Use of Coupled Al-Ag Bimetallic Cylindrical Nanoparticles to Improve the Photocurrent of a Thin-Film Silicon Solar Cell

In this paper, cylindrical shape coupled bimetallic plasmonic nanoparticles (NPs) were used to improve the performance of a thin-film silicon solar cell. Our design is based on the appropriate selection of the composition and morphology of the NPs to reach a cell with excellent optical properties. The specific interaction between the incident light and bimetallic NPs helps us to design better solar absorbers. Here, the FDTD method was used to evaluate the effect of cylindrical Al-Ag bimetallic NPs on the surface of a thin silicon absorber. At first, a unit cell with Al-Al paired nano-cylinders at the surface was evaluated and a photocurrent of 14.65 mA/cm² was obtained. In the case of a cell with paired Al-Ag bimetallic nano-cylinders, the photocurrent was increased to 16.15 mA/cm². This value was increased to 16.57 mA/cm² when paired polymetallic NPs were used. According to the results of this work, bimetallic and polymetallic nanoparticles can significantly improve the photocurrent of an ultra-thin silicon solar cell. The results of this work can be used to design better plasmonic-based light trapping systems for thin-film solar cells.

     

Numerical Study of Plasmonic Effects of Ag Nanoparticles Embedded in the Active Layer on Performance Polymer Organic Solar Cells

In this paper, the light absorption in the active layer of polymer solar cells (OPV) by using plasmonic nanocrystals with a hexagonal lattice structure is investigated. To study the relationship between the performance of the OPV solar cell and its active layer, a three-dimensional model of its morphology is utilized. Therefore, the three-dimensional (3D) finite-difference time-domain method and Lumerical software were used to measure the field distribution and light absorption in the active layer in terms of wavelength. OPV solar cells with bilayer and bulk heterojunction structured cells were designed using hexagonal lattice crystals with plasmonic nanoparticles, as well as core–shell geometry to govern a design to optimize light trapping in the active layer. The parameters of shape, material, periodicity, size, and the thickness of the active layer as a function of wavelength in OPV solar cells have been investigated. A very thin active layer and an ultra-thin shell were used to achieve the highest increase in optical absorption. The strong alternating electromagnetic field around the core–shell plasmonic nanoparticles resulting from the localized surface plasmon resonance (LSPR) suggested by the Ag plasmonic nanocrystals increased the intrinsic optical absorption in the active layer poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester (P3HT:PCBM). Based on the photovoltaic results, the short circuit current ranged from 19.7 to 26.7 mA/cm².

     

Morphology Optimization of Silver Nanoparticles Used to Improve the Light Absorption in Thin-Film Silicon Solar Cells

Plasmonics - Silver nanoparticle (NP) arrays are used as antireflection coating to enhance light trapping capability of thin-film silicon solar cells. In this paper, we theoretically investigate...     

Improvement on the Performance of InP/CdS Solar Cells with the Inclusion of Plasmonic Layer of Silver Nanoparticles

The effect of nano-Ag (n-Ag) plasmonic layer in InP/CdS solar cell structure was examined. An enhancement of short circuit current improving the overall cell efficiency was observed in InP/n-Ag/CdS cells. Location of the plasmonic layer in the above cell structure has been analyzed critically. The effect of introducing plasmonic layer on the overall performance of the cell has been studied in terms of the morphology, particle size distribution, optical absorption, I–V, C–V characteristics, and lifetime of the photo-generated carriers. Secondary ion mass spectroscopy (SIMS) studies were carried out for investigating possible interface alloying.     

Influence of Plasmonic Nanoparticles on the Performance of Colorimetric Cell Viability Assays

The conventional colorimetric assays based on measurement of the metabolic activity are routinely used to evaluate the cytotoxicity of nanomaterials (NMs). However, due to the varying absorbance properties of plasmonic NMs in the visible region of the spectrum, obtained results can be misleading. In this study, MTT, MTS, and WST-1 colorimetric cell viability assays were evaluated in the presence of gold (AuNPs) or silver nanoparticles (AgNPs). Since a living cell a complex system containing many molecular and ionic species, the plasmonic AuNP and AgNPs may selectively interact with intracellular components possessing thiol, amino, and carboxyl group moieties change the aggregation behavior of the NMs and thus their absorbance. A series of UV/Vis and DLS experiments were conducted to understand the interference possibility of the tested plasmonic NMs. The results show that the AuNPs and AgNPs do not have absorption at the wavelength where MTT formazan is measured while the both NPs may interfere with absorbance of MTS and WST-1 formazan.The overall assessments show that MTT assay is more suitable for the cell viability evaluation of spherical AuNPs and AgNPs with an average diameter of 50 nm. This study also suggests that a preliminary ex situ evaluation of plasmonic nanoparticles can provide valuable information for the suitability of the assay.     

