Bimetallic non-alloyed NPs for improving the broadband optical absorption of thin amorphous silicon substrates

We propose the use of bimetallic non-alloyed nanoparticles (BNNPs) to improve the broadband optical absorption of thin amorphous silicon substrates. Isolated bimetallic NPs with uniform size distribution on glass and silicon are obtained by depositing a 10-nm Au film and annealing it at 600°C; this is followed by an 8-nm Ag film annealed at 400°C. We experimentally demonstrate that the deposition of gold (Au)-silver (Ag) bimetallic non-alloyed NPs (BNNPs) on a thin amorphous silicon (a-Si) film increases the film''s average absorption and forward scattering over a broad spectrum, thus significantly reducing its total reflection performance. Experimental results show that Au-Ag BNNPs fabricated on a glass substrate exhibit resonant peaks at 437 and 540 nm and a 14-fold increase in average forward scattering over the wavelength range of 300 to 1,100 nm in comparison with bare glass. When deposited on a 100-nm-thin a-Si film, Au-Ag BNNPs increase the average absorption and forward scattering by 19.6% and 95.9% compared to those values for Au NPs on thin a-Si and plain a-Si without MNPs, respectively, over the 300- to 1,100-nm range.     

Improving the performance of inverted organic solar cells by embedding silica‐coated silver nanoparticles deposited by electron‐beam evaporation

Embedding metallic nanoparticles (MNPs) in organic solar cells (OSCs) is proposed as one of the promising strategies to enhance their photovoltaic performance owing to localized surface plasmon resonance, light scattering effects or a synergy of both effects derived from the MNPs. However, it has been demonstrated that MNPs wrapped by a thin dielectric silica shell can lead to better photovoltaic yield than bare MNPs due to the presence of the dielectric shell which avoids direct contact between the active layer and the MNPs, reducing the charge recombination and the exciton quenching loss at the metal surface. In this study, we report an alternative solution using an ultrathin dielectric layer coating silver nanoparticles (Ag NPs) for improving the performance of plasmonic inverted OSCs instead of the use of metal–dielectric core–shell NPs. A silica (SiO₂) layer 5 nm thick coating evaporated Ag NPs with an average size of 60 nm is deposited on top of the zinc oxide (ZnO) layer used as the electron transport layer, leading to a significant improvement in the short‐circuit current density (J_sc) and the power conversion efficiency (PCE) of the inverted OSCs. The electron‐beam evaporation method is employed for controlled deposition of Ag NPs and SiO₂ on the ZnO layer. The plasmonic devices resulted in an 18% and 14.1% enhancement of the J_sc and PCE, respectively, compared to reference devices. This increase of the photoelectric parameters in plasmonic devices is attributed not only to the plasmonic effects originating from the Ag NPs but also to the ultrathin silica layer which can contribute to facilitating charge extraction. © 2019 Society of Chemical Industry     

Antireflective silicon nanostructures with hydrophobicity by metal-assisted chemical etching for solar cell applications

We present broadband antireflective silicon (Si) nanostructures with hydrophobicity using a spin-coated Ag ink and by subsequent metal-assisted chemical etching (MaCE). Improved understanding of MaCE, by conducting parametric studies on optical properties, reveals a design guideline to achieve considerably low solar-weighted reflectance (SWR) in the desired wavelength ranges. The resulting Si nanostructures show extremely low SWR (1.96%) and angle-dependent SWR (<4.0% in the range of 0° to 60°) compared to that of bulk Si (SWR, 35.91%; angle-dependent SWR, 37.11%) in the wavelength range of 300 to 1,100 nm. Relatively large contact angle (approximately 102°) provides a self-cleaning capability on the solar cell surface.     

