This work concentrates on the design and implementation of aptamer-based electrochemical biosensors using a layer-by-layer approach for precise tracking of mucin-1 (MUC1), an important biomarker linked to breast cancer. The electrochemical biosensor was created by modifying a screen-printed carbon electrode (SPCE) with V2C MXene booster and gold nanoparticles (Au-NPs), along with Cd2+ integrated aptamer (AP) (SPCE/V2C-MXene/Au NPs/Cd2+-AP). This biosensor demonstrated high specificity and affinity for MUC1, establishing a sensitive quantification mechanism. The MXene nanolayer was produced and analyzed via TEM, XPS, SEM, AFM, BET, and MAP techniques. It served as a supportive material that enhanced electrochemical conductivity and allowed for the integration of the aptamer (AP) as the biological recognition component. The biosensor was constructed by immobilizing MUC1-specific aptamers onto the surfaces of SPCE/V2C-MXene/Au NPs, enabling selective recognition and binding with MUC1. The recorded signal, corresponding to Cd2+ integrated with AP at SPCE/V2C-MXene/Au NPs/Cd2+-AP, enabled quantitative assessment of MUC1 levels. The findings showed a linear concentration span of 1.0–500 pg/mL for detecting MUC1, achieving a detection limit of 3.45 fg/mL utilizing the SPCE/ V2C-MXene/Au NPs/Cd2+-AP biosensor. The SPCE/V2C-MXene/Au NPs/Cd2+-AP biosensor exhibited a good affinity for the detection of MUC1 in the presence of other breast cancer biomarkers, confirming its selectivity.

Quantum dot nanocomposite-based luminescent materials have gained attention for solid-state lighting and optical displays. This study presents a one-step, eco-friendly hydrothermal process to synthesize nitrogen, potassium, and calcium-doped carbon quantum dots (N, K, Ca-doped CQDs) from the flower extract of Mesembryanthemum crystallinum L. (ice plant). The CQDs were characterized using HRTEM, EDX, SAED, XPS, XRD, NMR, FTIR, zeta potential, UV–Vis, and photoluminescence spectroscopy. HRTEM revealed an average particle size of 4.6 nm, with a range of 2 to 7 nm. The CQDs exhibited a quantum yield of 20%, excellent water solubility, photostability, and greenish fluorescence under UV (365 nm). The fluorescence spectra were analyzed using CIE (Commission Internationale de l’Eclairage) chromaticity coordinates to determine the emitted color. The fluorescence emission behavior was influenced by solvent polarity, locally excited (LE) states, intramolecular charge transfer (ICT) processes, and hydrogen bonding. The hydrogen bonds between N, K, Ca-doped CQDs and DI water likely enhanced the stability of the ICT state, resulting in a red shift in fluorescence. Additionally, we developed an eco-friendly wheat-starch-based bioplastic nanocomposite by embedding the CQDs. The effects of CQD concentration and pH sensitivity on luminescent properties were explored. Finally, we demonstrated a practical application by designing a conceptual nameplate-like calligraphy using the optimized CQDs@bioplastic nanocomposite film (CQD concentration: 240 mg/mL, pH: 2.7), highlighting its potential for luminescent film applications.

The accurate detection of vital biomarkers such as Ascorbic Acid (AA), Uric Acid (UA) and Nitrite ( NO2 −) is crucial for human health surveillance. However, existing methods often struggle with concurrent detection and quantification of multiple species, highlighting the need for a more effective solution. To address this challenge, this study aimed to develop a multifunctional electrochemical sensor capable of parallel detection of AA, UA and NO2 − using a synergistic combination of Graphene Oxide (GO) and Cadmium Sulfide (CdS) materials. Notably, the fabricated CdS@GO/Glassy Carbon Electrode (GCE) exhibited exceptional electrochemical activity, as evidenced by Differential Pulse Voltammetry (DPV) analysis. The sensor demonstrated remarkable sensitivity (8.13, 10.12, and 9.05 μA·μM−1·cm−2) and ultra-low detection limits (0.034, 0.062, and 0.084 μM) for AA, UA and NO2 −, respectively. Furthermore, it successfully identified single molecules of each analyte in aqueous and biologic fluid samples, with recovery values comparable to those obtained using High-Performance Liquid Chromatography (HPLC) standard addition methods. The significance of this study lies in developing a novel CdS@ GO/GCE sensor that enables concurrent detection and quantification of multiple vital biomarkers, offering a promising tool for human health monitoring and diagnosis.

