Search

The widespread proliferation of water hyacinth ( Eichhornia crassipes ) in aquatic ecosystems has raised significant ecological, environmental, and socioeconomic concerns globally. These concerns include reduced biodiversity, impeded water transportation and recreational activities, damage to marine infrastructure, and obstructions in power generation dams and irrigation systems. This review critically evaluates the challenges posed by water hyacinth (WH) and investigates potential strategies for converting its biomass into value-added agricultural products, specifically nanonutrients-fortified, biochar-based, green fertilizer. The review examines various methods for producing functional nanobiochar and green fertilizer to enhance plant nutrient uptake and improve soil nutrient retention. These methods include slow or fast pyrolysis, gasification, laser ablation, arc discharge, or chemical precipitation used for producing biochar which can then be further reduced to nano-sized biochar through ball milling, a top-down approach. Through these means, utilization of WH-derived biomass in economically viable, eco-friendly, sustainable, precision-driven, and smart agricultural practices can be achieved. The positive socioeconomic impacts of repurposing this invasive aquatic plant are also discussed, including the prospects of a circular economy, job creation, reduced agricultural input costs, increased agricultural productivity, and sustainable environmental management. Utilizing WH for nanobiochar (or nano-enabled biochar) for green fertilizer production offers a promising strategy for waste management, environmental remediation, improvement of waterway transportation infrastructure, and agricultural sustainability. To underscore the importance of this work, a metadata analysis of literature carried out reveals that an insignificant section of the body of research on WH and biochar have focused on the nano-fortification of WH biochar for fertilizer development. Therefore, this review aims to expand knowledge on the upcycling of non-food crop biomass, particularly using WH as feedstock, and provides crucial insights into a viable solution for mitigating the ecological impacts of this invasive species while enhancing agricultural productivity., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2024 The Authors.)

Sensitive thermometry or thermography by responding to blackbody radiation is urgently desired in the intelligent information life, including scientific research, medical diagnosis, remote sensing, defense, etc. Even though thermography techniques based on infrared sensing have undergone unprecedented development, the poor compatibility with common optical components and the high diffraction limit impose an impediment to their integration into the established photonic integrated circuit or the realization of high-spatial-resolution and high-thermal-resolution imaging. In this work, we present a sensitive temperature-dependent visible photon detection in Bi-doped MAPbX 3 (X = Cl, Br, and I) and employ it for uncooled thermography. Systematic measurements reveal that the Bi dopant introduces trap states in MAPbX 3 , thermal energy facilitates the carriers jumping from trap states to the conduction band, while the vacancies of trap states ensure the sequential absorption of visible photons with energy less than the band gap. Subsequently, the change of response toward the visible photon is applied to construct the thermograph, and it possesses a specific sensitivity of 2.11% K -1 along temperature variation. As a result, our thermograph presents a temperature resolution of 0.21 nA K -1 , a high responsivity of 2.06 mA W -1 , and a high detectivity of 2.08 × 10 9 Jones at room temperature. Furthermore, remote thermal imaging is successfully achieved with our thermograph.

Narrowband photodetectors (NPDs) with the capability of detecting light within a selective wavelength range are in high demand for numerous emerging applications such as imaging systems, machine vision, and optical communication. Halide perovskite materials have been developed for eliminating the current complex filtering systems in NPDs due to their beneficial properties, while currently NPDs using perovskite materials are limited by hardly fully eliminated short wavelength response, low charge collection efficiency (CCE), complex fabrication process, and so forth. Herein, a series of perovskite single-crystalline heterojunctions (PSCHs) with a structure of Bi-MAPbX 3 /MAPbY 3 are fabricated by liquid phase epitaxy for filter-free narrowband detection. By varying the halide component in the PSCH, the PSCH-based NPDs can realize continuously tunable spectral response range from blue to NIR regions and ultra-narrow full width at half-maximum (FWHM) of <20 nm. Specifically, the PSCH-based NPD with a high CCE under a large electric filed shows a high spectra rejection ratio of >1000, a fast response speed with rise/fall time of ∼160/∼225 μs, and long-term stability more than 3 months in ambient air. This work provides a simple strategy for designing low-cost and high-performance filter-free NPDs with a tunable spectral response.

