Wearable thermoelectric devices offer a transformative approach to energy harvesting, providing sustainable solutions for powering next-generation technologies. In pursuit of efficient, flexible, biocompatible, and cost-effective thermoelectric materials, zinc oxide (ZnO) has emerged as a distinctive candidate due to its unique combination of favorable properties. This study explores the growth and optimization of ZnO nanorods on conductive carbon fabric (CF) using a simple microwave-assisted solvothermal technique. This method circumvents traditional complex processes that typically involve high temperatures or lengthy growth times, offering advantages such as rapid, uniform, and controllable volumetric heating. By systematically varying growth parameters, including microwave power and reaction time, we established conditions that promote the vertical alignment of ZnO nanorods, essential for enhancing thermoelectric performance. Structural and morphological analyses highlight the pivotal influence of the seed layer and growth parameters in achieving dense, uniform growth of ZnO nanorods. Interestingly, at higher microwave power levels, a transformation from nanorod structures to sheetlike morphologies was observed, likely due to Ostwald ripening, where larger particles grow at the expense of smaller ones. The optimized growth conditions for achieving superior growth and thermoelectric performance were identified as 15 min of growth at 100 W microwave power. Under these conditions, ZnO nanorods exhibited enhanced crystallinity and a higher growth rate, contributing to an improved thermoelectric power factor of 777 nW/mK2 at 373 K. This work underscores the importance of precise parameter control in tailoring ZnO nanostructures for wearable thermoelectric applications and demonstrates the potential of scalable, low-cost methods to achieve high-performance energy-harvesting materials.

Fossil fuels have a high energy density, meaning they contain a significant amount of energy per unit of volume, making them efficient for energy production and transport. Biodiesel is especially becoming a fossil fuel alternative and a key part of renewable energy. Several types of waste from homes, markets, street vendors, and other industrial places were collected and transesterified with Ni-doped ZnO nanoparticles for this study. These included castor oil, coffee grounds, eggshells, vegetable oil, fruit peels, and soybean oil. The Ni-doped ZnO’s were then calcined at 800 °C. The maximum conversion rate found in converting fruit peel waste into biodiesel is about 87.6%, and it was 89.6% when the oil-to-methanal ratio was about 1:2 and the reaction time was 140 min. This is the maximum biodiesel production compared to other wastes. Moreover, using vegetable oil with nanocatalyst, the maximum biodiesel production rate of about 90.58% was recorded with 15% catalyst loading, which is the maximum biodiesel production compared with the other wastes with nanocatalyst. Furthermore, at 75 °C and a concentration of catalyst of about 15% the maximum biodiesel production obtained by using castor oil is about 92.8%. It has the highest biodiesel yield compared with the yield recorded from other waste. The catalyst also demonstrated great stability and reusability for the synthesis of biodiesel. Using waste fruit peels with Ni-doped ZnO helps to progress low-cost and ecologically friendly catalyst for sustainable biodiesel production.

This study explored the development direction of punk fashion through 3D digital fashion design by analyzing the expressive characteristics and inherent meanings of the punk fashion expressed in Vivienne Westwood’s creations. To this end, the concept underlying punk and its expressive characteristics were examined, and the eco-friendly expressive attributes of punk fashion were scrutinized through photos of Vivienne Westwood’s collections. The analysis focused on 10 seasonal collections showcased over the past five years, from the designer’s 2018 S/S to 2022 F/W collections. The results revealed that Westwood’s punk expression was characterized by traditionality, eco-friendliness, playfulness, resistance, and deconstruction. Traditionality appeared in the form of a harmonious redesign of classics to create new works, while eco-friendliness was manifested through the use of slogans and eco-friendly materials and methods. Playfulness conveyed positive messages through comedic situations or characters, and resistance emerged as a means of delivering messages for improving social issues. Finally, the deconstruction of punk was reflected as resistance, boldly destroying fashion structures to express dissatisfaction with society. Punk design in fashion is one of the avenues in which designers effectively express the messages that they want to communicate to society. This study is significant, as it provides foundational data for exploring punk characteristic design strategies to be used in future fashion. The scope of application for 3D virtual clothing programs is expected to expand in the fashion industry, and continuous research on digital fashion design is anticipated.

Gold nanoparticles (Au NPs) decorated carbon nanofibers (CNFs) have been prepared by an electrospinning approach and then carbonized. The prepared Au-CNFs were employed to modifying a screen printed electrode (SPE) for simultaneous determination of ascorbic acid (AA), dopamine (DA) and uric acid (UA). Au NPs are uniformly dispersed on carbon nanofibers were confirmed by the structure and morphological studies. The modified electrodes were tested in cyclic voltammetry (CV), differential pulse voltammetry (DPV) and chronoamperometry (CA) to characterize their electrochemical responses. Compared to bare SPE, the Au-CNFs/SPE had a better sensing response to AA, DA, and UA. The electrochemical oxidation signal of AA, DA and UA are well separated into three distinct peaks with peak potential separation of 280 mV, 159 mV and 439 mV between AA-DA, DA-UA and AA-UA respectively in CV studies and the corresponding peak potential separation in DPV studies are 290 mV, 166 mV and 456 mV. The Au-CNFs/SPE has a wide linear response of AA, DA and UA in DPV analysis over the range of 5–40 μM ( R2 = 0.9984), 2–16 μM ( R2 = 0.9962) and 2–16 μM ( R2 = 0.9983) with corresponding detection limits of 0.9 μM, 0.4 μM and 0.3 μM at S/N = 3, respectively. The developed modified SPE based sensor exhibits excellent reproducibility, stability, and repeatability. The excellent sensing response of Au-CNFs could reveal to a promising approach in electrochemical sensor.