Quantifying spectral changes experienced by plasmonic nanoparticles in a cellular environment to inform biomedical nanoparticle design

Metal nanoparticles (NPs) scatter and absorb light in precise, designable ways, making them agile candidates for a variety of biomedical applications. When NPs are introduced to a physiological environment and interact with cells, their physicochemical properties can change as proteins adsorb on their surface and they agglomerate within intracellular endosomal vesicles. Since the plasmonic properties of metal NPs are dependent on their geometry and local environment, these physicochemical changes may alter the NPs'' plasmonic properties, on which applications such as plasmonic photothermal therapy and photonic gene circuits are based. Here we systematically study and quantify how metal NPs'' optical spectra change upon introduction to a cellular environment in which NPs agglomerate within endosomal vesicles. Using darkfield hyperspectral imaging, we measure changes in the peak wavelength, broadening, and distribution of 100-nm spherical gold NPs'' optical spectra following introduction to human breast adenocarcinoma Sk-Br-3 cells as a function of NP exposure dose and time. On a cellular level, spectra shift up to 78.6 ± 23.5 nm after 24 h of NP exposure. Importantly, spectra broaden with time, achieving a spectral width of 105.9 ± 11.7 nm at 95% of the spectrum''s maximum intensity after 24 h. On an individual intracellular NP cluster (NPC) level, spectra also show significant shifting, broadening, and heterogeneity after 24 h. Cellular transmission electron microscopy (TEM) and electromagnetic simulations of NPCs support the trends in spectral changes we measured. These quantitative data can help guide the design of metal NPs introduced to cellular environments in plasmonic NP-mediated biomedical technologies.     

Near-infrared optical absorption enhanced in black silicon via Ag nanoparticle-induced localized surface plasmon

Due to the localized surface plasmon (LSP) effect induced by Ag nanoparticles inside black silicon, the optical absorption of black silicon is enhanced dramatically in near-infrared range (1,100 to 2,500 nm). The black silicon with Ag nanoparticles shows much higher absorption than black silicon fabricated by chemical etching or reactive ion etching over ultraviolet to near-infrared (UV-VIS-NIR, 250 to 2,500 nm). The maximum absorption even increased up to 93.6% in the NIR range (820 to 2,500 nm). The high absorption in NIR range makes LSP-enhanced black silicon a potential material used for NIR-sensitive optoelectronic device.

PACS

78.67.Bf; 78.30.Fs; 78.40.-q; 42.70.Gi     

Luminescence nanothermometry with alkyl-capped silicon nanoparticles dispersed in nonpolar liquids

Silicon nanoparticles (Si NPs) with a diameter size ranging from 4 to 8 nm were successfully fabricated. They exhibit a visible photoluminescence (PL) due to the quantum confinement effect. Chemical functionalization of these Si NPs with alkyl groups allowed to homogeneously disperse them in nonpolar liquids (NPLs). In comparison to most of literature results for Si NPs, an important PL peak position variation with temperature (almost 1 meV/K) was obtained from 303 to 390 K. The influence of the liquid viscosity on the peak positions is also presented. These variations are discussed considering energy transfer between nanoparticles. The high PL thermal sensitivity of the alkyl-capped Si NPs paves the way for their future application as nanothermometers.     

An experimental and theoretical understanding of a UV photodetector based on Ag nanoparticles decorated Er-doped TiO2 thin film

