dyes 1a, b was constructed by using two azadipyrromethene units which were respectively modified with two hydrophobic alkyl and two hydrophilic oligo(ethylene glycol) chains. The spectroscopic and morphological studies revealed the consecutive self-assembly pathways of 1a in EtOH/H2O mixed solvent. The monomers of 1a firstly aggregated into the kinetic-controlled, nanodisc-shaped Agg. I upon cooling and the latter spontaneously transformed into the thermodynamically more stable Agg. II with a nanosheet morphology. While the non-fluorescent Agg. I displayed a broad absorption band (λmax = 594 nm), the Agg. II displayed a more intensive and narrowed J-band (λmax =693 nm) and a fluorescence band with a maximum at 760 nm (Фfl = 0.1), which could be ascribed to the J-aggregation induced emission enhancement. The kinetics of Agg. I to Agg. II transformation was further modulated by seed-initiated supramolecular polymerization with various ratios of Seedagg.II, in which the transformation rate was significantly increased by ca. 2 orders of magnitude compared to the spontaneous process. The supramolecular amphiphile 1b bearing longer hydrophilic chains formed only one type aggregate, which exhibited spectroscopic and morphological properties that were highly comparable with that of Agg. I.

Halogen-Dependent Circular Dichroism and Magneto-Photoluminescence Effects in Chiral 2D Lead Halide Perovskites.

Chiral lead halide perovskites (chiral LHPs) have emerged as one of the best candidates for opto-spintronics due to their large spin-orbit coupling (SOC) and unique chirality-induced spin selectivity (CISS) even in the absence of a magnetic field. Here, we report the impact of halide composition on circular dichroism (CD) and magneto-photoluminescence (PL) effects of chiral 2D LHPs (R/S-MBA)2PbBrxI4-x (MBA = C6H5CH2(CH3)NH3). By tuning the mixing ratio of Br/I halide anions, we find that (R/S-MBA)2PbBrxI4-x thin films exhibit tunable and wide wavelength range CD signals. Simultaneously, the main CD signals near the exciton absorption band gradually blue shift until they disappear. Moreover, the halogen-dependent negative magneto-PL effects of (R/S-MBA)2PbBrxI4-x thin films excited by left/right circularly polarized light can be detected at room temperature. We demonstrated that the halide composition can effectively modulate exciton splitting and chirality transfer in (R/S-MBA)2PbBrxI4-x owing to the chirality-induced SOC and crystalline structure transition, which lead to the adjustable CD signals. The interplay of Rashba-type band spin splitting and spin mixing among bright triplet exciton states is responsible for the halogen-dependent magneto-PL effect of chiral 2D LHPs. This study enables chiral 2D LHPs with CISS to be a new class of promising opto-spintronics materials for exploring high-performance spin-light-emitting diodes by halide engineering.

1,4-Benzodioxane Substituted Aza-BODIPY: Towards Photostable yet Efficient Triplet Photosensitizer.

We report herein the synthesis of aza-BODIPY substituted with 1,4-benzodioxane-6-yl substituents at 3,5 positions of the chromophore system. Both pyrrole rings of the aza-BODIPY in question were substituted with bromine atoms in order to induce highly desirable photophysical properties, such as highly populated excited triplet state (T1) and long excited triplet-state lifetime (τT) of 21 μs. The photosensitized oxygenation of a model compounds, viz. DPBF, points to a high singlet oxygen and/or other ROS formation quantum yield of 0.42. The photosensitizer studied exhibited an absorption band within the so-called "therapeutic window", with λabs 678 nm. As estimated by CV/DPV measurements the 1,4-benzodioxane-6-yl substituted aza-BODIPYs studied exhibited a multi-electron oxidations at a relatively low potentials (Eox), pointing to the very good electron-donating properties of these molecules. High photostability and thermal stability was observed for all compounds studied. The good singlet oxygen quantum yield measured combined with an exceptional photostability makes this aza-BODIPY a promising candidate for applications such as photocatalysis and photodynamic therapy (PDT).

The Extraction of Alcea Rosea Organic Dye and Its Characterization of Optical Properties

In the present study, the optical properties of a natural dye extracted from Alcea rosea flowers were investigated. The color extraction procedure was performed using a nontoxic solvent ethanol to enhance human safety and the ecological framework. Fourier transform infrared spectroscopy was employed to determine the functional groups of the natural dye obtained from Alcea rosea flowers. The optical properties of dye were achieved by the directed thin film using UV-Vis spectroscopy and analyzed absorption spectra, coefficients, refractive indices, extinction coefficients, and optical energy bandgap. A broad absorption band occurs over an extensive waveband with peak at 380 nm. The occurrence of a low indirect bandgap in a thin film was discerned at 3.9 eV, with Urbach energy noticed in a state of 0.23 eV.

