Influence of SiO<Subscript>2</Subscript> Spacer Layer Thickness on Performance of Plasmonic Textured Silicon Solar Cell

We investigated the effect of SiO₂ spacer layer thickness between the textured silicon surface and silver nanoparticles (Ag NPs) on solar cell performance using quantum efficiency analysis. Separation of Ag NPs from high index silicon with SiO₂ layer led to modified absorption and scattering cross-sections due to graded refractive index medium. The forward scattering from Ag NPs is very sensitive to SiO₂ layer thickness in plasmonic silicon cell performance due to the evanescent character of generated near-fields around the NPs. With the optimized ～30–40 nm SiO₂ spacer layer, we observed an enhancement of solar cell efficiency from ～8.7 to ～10 %, which is due to the photocurrent enhancement in the off-resonance surface plasmon region. We also estimated minority carrier diffusion lengths (L _eff) from internal quantum efficiency data, which are also sensitive to SiO₂ spacer layer thickness. We observed that the L _eff values are enhanced from ～356 to ～420 μm after placing Ag NPs on ～40 nm spacer layer due to improved forward (angular) scattering of light from the Ag NPs into silicon.     

Synthesis and X-ray crystal structure of [Ag(phendio)<Subscript>2</Subscript>]ClO<Subscript>4</Subscript> (phendio = 1,10-phenanthroline-5,6-dione) and its effects on fungal and mammalian cells

The Cu(II) and Ag(I) complexes, [Cu(phendio)₃](ClO₄)₂4H₂O and [Ag(phendio)₂]ClO₄ (phendio = 1,10-phenanthroline-5,6-dione), are prepared in good yield by reacting phendio with the appropriate metal perchlorate salt. The X-ray crystal structure of the Ag(I) complex shows it to have a pseudo tetrahedral structure. `Metal-free' phendio and the Cu(II) and Ag(I) phendio complexes strongly inhibit the growth of the fungal pathogen Candida albicans, and are more active than their 1,10-phenanthroline analogues. The simple Ag(I) salts, AgCH<sub>3</sub>CO<sub>2</sub>, AgNO<sub>3</sub> and AgClO<sub>4</sub>.H<sub>2</sub>O display superior anti-fungal properties compared to analogous simple Cu(II) and Mn(II) salts, suggesting that the nature of the metal ion strongly influences activity. Exposing C. albicans to `metal-free' phendio, simple Ag(I) salts and [Ag(phendio)₂]ClO₄ causes extensive, non-specific DNA cleavage. `Metal-free' phendio and [Ag(phendio)₂]ClO₄ induce gross distortions in fungal cell morphology and there is evidence for disruption of cell division. Both drugs also exhibit high anti-cancer activity when tested against cultured mammalian cells.     

Improving Efficiency of TiO<Subscript>2</Subscript>:Ag /Si Solar Cell Prepared by Pulsed Laser Deposition

Titanium dioxide (TiO₂) has been extensively studied and demonstrated to be suitable to enhance the efficiency of solar cell. In this work, TiO₂ is doped with silver nanoparticles (AgNP’s) on glass and the Si substrate by using Pulsed Laser Deposition (PLD) technique. UV–vis spectroscopy, X-ray diffraction (XRD), X-ray fluorescence (XRF), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Atomic Force Microscope (AFM), electrical conductivity (σ _dc), Hall coefficient (R_H), current–voltage (I–V), and capacity–voltage (C–V) characterizations have been used to examine the optical, the morphological, and the electrical properties of the films. It has been found that 5 wt.% (Ag) doped TiO₂ thin film has the most effect on efficiency of TiO₂:Ag /Si solar cell. The (I–V) characteristics showed that the (TiO₂) thin film enhances the efficiency of the (p–n) junction solar cell from 1.26 % pure TiO₂ to 7.19 % with doping of noble metal (Ag) representing improvement in the efficiency of solar cell leading to estimate empirical equations between efficiency, extinction coefficient, and energy band gap which have a total fit with the experimental data.     