Effective cooling strategies are critical for cultivating high-quality ornamental plants during the summer. The fan-and-pad cooling system reduces greenhouse temperatures by drawing air through wet pads, which humidify and cool the air, aided by fans on the opposite side. However, the paper-based pads (corrugated cellulose) used in this system have limited durability and degrade with prolonged use. Nanocomposite hydrogels, with their polymer-based structure, can absorb and retain moisture through swelling, presenting a promising alternative. This study examines the application of nanocomposite hydrogels, focusing on their hygroscopic properties and cooling efficiency under various temperatures and wind speeds. When treated with lithium chloride solutions at 25%, 50%, 75%, and 100% saturation, higher LiCl concentrations reduced weight but increased swelling capacity. Optimal cooling effects were achieved with wind speeds of 1.0 m/s at 25°C and 1.5 m/s at 35°C, with greater efficiency observed at lower wind speeds. These findings suggest that integrating nanocomposite hydrogels into cooling pads could enhance durability and reduce maintenance compared with conventional paper pads.

Herein, the electrochemical technique was employed to detect hydroquinone (HQ) using a modified glassy carbon electrode (GCE) with reduced graphene oxide (rGO) and silver (Ag)-decorated tin oxy-nanoparticles (SnONPs) to form Ag@SnONPs/ rGO nanocomposites (NC). The Ag@SnONPs/rGO nanocomposites were morphologically characterized using multiple analytical methods such as XRD, Raman, XPS, HR-SEM, and HR-TEM. This study revealed that Ag@SnONPs/rGO-NC exhibits excellent conductivity due to the presence of rGO that provides potential π–π interactions with SnONPs, while Ag enhances electron-transfer kinetics. This facilitates efficient charge transport within the sensor, thereby improving HQ adsorption. The key advantages of the sensor demonstrate a concentration of 0.5–200 μM, and a low detection limit value of 0.010 μM, and a high sensitivity value of 6.0746 μA μM−1 cm2. Under optimal conditions, the Ag@SnONPs/rGO sensor may be used to determine HQ and its concentration using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The Ag@SnONPs-rGO/GCE sensor demonstrated excellent reproducibility, repeatability, and stability. Moreover, the suggested bimetallic nanocomposite effectively determined the presence of HQ in water and cosmetic samples.

Wearable electronics have been the focus of considerable interest in various fields, such as human-machine interfaces, soft robotics, and medical treatments, due to their flexibility, stretchability, and light weight. To address the shortcomings of existing metal thin film-based wearable devices, stretchable conductive polymers have been developed. In particular, double networking hydrogels are being actively studied as a polymer with a three-dimensional stereoscopic structure that can be patterned. Nonetheless, they have shortcomings such as poor electrical properties and cumbersome manufacturing processes, making it difficult to apply them in electronic devices. Herein, we report 3D-printed stretchable electrodes enabled by a titanium/polyacrylamide-alginate-based hydrogel nanocomposite. This research suggests the strategy for resolving the challenges of high costs and complex fabrication processes associated with stretchable electrode, providing a solution to accelerate the commercialization of wearable electronic devices.

Graphene-based solar cells and supercapacitors integrated into photosupercapacitors represent a pioneering advancement. These devices leverage the exceptional properties of graphene, such as high conductivity and large surface area, to enhance both solar energy conversion and energy storage. The integration of these technologies into photosupercapacitors creates a multifunctional device capable of harnessing solar energy and storing it efficiently. This innovative approach holds promise for sustainable and versatile energy solutions, marking a significant step towards developing efficient and compact energy storage systems. This integration addresses the intermittent nature of solar power generation by providing a continuous and reliable power supply through energy storage. Supercapacitors are one such energy device with a high-power density and excellent specific capacitance which is integrated will a dye-sensitized solar cell (DSSC) comprising a single system of photosupercapacitor. A novel electrode material of NiO/CuO/Co3O4/rGO was synthesized which serves as the Pt-free counter electrode of DSSC and working or storage electrode of supercapacitor later was used as the intermediate electrode and storage electrode of a photosupercapacitor. The integrated photosupercapacitor device had a photovoltage of 0.81 V with arealspecific capacitance, energy and power density of 190.12 mF cm− 2, 17.325 μW h cm− 2 and 0.162 mW cm− 2, respectively. The device self-discharged in 385 s with an overall conversion efficiency of 2.17%, resulting in a self-charged energy device.

