Improving Water Retention in Sandy Soils with High-Performance Superabsorbents Hydrogel Polymer.

Improving the water retention capability of drained and sandy soils is vital for nurturing high-quality soil. This protective measure ensures the conservation of essential nutrients, such as fertilizers and organic matter; maintains soil quality; and prevents erosion. Superabsorbent hydrogels (SAHs) have emerged as promising solutions to boost water retention in sandy soils, typically characterized by a poor water-holding capacity. However, there is a noticeable gap in the existing literature regarding their potential to simultaneously achieve elevated swelling ratio (SR) and water retention ratio (WRR) levels. This study presents innovative SAH systems with the highest reported SR value yet, exceeding 10000 wt %, and remarkable WRR capability explicitly designed for agricultural use. These novel SAHs were synthesized using the chemical cross-linking polymerization method from polyacrylamide (PAM) polymer, employing various PAM ratios through a one-pot hydrothermal vessel method along with diverse drying techniques. The prepared hydrogels were characterized using various techniques, such as FTIR and DSC; unraveling insights into their structural properties; and the kinetics of the swelling process. Notably, these synthesized hydrogels exhibit robustness, maintaining structural integrity even under extreme conditions such as high temperatures or pressures. Our findings suggest immense potential for these hydrogels as soil enhancers in agriculture, offering a sustainable solution to bolster soil quality and nutrient preservation.

Blackberry Seeds-Derived Carbon as Stable Anodes for Lithium-Ion Batteries.

The suitability of biocarbons derived from blackberry seeds as anode materials in lithium-ion batteries has been assessed for the first time. Blackberry seeds have antibacterial, anticancer, antidysentery, antidiabetic, antidiarrheal, and potent antioxidant properties and are generally used for herbal medical purposes. Carbon is extracted from blackberries using a straightforward carbonization technique and activated with KOH at temperatures 700, 800, and 900 °C. The physical characterization demonstrates that activated blackberry seeds-derived carbon at 900 °C (ABBSC-900 °C) have well-ordered graphene sheets with high defects compared to the ABBSC-700 °C and ABBSC-800 °C. It is discovered that an ABBSC-900 °C is mesoporous, with a notable Brunauer-Emmett-Teller surface area of 65 m2 g-1. ABBSC-900 has good electrochemical characteristics, as studied under 100 and 1000 mA g-1 discharge conditions when used as a lithium intercalating anode. Delivered against a 500 mA g-1 current density, a steady reversible capacity of 482 mA h g-1 has been achieved even after 200 cycles. It is thought that disordered mesoporous carbon with a large surface area account for the improved electrochemical characteristics of the ABBSC-900 anode compared to the other ABBSC-700 and ABBSC-800 carbons. The research shows how to use a waste product, ABBSC, as the most desired anode for energy storage applications.

2D Hybrid Nanocomposite Materials (h-BN/G/MoS2) as a High-Performance Supercapacitor Electrode.

The nanocomposites of hexagonal boron nitride, molybdenum disulfide, and graphene (h-BN/G/MoS2) are promising energy storage materials. The originality of the current work is the first-ever synthesis of 2D-layered ternary nanocomposites of boron nitrate, graphene, and molybdenum disulfide (h-BN/G/MoS2) using ball milling and the sonication method and the investigation of their applicability for supercapacitor applications. The morphological investigation confirms the well-dispersed composite material production, and the ternary composite appears to be made of h-BN and MoS2 wrapping graphene. The electrochemical characterization of the prepared samples is evaluated by cyclic voltammetry and galvanostatic charge/discharge tests. With a high specific capacitance of 392 F g-1 at a current density of 1 A g-1 and an outstanding cycling stability with around 96.4% capacitance retention after 10,000 cycles, the ideal 5% BN_G@MoS2_90@10 composite demonstrates exceptional capabilities. Furthermore, a symmetric supercapacitor (5% BN_G@MoS2_90@10 composite) exhibits a 94.1% capacitance retention rate even after 10,000 cycles, an energy density of 16.4 W h kg-1, and a power density of 501 W kg-1. The findings show that the preparation procedure is safe for the environment, manageable, and suitable for mass production, which is crucial for advancing the electrode materials used in supercapacitors.