Tailored TiO2 Protection Layer Enabled Efficient and Stable Microdome Structured p‐GaAs Photoelectrochemical Cathodes

Group III–V compound semiconductors are a promising group of materials for photoelectrochemical (PEC) applications. In this work, a metal assisted wet etching approach is adapted to acquiring a large‐area patterned microdome structure on p‐GaAs surface. In addition, atomic layer deposition is used to deposit a TiO₂ protection layer with controlled thickness and crystallinity. Based on a PEC photocathode design, the optimal configuration achieves a photocurrent of ?5 mA cm^?2 under ?0.8 V versus Ag/AgCl in a neutral pH electrolyte. The TiO₂ coating with a particular degree of crystallization deposited via controlled temperature demonstrates a superior stability over amorphous coating, enabling a remarkably stable operation, for as long as 60 h. The enhanced charge separation induced by favorable band alignment between GaAs and TiO₂ contributes simultaneously to the elevated solar conversion efficiency. This approach provides a promising solution to further development of group III–V compounds and other photoelectrodes with high efficiency and excellent durability for solar fuel generation.     

A review of cardiovascular toxicity of TiO<Subscript>2</Subscript>, ZnO and Ag nanoparticles (NPs)

To ensure the safe use of nanoparticles (NPs) in modern society, it is necessary and urgent to assess the potential toxicity of NPs. Cardiovascular system is required for the systemic distribution of NPs entering circulation. Therefore, the adverse cardiovascular effects of NPs have gained extensive research interests. Metal based NPs, such as TiO₂, ZnO and Ag NPs, are among the most popular NPs found in commercially available products. They may also have potential applications in biomedicine, which could increase their contact with cardiovascular systems. This review aimed at providing an overview about the adverse cardiovascular effects of TiO₂, ZnO and Ag NPs. We discussed about the bio-distribution of NPs following different exposure routes. We also discussed about the cardiovascular toxicity of TiO₂, ZnO and Ag NPs as assessed by in vivo and in vitro models. The possible mechanisms and contribution of physicochemical properties of metal based NPs were also discussed.     

One-Step Preparation and Fluorescence Enhancement Effect in SiO2/Eu2+ Doped with Ag Nanowires

Eu²⁺ single-doped SiO₂ (SiO₂/Eu²⁺) and Eu²⁺, Ag nanowires co-doped SiO₂ (SiO₂/Eu²⁺–Ag) luminescent nanomaterials were prepared by an efficient one-step sol–gel method. Their microstructure and optical properties were characterized, and the fluorescence enhancement of Eu²⁺ by Ag nanowires was investigated. The experimental results indicate that the average diameter of Ag nanowires doped is 12.5 nm, and the length–diameter ratio is 30. The Ag nanowires cannot only enhance the light absorption of SiO₂/Eu²⁺ in the range of 230–350 nm, but also reduce the fluorescence lifetime of Eu²⁺. More importantly, the emission intensity is enhanced after doping Ag nanowires, and the red shift phenomenon of the emission spectrum is observed, red shift occurs between 10 and 56 nm. The highest fluorescence intensity is accessed under the Ag doping concentration of 0.10 %. Additionally, the emission of SiO₂/Eu²⁺ with 0.10 % of Ag doping at 456 nm is 16 times stronger than that of pure SiO₂/Eu²⁺. The present results indicate that the fluorescence enhancement is attributed to the local field enhancement and the increased radiative decay rates induced by Ag nanowires.     

Near-field Coupling Effect between Individual Au Nanospheres and their Supporting SiO<Subscript>2</Subscript>/Si Substrate

We studied the far-field optical reflection contrast spectroscopy (FORCS) properties of the following system: individual Au nanospheres (radius R) immobilized above Si substrate with different thicknesses (d) SiO₂ between them. We found that peaks in the FORCS red-shift exponentially with d decreasing. The near-field coupling between the Au nanosphere and its supporting substrate is revealed to contribute to this, while the coupling strength is demonstrated to decrease exponentially with a decay length of 0.30 in units of d/R. It qualitatively agrees well in magnitude with the near-field coupling between two noble metal nanoparticles consisting of a dimer. Our results demonstrate that the FORCS can provide insight into the near-field coupling, which is significant for their applications in nano-photonics, sensing, surface-enhanced spectrascopies, etc.     