Carbon fibers of polyacrylonitrile (PAN) type were coated with nickel nanoparticles using a chemical reduction method in alkaline hydrazine bath. The carbon fibers were firstly heated at 400 °C and then chemically treated in hydrochloric acid followed by nitric acid to clean, remove any foreign particles and functionalized its graphitic surfaces by introducing some functional groups. The functionalized carbon fibers were coated with nickel to produce 10 wt% Cf/Ni nanocomposites. The uncoated heat treated and the nickel coated carbon fibers were investigated by SEM, EDS, FTIR and XRD to characterize the particle size, morphology, chemical composition and the crystal structure of the investigated materials. The nickel nanoparticles were successfully deposited as homogeneous layer on the surface of the functionalized carbon fibers. Also, the deposited nickel nanoparticles have quazi-spherical shape and 128–225 nm median particle size. The untreated and the heat treated as well as the 10 wt% Cf/Ni nanocomposite particles were further reinforced in ethylene vinyl acetate (EVA) polymer separately by melt blending technique to prepare 0.5 wt% Cf-EVA polymer matrix stretchable conductive composites. The microstructures of the prepared polymer composites were investigated using optical microscope. The carbon fibers as well as the nickel coated one were homogenously distributed in the polymer matrix. The obtained samples were analyzed by TGA. The addition of the nickel coated carbon fibers to the EVA was improved the thermal stability by increasing the thermal decomposition temperature Tmax1 and Tmax2. The electrical and the mechanical properties of the obtained 10 wt% Cf/Ni nanocomposites as well as the 0.5 wt% Cf-EVA stretchable conductive composites were evaluated by measuring its thermal stability by thermogravimetric analysis (TGA), electrical resistivity by four probe method and tensile properties. The electrical resistivity of the fibers was decreased by coating with nickel and the 10 wt% Cf/Ni nanocomposites has lower resistivity than the carbon fibers itself. Also, the electrical resistivity of the neat EVA is decreased from 3.2 × 1010 to 1.4 × 104 Ω cm in case of the reinforced 0.5 wt% Cf/Ni-EVA polymer composite. However, the ultimate elongation and the Young’s modulus of the neat EVA polymer was increased by reinforcing with carbon fibers and its nickel composite.

해당 연구는 산업 폐수에서 염료를 효율적으로 제거하기 위한 고급 박막 나노복합체(TFN) 기반 나노여과막을 개 발하여 효과적인 폐수 처리 방법을 제시합니다. 최근 연구의 동향을 보면, 나노카본, 실리카 나노스피어, 금속-유기 프레임워 크(MOF) 및 MoS2와 같은 혁신적인 재료를 포함하는 TFN 막의 제조에 중점을 둡니다. 주요 목표는 염료 제거 효율을 향상 시키고 오염 방지 특성을 개선하며 염료/염 분리에 대한 높은 선택성을 유지하는 것입니다. 이 논문은 넓은 표면적, 기계적 견고성 및 특정 오염 물질 상호 작용 능력을 포함하여 이러한 나노 재료의 뚜렷한 이점을 활용하여 현재 나노여과 기술의 제 한을 극복하고 물 처리 문제에 대한 지속 가능한 솔루션을 제공하는 것을 목표로 합니다.

We have intended and preparation of hierarchically absorbent materials were covered with a NiMn2O4 and acts as a catalyst for azo dye degradation. The polyaromatic-based (PA) absorbent compounds were initially constructed by bromomethylated aromatic hydrocarbons which undergo self-polymerization in presence of ZnBr as a reagent and cross linker is bromomethyl methyl ether. The absorbent black materials with a 3D network were prepared by direct carbonization and activation of the as-prepared PA. The hydrothermal method was adapted for the preparation of carbon hybrid material C@NiMn2O4 powder's catalytic activity is effective in reducing p-nitrophenol to p-aminophenol and decolorizing carbon-based dyes like methyl orange (MO), methyl yellow (MY), and Congo red (CR) in aqueous media at 25 °C when NaBH4 is added. UV–visible spectroscopy was used to analyze the dyes' breakdown at regular interval.

Integration of noble metals on graphene is renowned for their catalytic and antioxidant prowess. However, utilization of toxic chemicals in the synthesis creates environmental pollution and poisonous nature of chemically synthesized materials. To address this, an economical and eco-friendly method for synthesizing graphene-gold (BRG-Au) nanocomposite by anchoring gold nanoparticles (Au NPs) onto reduced graphene oxide sheets using betel leaf extract as a reducing and stabilizing agent is presented. Comprehensive structural characterizations through UV–Visible, Raman, FT-IR, and XRD analyses confirm the successful formation of the BRG-Au nanocomposite. Morphological assessments utilizing FE-SEM and TEM techniques revealed the presence of transparent, twinkling graphene sheets embellished with 20 to 60 nm of Au NPs in various shapes, including spherical, triangular, pentagonal, circular, and trapezoids. The catalytic and antioxidant activities of the BRG-Au nanocomposite were thoroughly evaluated. In catalytic trials, the nanocomposite exhibited remarkable efficiency in the reduction of 4-nitrophenol to 4-aminophenol, accomplishing this transformation within a mere 30 min during the initial cycle and maintaining stable catalytic performance over three consecutive cycles. Additionally, antioxidant analyses employing Total Antioxidant Activity and 2,2-diphenyl-1-picrylhydrazyl methods demonstrated that BRG-Au nanocomposite possessed equal or superior antioxidant activity than the ascorbic acid standard. This research thus underscores the promising potential of environmentally benign synthesis method for graphene-gold nanocomposite with enhanced catalytic and antioxidant properties.