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Herein, we evaluate the conversion efficiency of dye-sensitized solar cells (DSSCs) photosensitized using two different natural dyes extracted from Alpinia purpurata and Alstroemeria flower petals. The appreciable absorption capacity of the extracts in the visible light region was examined through absorption spectroscopy. The functional groups of the corresponding pigments were identified through Fourier transform spectroscopy (FTIR) technique thus indicating the presence of cyanidin 3-glycosides and piperine in the flowers of Alstroemeria and Alpinia purpurata. The extracted dyes were immobilized on TiO2 on transparent conducting FTO glass, which were used as photoanode. The dye-coated TiO2 photoanode, pt photocathode and iodide/triiodide redox electrolyte assembled into a cell module was illuminated by a light source intensity 100 mW/cm2 to measure the photovoltaic conversion efficiency of DSSCs. The TiO2 anode and Pt counter electrode surface roughness and morphological studies were evaluated using atomic force microscope (AFM) and field emission scanning electron microscopy (FESEM), respectively. Through the photoelectric characterizations, it was promising to verify that the solar conversion efficiency was calculated with the photovoltaic cell sensitized by Alstroemeria and Alpinia purpurata. This was achieved with a yield (η) of 1.74% and 0.65%, with an open-circuit voltage (Voc) of 0.39 and 0.53 V, short-circuit current density (Jsc) of 2.04 and 0.49 mA/cm2, fill factor (FF) of 0.35 and 0.40, and Pmax of 0.280 and 0.100 mW/cm2, respectively. The results are promising and demonstrate the importance of the search for new natural dyes to be used in organic solar cells for the development of devices that generate electricity in a sustainable way.

In this paper, the electrochemical non-enzymatic detection of Riboflavin (RF) was proposed based on its catalytic reduction in a Thionine-coated Cadmium Selenide Quantum dots (TH@CdSe QDs)-modified paraffin wax-impregnated graphite electrode (PIGE) that was prepared using a novel approach. The synthesized TH@CdSe QDs were confirmed by UV-Vis spectroscopy, Confocal Raman Microscopy and High Resolution Transmission Electron Microscopy (HRTEM) studies. The electrochemical response of the TH@CdSe QDs-modified PIGE was studied by cyclic voltammetry. The voltammetric response of RF at the TH@CdSe QDs-modified PIGE showed higher current than the bare PIGE. Under optimum conditions, the electrocatalytic reduction currents of RF was found to be linearly related to its concentration over the range of 1.6 × 10−7 M to 1.4 × 10−4 M with a detection limit of 53 × 10−9 M (S/N = 3). The TH@CdSe QDs-modified PIGE was utilized as an amperometric sensor for the detection of RF in flow systems was performed by carrying out hydrodynamic and chronoamperometric experiments. The TH@CdSe QDs-modified PIGE showed very good stability and a longer shelf life. The applicability of the fabricated electrode was justified by the quantification of RF in commercial tablets.

Abstract Energy crisis and environmental pollution have been one of the major global issues. In this regard, the search for new energy storage materials is cheap, flexible and high-performance supercapacitors electrode which has become intensive. Also, reducing the amount of organic dyes polluting in water is a great significance. Herein, one-step electropolymerization of methylene blue on carbon fiber and the resulting films were applied to the supercapacitor. The high performance is associated to the outstanding conductivity, electrochemical stability and superior mechanical flexibility of carbon fiber. A new flexible electrode for supercapacitors was successfully fabricated by demonstrating with a good electrochemical performance and a promising alternative to reduce the water pollution.

In this manuscript, we are reporting for the first time one dimensional (1D) cerium hydrogen phosphate (Ce(HPO4)2.xH2O) electrode material for supercapacitor application. In short, a simple hydrothermal technique was employed to prepare Ce(HPO4)2.xH2O. The maximum surface area of 82 m2 g−1 was obtained from nitrogen sorption isotherm. SEM images revealed Ce(HPO4)2.xH2O exhibited a nanorod-like structure along with particles and clusters. The maximum specific capacitance of 114 F g−1 was achieved at 0.2 A g−1 current density for Ce(HPO4)/NF electrode material in a three-electrode configuration. Furthermore, the fabricated symmetric supercapacitor (SSC) based on Ce(HPO4)2.xH2O//Ce(HPO4)2.xH2O demonstrates reasonable specific energy (2.08 Wh kg−1), moderate specific power (499.88 W kg−1), and outstanding cyclic durability (retains 92.7% of its initial specific capacitance after 5000 GCD cycles).