Sequential interactions of silver–silica nanocomposite (Ag–SiO2NC) with cell wall,metabolism and genetic stability of Pseudomonas aeruginosa,a multiple antibiotic‐resistant bacterium

The study was carried out to understand the effect of silver–silica nanocomposite (Ag–SiO₂NC) on the cell wall integrity, metabolism and genetic stability of Pseudomonas aeruginosa, a multiple drug‐resistant bacterium. Bacterial sensitivity towards antibiotics and Ag–SiO₂NC was studied using standard disc diffusion and death rate assay, respectively. The effect of Ag–SiO₂NC on cell wall integrity was monitored using SDS assay and fatty acid profile analysis, while the effect on metabolism and genetic stability was assayed microscopically, using CTC viability staining and comet assay, respectively. Pseudomonas aeruginosa was found to be resistant to β‐lactamase, glycopeptidase, sulfonamide, quinolones, nitrofurantoin and macrolides classes of antibiotics. Complete mortality of the bacterium was achieved with 80 μg ml^?1 concentration of Ag–SiO₂NC. The cell wall integrity reduced with increasing time and reached a plateau of 70% in 110 min. Changes were also noticed in the proportion of fatty acids after the treatment. Inside the cytoplasm, a complete inhibition of electron transport system was achieved with 100 μg ml^?1 Ag–SiO₂NC, followed by DNA breakage. The study thus demonstrates that Ag–SiO₂NC invades the cytoplasm of the multiple drug‐resistant P. aeruginosa by impinging upon the cell wall integrity and kills the cells by interfering with electron transport chain and the genetic stability.

Significance and Impact of Study

Although the synthesis, structural characteristics and biofunction of silver nanoparticles are well understood, their application in antimicrobial therapy is still at its infancy as only a small number of microorganisms are tested to be sensitive to nanoparticles. A thorough knowledge of the mode of interaction of nanoparticles with bacteria at subcellular level is mandatory for any clinical application. The present study deals with the interactions of Ag–SiO2NC with the cell wall integrity, metabolism and genetic stability of Pseudomonas aeruginosa, which would contribute substantially in strengthening the therapeutic applications of silver nanoparticles.     

Surface Plasmon Resonance Enhanced Faraday Rotation in Fe3O4/Ag Nanoparticles Doped Diamagnetic Glass

Diamagnetic TeO₂-PbO-B₂O₃ glasses were melt-quenching fabricated and characterized for Fe₃O₄/Ag nanoparticles doping through radio-frequency sputtering and thermal treatment techniques. The surface plasmon resonance influenced structure, composition, optical, and magneto optical properties of Fe₃O₄/Ag doped glasses were investigated through XRD, SEM, XPS analysis, and Faraday rotation measurement. The optimized sputtering and thermal conditions Fe₃O₄ and Ag nanoparticles were obtained. Under the optimized conditions, a great enhancement of Faraday rotation, thermal property, and big UV cutoff red-shift due to the excited surface plasma’s resonance effect was achieved in diamagnetic glass.

     

Optimization of Electrodeposited p‐Doped Sb2Te3 Thermoelectric Films by Millisecond Potentiostatic Pulses

A systematic optimization of p‐type Sb₂Te₃ thermoelectric films made by potentiostatic electrodeposition on Au and stainless steel substrates is presented. The influence of the preparative parameters of deposition voltage, concentration, and the deposition method are investigated in a nitric acid solution. As a postdeposition step, the influence of annealing the films is investigated. The use of a potential‐controlled millisecond‐pulsed deposition method could improve both the morphology and the composition of the films. The samples are characterized in terms of composition, crystallinity, Seebeck coefficient, and electrical resistivity. Pulsed‐deposited films exhibit Seebeck coefficients of up to 160 μV K^?1 and an electrical conductivity of 280 S cm^?1 at room temperature, resulting in power factors of about 700 μW m^?1 K^?2. After annealing, power factors of maximum 852 μW m^?1 K^?2 are achieved. Although the annealing of DC‐deposited films significantly increased the power factor, they do not reach the values of the pulsed‐deposited films in the preannealing state. Structural analysis is performed with X‐ray diffraction and shows the crystalline structure of Sb₂Te₃ films. The performance is tuned by annealing of deposited films up to 300 °C under He atmosphere while performing in‐situ X‐ray diffraction and resistivity measurements. The chemical analysis of the films is performed by inductively coupled plasma optical emission spectroscopy (ICP‐OES) as well as scanning electron microscope energy dispersive X‐ray analysis (SEM‐EDX).     