JWST/NIRSpec Observations of Brown Dwarfs in the Orion Nebula Cluster

We have used the multiobject mode of the Near-Infrared Spectrograph (NIRSpec) on board the James Webb Space Telescope (JWST) to obtain low-resolution 1–5 μm spectra of 22 brown dwarf candidates in the Orion Nebula Cluster, which were selected with archival images from the Hubble Space Telescope. One of the targets was previously classified as a Herbig–Haro (HH) object and exhibits strong emission in H i, H2, and the fundamental band of CO, further demonstrating that HH objects can have bright emission in that CO band. The remaining targets have late spectral types (M6.5 to early L) and are young based on gravity-sensitive features, as expected for low-mass members of the cluster. According to theoretical evolutionary models, these objects should have masses that range from the hydrogen burning limit to 0.003–0.007 M ⊙. Two of the NIRSpec targets were identified as proplyds in earlier analysis of Hubble images. They have spectral types of M6.5 and M7.5, making them two of the coolest and least massive known proplyds. Another brown dwarf shows absorption bands at 3–5 μm from ices containing H2O, CO2, OCN−, and CO, indicating that it is either an edge-on class II system or a class I protostar. It is the coolest and least massive object that has detections of these ice features. In addition, it appears to be the first candidate for a protostellar brown dwarf that has spectroscopy confirming its late spectral type.

Radiopaque Polyurethanes Containing Barium Sulfate: A Survey on Thermal, Rheological, Physical, and Structural Properties

Radiopaque polyurethanes are extensively used in biomedical fields owing to their favorable balance of properties. This research aims to investigate the influence of particle concentration on various properties, including rheological, radiopacity, structural, thermal, and mechanical attributes, with a thorough analysis. The findings are benchmarked against a commercial product (PL 8500 A) that contains 10% weight barium sulfate. Two more thermoplastic polyurethanes (TPU) were formulated with two different concentrations of barium sulfate (10 wt.% and 20 wt.%) and compared to the commercially available product. FTIR demonstrated similar absorption bands among all samples, indicating that the fabrication method did not impact the TPU matrix. DSC indicated a predominantly amorphous structure for PL 8500 A compared to the other samples, while the kinetic degradation was more influenced by the higher barium sulfate content. The rheological analysis showed a decrease in the complex viscosity and storage modulus with the radiopacifier and an increase in the radiopacity, as demonstrated by the X-radiography. X-ray microtomography showed a more spherical particle format with a heterogeneous particle structure for PL 8500 A compared to the other polyurethanes. These findings enhance the comprehension of the structure–property relationships inherent in these materials and facilitate the development of customized materials for targeted applications.

Microwave Absorption and Magnetic Properties of M-Type Hexagonal Ferrite Ba0.95Ca0.05Fe12−xCoxO19 (0 ≤ X ≤ 0.4) at 1–18 GHz

In order to improve the microwave-absorption performance of barium ferrite and broaden its microwave-absorption band, BaFe12O19, Ba0.95Ca0.05Fe12O19, and Ba0.95Ca0.05Fe12−xCoxO19 (x = 0.1, 0.2, 0.3 and 0.4, respectively) hexaferrites were synthesized by the solid-state reaction method, and the influence of Co ion substitution on the phase composition, microstructure, magnetic properties, and microwave-absorption ability of the ferrites in this system was studied. Introducing minor Co ions (x < 0.2) facilitated sintering and grain growth. At x ≥ 0.2, XRD revealed the emergence of the Co2X phase alongside the BaM phase. Increasing Co ion concentration and the secondary X-phase led to slight reductions in saturation magnetization (69 to 63.5 emu/g) and substantial decline in coercivity (2107.02 to 111.21 Oe), attributed to grain size growth and Co2X’s soft magnetic nature. Notably, Co2X incorporation significantly enhanced the microwave absorption and provided a tunable absorption band from the Ku to the C band. For a sample with a thickness of 2.0 mm and a doping level of x = 0.2, a minimum reflection loss of −59.5 dB was achieved at 8.92 GHz, with an effective absorption bandwidth of 3.31 GHz (7.07–10.38 GHz). The simple preparation method and good performance make Ba0.95Ca0.05Fe12−xCoxO19 (x = 0.1, 0.2, 0.3 and 0.4, respectively) hexaferrites promising microwave-absorbing materials.

