Picosecond nonlinear optical studies of gold nanoparticles synthesised using coriander leaves (Coriandrum sativum)

The results are presented from the experimental picosecond nonlinear optical (NLO) studies of gold nanoparticles synthesised using coriander leaf (Coriandrum sativum) extract. Nanoparticles with an average size of ～30?nm (distribution of 5–70?nm) were synthesised according to the procedure reported by Narayanan et al. [Mater. Lett. 2008, 62, 4588–4591]. NLO studies were carried out using the Z-scan technique using 2?ps pulses near 800?nm. Open-aperture data suggested saturation absorption as the nonlinear absorption mechanism, whereas closed-aperture data suggested a positive nonlinearity. The magnitude of third-order nonlinearity was estimated to be (3.3?±?0.6)?×?10^?13?esu. A solvent contribution to the nonlinearity was also identified and estimated. A comparison is attempted with some recently reported NLO studies of similar gold nanostructures.     

Biostabilised icosahedral gold nanoparticles: synthesis,cyclic voltammetric studies and catalytic activity towards 4-nitrophenol reduction

A green and cost-effective biosynthetic approach for the preparation of icosahedral gold nanoparticles (AuNPs) using an aqueous leaf extract of Polygonum minus as reducing and stabilising factor is described. The reduction of Au³⁺ ions to elemental Au rapidly occurred and is completed within 20 minutes at room temperature. The size of the nanoparticles is highly sensitive to the AuCl₄^?/leaf extract concentration ratio and pH. Transmission electron microscopy and X-ray diffraction data indicated that the nanoparticles were in a crystalline shape (face-centred cubic), mostly icosahedral and nearly monodispersed with an average size of 23 nm. Cyclic voltammetric studies suggested that flavonoids, such as quercetin and myricetin present in the leaf extract had a tendency to donate electrons to Au³⁺ ions and the formation of elemental Au was possible due to the transfer of electrons from these flavonoids to Au³⁺ ions. Infrared absorption of the AuNPs and the leaf extract revealed that the oxidised (quinone) form of quercetin and myricetin were presumably the main stabilising agents in the formation of stable nanoparticles. The present biosynthesis of AuNPs was simple, rapid, cost-effective and environmentally friendly. The newly prepared biostabilised icosahedral AuNPs show good catalytic activity in the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP).     

Comparative study of synthesized silver and gold nanoparticles using leaves extract of <Emphasis Type="Italic">Bauhinia tomentosa</Emphasis> Linn and their anticancer efficacy

Nanotechnology is an emerging field in science and technology, which can be applied to synthesize new materials at the nanoscale level. The present investigation aimed at comparing the synthesis, characterization and in vitro anticancer efficacy of synthesized silver and gold nanoparticles using leaves extract of Bauhinia tomentosa Linn. Silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs) were synthesized using aqueous extract of leaves with solution of silver nitrate (AgNO₃, 1 mM) and chloroauric acid (HAuCl₄?3H₂O, 1 mM), respectively. The synthesized nanoparticles were characterized using UV–visible spectrophotometry, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive analysis of X-rays, X-ray diffraction, thermogravimetric analysis and cyclic voltammetry, which confirmed the reduction of Ag⁺ ions to Ag⁰ and Au³⁺ ions to Au ⁰ . The in vitro anticancer efficacy of AgNPs, AuNPs and aqueous extract of leaves confirmed by MTT assay exhibited IC₅₀ concentrations of 28.125, 46.875 and 50 μg ml^?1 for lung A-549 cells, 103.125, 34.375 and 53.125 μg ml^?1 for HEp-2 cells and 62.5, 23.4 and 13.26 μg ml^?1 for MCF-7 cells, respectively. The concentrations indicate that both silver and gold nanoparticles as well as aqueous extract of leaves exhibited high anticancer efficacy.     