Flexible and Freestanding MoS2/Graphene Composite for High-Performance Supercapacitors.

Two-dimensional atomically thick materials such as graphene and layered molybdenum disulfide (MoS2) have been studied as potential energy storage materials because of their high specific surface area, potential redox activity, and mechanical flexibility. However, because of the layered structure restacking and poor electrical conductivity, these materials are unable to attain their full potential. Composite electrodes made of a mixture of graphene and MoS2 have been shown to partially resolve these issues in the past, although their performance is still limited by inadequate mixing at the nanoscale. Herein, we report three composites via a simple ball-milling method and analyze supercapacitor electrodes. Compared with pristine graphene and MoS2, the composites showed high capacitance. The as-obtained MoS2@Graphene composite (1:9) possesses a high surface area and uniform dispersion of MoS2 on the graphene sheet. The MoS2@Graphene (1:9) composite electrode has a high specific capacitance of 248 F g-1 at 5 A g-1 in an electrochemical supercapacitor compared with the other two composites. Simultaneously, the flexible symmetric supercapacitor device prepared demonstrated superior flexibility and a long lifespan (93% capacitance retention after 8000 cycles) with no obvious changes in performance under different angles. In portable and wearable energy storage devices, the current experimental results will result in scalable, freestanding hybrid electrodes with improved, flexible, supercapacitive performance.

Dendritic Mesoporous Organosilica Nanoparticles with Photosensitizers for Cell Imaging, siRNA Delivery and Protein Loading.

Dendritic mesoporous organosilica nanoparticles (DMON) are a new class of biodegradable nanoparticles suitable for biomolecule delivery. We studied the photochemical internalization (PCI) and photodynamic therapy (PDT) of DMON to investigate new ways for DMON to escape from the endosomes-lysosomes and deliver biomolecules into the cytoplasm of cells. We added photosensitizers in the framework of DMON and found that DMON were loaded with siRNA or FVIII factor protein. We made four formulations with four different photosensitizers. The photosensitizers allowed us to perform imaging of DMON in cancer cells, but the presence of the tetrasulfide bond in the framework of DMON quenched the formation of singlet oxygen. Fortunately, one formulation allowed us to efficiently deliver proapoptotic siRNA in MCF-7 cancer cells leading to 31% of cancer cell death, without irradiation. As for FVIII protein, it was loaded in two formulations with drug-loading capacities (DLC) up to 25%. In conclusion, DMON are versatile nanoparticles capable of loading siRNA and delivering it into cancer cells, and also loading FVIII protein with good DLC. Due to the presence of tetrasulfide, it was not possible to perform PDT or PCI.

Custom-made holey graphene via scanning probe block co-polymer lithography.

Oxidative chemical etching of metal nanoparticles (NPs) to produce holey graphene (hG) suffers from the presence of aggregated NPs on the graphene surface triggering heterogeneous etching rates and thereby producing irregular sized holes. To encounter such a challenge, we investigated the use of scanning probe block co-polymer lithography (SPBCL) to fabricate precisely positioned silver nanoparticles (AgNPs) on graphene surfaces with exquisite control over the NP size to prevent their aggregation and consequently produce uniformly distributed holes after oxidative chemical etching. SPBCL experiments were carried out via printing an ink suspension consisting of poly(ethylene oxide-b-2-vinylpyridine) and silver nitrate on a graphene surface in a selected pattern under controlled environmental and instrumental parameters followed by thermal annealing in a gaseous environment to fabricate AgNPs. Scanning electron microscopy revealed the uniform size distribution of AgNPs on the graphene surface with minimal to no aggregation. Four main sizes of AgNPs were obtained (37 ± 3, 45 ± 3, 54 ± 2, and 64 ± 3 nm) via controlling the printing force, z-piezo extension, and dwell time. Energy dispersive X-ray spectroscopy analysis validated the existence of elemental Ag on the graphene surface. Subsequent chemical etching of AgNPs using nitric acid (HNO3) with the aid of sonication and mechanical agitation produced holes of uniform size distribution generating hG. The obtained I D/I G ratios ≤ 0.96 measured by Raman spectroscopy were lower than those commonly reported for GO (I D/I G > 1), indicating the removal of more defective C atoms during the etching process to produce hG while preserving the remaining C atoms in ordered or crystalline structures. Indeed, SPBCL could be utilized to fabricate uniformly distributed AgNPs of controlled sizes on graphene surfaces to ultimately produce hG of uniform hole size distribution.

