Investigation of the optical gain and noise figure for multi-channel amplification in EDFA under optimized pump condition

We present the results of an investigation of optical gain and noise figure for simultaneous multi-channel amplification of an erbium doped fibre amplifier (EDFA) under optimized pump condition. Different pump configurations with varying input signal levels show interesting features on gain flatness. In the experiment, population inversion along the fibre length which determines the gain-spectra and noise characteristics of the amplifier is adjusted through optimized fibre length and injected pump power in order to minimize the gain-tilt at C-band. It is observed that bi-directional pumping manifests the best combination of low noise and high gain of EDFA which are useful as in-line repeaters in WDM network. We obtain 30 ± 1.5 dB intrinsically flat small signal gain from 1538 nm to 1558 nm band of wavelength with noise figure <4 dB for 16-channel simultaneous amplification in a single stage EDFA without gain flattening filter.     

Perfect fluid dark matter

Taking the flat rotation curve as input and treating the matter content in the galactic halo region as perfect fluid we obtain a space–time metric at the galactic halo region in the framework of general relativity. We find that the resultant space–time metric is a non-relativistic dark matter induced space–time embedded in a static Friedmann–Lemaître–Robertson–Walker universe i.e. the flat rotation curve not only leads to the existence of dark matter but also suggests about the background geometry of the universe. Within its range of validity the flat rotation curve and the demand that the dark matter to be non-exotic together indicate for a (nearly) flat universe as favored by the modern cosmological observations. We obtain the expressions for energy density and pressure of dark matter there and consequently the equation of state of dark matter. Various other aspects of the solutions are also analyzed.     

Investigation of nuclear quantum effect on the hydrogen bonds of ammonium dihydrogen phosphate using single-crystal neutron diffraction and theoretical modelling

The heterostructure of patterned CdS / CdTe thin films with back contact have been devised with electron beam lithography and fabricated using sputter deposition technique. The metallic contacts for n-CdS and p-CdTe are patterned such that both are placed at the bottom of the cell. This avoids losses due to contact shading and increases absorption in the window layer. Patterning of the device surface helps in increasing the junction area which can modulate the absorption of more number of photons due to total internal reflection. Computing the surface area between a planar and a patterned device has revealed 133% increase in the junction area. The physical and optical properties of the sputter-deposited CdS / CdTe layers are also presented. J–V characteristics of the solar cell showed the fill factor to be 25.9%, open circuit voltage to be 17 mV and short-circuit current density to be \(113.68~\hbox {A}/\hbox {m}^{2}\). The increase in surface area is directly related to the increase in the short circuit current of the photovoltaic cell, which is observed from the results of simulated model in Atlas / Silvaco.     

Tamarind seed skin-derived fiber-like carbon nanostructures as novel anode material for lithium-ion battery

Demand of low-cost carbonaceous anode materials for lithium-ion batteries has led to the development of anode materials from different bio-sources. In this regard, tamarind seed (skin) was used as a precursor to prepare disordered carbon as an anode material for lithium-ion batteries. The carbon was prepared through simple hydrothermal method and was characterized by X-ray diffraction (XRD), Raman spectroscopy, Brunauer–Emmett–Teller (BET) measurements, field emission scanning electron microscopy (FE-SEM), and transmission electron microscopy (TEM) techniques. It exhibited amorphous carbon particles arranged in a fiber-like morphology with high surface area of 508 m² g^?1. The binder content was optimized for the carbon to achieve high and stable capacity. Electrochemical performance of the as-prepared carbon with optimized binder content showed a stable reversible specific capacity of 224 mAhg^?1 after 300 cycles at 1 C-rate. The stable cycling performance of carbon at high current rate is explained by electrochemical impedance spectroscopy (EIS) and FE-SEM data of cycled electrodes. The low cost and stable specific capacity make the carbon as potential anode material for lithium-ion battery.

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Graphical abstract Fiber-like carbon nanostructures from tamarind seed (skin) (TDC) via simple and effective hydrothermal method and its application as a novel anode material for lithium-ion battery.

     