Green synthesis of gold nanoparticles using ethanolic leaf extract of Centella asiatica

Here, we report a novel use of the ethanolic leaf extract of Centella asiatica to produce gold nanoparticles by reduction of AuCl₄⁻ ions. The phytochemicals present in the leaf extract served as effective reducing and capping agent. The gold nanoparticles obtained were characterized by UV-visible spectra, transmission electron microscopy (TEM) and X-ray diffraction (XRD). TEM studies showed the particles to be of various shapes and sizes. Selected-area electron diffraction (SAED) pattern and high-resolution TEM image confirmed a fcc phase and high crystallinity of the particles. The XRD patterns showed a (1 1 1) preferential orientation of the gold nanoparticles. Fourier transform infra-red spectroscopy (FTIR) measurements showed the GNPs having a coating of phenolic compounds indicating a possible role of biomolecules responsible for capping and efficient stabilization of the gold nanoparticles. As no synthetic reagents were used in this method, the synthesized gold nanoparticles have potential for application in bio-molecular imaging and therapy.     

Photocatalytic degradation of ciprofloxacin pollutant and in-vitro cytotoxic activity of gold nanoparticles using seed extract of Abrus precatorius

Synthesis of nanoparticles from plant extract is a very simple reliable, rapid, affordable and un-hazardous technique. In the present exploration, gold nanoparticles (Au NPs) were rapidly synthesized using seed extract of Abrus precatorius. The prepared nanomaterials were systematically proved by FTIR, UV–Visible, Powder-XRD, SEM, EDAX and TEM analyses. The formation of Au NPs was primarily identified by the colour change from yellow to purple within 5 min and which showed a surface Plasmon peak around 535 nm. The dimension of the gold nanoparticles was found to be in the range of 10–20 nm. The particles were poly-dispersed with a triangular, spherical and hexagonal shape. The gold nanoparticles were used to degrade the antibiotic drug ciprofloxacin (CIP) with an efficiency of above 95%. Moreover, the bio-synthesized gold nanoparticles had been assessed for their in-vitro cytotoxic activity on human breast cancer cells (MCF-7) lines. The colorimetric 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay was used to evaluate the Inhibitory Concentration (IC₅₀) value. The IC₅₀ value is 37?±?1.5 µg/mL. In future, this can be used for breast cancer therapy.

     

Fabrication of novel GMO/Eudragit E100 nanostructures for enhancing oral bioavailability of carvedilol

In the present work, novel nanostructures comprising of glyceryl monooleate (GMO) and Eudragit E100 were prepared using high intensity ultrasonic homogenization. 3² Factorial design approach was used for optimization of nanostructures. Results of regression analysis revealed that the amount of GMO and Eudragit E100 had a drastic effect on particle size and percent entrapment efficiency. Optimized carvedilol-loaded nanostructures (Car-NS) were characterized by FTIR, TEM, DSC, in vitro drug release study. Pharmacokinetic parameters such as C_max, T_max, Ke, Ka, V_d and AUC were estimated for Car-NS upon its oral administration in Sprague-Dawley rats. Particle size of Car-NS was found to be 183?±?2.43?nm with an entrapment efficiency of 81.4?±?0.512%. FTIR studies revealed loading and chemical compatibility of carvedilol with the components of nanostructures. DSC thermograms did not show endothermic peak for melting of carvedilol which could be attributed to solubilization of carvedilol in molten GMO during DSC run. The prepared Car-NS released carvedilol in sustained manner over a period of 10 h as suggested by in vitro drug release study. The pharmacokinetic study of Car-NS showed significant improvement in C_max (two fold, p?p?相似文献   

Green synthesis of silver nanoparticles using Nervalia zeylanica leaf extract and evaluation of their antioxidant,catalytic, and antimicrobial potentials

ABSTRACT

Here we report a simple, one-pot, inexpensive, and eco-friendly method for the synthesis of silver nanoparticles. The leaf extract of a medicinal plant Nervalia zeylanica was used as reducing and stabilizing agent for the synthesis of nanoparticles by microwave-assisted strategy. The nanoparticles show characteristic surface plasmon peak at 468?nm in UV–vis absorption spectrum. The involvement of phytochemicals in the reduction and stabilization of nanoparticles was confirmed by FTIR analysis. Using X-ray diffraction analysis, the crystalline nature of the nanoparticles was demonstrated. Transmission electron microscopic analysis shows that the nanoparticles were in spherical shape with average particle size of 34.2?nm. The antioxidant studies were performed by the 1,1-diphenyl-2-picryl hydrazyl method. The nanoparticles show excellent scavenging activities than the leaf extract. The IC₅₀ values of silver nanoparticles and the leaf extract, respectively, were 15.20 and 92.83?µg?mL^?1. The catalytic activities of synthesized nanoparticles were examined by using them in the reduction of organic dyes. The nanoparticles show excellent catalytic activities and follow pseudo-first-order kinetics. The antimicrobial activities of nanoparticles were analyzed by an agar well diffusion method against six microbial strains and found that the nanoparticles were highly toxic against all the tested microbial strains.     