Insight into thermo-mechanical enhancement of polymer nanocomposites coated microsand proppants for hydraulic fracturing.

The present work reports the fabrication of ultra-high strength microsand proppants (100 mesh) through a polymer nanocomposite dual coating approach and gives insight into their thermo-mechanical reinforcements. The dual coating can be of 3D-cross-linked poly(styrene-methyl methacrylate)/divinylbenzene) (PS-PMMA/DVB) porous network and thermally cross-linked epoxy with graphene nanosheets. The inner layer of PS-PMMA/DVB was prepared using bulk polymerization of styrene (S) and methyl methacrylate (MMA) at 70 °C with a free radical initiator azobisisobutyronitrile (AIBN). The outer layer was prepared by mixing epoxy resin, a cross-linker, and commercial graphene (CG) followed by thermally curing the mixture. The dual-coated microsand proppants exhibited enhanced mechanical characteristics of elastic modulus (E) as high as 7.78 GPa, hardness (H) of 0.35 GPa, and fracture toughness (Kc) of 3.19 MPa m1/2 along with largely improved thermal properties. Moreover, the dual-coated microsand proppants exhibit a very high-stress resistance up to 14000 psi, and to the best of our knowledge, this is the highest stress resistance value attained for the modified sand-based proppants so far.

PEG Coated Fe3O4/RGO Nano-Cube-Like Structures for Cancer Therapy via Magnetic Hyperthermia.

Superparamagnetic iron oxide nanoparticles (SPIONs) have high saturation magnetization and are promising candidates for hyperthermia. They may act as magnetic heating agents when subjected to magnetic field in nano-based hyperthermia. In this work, cube-like Fe3O4 nanoparticles (labelled as cubic SPIONs) with reduced graphene oxide (RGO) nanocomposites were prepared by a microwave hydrothermal method. The shape and size of magnetic nanoparticles were controlled by varying synthesis parameters, including reaction time, pressure and microwave power. This study successfully synthesized cubic SPIONs nanocomposites with an average particle size between 24-34 nm. Poly-(ethylene) glycol (PEG) was used as a coating material on SPIONs to enhance biocompatibility. The RGO sheets provided a high surface area-to-volume ratio for SPIONs to be dispersed on their surface, and hence, they prevented aggregation of the SPIONs in the nanocomposites. Magnetically induced heating studies on the optimized nanocomposite (Fe3O4/RGO/PEG) demonstrated heating capabilities for magnetic hyperthermia application with a promising specific absorption rate (SAR) value of 58.33 W/g in acidic solution. Cytotoxicity tests were also performed to ensure low nanoparticle toxicity before incorporation into the human body. The results of the standard assay for the toxicity determination of the nanocomposites revealed over 70% cell survival after 48 h, suggesting the feasibility of using the synthesized nanocomposites for magnetic hyperthermia.

Microwave Irradiation Synthesis and Characterization of Reduced-(Graphene Oxide-(Polystyrene-Polymethyl Methacrylate))/Silver Nanoparticle Nanocomposites and their Anti-Microbial Activity.