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.     

A New GaAs Metal-Semiconductor-Metal Photodetector Based on Hybrid Plasmonic Structure to Improve the Optical and Electrical Responses

In this article, a new hybrid plasmonic based metal-semiconductor-metal photodetector (MSM-PD) is proposed. A subwavelength slit, the metal nanoscale gratings, and the metal pads which are extended into the absorption layer are used in a basic hybrid plasmonic structure to enhance the absorption coefficient. The finite-difference time-domain (FDTD) method is used to simulate the new structure. The absorption coefficient of the hybrid plasmonic MSM-PD becomes 42 times greater than that of the conventional plasmonic MSM-PD made of only subwavelength slit, which is known as the reference structure. This result is equivalently about 1.5 times greater than that of a recently reported structure. It is also demonstrated that the quantum efficiency of the proposed structure is 10 times more, if compared with the reference one. Moreover, considering the incident light modulation frequency, the frequency response of the hybrid plasmonic MSM-PD is improved, where the cutoff frequency is increased 22 times greater than that of the reference MSM-PD.     

Theoretical Study of the Anchoring Influence on Plasmonic Resonance Tunability of Metallic Nanoparticles Embedded in a Liquid Crystal Cell

In this paper, the localized surface plasmon resonance (LSPR) peak position of an ordered gold nanoparticles array embedded in a nematic liquid crystal (LC) media is investigated using finite-difference time-domain method. The influence of the anchoring effects between nematic LC molecules and glass substrate on the shift of LSPR wavelength is taken into account, and results are compared with the case of a perfect alignment of the LC molecules.     

Study on the Plasmonic Properties of Ag-coated Spherical Dielectric Nanoparticles by Finite-Difference Time-Domain Calculations

Plasmonics - The optical properties of nanostructures are rather important for designing plasmonic devices. In this work, the plasmonic properties of Ag-coated spherical dielectric nanoparticles...     

Improved Method of Study on the Photothermal Effect of Plasmonic Nanoparticles by Dynamic IR Thermography

Efficient heat generation by plasmon-resonant gold nanoparticles, together with their biocompatibility and high specificity of biomolecular recognition, opens new possibilities for applications in biomedical applications. In this work, we present an improved method of monitoring surface temperature changes subjected to external stimulation by dynamic IR thermography. The method is based on the careful analysis of an IR image sequence recorded before, during, and after the stimulation that allows one to select areas with significant temperature variation and evaluate temporal behavior of the surface temperature. The method was applied for the experimental study on the photothermal effect in a gold hydrosol containing hollow gold nanoparticles heated with laser beam. Under these conditions, it was seen that the surface temperature of the gold hydrosol (measured with a FLIR SC655 InfraRed Camera, resolution 640 × 480 pixels) under the laser beam gradually increases and reaches a saturation level. It was shown that the developed method is capable of producing a quantitative analysis of the changes in the surface temperature distribution of the gold hydrosol, as well as characterizing the photothermal properties of the nanoparticles.