Biosynthesis of gold nanoparticles using marine bacteria and Box–Behnken design optimization

Gold nanoparticles are exciting materials because of their potential applications in optics, electronics, biomedical, and pharmaceutical fields. In recent years, environmentally friendly, low-cost biosynthesis methods with bio-applicable features have continued to be developed for the synthesis of gold nanoparticles. In the present study, an actinobacterial strain was isolated from the Petrosia ficiformis (Poiret 1798) sponge, which was collected from a marine environment, and the gold nanoparticle synthesis was performed for the first time from the bacteria type belonging to the Citricoccus genus. The synthesis conditions were optimized using the Box–Behnken experimental design, with a statistical method that included three independent variables (temperature, time, and mixture ratio) to affect the synthesis at three levels (+1, 0, and ?1). Accordingly, the conditions proposed for the biosynthesis of gold nanoparticles at the maximum optical density values that are specific for the Citricoccus sp. K1D109 strain were estimated as 35°C temperature, 24?h, and 1/5 mixture ratio (cell-free extract/HAuCl₄?·?3H₂O). When recommended conditions were applied, it was determined that the maximum absorbance of the synthesized gold nanoparticles is 1.258 at 545?nm, and their sizes are in the range of 25–65?nm, according to transmission electron microscopy (TEM) data.     

Microbial Synthesis of Multishaped Gold Nanostructures

The development of methodologies for the synthesis of nanoparticles of well‐defined size and shape is a challenging one and constitutes an important area of research in nanotechnology. This Full Paper describes the controlled synthesis of multishaped gold nanoparticles at room temperature utilizing a simple, green chemical method by the interaction of chloroauric acid (HAuCl₄ · 3H₂0) and cell‐free extract of the fungal strain Rhizopus oryzae. The cell‐free extract functions as a reducing, shape‐directing, as well as stabilizing, agent. Different shapes of gold nanocrystals, for example, triangular, hexagonal, pentagonal, spherical, spheroidal, urchinlike, two‐dimensional nanowires, and nanorods, are generated by manipulating key growth parameters, such as gold ion concentration, solution pH, and reaction time. The synthesized nanostructures are characterized by UV/Vis and Fourier‐transform infrared spectroscopy, transmission electron microscopy, and energy dispersive X‐ray analysis studies. Electron diffraction patterns reveal the crystalline nature of the nanoparticles and a probable mechanism is proposed for the formation of the different structural entities.     

Ferrocene‐Incorporated Cobalt Sulfide Nanoarchitecture for Superior Oxygen Evolution Reaction

Here, ferrocene(Fc)‐incorporated cobalt sulfide (Co_xS_y) nanostructures directly grown on carbon nanotube (CNT) or carbon fiber (CF) networks for electrochemical oxygen evolution reaction (OER) using a facile one‐step solvothermal method are reported. The strong synergistic interaction between Fc‐Co_xS_y nanostructures and electrically conductive CNTs results in the superior electrocatalytic activity with a very small overpotential of ≈304 mV at 10 mA cm^?2 and a low Tafel slope of 54.2 mV dec^?1 in 1 m KOH electrolyte. Furthermore, the Fc‐incorporated Co_xS_y (FCoS) nanostructures are directly grown on the acid pretreated carbon fiber (ACF), and the resulting fabricated electrode delivers excellent OER performance with a low overpotential of ≈315 mV at 10 mA cm^?2. Such superior OER catalytic activity can be attributed to 3D Fc‐Co_xS_y nanoarchitectures that consist of a high concentration of vertical nanosheets with uniform distribution of nanoparticles that afford a large number of active surface areas and edge sites. Besides, the tight contact interface between ACF substrate and Fc‐Co_xS_y nanostructures could effectively facilitate the electron transfer rate in the OER. This study provides valuable insights for the rational design of energy storage and conversion materials by the incorporation of other transition metal into metal sulfide/oxide nanostructures utilizing metallocene.     