Assessing the in vitro toxicity of the lunar dust environment using respiratory cells exposed to Al<Subscript>2</Subscript>O<Subscript>3</Subscript> or SiO<Subscript>2</Subscript> fine dust particles

Prior chemical and physical analysis of lunar soil suggests a composition of dust particles that may contribute to the development of acute and chronic respiratory disorders. In this study, fine Al₂O₃ (0.7 μm) and fine SiO₂ (mean 1.6 μm) were used to assess the cellular uptake and cellular toxicity of lunar dust particle analogs. Respiratory cells, murine alveolar macrophages (RAW 264.7) and human type II epithelial (A549), were cultured as the in vitro model system. The phagocytic activity of both cell types using ultrafine (0.1 μm) and fine (0.5 μm) fluorescent polystyrene beads was determined. Following a 6-h exposure, RAW 264.7 cells had extended pseudopods with beads localized in the cytoplasmic region of cells. After 24 h, the macrophage cells were rounded and clumped and lacked pseudopods, which suggest impairment of phagocytosis. A549 cells did not contain beads, and after 24 h, the majority of the beads appeared to primarily coat the surface of the cells. Next, we investigated the cellular response to fine SiO₂ and Al₂O₃ (up to 5 mg/ml). RAW 264.7 cells exposed to 1.0 mg/ml of fine SiO₂ for 6 h demonstrated pseudopods, cellular damage, apoptosis, and necrosis. A549 cells showed slight toxicity when exposed to fine SiO₂ for the same time and dose. A549 cells had particles clustered on the surface of the cells. Only a higher dose (5.0 mg/ml) of fine SiO₂ resulted in a significant cytotoxicity to A549 cells. Most importantly, both cell types showed minimal cytotoxicity following exposure to fine Al₂O₃. Overall, this study suggests differential cellular toxicity associated with exposure to fine mineral dust particles.     

Evaluation of the antibacterial activity and treatment of acne with SiO<Subscript>2</Subscript>-ionized loess

SiO₂-ionized loess was prepared from the reaction of loess and sodium hydroxide at 1,400°C for 2 h. The antibacterial activity of SiO₂-ionized loess against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, Pseudomonas aerusinosa, and Propionobacterium acnes causing acne was examined by comparing the results against those of untreated loess, and treatment efficacy was examined for treating acne using soap containing SiO₂-ionized loess. The minimum inhibitory concentration value of SiO₂-ionized loess against S. aureus, P. aerusinosa, B. subtilis, E. coli, and P. acne was 10.0, 10.0, 2.5, 5.0, and 2.5 mg/mL, respectively. However, medium containing untreated loess had no antimicrobial activity. A treatment efficacy test revealed that acne symptoms decreased as the duration of using soap containing SiO₂-ionized loess increased.     

Quantifying the Usefulness of Oxide-Encapsulated Silver Nanoparticles in Semiconducting Films

Incorporating plasmonic nanoparticles (NPs) in an organic solar cell (OSC) can improve device performance. In our simulation studies, at NP resonance, absorption in poly(3-hexythiophene)/phenyl-C61-butyric acid methyl ester (P3HT/PCBM) can be increased by encapsulating 50 nm Ag NPs with Al₂O₃, HfO₂, MoO₃, and SiO₂. At Ag NP resonance, when the oxide thickness is significant enough, oxides with high relative permittivity induces a higher electric field enhancement at the metal/dielectric interface. This is translated to improved absorption in the polymer layer. By integrating against AM1.5G, overall absorption in P3HT/PCBM is improved when incorporating Ag NPs encapsulated with a thin oxide shell into the polymer film. However, polymeric absorption loss is induced for oxide-encapsulated Ag NPs if MoO₃ and SiO₂ shells are more than 5 nm. For Al₂O₃ and HfO₂, Ag NPs should not be encapsulated with shells thicker than 10 nm. Modeling studies are also extended to absorption in a CH₃NH₃PbI₃ perovskite layer. It is revealed that both Al₂O₃ and HfO₂ have an optimal shell thickness of about 20 nm to ensure maximum absorption in CH₃NH₃PbI₃. The results can be utilized as a useful guideline when designing photovoltaics from an optical point of view.     