Herein, we report a facile process for the preparation of styrene and methyl-methacrylate copolymer nanocomposites containing reduced graphene oxide and silver nanoparticles ((R-(GO-(PS-PMMA))/AgNPs)) by using (i) microwave irradiation (MWI) to obtain R-(GO-(PS-PMMA))/AgNPs and (ii) the in situ bulk polymerization technique to produce RGO/AgNPs-(PS-PMMA). Various characterization techniques, including FT-IR, XPS, Raman spectroscopy, XRD, SEM, HR-TEM, DSC, and TGA analysis, were used to characterize the prepared nanocomposites. The Berkovich nanoindentation method was employed to determine the hardness and elastic modulus of the nanocomposites. The results showed that the MWI-produced nanocomposites were found to have enhanced morphological, structural, and thermal properties compared with those of the nanocomposites prepared by the in situ method. In addition, the antibacterial activity of the prepared nanocomposites against the E. coli HB 101 K-12 was investigated, whereby an inhibition zone of 3 mm (RGO/AgNPs-(PS-PMMA) and 27 mm (R-(GO-(PS-PMMA))/AgNPs) was achieved. This indicates that the MWI-prepared nanocomposite has stronger antibacterial activity than the in situ-prepared nanocomposite.

Two dimensional (2D) reduced graphene oxide (RGO)/hexagonal boron nitride (h-BN) based nanocomposites as anodes for high temperature rechargeable lithium-ion batteries.

With lithium-ion (li-ion) batteries as energy storage devices, operational safety from thermal runaway remains a major obstacle especially for applications in harsh environments such as in the oil industry. In this approach, a facile method via microwave irradiation technique (MWI) was followed to prepare Co3O4/reduced graphene oxide (RGO)/hexagonal boron nitride (h-BN) nanocomposites as anodes for high temperature li-ion batteries. Results showed that the addition of h-BN not only enhanced the thermal stability of Co3O4/RGO nanocomposites but also enhanced the specific surface area. Co3O4/RGO/h-BN nanocomposites displayed the highest specific surface area of 191 m2/g evidencing the synergistic effects between RGO and h-BN. Moreover, Co3O4/RGO/h-BN also displayed the highest specific capacity with stable reversibility on the high performance after 100 cycles and lower internal resistance. Interestingly, this novel nanocomposite exhibits outstanding high temperature performances with excellent cycling stability (100% capacity retention) and a decreased internal resistance at 150 °C.

Novel Synthesis of Holey Reduced Graphene Oxide/Polystyrene (HRGO/PS) Nanocomposites by Microwave Irradiation as Anodes for High-Temperature Lithium-Ion Batteries.

To overcome the risk of exothermic lithium-ion battery overheating reactions, we fabricated a novel, high-temperature-stable anode material composed of holey reduced graphene oxide/polystyrene (HRGO/PS) nanocomposites synthesized through in situ bulk polymerization in the presence of HRGO via microwave irradiation. The HRGO/PS nanocomposites were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, Raman spectroscopy, and electron microscopy analyses including field-emission scanning electron microscopy and transmission electron microscopy. All characterization studies demonstrated homogenous dispersion of HRGO in the PS matrix, which enhanced the thermal and electrical properties of the overall nanocomposites. These novel HRGO/PS nanocomposites exhibited excellent electrochemical responses, with reversible charge/discharge capacities of 92.1/92.78 mA·h/g at a current density of 500 mA/g with ~100% capacity retention and ~100% coulombic efficiency at room temperature. Furthermore, an examination of the electrochemical properties of these nanocomposites at 110 °C showed that HRGO/PS nanocomposites still displayed good charge/discharge capacities with stable cycle performances for 150 cycles.

Polymeric Reactor for the Synthesis of Superparamagnetic-Thermal Treatment of Breast Cancer.