Copper, silver, and gold-reduced graphene oxide nanocomposite (Cu-rGO, Ag-rGO, and Au-rGO) were fabricated via the hydrothermal method, which shows unique physiochemical properties. Environment friendly electromagnetic radiation was employed to synthesize rGO from GO. The nonlinear optical phenomenon of noble metal decorated rGO is predominantly due to excited state absorption, which arises from surface plasmon resonance and increases in defects at the surface due to Cu, Ag, and Au incorporation. It is found that the third-order nonlinear absorption coefficient was in the order of 10− 10 m/W, with notable enhancements in the third-order properties of Au-rGO compared to other nanocomposites and their respective counterparts. Functionalizing rGO induces defect states ( sp3), increasing NLO response. Cu, Ag, and Au exhibit higher Surface-Enhanced Raman Scattering (SERS) activity due to rGO-induced structural modifications. SERS signals are influenced by dominant signals from Au nanorods. The electronic structures for pure and doped rGO were investigated through Density Functional Theory (DFT). The computed partial density of states (PDOS) confirms the enhancement of the state in Au-doped rGO is due to the charge transference from Au to C 2p orbital. The optical absorption spectra and PDOS reveal the possibility of free carrier absorption enhancement in Au which validates experimentally observed higher two-photon absorption (β) value of Au-doped rGO. The tuning of nonlinear optical and SERS behaviour with variation in the noble metal upon rGO provides an easy way to attain tuneable properties which are exceedingly required in both optoelectronics and photonics applications.

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.

Metal-free N–S- and N–P-doped nanocarbon (SCNP and PCNP) electrocatalysts prepared through sustainable microwaveassisted synthesis using hemigraphis alternata plant leaves. The prepared heteroatom-doped nanocarbon materials are active catalysts for the two-electron oxygen reduction reaction (ORR) to produce 65–70% of hydrogen peroxide. As evidenced from the XPS, most proportion of the doped heteroatoms contain the oxygen functional groups in the nanocarbons. These attributes are the critical factors to see the selective two-electron transfer ORR for the PCNP and SCNP. This approach shed light on the critical role of dual heteroatoms doping and the oxygen functionalities in nanocarbon towards the selectivity of ORR. We believe that this method would allow the preparation of heteroatom that contains oxygen functionalities. Our work paves a sustainable way of preparation of nanocarbon based ORR catalysts that are only selective for two-electron transfer process.

The most significant threat to the ecosystem is emerging pollutants, which are becoming worse each year and harming the planet severely and permanently. Many organic and inorganic contaminants are present and persistent due to various world events and population growth. As a result, there is a greater need for new technology and its application to address the problems caused by developing pollutants. Carbon composite nanomaterials have significant potential in the fight against numerous environmental contaminants due to their distinctive attributes. This review discusses the reports of customized carbon composite nanomaterials to meet the need for specific elimination of emerging contaminants. Physical and chemical features such as high surface area, conductivity (thermal and electrical), and vibroelectronic properties, size, shape, porosity, and composite nature are making these tailored materials of carbon-based nanomaterials an emerging and sustainable tool to remove persistent compounds like emerging contaminants in aqueous solution. Different composite materials are well discussed in this review, along with their adsorption efficiency of diverse emerging contaminants, including Bisphenol A, estradiol, metformin, etc. This review provides insight into the recent trends limited to 2017–2023. The limitations of carbon-based nanomaterials, such as regeneration and cost-effectiveness, have also been overcome in recent years by diverse modifications in the production process, which can be further improved to make these materials well suited for an extended group of emerging contaminants.

Graphene quantum dots (GQDs) are zero-dimensional carbonous materials with exceptional physical and chemical properties such as a tuneable band gap, good conductivity, quantum confinement, and edge effect. The introduction of GQDs in various layers of solar cells (SCs) such as hole transport layer (HTL), electron transport materials (ETM), cathode interlayer (CIL), photoanode materials (PAM), counter electrode (CE), and transparent conducting electrode (TCE) could improve the solar energy (SE) harvesting, separation and transportation of electrons and hole, thus ultimately enhance the overall performance and stability of SCs. The incorporation of GQDs in various layers such as HTL, ETM, CIL, PAM, CE, and TCE achieved photo conversion efficiencies (PCEs) of 18.63, 21.1, 12.81, 9.41, 8.1, and 3.66%, respectively. Furthermore, GQDs improved stabilities such as resistance to degradation for HTL (up to 77%), ETM (80%), resistance to UV light for ETM (94%), resistance to temperature in ETM (90%), and bending stabilities after 1000 cycles for HTL (88%) and for TCE (90%). There are reviews focused on the utilization of different carbon-structured materials such as graphene, carbon nanotubes (CNT), fullerenes, and carbon dots in SCs applications. More specifically, the utilization of GQDs for SCs is limited and yet to be explored in greater detail. This review mainly focuses on the recent advancement of various techniques of production of GQDs synthesis, utilization of GQDs in various layers like HTL, ETM, CIL, PAM, CE, and TCE for the enhancement of PCE, and the stability of SCs. As a result, we believe that an exclusive study on GQDs-sensitized solar cells (GQDSSCs) could provide an in-depth analysis of the recent progress, achievements, and challenges.