In this study, sustainable, low-cost, and environmentally friendly biomass (Terminalia chebula) was employed as a precursor for the formation of nitrogen-doped carbon dots (N-CDs). The hydrothermally assisted Terminalia chebula fruit-derived N-CDs (TC-CDs) emitted different bright fluorescent colors under various excitation wavelengths. The prepared TC-CDs showed a spherical morphology with a narrow size distribution and excellent water dispensability due to their abundant functionalities, such as oxygen- and nitrogen-bearing molecules on the surfaces of the TC-CDs. Additionally, these TC-CDs exhibited high photostability, good biocompatibility, very low toxicity, and excellent cell permeability against HCT-116 human colon carcinoma cells. The cell viability of HCT-116 human colon carcinoma cells in the presence of TC-CDs aqueous solution was calculated by MTT assay, and cell viability was higher than 95%, even at a higher concentration of 200 μg mL−1 after 24 h incubation time. Finally, the uptake of TC-CDs by HCT-116 human colon carcinoma cells displayed distinguished blue, green, and red colors during in vitro imaging when excited by three filters with different wavelengths under a laser scanning confocal microscope. Thus, TC-CDs could be used as a potential candidate for various biomedical applications. Moreover, the conversion of low-cost/waste natural biomass into products of value promotes the sustainable development of the economy and human society.

Supercapacitors (SCs), also known as ultracapacitors, should be one of the most promising contenders for meeting the needs of human viable growth owing to their advantages: for example, excellent capacitance and rate efficiency, extended durability, and cheap materials price. Supercapacitor research on electrode materials is significant because it plays a vital part in the performance of SCs. Polyaniline (PANI) is an exceptional candidate for energy-storage applications owing to its tunable structure, multiple oxidation/reduction reactions, cheap price, environmental stability, and ease of handling. With their exceptional morphology, suitable functional linkers, metal sites, and high specific surface area, metal–organic frameworks (MOFs) are outstanding materials for electrodes fabrication in electrochemical energy storage systems. The combination of PANI and MOF (PANI/MOF composites) as electrode materials demonstrates additional benefits, which are worthy of exploration. The positive impacts of the two various electrode materials can improve the resultant electrochemical performances. Recently, these kinds of conducting polymers with MOFs composites are predicted to become the next-generation electrode materials for the development of efficient and well-organized SCs. The recent achievements in the use of PANI/MOFs-based electrode materials for supercapacitor applications are critically reviewed in this paper. Furthermore, we discuss the existing issues with PANI/MOF composites and their analogues in the field of supercapacitor electrodes in addition to potential future improvements.

Exploring faster, safer, and more efficient energy storage devices will motivate scientists to develop novel energy storage products with high performance. Herein, we report porous NiO nanoparticles have been prepared by a simple hydrothermal method with CTAB and laboratory tissue paper as a template followed by calcination at three different temperatures (300, 500, and 700 °C). The electrochemical characteristics of the prepared materials were examined in a three-electrode cell configuration using aqueous potassium hydroxide (2.0 M KOH) electrolyte. The NiO-300 electrode displayed the supreme capacitance of 568.7 F g−1 at 0.5 A g−1. The fascinating NiO morphology demonstrates a crucial part in offering simple ion transport, shortening electron, and ion passage channels and rich energetic spots for electrochemical reactions. Finally, the asymmetric supercapacitor (ASC), NiO//AC was constructed using positive and negative electrode materials of NiO-300 and activated carbon (AC), respectively. The assembled ASC displayed excellent supercapacitive performance with a high specific energy (52.4 Wh kg−1), specific power (800 W kg−1), and remarkable cycle life. After quick charging (25 s), such supercapacitors in the series will illuminate the light emitting diode for an extended time, suggesting improvements in energy storage, scalable integrated applications, and ensuring business efficacy. This work will lead to a new generation of high-performance ASCs to portable electronic displays and electric automobiles.