Dual-mode photodetectors (PDs) have attracted increasing interest owing to their potential optoelectrical applications. However, the widespread use of PDs is still limited by the high cost of epitaxial semiconductors. In contrast, the solution processability and wide spectral tunability of perovskites have led to the development of various inexpensive and high-performance optoelectronic devices. In this study, we develop a high-performance electronically modulated dual-mode PD with near-infrared (NIR) narrowband and visible light broadband detection based on organic-inorganic hybrid methylammonium lead halide perovskite (MAPbX 3 ; MA = CH 3 NH 3 and X = Cl, Br, and I) single crystals with a pnp configuration. The operating mode of the dual-mode PD can be switched according to voltage bias polarity because the photon absorption region and carrier transport performance are tuned at different bias voltages. The dual-mode PD exhibits a NIR light responsivity of 0.244 A/W and a narrow full width at half-maximum of ∼12 nm at 820 nm at positive voltages and an average visible light responsivity of ∼0.13 A/W at negative voltages. The detectivities of both modes are high (∼10 12 Jones), and the linear dynamic range is wide (>100 dB). Our study provides a new method for fabricating multifunctional PDs and can expand their application in integrated imaging systems.

Waste water remediation of toxic metals and dyes could be complex to achieve owing to several factors. Various techniques have been developed for the removal of these pollutants. However, the success of these water treatment techniques mainly depends on the choice of appropriate media. Most of the commercial and chemically synthesized materials for water treatment create additional hazards due to the leaching of toxic chemicals into the process water. Consequently, studies on the development of better materials which could achieve high efficiency without posing any health risk led to the exploration of non-toxic composite materials such as those composed of cellulose and metal oxides. The focus is on the choice of materials and the best methods that allows their combination in order to address the pollution caused by heavy metals and dyes. This review critically analyses or assess the use of cellulose incorporated with metal oxides in the removal of toxic metals and dyes from industrial effluent. The nanocomposites have been accepted as a technique that circumvents the problems associated with the use of only metal oxides in water purification. They provide a platform for an improvement in the hydrophobicity of the composite with concomitant efficiency in adsorption and photocatalysis., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Introducing hole/electron transporting and blocking layers is considered to enhance the performance of electronic devices based on organic-inorganic hybrid halide perovskite single crystals (PSCs). In many photodiodes, the hole/electron transporting or blocking materials are spin-coated or thermal-evaporated on PSC to fabricate heterojunctions. However, the heterojunction interfaces due to lattice mismatch between hole/electron, transporting or blocking materials and perovskites easily form traps and cracks, which cause noise and leakage current. Besides, these low-mobility transporting layers increase the difficulty of transporting carriers generated by photons to the electrode; hence, they also increase the response time for photo detection. In the present study, MAPbCl 3 -MAPbBr 2.5 Cl 0.5 heterojunction interfaces were realized by liquid-phase epitaxy, in which MAPbBr 2.5 Cl 0.5 PSC acts as an active layer and MAPbCl 3 PSC acts as a hole blocking layer (HBL). Our PIN photodiodes with epitaxial MAPbCl 3 PSC as HBL show better performance in dark current, light responsivity, stability, and response time than the photodiodes with spin-coated organic PCBM as HBL. These results suggest that the heterojunction interface formed between two bulk PSCs with different halide compositions by epitaxy growth is very useful for effectively blocking the injected charges under high external electric field, which could improve the collection of photo-generated carriers and hereby enhance the detection performance of the photodiode. Furthermore, the PIN photodiodes made of PSC with epitaxial HBL show the sensitivities of 7.08 mC Gy air -1 cm -2 , 4.04 mC Gy air -1 cm -2 , and 2.38 mC Gy air -1 cm -2 for 40-keV, 60-keV, and 80-keV X-ray, respectively., (Copyright © 2020 Pan, Wang, Xu, Li, Elemike, Shuja, Li, Zhang, Chen, Zhao and Lei.)

Production and use of metallic nanoparticles have increased dramatically over the past few years and design of nanomaterials has been developed to minimize their toxic potencies. Traditional chemical methods of production are potentially harmful to the environment and greener methods for synthesis are being developed in order to address this. Thus far phytosynthesis have been found to yield nanomaterials of lesser toxicities, compared to materials synthesized by use of chemical methods. In this study nanoparticles were synthesized from an extract of leaves of golden rod (Solidago canadensis). Silver (Ag), gold (Au) and Ag-Au bimetallic nanoparticles (BNPs), synthesized by use of this "green" method, were evaluated for cytotoxic potency. Cytotoxicity of nanomaterials to H4IIE-luc (rat hepatoma) cells and HuTu-80 (human intestinal) cells were determined by use of the xCELLigence real time cell analyzer. Greatest concentrations (50 µg/mL) of Ag and Ag-Au bimetallic were toxic to both H4IIE-luc and HuTu-80 cells but Au nanoparticles were not toxic. BNPs exhibited the greatest toxic potency to these two types of cells and since AuNPs caused no toxicity; the Au functional portion of the bimetallic material could be assisting in uptake of particles across the cell membrane thereby increasing the toxicity.