Glancing angle deposition (GLAD) was employed to synthesise plasmonic Silver (Ag) nanoparticles (NPs) on the chemically prepared Erbium-doped Titanium dioxide (Er:TiO₂) thin films (TFs). The impact of using Ag NPs on the morphological, optical, and electrical aspects of Er:TiO₂ TFs were sequentially analysed. From the field emission scanning electron microscopy (FESEM) image, the Ag NPs appeared spherical and uniformly distributed on the Er:TiO₂ TFs. The size (diameter) of the maximum number of Ag NPs was ~15 nm (calculated from FESEM image). Energy dispersive X-ray (EDX) spectra assured the presence of Ag NPs on the TFs. X-ray diffraction (XRD) pattern for Ag NPs decorated Er:TiO₂ TFs closely resembled the face centred cubic crystal structure of Ag NPs and body centred tetragonal Ag–O compound. The optical spectroscopy (UV–visible diffuse reflectance and photoluminescence) elucidated that the absorption of light was significantly enhanced in the UV–visible spectral range for the TFs in which Ag NPs were sandwiched between Er:TiO₂ TF layers (Er:TiO₂/Ag NPs/Er:TiO₂). The Schottky contact-based Au/Er:TiO₂/Si photodetector (PD) and Au/Er:TiO₂/Ag NPs/Er:TiO₂/Si (plasmonic) PD were constructed. The plasmonic PD offered a better photo-responsivity of ~4.5 fold higher as compared to Er:TiO₂ TF-based PD upon 380 nm illumination under ?6 V bias. An increase in detectivity and a decrease in noise equivalent power was observed for the plasmonic device compared to Er:TiO₂ device in the UV region. A theoretical approach had been adopted to calculate the wavelength-dependent responsivity for both devices. Further, the important parameters like photoconductive gain, electron transit time and electron mobility were calculated by simulating the experimental responsivity curves of the devices. These parameters exhibited improvement in the UV regime for the plasmonic PD. The fast temporal response with short rise and decay time proves the excellent efficiency of the plasmonic UV PD.     

Performance enhancement of ITO/oxide/semiconductor MOS-structure silicon solar cells with voltage biasing

In this study, we demonstrate the photovoltaic performance enhancement of a p-n junction silicon solar cell using a transparent-antireflective ITO/oxide film deposited on the spacing of the front-side finger electrodes and with a DC voltage applied on the ITO-electrode. The depletion width of the p-n junction under the ITO-electrode was induced and extended while the absorbed volume and built-in electric field were also increased when the biasing voltage was increased. The photocurrent and conversion efficiency were increased because more photo-carriers are generated in a larger absorbed volume and because the carriers transported and collected more effectively due to higher biasing voltage effects. Compared to a reference solar cell (which was biased at 0 V), a conversion efficiency enhancement of 26.57% (from 12.42% to 15.72%) and short-circuit current density enhancement of 42.43% (from 29.51 to 42.03 mA/cm²) were obtained as the proposed MOS-structure solar cell biased at 2.5 V. In addition, the capacitance-volt (C-V) measurement was also used to examine the mechanism of photovoltaic performance enhancement due to the depletion width being enlarged by applying a DC voltage on an ITO-electrode.     

Porous Polydimethylsiloxane/Au Composites as Solar-Light Absorbers for Light-Driven Thermoelectric Applications

Solar thermoelectric (TE) generators may potentially provide a viable alternative to photovoltaic devices for producing electrical energy from renewable sources. In this approach, the conversion of solar radiation into heat is essential to enhance the performance of TE devices, which necessitates the development of efficient solar light absorbers. Metal nanoparticles (NPs) have gained much attention in this regard because they can convert light into heat via plasmon-mediated photothermal effects. In this study, porous nanocomposites comprising polydimethylsiloxane (PDMS) and Au NPs are prepared. In the PDMS/Au composites, the narrow extinction spectrum of Au NPs is extended over longer wavelengths by plasmonic hybridization to promote the light absorption property of the NPs. In addition, the porous structure induces strong scattering of incident light, which further enhances the absorption efficiency of the Au NPs. Consequently, the plasmon-mediated photothermal effects of Au NPs are noticeably enhanced and increased the temperature of the PDMS/Au composites to as high as 75.7 °C under artificial solar radiation, compared to 42.1 °C without the Au NPs. By applying the PDMS/Au composites to commercial TE devices, the electrical performance of the TE devices is enhanced by approximately threefold.     

Thin and long silver nanowires self-assembled in ionic liquids as a soft template: electrical and optical properties

Thin and long silver nanowires were successfully synthesized using the polyvinylpyrrolidone (PVP)-assisted polyol method in the presence of ionic liquids, tetrapropylammonium chloride and tetrapropylammonium bromide, which served as soft template salts. The first step involved the formation of Ag nanoparticles with a diameter of 40 to 50 nm through the reduction of silver nitrate. At the growing stage, the Ag nanoparticles were converted into thin and long one-dimensional wires, with uniform diameters of 30 ± 3 nm and lengths of up to 50 μm. These Ag nanowires showed an electrical conductivity of 0.3 × 10⁵ S/cm, while the sheet resistance of a two-dimensional percolating Ag nanowire network exhibited a value of 20 Ω/sq with an optical transmittance of 93% and a low haze value.     