The nanostructured dysprosium oxide ( Dy2O3) was synthesized by the co-precipitation method and incorporated with graphitic carbon nitride (g-C3N4) using the ultrasonication method. The resultant product is denoted as Dy2O3/ g-C3N4 nanocomposite which was further used for electrochemical sensing of riboflavin (RF). The physicochemical properties of Dy2O3/ g-C3N4 nanocomposite were examined using several characterization techniques. The obtained results exhibit the nanocomposite formation with the preferred elemental compositions, functional groups, crystalline phase and desired surface morphology. The electrocatalytic performance of Dy2O3/ g-C3N4 nanocomposite was scrutinized with a glassy carbon electrode (GCE) via differential pulse voltammetry (DPV) and cyclic voltammetry (CV) techniques with the conventional three-electrode system. The modified electrode distributes more active surface area suggesting high electrocatalytic activity for the RF detection with two linear ranges (0.001–40 μM and 40–150 μM), a low detection limit of 48 nM and sound sensitivity (2.5261 μA μM−1 cm− 2). Further, the designed sensor possesses high selectivity, excellent stability, repeatability and reproducibility. Finally, the fabricated sensor was successfully estimated for the detection of RF in actual food sample analysis using honey and milk with better recovery.

The dyeing process is a very important unit operation in the leather and textile industries; it produces significant amounts of waste effluent containing dyes and poses a substantial threat to the environment. Therefore, degradation of the industrial dye-waste liquid is necessary before its release into the environment. The current is focusing on the reduction of pollutant loads in industrial wastewater through remediating azo and thiazine dyes (synthetic solutions of textile dye consortium). The current research work is focused on the degradation of dye consortium through photo-electro-Fenton (PEF) processes via using dimensionally stable anode (Ti) and graphite cathode. The ideal conditions, which included a pH of 3, 0.1 (g/L) of textile dye consortium, 0.03 (g/L) of iron, 0.2 (g/L) of H2O2, and a 0.3 mAcm-2 of current density, were achieved to the removal of dye consortium over 40 min. The highest dye removal rate was discovered to be 96%. The transition of azo linkages into N2 or NH3 was confirmed by Fourier transforms infra-red spectroscopic analysis. PEF process reduced the 92% of chemical oxygen demand (COD) of textile dye consortium solution, and it meets the kinetics study of the pseudo-first-order. The degradation of dye through the PEF process was evaluated by using the cyclic voltammetric method. The toxicity tests showed that with the treated dye solution, seedlings grew well.

The mechanism of resonant light scattering in single-layer graphene is discussed. A new concept of electron–hole selfphotorecombination is proposed, which makes it possible to clearly separate the phenomena of resonant light scattering and resonant photoluminescence. It is established that Rayleigh resonant radiation has been found to consist of virtual and non-virtual components. It has been shown that Rayleigh radiation is mainly caused by resonant non-virtual optical transitions. The band of Rayleigh radiation due to resonant virtual transitions is quite wide, and the intensity is extremely low. On the basis of the presented theory, the results of numerical estimates of the linewidth and intensity of the Rayleigh band of single-layer graphene are in fairly good agreement with the experimental data.

Graphene oxide (GO) and ultrafine slag (UFS) have been applied to reinforce cement mortar cubes (CMC) in this research. The consequences of GO and UFS on the mechanical attributes of the CMC were explored through experimental investigations. Established on the results, at the 28 days of hydration, the CMC compressive and flexural strength with 0.03% of GO and 10% UFS were 89.8 N/mm2 and 9.1 N/mm2, respectively. Furthermore, the structural changes of CMC with GO and UFS were qualitatively analysed with instrumental techniques such as scanning electron microscope (SEM), X-ray fluorescence (XRF), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), FT Raman spectroscopy, atomic force microscopy (AFM), and 27Al, 29Si-Nuclear magnetic resonance spectroscopy (NMR). SEM results reported that GO and UFS formed an aggregated nanostructure that improved the microstructural properties of the CMC. TGA analysis revealed the quantum of calcium hydrate and bound water accomplished by supplementing GO bound to the UFS aggregates. FT-IR analysis of the CMC samples confirmed the ‘O-’comprising functional groups of GO which expedited the formation of complexes between calcium carbonate ( CaCO3) and UFS. 0.03% GO was the optimum dosage that enhanced the compressive and flexural attributes when combined with 10% UFS in CMC.