Herein, Sargassum coreanum (marine algae)-mediated silver nanoparticles (AgNPs) were successfully synthesized by a simple reduction method. The synthesized AgNPs were characterized using ultraviolet-visible spectroscopy, attenuated total reflection Fourier transformed infrared spectroscopy, X-ray diffractometry, field emission scanning electron microscopy (FESEM) with energy-dispersive X-ray (EDX) spectroscopy, and high-resolution transmission electron microscopy (HR-TEM) analysis. The acquired colloidal AgNPs were strongly absorbed around 420 nm and displayed brown color under visible light. The XRD pattern of AgNPs exposed their face-centered cubic geometry along with crystalline nature. The HRTEM images of synthesized AgNPs confirmed the mean particle size of 19 nm with a distorted spherical shape, and the calculated interlayer distance (d-spacing value) was about 0.24 nm. Further, the catalytic degradation of methylene blue using sodium borohydride and AgNPs was monitored using UV–vis spectroscopy. The result revealed that AgNPs performed as a superior catalyst, which completely degraded MB in 20 min. The rate constant for MB degradation was calculated to be 0.106 min−1, demonstrating that the marine algae-mediated AgNPs had outstanding catalytic activity. This approach is easy and environmentally benign, which can be applied for environmental-based applications such as dye degradation and pollutant detoxification.

This paper’s emphasis is on the development of a fluorescent chemosensor for Fe3+ ions in an aqueous solution, using hydrophilic carbon dots (O-CDs). A simple, cost-effective, and environmentally friendly one-step hydrothermal synthesis method was used to synthesize fluorescent hydrophilic O-CDs from Oxalis corniculata (Family; Oxalidaceae). The graphitic structure and size distribution of the O-CDs was verified by X-ray diffraction, Raman spectroscopy, and high-resolution transmission electron microscopy studies. The resulting O-CDs had a near-spherical shape and an adequate degree of graphitization at the core, with an average diameter of 4.5 nm. X-ray photoelectron and Fourier transform infrared spectroscopy methods revealed the presence of several hydrophilic groups (carbonyl, amine, carboxyl, and hydroxyl, along with nitrogen and oxygen-rich molecules) on the surface of O-CDs. The synthesized hydrophilic O-CDs with excitation wavelength-dependent emission fluorescence characteristics showed a high quantum yield of about 20%. Besides this, the hydrophilic O-CDs exhibited a bright and controllable fluorescence with prolonged stability and photo-stability. These fluorescent hydrophilic O-CDs were used as a nanoprobe for the fluorometric identification of Fe3+ ions in an aqueous solution, with high sensitivity and selectivity. By quenching the blue emission fluorescence of this nanosensor, a highly sensitive Fe3+ ion in the range of 10–50 µM with a minimum detection limit of 0.73 µM was achieved. In addition, the developed nanosensor can be used to sense intracellular Fe3+ ions with high biocompatibility and cellular imaging capacity, and it has a lot of potential in biomedical applications.

Recently, the use of natural products for the synthesis of carbon dots (CDs) has received much attention. Herein, leftover kiwi (Actinidia Deliciosa) fruit peels were successfully turned into beneficial fluorescent carbon dots (KN-CDs) via the hydrothermal-carbonization route. KN-CDs 1 and KN-CDs 2 were prepared without and with ammonium hydroxide, respectively. KN-CDs 1 and KN-CDs 2 were systematically characterized by various analytical techniques. Synthesized KN-CDs showed spherical-shaped morphology with narrow size distribution and excellent optical properties with excitation-independent behaviors. The quantum yields of KN-CDs 1 and KN-CDs 2 were calculated as 14 and 19%, respectively. Additionally, the KN-CDs possess excellent prolonging and photostability. Because of the excellent optical properties of KN-CDs, they were utilized as fluorescent sensors. The strong fluorescence of the KN-CDs was selectively quenched by Fe3+ ion, and quenching behavior showed a linear correlation with the concentrations of Fe3+ ion. KN-CDs 1 and KN-CDs 2 showed the detection of Fe3+ ions within the concentration range of 5–25 µM with the detection limit of 0.95 and 0.85 µM, respectively. Based on the turn-off sensing by the detection of Fe3+ ions, KN-CDs would be a promising candidate as a selective and sensitive fluorescent sensor.