     

A Novel Strategy to Improve the Therapeutic Efficacy of Gemcitabine for Non-Small Cell Lung Cancer by the Tumor-Penetrating Peptide iRGD

Non-small cell lung cancer (NSCLC) is the most common type of lung cancer, comprising approximately 75–80% of all lung cancers. Gemcitabine is an approved chemotherapy drug for NSCLC. The objective of this study was to develop a novel strategy to improve the therapeutic efficacy of Gemcitabine for NSCLC by the co-administered iRGD peptide. We showed that the rates of positive expression of αvβ3, αvβ5 and NRP-1 in the A549 cell line were 68.5%, 35.3% and 94.5%, respectively. The amount of Evans Blue accumulated in the tumor of Evans Blue+iRGD group was 2.5 times that of Evans Blue group. The rates of growth inhibition of the tumors of the iRGD group, the Gemcitabine group and the Gemcitabine+iRGD group were 8%, 59.8% and 86.9%, respectively. The results of mechanism studies showed that PCNA expression in the Gemcitabine+iRGD group decreased 71.5% compared with that in Gemcitabine group. The rate of apoptosis in the Gemcitabine+iRGD group was 2.2 time that of the Gemcitabine group. Therefore, the tumor-penetrating Peptide iRGD can enhance the tumor-penetrating ability and therapeutic efficacy of Gemcitabine in the A549 xenograft. The combined application of Gemcitabine with iRGD may be a novel strategy to enhance the clinical therapeutic efficacy of Gemcitabine in patients with NSCLC.     

A Comparative Study of the Effects of Nontoxic Chloride Treatments on CdTe Solar Cell Microstructure and Stoichiometry

This work presents the first systematic comparison of the effects of a range of chlorides (CdCl₂, MgCl₂, NaCl, and NH₄Cl) on the microstructure and chemical composition of CdTe/CdS/ZnO/SnO₂ solar cells, providing valuable insight to the ubiquitous Cl‐activation process. Using X‐ray diffraction, it is shown that CdCl₂ induces the greatest extent of recrystallization (standard deviation of texture coefficients, σ, reduces from 0.93 for as‐grown CdTe to 0.43) and minimizing stress (from 178 MPa for as‐grown material to zero). MgCl₂ treatment also yields significant randomization of the CdTe texture (σ = 0.55) but NaCl treatment does not (σ = 1.10). A strong correlation between the extent of metallurgical changes induced by the chloride treatment (and consequently, device efficiency) and the dissociation energy of the cationCl bond is shown, thereby accounting for the ineffectiveness of NaCl (bond energy = 4.3 eV). From this, a mechanism for Cl activation is postulated. By X‐ray photoelectron spectroscopy it is also shown that the Te/Cd ratio at the back surface, and the Cl content at the CdTe–CdS interface, are both higher following CdCl₂‐ and MgCl₂ treatments (Te/Cd = 1.3–1.4, and 1–2 at% Cl) than following NaCl treatment (Te/Cd = 1.1, and 0 at% Cl).     

A Novel Approach to the Study of Kinetically Changing Cell Populations

A method is described for estimating changes in cell cycle times during periods of rapid change in proliferation rate. This method, which depends upon the interpretation of pre- and post-velocity sedimentation fractionation continuous thymidine labelling patterns, exploits the relationship between sedimentation rate and cell cycle location. By this means, cycle times can be estimated under conditions that are difficult (if not impossible) to analyse by FLM methods.     

Improving the Performance and Stability of Inverted Planar Flexible Perovskite Solar Cells Employing a Novel NDI‐Based Polymer as the Electron Transport Layer

A new naphthalene diimide (NDI)‐based polymer with strong electron withdrawing dicyanothiophene (P(NDI2DT‐TTCN)) is developed as the electron transport layer (ETL) in place of the fullerene‐based ETL in inverted perovskite solar cells (Pero‐SCs). A combination of characterization techniques, including atomic force microscopy, scanning electron microscopy, grazing‐incidence wide‐angle X‐ray scattering, near‐edge X‐ray absorption fine‐structure spectroscopy, space‐charge‐limited current, electrochemical impedance spectroscopy, photoluminescence (PL), and time‐resolved PL decay, is used to demonstrate the interface phenomena between perovskite and P(NDI2DT‐TTCN) or [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM). It is found that P(NDI2DT‐TTCN) not only improves the electron extraction ability but also prevents ambient condition interference by forming a hydrophobic ETL surface. In addition, P(NDI2DT‐TTCN) has excellent mechanical stability compared to PCBM in flexible Pero‐SCs. With these improved functionalities, the performance of devices based on P(NDI2DT‐TTCN) significantly outperform those based on PCBM from 14.3 to 17.0%, which is the highest photovoltaic performance with negligible hysteresis in the field of polymeric ETLs.