Engineered superparamagnetic iron oxide nanoparticles (SPIONs) have been studied extensively for their localized homogeneous heat generation in breast cancer therapy. However, challenges such as aggregation and inability to produce sub-10 nm SPIONs limit their potential in magnetothermal ablation. We report a facile, efficient, and robust in situ method for the synthesis of SPIONs within a poly(ethylene glycol) (PEG) reactor adsorbed onto reduced graphene oxide nanosheets (rGO) via the microwave hydrothermal route. This promising modality yields crystalline, stable, biocompatible, and superparamagnetic PEGylated SPION-rGO nanocomposites (NCs) with uniform dispersibility. Our findings show that rGO acts as a breeding ground for the spatially distributed nanosites around which the ferrihydrite seeds accumulate to ultimately transform into immobilized SPIONs. PEG, in parallel, acts as a critical confining agent physically trapping the accumulated seeds to prevent their aggregation and create multiple domains on rGO for the synthesis of quantum-sized SPIONs (9 ± 1 nm in diameter). This dual functionality (rGO and PEG) exhibits a pronounced effect on reducing both the aggregation and the sizes of fabricated SPIONs as confirmed by the scanning transmission electron microscopy images, dynamic light scattering analyses, and the specific absorption rates (SARs). Reduced aggregation lowered the toxicity of NCs, where PEGylated SPION-rGO NCs are more biocompatible than PEGylated SPIONs, showing no significant induction of cell apoptosis, mitochondrial membrane injury, or oxidative stress. Significantly less lactate dehydrogenase release and hence less necrosis are observed after 48 h exposure to high doses of PEGylated SPION-rGO NCs compared with PEGylated SPIONs. NCs induce local heat generation with a SAR value of 1760 ± 97 W/g, reaching up to 43 ± 0.3 °C and causing significant MCF-7 breast tumor cell ablation of about 78 ± 10% upon applying an external magnetic field. Collectively, rGO and PEG functionalities have a synergistic effect on improving the synthesis, stability, biocompatibility, and magnetothermal properties of SPIONs.

Template Assisted Microwave Synthesis of rGO-ZrO2 Composites: Efficient Photocatalysts Under Visible Light.

In this research, cetyltetraethyl ammonium bromide template assisted microwave procedure was utilized to synthesize reduced graphene oxide-zirconia (rGO-ZrO2) nanocomposites by varying the rGO composition (1, 2, 5 and 10 wt%). The physico-chemical characteristics of the nanocomposites were studied using X-ray diffraction (XRD), Raman, differential scanning calorimetry (DSC), scanning electron microscopy (SEM), diffusive reflectance ultraviolet-visible (DRUV-vis), X-ray photoelectron spectroscopy (XPS) and N2-physisorption techniques. The results from XRD, Raman and DSC studies indicate that the increase in rGO concentration resulted in the delay in ZrO2 crystallization temperature and alteration of ZrO2 phase from monoclinic to tetragonal due to an effective incorporation of rGO nanosheets in ZrO2 structure. The rGO loading also have an influence in the morphology of nanocomposites, as sample with 10 wt% rGO possessed unique monolith like morphology with macro pores. All the nanocomposites were utilized as photocatalysts for degradation of crystal violet dye in visible light irradiation. The rGO-ZrO2 nanocomposites showed high reaction rates; the nanocomposite with 5 wt% rGO showed the superior photocatalytic performance as this sample possessed low band gap energy, high surface area, pore volume and presence of surface rGO-ZrO2 interactive species as well as the reactive -OH groups. In addition, the synthesized nanocomposites exhibited excellent recyclability for photocatalytic degradation.

Enhanced Electrochemical performance at high temperature of Cobalt Oxide/Reduced Graphene Oxide Nanocomposites and its application in lithium-ion batteries.

We report a microwave irradiation method for the preparation of reduced graphene oxide (RGO) based Co3O4 nanocomposites as anodes for lithium-ion (li-ion) batteries. The Co3O4/RGO nanocomposites displayed good electrochemical behavior as anodic materials for li-ion batteries when compared to pure Co3O4. The Co3O4/RGO nanocomposites with low RGO content resulted in stable electrochemical performance with 100% coulombic efficiency at a high current density of 500 mA/g for 50 cycles. The enhanced capacity of the Co3O4/RGO nanocomposites is due to the incorporation of RGO, which resulted in a four times larger surface area than that of Co3O4. This increased surface area could facilitate the absorption of more lithium ions, resulting in excellent electrochemical performance. Interestingly, the novelty of this work is that the designed li-ion batteries showed stable electrochemical performance even at a high temperature of 100 °C, which might be useful for rechargeable battery applications in a wide temperature range.