The growth of industry fulfills our necessity and promotes economic development. However, pollutants from such industries pollute water bodies which pose a high risk for living organisms. Thus, researchers have been urged to develop an efficient method to remove toxic heavy metal ions from water bodies. The adsorption method shows promising results for the removal of heavy metal ions and is easy to operate on a large scale, thus can be applied to practical applications. Numerous adsorbents were developed and reported, among them hydrogels, which attract great attention because of the reusability, ease of preparation, and handling. Hydrogels are generally prepared by the cross-linking of polymers that result in a three-dimensional structure, showing high porosity and high functionality. They are hydrophilic in nature because of the functional groups, and are non-toxic. Thus, this review provides various methods of hydrogel adsorbents preparation and summarizes recent progress in the use of hydrogel adsorbents for the removal of heavy metal ions. Further, the mechanism involved in the removal of heavy metal ions is briefly discussed. The most recent studies about the adsorption method for the treatment of heavy metal ions contaminated water are presented.

Integration of materials acts as a bridge between the electronic and biological worlds, which has revolutionized the development of bioelectronic devices. This review highlights the rapidly emerging field of switchable interface and its bioelectronics applications. This review article highlights the role and importance of two-dimensional (2D) materials, especially graphene, in the field of bioelectronics. Because of the excellent electrical, optical, and mechanical properties graphene have promising application in the field of bioelectronics. The easy integration, biocompatibility, mechanical flexibility, and conformity add impact in its use for the fabrication of bioelectronic devices. In addition, the switchable behavior of this material adds an impact on the study of natural biochemical processes. In general, the behavior of the interfacial materials can be tuned with modest changes in the bioelectronics interface systems. It is also believed that switchable behavior of materials responds to a major change at the nanoscale level by regulating the behavior of the stimuli-responsive interface architecture.

Summary: Nowadays, intrusion detection systems (IDSs) enabled with computational intelligence for electing the suitable classifiers to learn the patterns of various types of network attacks are under study. Selection mechanism of single or ensemble classifiers based on performance and ranking is to be enabled in the IDS framework to make accurate pattern predictions. A new anomaly based network intrusion detection system framework is proposed using context adaptive classification through the technique for order of preference by similarity to ideal solution (TOPSIS) ranking mechanism with hierarchy based chi‐square and bat algorithms for feature selection. Parameters like accuracy, false positive rate (FPR), and classification model building time are explored for choosing the best and situation aware classifiers using TOPSIS. For experimentation, NSL‐KDD and UNSW‐NB15 datasets are used. The proposed system opts decision tree (DT) algorithm for NSL‐KDD and produces 98.77% accuracy, 0.03% FPR with 8 features. Ensemble learner is selected for the UNSW‐NB15 dataset using DT and support vector machine classifiers with 9 features. Combined classifier predicts 89.43% accuracy and 3.215% FPR. Experimentation on the proposed methodology with the state of the art approaches produces promising results. [ABSTRACT FROM AUTHOR]

A recent challenge in information technology is to protect secret data and preserve the ownership of a product. There are many duplicate products being released on a daily basis. Owners have a high risk in proving their products. Watermarking is a technique used to preserve ownership by hiding the owner's information in their products. The proposed hypothesis-based vertex shifting algorithm embeds 2D secret logos in 3D cover objects. The 3D objects are represented using vertices and facets. 3D watermarking faces various challenges and one among them is capacity. In this work, capacity is addressed by using a hypothesis-based vertex shift method that enables the embedding process for all the coordinates of the vertex. The method works by partitioning the vertex based on a shift factor called svalue. The svalue is chosen based on the visual quality of the watermarked object. The metrics used for testing are bit error rate for the recovered watermark, peak-to-signal noise ratio, and vertex signal-to-noise ratio (VSNR) of the watermarked 3D image. The proposed algorithm shows that a maximum of 3 bits can be embedded in a vertex when compared with the existing algorithms. The VSNR value of the proposed algorithm is high (125.87) compared to the existing algorithms. This shows that the algorithm withstands visual quality inspection. Hence, it is a robust watermarking algorithm for embedding secret logos into 3D objects with better visual quality and higher resilience against translation and uniform scaling attacks. [ABSTRACT FROM AUTHOR]