Simulation and optical spectroscopy of a DC discharge in a CH<Subscript>4</Subscript>/H<Subscript>2</Subscript>/N<Subscript>2</Subscript> mixture during deposition of nanostructured carbon films

Two-dimensional numerical simulations of a dc discharge in a CH₄/H₂/N₂ mixture in the regime of deposition of nanostructured carbon films are carried out with account of the cathode electron beam effects. The distributions of the gas temperature and species number densities are calculated, and the main plasmachemical kinetic processes governing the distribution of methyl radicals above the substrate are analyzed. It is shown that the number density of methyl radicals above the substrate is several orders of magnitude higher than the number densities of other hydrocarbon radicals, which indicates that the former play a dominant role in the growth of nanostructured carbon films. The model is verified by comparing the measured optical emission profiles of the H(n ≡ 3), C ₂ ^* , CH*, and CN* species and the calculated number densities of excited species, as well as the measured and calculated values of the discharge voltage and heat fluxes onto the electrodes and reactor walls. The key role of ion–electron recombination and dissociative excitation of H₂, C₂H₂, CH₄, and HCN molecules in the generation of emitting species (first of all, in the cold regions adjacent to the electrodes) is revealed.     

Optical Absorption Modeling of Plasmonic Organic Solar Cells Embedding Silica-Coated Silver Nanospheres

We numerically study plasmonic solar cells in which a square periodic array of core–shell Ag@SiO₂ nanospheres (NSs) are placed on top of the indium tin oxide (ITO) layer using a 3D finite-difference time-domain (FDTD) method. We investigate the influence of various parameters such as the periodicity of the array, the Ag core diameter, the active layer thickness, the shell thickness, and the refractive index of the shell materials on the optical performance of the organic solar cells (OSC). Our results show that the optimal periodicity of the array of NSs is dependent on the size of Ag core NSs in order to maximize optical absorption in the active layer. A very thin active layer (<70 nm) and an ultrathin (<5 nm) SiO₂ shell are needed in order to obtain the highest optical absorption enhancement. Strong electric field localization is observed around the plasmonic core–shell nanoparticles as a result of localized surface plasmon resonance (LSPR) excited by Ag NSs with and without silica shell. Embedding 50 nm Ag NSs with 1-nm-thick SiO₂ shell thickness on top of ITO leads to an enhanced intrinsic optical absorption in a 40-nm-thick poly(3-hexylthiophene):phenyl-C₆₁-butyric acid methyl ester (P3HT:PCBM) active layer by 24.7% relative to that without the NSs. The use of 1-nm-thick ZnO shell instead of SiO₂ leads to an enhanced intrinsic absorption in a 40-nm-thick P3HT:PCBM active layer by 27%.

     

Photo‐Electrical Characterization of Silicon Micropillar Arrays with Radial p/n Junctions Containing Passivation and Anti‐Reflection Coatings

In order to assess the contributions of anti‐reflective and passivation effects in microstructured silicon‐based solar light harvesting devices, thin layers of aluminum oxide (Al₂O₃), silicon dioxide (SiO₂), silicon‐rich silicon nitride (SiN_x), and indium tin oxide (ITO), with a thickness ranging from 45 to 155 nm, are deposited onto regularly packed arrays of silicon micropillars with radial p/n junctions. Atomic layer deposition of Al₂O₃ yields the best conformal coating over the micropillars. The fact that layers made by low‐pressure chemical vapor deposition (SiO₂ and SiN_x) are not conformally deposited on the sidewalls of the Si micropillars do not influence the photoelectrical efficiency. For ITO, a change in composition along the micropillar height is measured, which leads to poor performance. For Al₂O₃, deconvolution of the contributions of passivation and anti‐reflection to the overall efficiency gain exhibits the importance of passivation in micro/nano‐structured Si devices. Al₂O₃‐coated samples perform the best, for both n/p and p/n configured pillars, yielding (relative) increases of 116% and 37% in efficiency of coated versus non‐coated samples for p‐type and n‐type base micropillar arrays, respectively.     