Synthesis of cube-shaped gold nanostructures by electron irradiation

The needle-like gold nanostructures were synthesized by using chloroauric acid (HAuCl₄) as a metal precursor and sodium borohydride (NaBH₄) as the reducing agent. These needle-like nanostructures of gold were irradiated with high energy electrons (E ~ 6 MeV, ? ~ 10¹² e cm⁻² s⁻¹). The pre- and post-irradiated gold nanostructures were characterized by Scanning Electron Microscopy (SEM), UV-vis spectroscopy, X-ray Diffraction (XRD) and contact angle measurement (GBX-Model Digidrop) techniques. The results of the SEM revealed that after electron irradiation, the needle-like gold structures got fragmented into identical cube-shaped gold nanostructures, though of different sizes. The XRD analysis indicated that the average crystallite size of the gold nanostructures remained unchanged even after irradiation with high energy electrons. A glass surface showed hydrophilic behavior when coated with needle-like nanostructures and became ultra hydrophilic when coated with cube-shaped gold nanostructures.     

Hybrid PdAg alloy-Au nanorods: Controlled growth, optical properties and electrochemical catalysis

Controllable growth of high-quality hybrid nanostructures is highly desirable for the fabrication of hierarchical, complex and multifunctional devices. Here, PdAg alloys have been controllably grown at different locations on gold nanorods, producing dumbbell-like nanostructures with PdAg at the ends of the gold nanorods or branched nanostructures with PdAg grown almost perpendicular to the gold nanorods. The nucleation sites of PdAg alloys on the gold nanorods can be effectively tuned by varying the concentrations of H2PdC14, AgNO3 and cetyltrimethylammonium bromide （CTAB）. The dumbbell-like and branched nanostructures were characterized by transmission electron microscopy （TEM）, high-resolution TEM （HRTEM）, line-scanning energy-dispersive X-ray spectros-copy （EDS）, X-ray photoelectron spectroscopy （XPS） and UV-Vis absorption spectroscopy. Their electrocatalytic performance was evaluated using ethanol oxidation as a probe reaction. The dumbbelMike nanostructures show a better anti-poisoning performance, but a worse electrochemical activity than the branched ones. The results provide guidelines for the controlled growth of complicated nanostructures for either fundamental studies or potential applications.     

Phytosynthesis of gold nanoparticles using leaf extract of Coleus amboinicus Lour

Present study reports a green chemistry approach for the biological synthesis of gold nanoparticles by using the leaf extract of Coleus amboinicus Lour. The nanoparticles were structurally characterized by UV–Vis spectroscopy, XRD, TEM and SAED analyses. Elemental and vibrational analyses were done with EDAX and FT–IR spectroscopies respectively. Bioreduction of gold ions by C. amboinicus leaf extract resulted in the synthesis of spherical, truncated triangle, triangle, hexagonal and decahedral nanoparticles. These nanoparticles showed an absorption peak at 536 nm in UV–Vis spectrum corresponding to the plasmon resonance of gold nanoparticles. The size of gold nanoparticles ranged from 4.6 to 55.1 nm. FT–IR spectrum confirmed the involvement of aromatic amines, amide (II) groups and secondary alcohols in capping and reduction of gold nanoparticles. Extracellular synthesis of gold nanoparticles is a simple, cheap and environmentally benign alternative to physical and chemical procedures.     