Bowl‐Shaped Anthracene‐Fused Antiaromatic Ni(II) Norcorrole: Synthesis, Structure, Assembly with C60, and Photothermal Conversion

The synthesis of bowl‐shaped antiaromatic molecules represents a formidable challenge, because the molecular distortion further destabilizes these already inherently reactive molecules. Here, we report the synthesis and properties of bowl‐shaped fused anthrylnorcorroles that exhibit near‐infrared (NIR) absorption reaching 1900 nm. The oxidation of meso‐anthryldibromodipyrrin provides fused anthryldibromodipyrrin, which was converted to the fused mono‐ and bisanthrylnorcorroles through Ni(0)‐mediated intramolecular coupling with a bis(dibromodipyrrin) Ni(II) complex. Single‐crystal X‐ray diffraction analyses revealed bowl‐shaped structures for the fused mono‐ and bisanthrylnorcorroles, which enables them to act as suitable receptors for C60 with bonding constants of 2.89 × 103 M–1 and 1.59 × 103 M–1, respectively. The formation of a 1:1 complex between the fused monoanthrylnorcorrole and C60 was confirmed by single‐crystal X‐ray diffraction analysis. The effective expansion of the π‐conjugation through the triple fusion of the norcorrole with the anthracene units substantially enhances the near‐infrared absorption bands, which endows these anthrylnorcorroles with effective photothermal conversion.

Bowl-Shaped Anthracene-Fused Antiaromatic Ni(II) Norcorrole: Synthesis, Structure, Assembly with C60, and Photothermal Conversion.

The synthesis of bowl-shaped antiaromatic molecules represents a formidable challenge, because the molecular distortion further destabilizes these already inherently reactive molecules. Here, we report the synthesis and properties of bowl-shaped fused anthrylnorcorroles that exhibit near-infrared (NIR) absorption reaching 1900 nm. The oxidation of meso-anthryldibromodipyrrin provides fused anthryldibromodipyrrin, which was converted to the fused mono- and bisanthrylnorcorroles through Ni(0)-mediated intramolecular coupling with a bis(dibromodipyrrin) Ni(II) complex. Single-crystal X-ray diffraction analyses revealed bowl-shaped structures for the fused mono- and bisanthrylnorcorroles, which enables them to act as suitable receptors for C60 with bonding constants of 2.89 × 103 M-1 and 1.59 × 103 M-1, respectively. The formation of a 1:1 complex between the fused monoanthrylnorcorrole and C60 was confirmed by single-crystal X-ray diffraction analysis. The effective expansion of the π-conjugation through the triple fusion of the norcorrole with the anthracene units substantially enhances the near-infrared absorption bands, which endows these anthrylnorcorroles with effective photothermal conversion.

Synthesis and characterization of new organometallic lanthanides metal complexes for photodynamic therapy

New Schiff base ligand: 4-methoxy salicaldhyde-2-2-phenyl-hydrazono acetaldehíyde prepared by facile method. The molecular structures characterized by elemental analysis and proton magnetic resonance spectra (1H-NMR spectra). This spectra at the chemical shifts (3.5–10.39 ppm) confirmed the types and the numbers of protons. The sharp melting point at the range 110–112 °C confirmed purity. New optically active metal (samarium, terbium and gadolinium) complexes of the Schiff base synthesized in a one pot reaction. Vibrational IR spectra confirmed functional groups. Scanning electron microscopy micrographs confirmed that the modified microstructure of the metal complexes differed in morphology than the ligand. Powder X-ray diffraction patterns confirmed good crystalline structure. The optically activity of the solid metal complexes confirmed from electronic absorption spectra. The UV absorbance band at the wavelength range 280–390 nm and the intense phosphorescence bands up to 830 nm enabled application in photo dynamic therapy for apoptosis cancer cells by conversion triplet oxygen in the tissues into reactive singlet oxygen. Low charge transfer energy: 2.59–2.61 eV, high molar extinction coefficients (ε) at the order of magnitude \\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\:{10}^{6}$$\\end{document} M− 1 cm− 1 and the intense phosphorescence bands reflected good photodynamic activity. The metal complexes are thermally stable.