Magnetic properties of superparamagnetic nanoparticles loaded into silicon nanotubes

In this work, the magnetic properties of silicon nanotubes (SiNTs) filled with Fe₃O₄ nanoparticles (NPs) are investigated. SiNTs with different wall thicknesses of 10 and 70 nm and an inner diameter of approximately 50 nm are prepared and filled with superparamagnetic iron oxide nanoparticles of 4 and 10 nm in diameter. The infiltration process of the NPs into the tubes and dependence on the wall-thickness is described. Furthermore, data from magnetization measurements of the nanocomposite systems are analyzed in terms of iron oxide nanoparticle size dependence. Such biocompatible nanocomposites have potential merit in the field of magnetically guided drug delivery vehicles.

PACS

61.46.Fg; 62.23.Pq; 75.75.-c; 75.20.-g     

金纳米颗粒掺杂导电聚合物对有机-硅杂化光伏电池性能的影响研究

本研究将金纳米颗粒掺入聚3, 4-乙烯二氧噻吩:聚苯乙烯磺酸（PEDOT:PSS）薄膜中,制备了有机-硅杂化光伏电池。与纯PEDOT:PSS-硅电池相比,掺入金纳米颗粒制备的杂化光伏电池的光电转化效率（PCE）提高了23%,达到12.85%。电池的电流密度-电压曲线（J-V）、外量子效率（EQE）和电容-电压曲线（C-V）测试结果表明,掺入金纳米颗粒后电池性能提高的主要原因在于电池的光学性能和电学性能得到了改善：在金纳米颗粒的等离子共振区域,电池对光的反射性能降低;金纳米颗粒还能提高PEDOT:PSS薄膜的导电率、增加该电池的内建电场,因此极大减少了电荷在传输过程中的损失,提高了电池中电荷的传输和收集效率。     

Plasmonic Effects of Infiltrated Silver Nanoparticles Inside TiO2 Film: Enhanced Photovoltaic Performance in DSSCs

The plasmonic effects of infiltrated silver (Ag) nanoparticles, with different contents, inside a nanostructured TiO₂ film on the photovoltaic performance of dye‐sensitized solar cells (DSSCs) are explored. The synthesized Ag nanoparticles are immobilized onto deposited TiO₂ nanoparticles by a new strategy using 3‐mercaptopropionic acid (MPA), a bifunctional linker molecule. Transmission electron microscope (TEM) images show that monodispersed Ag and polydispersed TiO₂ nanoparticles have an average diameter of 12 ± 3 nm and 5 ± 1 nm, respectively. Moreover, Fourier transform infrared spectroscopy (FTIR) analysis reveals that Ag nanoparticles were successfully functionalized and capped with MPA. Optical studies on the MPA‐capped Ag nanoparticles inside TiO₂ film show an increase in the total absorbance of the electrode. Moreover, EIS measurements confirm that MPA‐capped Ag nanoparticles inhibit the charge recombination and improve the stability of nanoparticles in I₃^?/I^? electrolyte. The DSSC assembled with optimal content of MPA‐capped Ag nanoparticles demonstrated an enhanced power conversion efficiency (8.82% ± 0.07%) compared with the pure TiO₂ (7.30% ± 0.05%). The increase in cell efficiency was attributed to the enhanced dye light absorption in strength and spectral range due to the surface plasmon resonance of MPA‐capped Ag nanoparticles in the photoanode.     