Ultrahigh Responsivity UV Photodetector Based on Cu Nanostructure/ZnO QD Hybrid Architectures

Strong near‐surface electromagnetic field formed by collective oscillation of electrons on Cu nanostructure a shows a strong dependence on geometry, offering a promising approach to boost the light absorption of ZnO photoactive layers with enhanced plasmon scattering. Here, a facile way to fabricate UV photodetectors with tunable configuration of the self‐assembled Cu nanostructures on ZnO thin films is reported. The incident lights are effectively confined in ZnO photoactive layers with the existence of the uplayer Cu nanostructures, and the interdiffusion of Cu atoms during fabrication of the Cu nanostructures can improve the carrier transfer in ZnO thin films. The optical properties of the hybrid architectures are successfully tailored over a control of the geometric evolution of the Cu nanostructures, resulting in significantly enhanced photocurrent and responsivity of 2.26 mA and 234 A W^?1 under a UV light illumination of 0.62 mW cm^?2 at 10 V, respectively. The photodetectors also exhibit excellent reproducibility, stability, and UV–visible rejection ratio (R_{370 nm}/R_{500 nm}) of ≈370, offering an approach of high‐performance UV photodetectors for practical applications.     

Comparison of antibacterial activity of Ag nanoparticles synthesized from leaf extract of Parthenium hystrophorus L in aqueous media and Gentamicin sulphate: in-vitro

Monodisperse silver (Ag) nanoparticles were synthesized by using Parthenium hystrophorus L leaf extract in aqueous media. The synthesized nanoparticles were characterized by using UV-vis spectrophotometer, X-ray diffracto-meter (XRD), transmission electron microscope (TEM), and dynamics light scattering (DLS). Size-dependent antibacterial activities of Ag nanoparticles were tested against Gram negative Pseudomonas aeruginosa and Gram positive Staphylococcus aureus. Ag nanoparticles having 20?±?2?nm size in diameter show maximum zone of inhibition (23?±?2.2?mm) in comparison to 40?nm and 70?nm diameter nanoparticles for Pseudomonas aeruginosa. The zone of inhibition against Staphylococcus aureus were 19?±?1.8?mm, 15?±?1.5?mm and 11?±?1?mm for 20?nm, 40?nm, and 70?nm, respectively. In addition, affect of concentration of 20?nm size Ag nanoparticles on Bacillus cereus, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus species were also reported and results were compared with 10?µg/ml dose of Gentamicin sulphate. The Parthenium hystrophorus L leaf extract capped 20?±?2?nm Ag nanoparticles (7.5?µg/ml) shows statistically significant antibacterial activity than Gentamicin sulphate (10?µg/ml) against Staphylococcus aureus.     

Green fabricated CuO nanobullets via Olea europaea leaf extract shows auspicious antimicrobial potential

In present investigation, copper oxide (CuO) nanostructures have been prepared via green chemistry. Olea europaea leaf extract act as strong chelating agent for tailoring physical as well as bio‐medical characteristics of CuO at the nano‐size. Physical characterisation such as scanning electron microscope analysis depicts the formation of homogenised spherical shape nanoparticles (NPs) with average size of 42 nm. X‐ray diffraction and Fourier transform infrared spectroscopy further confirmed the crystalline pure phase and monoclinic structure. High performance liquid chromatography (HPLC) testing is performed to evaluate the relative concentration of bioactive molecules in the O. europaea leaf extract. From HPLC results capping action of organic molecules around CuO‐NPs is hypothesised. The antimicrobial potency of biosynthesised CuO‐NPs have been evaluated using colony forming unit (CFU) counting assay and disc diffusion method which shows a significant zone of inhibition against bacterial and fungal strains may be highly potential for future antimicrobial pharmaceutics. Furthermore, reduction of various precursors by plant extract will reduce environmental impact over chemical synthesis.Inspec keywords: copper compounds, antibacterial activity, biochemistry, nanoparticles, nanomedicine, biomedical materials, chromatographyOther keywords: CuO, size 42 nm, chemical synthesis, antimicrobial pharmaceutics, bacterial strain, fungal strain, disc diffusion method, colony forming unit counting assay, biosynthesised CuO‐NP, bioactive molecules, high‐performance liquid chromatography testing, monoclinic structure, crystalline pure phase, Fourier transform infrared spectroscopy, X‐ray diffraction, homogenised spherical shape nanoparticles, scanning electron microscope analysis, CuO biomedical characteristics, chelating agent, green fabricated CuO nanobullets, green chemistry, copper oxide nanostructures, antimicrobial potential, Olea europaea leaf extract     