Designed Synthesis of Nanostructured Magnetic Hydroxyapatite Based Drug Nanocarrier for Anti-Cancer Drug Delivery toward the Treatment of Human Epidermoid Carcinoma.

Superparamagnetic Fe3O4 nanoparticles on hydroxyapatite nanorod based nanostructures (Fe3O4/HAp) were synthesized using hydrothermal techniques at 180 °C for 12 h and were used as drug delivery nanocarriers for cancer cell therapeutic applications. The synthesized Fe3O4/HAp nanocomposites were characterized by X-ray diffraction analysis (XRD), Field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET)-analysis, and vibrating sample magnetometry (VSM). The morphologies of the Fe3O4/HAp nanocomposites show 15 nm Fe3O4 nanoparticles dispersed in the form of rods. The BET result shows that the synthesized samples have a high specific surface area of 80 m² g-1 with mesoporous structures. Magnetic measurements revealed that the sample has high saturation magnetization of 18 emu/g with low coercivity. The Fe3O4/HAp nanocomposites had a large specific surface area (SSA), high mesoporous volume, and good magnetic property, which made it a suitable nanocarrier for targeted drug delivery systems. The chemotherapeutic agent, andrographolide, was used to investigate the drug delivery behavior of the Fe3O4/HAp nanocomposites. The human epidermoid skin cancer cells (A431) were used as the model targeting cell lines by treating with andrographolide loaded Fe3O4/HAp nanosystems and were further evaluated for their antiproliferative activities and the induction of apoptosis. Also, the present nanocomposite shows better biocompatibility, therefore it can be used as suitable drug vehicle for cancer therapy applications.

Biogenic synthesis of Zinc oxide nanostructures from Nigella sativa seed: Prospective role as food packaging material inhibiting broad-spectrum quorum sensing and biofilm.

Bacterial spoilage of food products is regulated by density dependent communication system called quorum sensing (QS). QS control biofilm formation in numerous food pathogens and Biofilms formed on food surfaces act as carriers of bacterial contamination leading to spoilage of food and health hazards. Agents inhibiting or interfering with bacterial QS and biofilm are gaining importance as a novel class of next-generation food preservatives/packaging material. In the present study, Zinc nanostructures were synthesised using Nigella sativa seed extract (NS-ZnNPs). Synthesized nanostructures were characterized hexagonal wurtzite structure of size ~24 nm by UV-visible, XRD, FTIR and TEM. NS-ZnNPs demonstrated broad-spectrum QS inhibition in C. violaceum and P. aeruginosa biosensor strains. Synthesized nanostructures inhibited QS regulated functions of C. violaceum CVO26 (violacein) and elastase, protease, pyocyanin and alginate production in PAO1 significantly. NS-ZnNPs at sub-inhibitory concentrations inhibited the biofilm formation of four-food pathogens viz. C. violaceum 12472, PAO1, L. monocytogenes, E. coli. Moreover, NS-ZnNPs was found effective in inhibiting pre-formed mature biofilms of the four pathogens. Therefore, the broad-spectrum inhibition of QS and biofilm by biogenic Zinc oxide nanoparticles and it is envisaged that these nontoxic bioactive nanostructures can be used as food packaging material and/or as food preservative.

Low temperature growth of ZnO nanotubes for fluorescence quenching detection of DNA.