Study of Design Tunable Optical Sensor and Monochromatic Filter of the One-Dimensional Periodic Structure of TiO2/MgF2 with Defect Layer of Liquid Crystal (LC) Sandwiched with Two Silver Layers

In this paper, we have inspected the optical characteristics of one-dimensional periodic structure (1DPS) of TiO₂ and MgF₂ dielectric materials with defect layer of liquid crystal (LC) sandwiched with two silver layers, i.e., (TiO₂|MgF₂)³|Ag|LC|Ag|(TiO₂/MgF₂)³ using transfer matrix method (TMM). The optical tunable properties of considered periodic structures investigated at different incident angles and temperatures for TE and TM modes. Our study shows that absorption peak of 1DPS varies with incident angle and temperature. The defect layer (Ag-LC-Ag), sandwiched LC within two metallic (Ag) layers, exhibits the surface plasmon waves at the metal LC interfaces. The effect of surface plasmon waves can be better understand through the optical sensing property of such defect periodic structure. The detailed study concludes that such a type of one-dimensional periodic structure (1DPS) may be useful to design a tunable sensor and monochromatic filter.

     

Comparative behavior of Pd and Ag deposition phenomenon on clean α-Al2O3 (001) surface—A first principle study

The nature of bonding at the interface between deposited silver/palladium and clean Al-terminated (001) surface of α-Al₂O₃ has been investigated using a periodic ab initio method. Substantial inter-planar relaxations within the alumina were found at both the interfaces and the bulk. The periodic calculation with both Ag and Pd deposition shows that 10% of loading on alumina results maximum stability. Surface energy and work function calculations were performed to propose the stability for the metals on the studied surfaces. The deposited Ag forms a three-dimensional (3-D) cluster on top of the alumina surface. The Pd cluster formed on the alumina surface is two-dimensional (2-D) and is distorted to accommodate the Ag cluster in its domain. A further low index calculation can explain the reason for a higher stability of the membrane generated over alumina support with silver and palladium. The results are discussed in view of the existing experimental data and models of metal-oxide interface and a reason for the difference of activity of the metal interaction with alumina surface is postulated.     

Molecular properties of metal difluorides and their interactions with CO<Subscript>2</Subscript> and H<Subscript>2</Subscript>O molecules: a DFT investigation

A computational study of metal difluorides (MF₂; M = Ca to Zn) and their interactions with carbon dioxide and water molecules was performed. The structural parameter values obtained and the results of AIM analysis and energy decomposition analysis indicated that the Ca–F bond is weaker and less ionic than the bonds in the transition metal difluorides. A deformation density plot revealed the stablizing influence of the Jahn–Teller effect in nonlinear MF₂ molecules (e.g., where M= Sc, Ti, Cr). An anaysis of the metal K-edge peaks of the difluorides showed that shifts in the edge energy were due to the combined effects of the ionicity, effective nuclear charge, and the spin state of the metal. The interactions of CO₂ with ScF₂ (Scc3 geometry) and TiF₂ (Tic2 geometry) caused CO₂ to shift from its usual linear geometry to a bent geometry (η²(C=O) binding mode), while it retained its linear geometry (η¹(O) binding mode) when it interacted with the other metal difluorides. Energy decomposition analysis showed that, among the various geometries considered, the Scc3 and Tic2 geometries possessed the highest interaction energies and orbital interaction energies. Heavier transition metal difluorides showed stronger affinities for H₂O, whereas the lighter transition metal (Sc and Ti) difluorides preferred CO₂. Overall, the results of this study suggest that fluorides of lighter transition metals with partially filled d orbitals (e.g., Sc and Ti) could be used for CO₂ capture under moist conditions.

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Graphical abstract Interaction of metal difluorides with carbon dioxide and water