Graphene pixel based broadband polarization insensitive THz absorber

Abstract Suppressing undesired radiation and eliminating stray radiation in a high-frequency circuit might be challenging. Ultra-high frequency (UHF) electromagnetic wave absorbers are finding new applications in both the military and civilian domains. Obtaining an ultra-wide absorption band in a thin, single-layer Terahertz absorber becomes difficult. Also, achieving perfect absorption bandwidth on transverse electric (TE) and transverse magnetic (TM) mode is very sensitive. This paper presents a polarization-independent graphene-based absorbers with a near unity absorption band of 2.32 THz and 3.78 THz in a lower mid-infrared regime. The structure’s unit cell consists of cross-slot circular patches with Au as a ground separated by SiO2. To improve the absorption band another graphene layer was placed between the top and dielectric material. The absorber is polarization independent under normal incidence because of the deposited graphene structure’s fourfold symmetry. Both TE and TM polarizations were investigated, with wide-band absorption observed up to 60° incident angles in both cases. In terms of the lowest frequency of absorption, the prototype is deemed to be as thin as ∼ 0.1 λ max for both absorbers. Similarly, the effective homogeneity criteria in the subwavelength region are supported by the unit cell’s period of ∼ 0.1 λ max . The proposed absorber-2 shows 10 % higher FBW than existing work.

Novel Structures for PV Solar Cells: Fabrication of Cu/Cu2S-MWCNTs 1D-Hybrid Nanocomposite

The production of cost-effective novel materials for PV solar cells with long-term stability, high energy conversion efficiency, enhanced photon absorption, and easy electron transport has stimulated great interest in the research community over the last decades. In the presented work, Cu/Cu2S-MWCNTs nanocomposites were produced and analyzed in the framework of potential applications for PV solar cells. Firstly, the surface of the produced one-dimensional Cu was covered by Cu2S nanoflake. XRD data prove the formation of both Cu and Cu2S structures. The length and diameter of the one-dimensional Cu wire were 5–15 µm and 80–200 nm, respectively. The thickness of the Cu2S nanoflake layer on the surface of the Cu was up to 100 nm. In addition, the Cu/Cu2S system was enriched with MWCNTs. MWCNs with a diameter of 50 nm interact by forming a conductive network around the Cu/Cu2S system and facilitate quick electron transport. Raman spectra also prove good interfacial coupling between the Cu/Cu2S system and MWCNTs, which is crucial for charge separation and electron transfer in PV solar cells. Furthermore, UV studies show that Cu/Cu2S-MWCNTs nanocomposites have a wide absorption band. Thus, MWCNTs, Cu, and Cu2S exhibit an intense absorption spectrum at 260 nm, 590 nm, and 972 nm, respectively. With a broad absorption band spanning the visible–infrared spectrum, the Cu/Cu2S-MWCNTs combination can significantly boost PV solar cells’ power conversion efficiency. Furthermore, UV research demonstrates that the plasmonic character of the material is altered fundamentally when CuS covers the Cu surface. Additionally, MWCN-Cu/Cu2S nanocomposite exhibits hybrid plasmonic phenomena. The bandgap of Cu/Cu2S NWs was found to be approximately 1.3 eV. Regarding electron transfer and electromagnetic radiation absorption, the collective oscillations in plasmonic metal-p-type semiconductor–conductor MWCNT contacts can thus greatly increase energy conversion efficiency. The Cu/Cu2S-MWCNTs nanocomposite is therefore a promising new material for PV solar cell application.

Non-alternant Benzodifluoranthene Tetraimides from 7,8,9,10-Fluoranthene Diimides: Synthesis, Structure, and Optical-Limiting Properties.

A novel tetraimide-functionalized non-alternant π-conjugated system, namely, benzodifluoranthene tetraimides (BDFTI), has been designed and synthesized through highly efficient UV-photocyclization of a vinyl-bridged fluoranthene diimide dimer (i.e., FDI-V). The synthesis of FDI-V starts from a straightforward three-step route to produce novel 7,8,9,10-fluoranthene diimide (FDIs) building-blocks, followed by nearly complete bromination and then Stille-coupling reaction to give the desired dimer. The analysis by X-ray crystallography confirms a near-coplanar geometry for FDIs, while BDFTI shows a U-shaped and distorted backbone configuration proven by theoretical optimizations. The tetraimide BDFTI exhibits several advantages over the FDI cores, including an extended absorption band and a red-shift in photoluminescence spectra. This enhancement can be attributed to the presence of additional electron-deficient imide units, which promotes increased intramolecular charge transfer and improved electron affinity. All the imides show a local aromatic characteristic owing to the incorporation of pentagon rings in the π-frameworks. The fully fused BDFTI exhibits nonlinear optical properties as analyzed by the open-aperture Z-scan technique, demonstrating superior optical-limiting performance compared to vinyl-bridged FDI-V. The versatile UV-photocyclization chemistries provide a pathway for developing complex and unique multiimide-functionalized π-conjugated systems, paving the way for creating high-performance optical-limiting materials.