In this study, French marigold's leaf and flower were used for the synthesis of silver nanoparticles (SNPs) in order to explore their potentials towards bioreduction of Ag + to Agᵒ. The as-synthesised SNPs were characterised using UV-Vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction, transmission electron microscopy, and zeta-potential analysis. The results obtained showed that the particles are polydispersed with sizes in the range 15.8-42.8 nm. The bioreduction was believed to be due to the amides, aldehyde functional groups, and essential oils present in the extracts as confirmed by the FTIR analysis. The growth mechanism involved in the reaction was studied which revealed oriented attachment (OA) onwards Ostwald ripening in the case of the flower-mediated synthesis and typical OA in the leaf-mediated synthesis. The studied kinetics of the particle formation showed that the reaction is possibly a pseudo-first-order reaction with some diffusion-controlled mechanism which is driven by high surface area to volume ratio in both the leaf- and flower-mediated synthesis.

In this study, the conversion of silver ions into ∼30.74 nm sized silver nanoparticles (AgNPs) was achieved in 30 min at a reaction temperature of 80-90°C in aqueous leaf extract of Artemisia afra . The synthesised AgNPs showed surface plasmon resonance in the range of 423-438 nm. Spherical and face-centred cubic nanoparticles were confirmed by transmission electron microscope (TEM) and X-ray diffraction (XRD) analysis, respectively. Fourier transform infra-red (FTIR) results indicated that the obtained nanoparticles were stabilised and capped through the carbonyl and carboxylate ion groups possibly from flavonoids, terpenoids, phenolics and esters content of the extracts. In addition, the AgNPs were assessed for their biological potentials against some microbes and, also, their free radical scavenging ability was established. The AgNPs exhibited interesting antimicrobial and antioxidant properties better than the aqueous extract of A. afra.

Three Schiff base compounds, N 1 ,N 2 -bis(3-nitrobenzylidene)phenylene diamine (NBBA), 2-methyl- N -(3-nitrobenzylidene)aniline (MNBA) and N -(2-chlorobenzylidene)-4-nitroaniline (CBNA) were synthesized, characterised and applied for the first time as potential mild steel (MS) corrosion inhibitors in 1 M HCl at 30 °C. Fourier transform infra-red (FTIR), 1 H, 13 C Nuclear magnetic resonance (NMR) and Mass spectrometry (MS) were used for the characterisation of the compounds. The electrochemical studies and evaluation of corrosion inhibition potency were achieved using potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) techniques. Density functional theory (DFT) calculations were further employed to describe the electronic distribution on the molecules and potential sites that aided corrosion inhibition. The results of the employed characterisation techniques confirmed the proposed structures of the compounds with the MS revealing the exact molecular mass of the compounds. Electrochemical results showed that the trend in inhibition efficiency of the three compounds was in the order: MNBA > NBBA > CBNA. MNBA recorded the highest inhibition efficiency at 100 ppm. Corrosion kinetics of the set of inhibitors was found to prefer the Langmuir adsorption isotherm with both physisorption and chemisorption mechanisms as revealed by ΔG values. In an effort to develop efficient corrosion inhibitors with non-toxic effect, low cost and multiple adsorption centres, these Schiff bases are presented.

The study of Lasienthera africanum as corrosion inhibitor for A6063 grade aluminum alloy in 1.0 M HCl acid solution using weight loss method of corrosion study was investigated at 30 °C and 40 °C to check its degradation trend at high varying temperature application. The results revealed that L. africanum in 1.0 M acidic environment decreased the corrosion rate at various concentrations considered. Inhibitor efficiency (IE) as high as 98.7 and 94.9% both at 30 °C and 40 °C respectively, was observed.