In this work, large-scale and single-crystalline ZnO nanotubes were fabricated by a simple technique from an aqueous solution at a low temperature of 65 °C. According to detailed morphology, structural and compositional analyses showed that the ZnO nanotubes [diameter ~200 nm (wall thickness ~50 nm); length ~1 µm] have single-crystallite with wurtzite structure. As-prepared ZnO nanotubes showed an effective fluorescence quenching for the detection of calf thymus DNA. In particular, increasing DNA concentrations (5-50 µM) into the fixed concentration of ZnO nanotubes (50 µM) progressively quenched the intrinsic fluorescence of nanotubes, which showed that the nanotubes fluorescence was efficiently quenched upon binding to DNA. At the highest ZnO-DNA molar ratios of 1:1.8, around 50.1 % of fluorescence quenching of DNA was observed. Significance of this study provides simple, cost-effective, and low temperature synthesis of ZnO nanotubes revealed better fluorescence property toward a platform of DNA sensor. ZnO nanotubes with diameter of ~200 nm (wall thickness ~50 nm) and length of about 1 µm prepared at low temperature (65 °C) showed fluorescence was efficiently quenched upon binding to DNA. In particular, around 50.1 % of DNA fluorescence quenching at the highest ZnO-DNA molar ratios of 1:1.8 was observed.

Novel synthesis of holey reduced graphene oxide (HRGO) by microwave irradiation method for anode in lithium-ion batteries.

In this work, holey reduced graphene oxide (HRGO) was synthesized by the deposition of silver (Ag) nanoparticles onto the reduced graphene oxide (RGO) sheets followed by nitric acid treatment to remove Ag nanoparticles by microwave irradiation to form a porous structure. The HRGO were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), ultra violet-visible spectroscopy (UV-Vis), thermogravimetric analysis (TGA), and Raman spectroscopy. These novel HRGO exhibited high rate capability with excellent cycling stability as an anode material for lithium-ion batteries. The results have shown an excellent electrochemical response in terms of charge/discharge capacity (423 mAh/g at 100 mA/g). The cyclic performance was also exceptional as a high reversible capacity (400 mAh/g at 100 mA/g) was retained for 100 charge/discharge cycles. This fascinating electrochemical performance can be ascribed to their specific porous structure (2-5 nm pores) and high surface area (457 m(2)/g), providing numerous active sites for Li(+) insertion, high electrical conductivity, low charge-transfer resistance across the electrolyte-electrode interface, and improved structural stability against the local volume change during Li(+) insertion-extraction. Such electrodes are envisioned to be mass scalable with relatively simple and low-cost fabrication procedures, thereby providing a clear pathway toward commercialization.

Novel Biomimatic Synthesis of ZnO Nanorods Using Egg White (Albumen) and Their Antibacterial Studies.

Zinc oxide (ZnO) is well-recognized as a biocompatible multifunctional material with outstanding properties as well as low toxicity and biodegradability. In this work, a simple and versatile technique was developed to prepare highly crystalline ZnO nanorods by introducing egg white to a bio-inspired approach. X-ray diffraction (XRD) and selected area electron diffraction (SAED) pattern results indicated that the ZnO nanorods have single phase nature with the wurtzite structure. Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) results showed the nanometer dimension of the nanorods. Raman, FTIR, and TGA/DTA analyses revealed the formation of wurtzite ZnO. The antibacterial properties of ZnO nanorods were investigated using both Gram-positive and Gram-negative microorganisms. These studies demonstrate that ZnO nanorods have a wide range of antibacterial activities toward various microorganisms that are commonly found in environmental settings. Survival ratio of bacteria decreased with increasing powder concentration, i.e., increase in antibacterial activity. The antibacterial activity of the ZnO nanorods toward Pseudomonas aeruginosa was stronger than that of Escherichia coli and Staphylococcus aureus. Surprisingly, the antibacterial activity did not require specific UV activation using artificial lamps, rather activation was achieved under ambient lighting conditions. Overall, the experimental results suggest that ZnO nanorods could be developed as antibacterial agents against a wide range of microorganisms to control and prevent the spreading and persistence of bacterial infections. This research introduces a new concept to synthesize ZnO nanorods by using egg white as a biological template for various applications including food science, animal science, biochemistry, microbiology and medicine.