Agglomeration behavior of lipid-capped gold nanoparticles

The current investigation deciphers aggregation pattern of gold nanoparticles (AuNPs) and lipid-treated AuNPs when subjected to aqueous sodium chloride solution with increasing ionic strengths (100–400 nM). AuNPs were synthesized using 0.29 mM chloroauric acid and by varying the concentrations of trisodium citrate (AuNP1 1.55 mM, AuNP2 3.1 mM) and silver nitrate (AuNP3 5.3 μM, AuNP4 10.6 μM) with characteristic LSPR peaks in the range of 525–533 nm. TEM analysis revealed AuNPs to be predominantly faceted nanocrystals with the average size of AuNP1 to be 35?±?5 nm, AuNP2 15?±?5 nm, AuNP3 30?±?5 nm, and AuNP4 30?±?5 nm and the zeta-average for AuNPs were calculated to be 31.23, 63.80, 26.08, and 28 nm respectively. Induced aggregation was observed within 10 s in all synthesized AuNPs while lipid-treated AuNP2 (AuNP2-L) was found to withstand ionic interferences at all concentration levels. However, lipid-treated AuNPs synthesized using silver nitrate and 1.55 mM trisodium citrate (AuNP3, AuNP4) showed much lower stability. The zeta potential values of lipid-treated AuNPs (AuNP1-L-1x/200, ??17.93?±?1.02 mV; AuNP2-L-1x/200, ??21.63?±?0.70; AuNP3-L-1x/200, ??14.54?±?0.90; AuNP3-L-1x/200 ??13.77?±?0.83) justified these observations. To summarize, AuNP1 and AuNP2 treated with lipid mixture 1 equals or above 1x/200 or 1x/1000 respectively showed strong resistance against ionic interferences (up to 400 mM NaCl). Use of lipid mixture 1 for obtaining highly stable AuNPs also provided functional arms of various lengths which can be used for covalent coupling.

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Graphical abstract Agglomeration behavior of gold nanoparticles before and after lipid capping

     

Long-Term Stability Analysis of 3D and 2D/3D Hybrid Perovskite Solar Cells Using Electrochemical Impedance Spectroscopy

Despite the remarkable progress in perovskite solar cells (PSCs), their instability and rapid degradation over time still restrict their commercialization. A 2D capping layer has been proved to overcome the stability issues; however, an in-depth understanding of the complex degradation processes over a prolonged time at PSC interfaces is crucial for improving their stability. In the current work, we investigated the stability of a triple cation 3D ([(FA_0.83MA_0.17)Cs_0.05]Pb(I_0.83Br_0.17)₃) and 2D/3D PSC fabricated by a layer-by-layer deposition technique (PEAI-based 2D layer over triple cation 3D perovskite) using a state-of-art characterization technique: electrochemical impedance spectroscopy (EIS). A long-term stability test over 24 months was performed on the 3D and 2D/3D PSCs with an initial PCE of 18.87% and 20.21%, respectively, to suggest a more practical scenario. The current-voltage (J-V) and EIS results showed degradation in both the solar cell types; however, a slower degradation rate was observed in 2D/3D PSCs. Finally, the quantitative analysis of the key EIS parameters affected by the degradation in 3D and 2D/3D PSCs were discussed.     

Microwave-assisted rapid and efficient synthesis of chromene-fused pyrrole derivatives through multicomponent reaction and evaluation of antibacterial activity with molecular docking investigation

The current study aimed to identify a new strategy of FeCl₃ catalyzed multicomponent synthesis of substituted 2H-chromene–fused pyrrole derivatives. A series of chromene-based pyrrole prepared by employing an array of 3-nitro-2H-chromenes, aniline, and acetylacetone in toluene under microwave irradiation. Using FeCl₃ as a prompt catalyst and microwave irradiation to synthesize 2H-chromene–fused pyrrole motifs significantly reduces the reaction time and facilitates to high yields (83%-95%). Structure of all synthesized compounds analyzed by spectroscopic analysis. One-pot reaction, short reaction period, and simple experimental procedure are the fascinating properties associated with this protocol. The in vitro antibacterial activity of the entire series was assessed against Staphylococcus aureus and Escherichia coli. Out of all the compounds, 15b and 15h revealed most excellent potency against both the bacterial strains relative to the reference gentamicin. Docking study was employed to determine the possible binding orientation of DNA gyrase with the active sites of chromene-fused pyrrole analog. The docking results show that compounds 15b and 15h have higher binding affinity with energy −8.00 and −8.80 kcal/mol. These results illuminate the mode of binding progression and provide an esteemed pathway for the design and the structural modification of chromene-fused pyrroles as a newly advanced class of antibacterial agent.     

Catalytic Approaches for the Direct Heterofunctionalization of Aliphatic Carboxylic Acids and Their Equivalents with Group 16 Elements

In contrast to traditional multistep synthesis, modern organic synthesis extensively depends on the direct functionalization of unactivated C?H bonds for the construction of various C?C and C‐heteroatom bonds in atom‐ and step‐economic manner. Common aliphatic substrates, e. g. carboxylic acids and their synthetic equivalents, are regiospecifically functionalized based on either a directed approach, in which the polar directing group assists to functionalize a specific C?H bond positioned at β‐ and γ‐carbon centers, or a non‐directed approach typically leading to α‐functionalization. While numerous reviews on catalytic C?H functionalization have appeared, a concise review on the direct C(sp³)?H heterofunctionalization of carboxylic acid synthons with Group 16 elements has been awaited. The recent advances on the direct oxy‐functionalization and chalcogenation of aliphatic carboxylic acid synthons enabled by transition metal, organo‐ and photocatalysts are described herein.