Nanoscience and nanotechnology represent new and enabling platforms that promise to provide broad range of novel and improved technologies for environmental, biological and other scientific applications. This study reports the synthesis of silver nanoparticles mediated by aqueous leaf extract of Lippia citriodora at two different temperatures of 50°C and 90°C. The synthesis of colloidal silver nanoparticles (AgNPs) was monitored by the use of UV-visible spectroscopy at different temperatures and time intervals. The surface plasmon bands (SPBs) showed peaks between 417 and 421nm at 90°C and around 430nm at 50°C, indicating a red shift at lower temperature. Fourier transform infrared (FTIR) analysis of the nanoparticles showed the presence of similar peaks found in the spectra of the plant extract. The size of the AgNPs was confirmed by transmission electron microscopy (TEM) which indicated an average size of 23.8nm (90°C) and 25nm (50°C). The nanoparticles showed better antimicrobial activities when compared to the crude plant extract against several screened pathogens: Gram negative (Escherichia coli, and Salmonella typhi) and Gram positive (Bacillus subtilis and Staphylococcus aureus) strains and a fungi organism; Candida albicans. In addition, the AgNPs showed good larvicidal efficacy against early 4th instar of Culex quinquefasciatus (a vector of lymphatic filariasis). Finally, the nanoparticles exhibited photocatalytic properties on an industrial waste pollutant, methylene blue., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Synthesis of metallic and semiconductor nanoparticles through physical and chemical routes has been extensively reported. However, green synthesized metal nanoparticles are currently in the limelight due to the simplicity, cost-effectiveness and eco-friendliness of their synthesis. This study explored the use of aqueous leaf extract of Costus afer in the synthesis of silver nanoparticles (CA-AgNPs). The optical and structural properties of the resulting silver nanoparticles were studied using UV-visible spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Fourier transform infra-red spectrophotometer (FTIR). TEM images of the silver nanoparticles confirmed the existence of monodispersed spherical nanoparticles with a mean size of 20 nm. The FTIR spectra affirmed the presence of phytochemicals from the Costus afer leaf extract on the surface of the silver nanoparticles. The electrochemical characterization of a CA-AgNPs/multiwalled carbon nanotubes (MWCNT)-modified electrode was carried out to confirm the charge transfer properties of the nanocomposites. The comparative study showed that the CA-AgNPs/MWCNT-modified electrode demonstrated faster charge transport behaviour. The anodic current density of the electrodes in Fe(CN)₆] 4- /[Fe(CN)₆] 3- redox probe follows the order: GCE/CA-Ag/MWCNT (550 mA/cm²) > GCE/MWCNT (270 mA/cm²) > GCE (80 mA/cm²) > GCE/CA-Ag (7.93 mA/cm²). The silver nanoparticles were evaluated for their antibacterial properties against Gram negative ( Escherichia coli, Klebsiella pneumonia, Pseudomonas aeruginosa ) and Gram positive ( Bacillus subtilis and Staphylococcus aureus ) pathogens. The nanoparticles exhibited better inhibition of the bacterial strains compared to the precursors (leaf extract of Costus afer and silver nitrate). Furthermore, the ability of the nanoparticles to scavenge DPPH radicals at different concentrations was studied using the DPPH radical scavenging assay and compared to that of the leaf extract and ascorbic acid. The nanoparticles were better DPPH scavengers compared to the leaf extract and their antioxidant properties compared favorably the antioxidant results of ascorbic acid. The green approach to nanoparticles synthesis carried out in this research work is simple, non-polluting, inexpensive and non-hazardous.

The health challenges associated with pathogens and ectoparasites highlight the need for effective control approaches. Metal nanoparticles have been proposed as highly effective tools towards combatting different microbial organisms and parasites. The present work reports the antimicrobial and larvicidal potential of biosynthesized Ag/Ag₂O nanoparticles using aqueous leaf extract of Eupatorium odoratum (EO). The constituents of the leaf extract act as both reducing and stabilizing agents. The UV-VIS spectra of the nanoparticles showed surface plasmon resonance. The particle size and shape of the nanoparticles was analysed by transmission electron microscopy (TEM). The larvicidal study was carried out using third and fourth instar Culex quinquefasciatus larvae. The mosquito larvae were exposed to varying concentrations of plant extract (EO) and the synthesized nanoparticles, and their percentage of mortality was accounted for at different time intervals of 12 h and 24 h periods of exposure. The nanoparticles were more lethal against third and fourth instars of Culex quinquefasciatus larvae at the 24 h period of exposure with lower lethal concentration values (LC50 = 95.9 ppm; LC90 = 337.5 ppm) and (LC50 = 166.4 ppm; LC90 = 438.7 ppm) compared to the plant extract (LC50 = 396.8 ppm; LC90 = 716.8 ppm and LC50 = 448.3 ppm; LC90 = 803.9 ppm, respectively). The antimicrobial properties of the nanoparticles were established against different clinically-isolated microbial strains and compared to that of the plant extract (EO) and standard antimicrobial drugs. The nanoparticles were generally more active than the plant extract against the selected microbial organisms. The Gram-negative bacterial strains Escheerichua coli and Salmonella typhi were more susceptible towards the nanoparticles compared to the Gram-positive strains and the fungal organism.