Microwave-assisted green synthesis of Ag/reduced graphene oxide nanocomposite as a surface-enhanced Raman scattering substrate with high uniformity

A nanocomposite of silver nanoparticles/reduced graphene oxide (Ag/rGO) has been fabricated as a surface-enhanced Raman scattering (SERS) substrate owing to the large surface area and two-dimensional nanosheet structure of rGO. A facile and rapid microwave-assisted green route has been used for the formation of Ag nanoparticles and the reduction of graphene oxide simultaneously with L-arginine as the reducing agent. By increasing the cycle number of microwave irradiation from 1 and 4 to 8, the mean diameters of Ag nanoparticles deposited on the surface of rGO increased from 10.3 ± 4.6 and 21.4 ± 10.5 to 41.1 ± 12.6 nm. The SERS performance of Ag/rGO nanocomposite was examined using the common Raman reporter molecule 4-aminothiophenol (4-ATP). It was found that the Raman intensity of 4-ATP could be significantly enhanced by increasing the size and content of silver nanoparticles deposited on rGO. Although the Raman intensities of D-band and G-band of rGO were also enhanced simultaneously by the deposited Ag nanoparticles which limited the further improvement of SERS detection sensitivity, the detectable concentration of 4-ATP with Ag/rGO nanocomposite as the SERS substrate still could be lowered to be 10⁻¹⁰ M and the enhancement factor could be increased to 1.27 × 10¹⁰. Furthermore, it was also achievable to lower the relative standard deviation (RSD) values of the Raman intensities to below 5%. This revealed that the Ag/rGO nanocomposite obtained in this work could be used as a SERS substrate with high sensitivity and homogeneity.     

Periodic nano/micro-hole array silicon solar cell

In this study, we applied a metal catalyst etching method to fabricate a nano/microhole array on a Si substrate for application in solar cells. In addition, the surface of an undesigned area was etched because of the attachment of metal nanoparticles that is dissociated in a solution. The nano/microhole array exhibited low specular reflectance (<1%) without antireflection coating because of its rough surface. The solar spectrum related total reflection was approximately 9%. A fabricated solar cell with a 40-μm hole spacing exhibited an efficiency of 9.02%. Comparing to the solar cell made by polished Si, the external quantum efficiency for solar cell with 30 s etching time was increased by 16.7%.     

Evaluation of the Cytotoxic Behavior of Fungal Extracellular Synthesized Ag Nanoparticles Using Confocal Laser Scanning Microscope

Silver nanoparticles have been synthesized by subjecting a reaction medium to a Fusarium oxysporum biomass at 28 °C for 96 h. The biosynthesized Ag nanoparticles were characterized on the basis of their anticipated peak at 405 nm using UV-Vis-NIR spectroscopy. Structural confirmation was evident from the characteristic X-ray diffraction (XRD) pattern, high-resolution transmission electron Microscopy (HRTEM) and the particle size analyzer. The Ag nanoparticles were of dimension 40 ± 5 nm and spherical in shape. The study mainly focused on using the confocal laser scanning microscope (CLSM) to examine the cytotoxic activities of fungal synthesized Ag nanoparticles on a human breast carcinoma cell line MCF7 cell, which featured remarkable vacuolation, thus indicating a potent cytotoxic activity.     

Micro- and nanotopographies for photoelectrochemical energy conversion. I: The photovoltaic mode

The development of an efficient photovoltaic electrochemical solar cell with n-Si (1 0 0) based on the nanoemitter concept is described. The corresponding structure results from the self-organized formation of nanopores in about 10 nm thick silicon oxide during photocurrent oscillations in dilute fluoride containing solutions. The oscillations occur at higher anodic potentials and, due to the stress between Si and its anodic oxide, nanopores form in the oxide. Site selective metal electrodeposition (Pt) into those pores that have contact to the Si substrate and immersion into an acidic iodine-iodide redox electrolyte gives efficiencies in the range of 10%. Model experiments on the electrodeposition of Pt nanoparticles on n-Si (1 1 1) using photoelectron spectroscopy, performed with synchrotron radiation and atomic force microscopy in the contact- and tapping mode show that upon Pt deposition, silicon oxide is formed and step-bunching is observed. Mechanistic models are presented that explain the observed features. Scanning tunnelling experiments are performed with the tip on top of Pt nanoparticles. The resulting local I–V characteristics are interpreted based on a modified MOS (metal-oxide-semiconductor) model.     

Ag and Si Codoped Phosphate Glasses: Plasmonic Nanocomposites with Enhanced UV Transparency

The use of silicon powder to produce plasmonic Ag nanocomposite phosphate glasses which also exhibit improved transparency in the ultraviolet (UV) is proposed. Ag₂O/Si codoped glasses were prepared in a barium‐phosphate matrix by a simple melt‐quench method in ambient atmosphere. The as‐prepared glasses exhibit enhanced UV transparency, whereby the surface plasmon resonance of Ag nanoparticles (NPs) is manifested for the glasses with higher Ag₂O contents. ³¹P nuclear magnetic resonance spectroscopy is consistent with the formation of P–O–Si bonds, thus suggesting their possible role on the improved UV light transmission. Consequently, a model was presented accounting for the influence of silicon on the polymerization of the phosphate network concomitant with the creation of highly reactive oxygen species. Further exploiting the proposed reactive species, a real‐time spectroscopic study of the plasmonic response of Ag NPs in Ag/Si codoped glass samples was carried out during an in situ thermal processing. The temperature dependence of the Ag particle precipitation was studied in the 400°C–430°C range, from which an Arrhenius‐type plot allowed for estimating the activation energy of the process at 3.42 (±0.38) eV. Ultimately, the vanishing of the luminescence ascribed to Ag⁺ ions was observed in a heat‐treated sample, consistent with the high reactivity acquired by the glass matrix. Silicon thus appears promising for producing UV transparent glasses for high‐performance optics and for the reduction of Ag⁺ ions to produce Ag nanocomposites valuable for photonic (nanoplasmonic) applications.     

Naturally inspired SERS substrates fabricated by photocatalytically depositing silver nanoparticles on cicada wings

Densely stacked Ag nanoparticles with an average diameter of 199 nm were effectively deposited on TiO₂-coated cicada wings (Ag/TiO₂-coated wings) from a water-ethanol solution of AgNO₃ using ultraviolet light irradiation at room temperature. It was seen that the surfaces of bare cicada wings contained nanopillar array structures. In the optical absorption spectra of the Ag/TiO₂-coated wings, the absorption peak due to the localized surface plasmon resonance (LSPR) of Ag nanoparticles was observed at 440 nm. Strong Surface-enhanced Raman scattering (SERS) signals of Rhodamine 6G adsorbed on the Ag/TiO₂-coated wings were clearly observed using the 514.5-nm line of an Ar⁺ laser. The Ag/TiO₂-coated wings can be a promising candidate for naturally inspired SERS substrates.     

Optimum deposition conditions of ultrasmooth silver nanolayers

Reduction of surface plasmon-polariton losses due to their scattering on metal surface roughness still remains a challenge in the fabrication of plasmonic devices for nanooptics. To achieve smooth silver films, we study the dependence of surface roughness on the evaporation temperature in a physical vapor deposition process. At the deposition temperature range 90 to 500 K, the mismatch of thermal expansion coefficients of Ag, Ge wetting layer, and sapphire substrate does not deteriorate the metal surface. To avoid ice crystal formation on substrates, the working temperature of the whole physical vapor deposition process should exceed that of the sublimation at the evaporation pressure range. At optimum room temperature, the root-mean-square (RMS) surface roughness was successfully reduced to 0.2 nm for a 10-nm Ag layer on sapphire substrate with a 1-nm germanium wetting interlayer. Silver layers of 10- and 30-nm thickness were examined using an atomic force microscope (AFM), X-ray reflectometry (XRR), and two-dimensional X-ray diffraction (XRD2).

PACS

63.22.Np Layered systems; 68. Surfaces and interfaces; thin films and nanosystems (structure and nonelectronic properties); 81.07.-b Nanoscale materials and structures: fabrication and characterization