Sustainable Synthesis of Co@NC Core Shell Nanostructures from Metal Organic Frameworks via Mechanochemical Coordination Self‐Assembly: An Efficient Electrocatalyst for Oxygen Reduction Reaction

Herein, a new type of cobalt encapsulated nitrogen‐doped carbon (Co@NC) nanostructure employing Zn_xCo_1?x(C₃H₄N₂) metal–organic framework (MOF) as precursor is developed, by a simple, ecofriendly, solvent‐free approach that utilizes a mechanochemical coordination self‐assembly strategy. Possible evolution of Zn_xCo_1?x(C₃H₄N₂) MOF structures and their conversion to Co@NC nanostructures is established from an X‐ray diffraction technique and transmission electron microscopy analysis, which reveal that MOF‐derived Co@NC core–shell nanostructures are well ordered and highly crystalline in nature. Co@NC–MOF core–shell nanostructures show excellent catalytic activity for the oxygen reduction reaction (ORR), with onset potential of 0.97 V and half‐wave potential of 0.88 V versus relative hydrogen electrode in alkaline electrolyte, and excellent durability with zero degradation after 5000 potential cycles; whereas under similar experimental conditions, the commonly utilized Pt/C electrocatalyst degrades. The Co@NC–MOF electrocatalyst also shows excellent tolerance to methanol, unlike the Pt/C electrocatalyst. X‐ray photoelectron spectroscopy (XPS) analysis shows the presence of ORR active pyridinic‐N and graphitic‐N species, along with CoN_x? C_y and Co? N_x ORR active (M–N–C) sites. Enhanced electron transfer kinetics from nitrogen‐doped carbon shell to core Co nanoparticles, the existence of M–N–C active sites, and protective NC shells are responsible for high ORR activity and durability of the Co@NC–MOF electrocatalyst.     

Response of low-grade gold ore to cyanidation and thiourea leaching

In this study, leaching tests were conducted on representative samples provided from Hamze-Qarnein gold deposit with grade of 0.8?ppm using cyanidation and thiourea leaching. Effective parameters including particle size, reagent concentration, oxidant concentration, pH, and dissolution time were examined in both cyanidation and acidic extraction with thiourea. Gold recovery and reagent consumptions (lime, cyanide, thiourea, ferric sulfate, and sulfuric acid) were measured under different leaching conditions. The results showed that cyanidation method was efficient with 95.21% gold recovery with following conditions: d₈₀?=?63?µm, pH 10.5, cyanide consumption of 1.23?kg/t, and 12?h cyanidation time. The acidic leaching using thiourea, required more chemical reagents and maximum gold recovery of 90.48% was achieved with thiourea consumption, leaching time, and pH equal to 13.32?kg/t, 5?h, and 1.7, respectively. According to the results, there was an interaction between ferric sulfate and thiourea concentrations and modeling of this process utilizing historical data design confirmed that the most effective parameter was the molar ratio of ferric sulfate to thiourea. Maximum recovery of gold obtained at molar ratio of 1/1. In addition, based on the experimental results, kinetics parameters of first-order reaction for gold dissolution were determined for cyanidation and thiourea leaching separately; therefore, for cyanidation, R_∞ and K were 95.59% and 0.59?h^?1 respectively, while R_∞ and K were in order of 78% and 0.87?h^?1 for acidic leaching using thiourea.     

Phytosynthesis of Cu/rGO using Euphorbia cheiradenia Boiss extract and study of its ability in the reduction of organic dyes and 4‐nitrophenol in aqueous medium

For the first time, copper nanoparticles (Cu NPs) superficially deposited on reduced graphene oxide (rGO) using Euphorbia cheiradenia Boiss leaf aqueous media. A beneficial series of analytical methods was used to characterise E. cheiradenia Boiss leaf extract and involved nanostructures. The Cu/rGO nanocomposite (NC) obtained from the conversion of Cu²⁺ ions to Cu NPs and GO to rGO undergoes the plant extract and used as a heterogeneous and reusable nanocatalyst for the destruction of 4‐nitrophenol, rhodamine B, methylene blue, methyl orange and congo red using sodium borohydride at ambient temperature. In addition, Cu/rGO NC has reusability for many times in the reduction reactions with no decreasing of its catalytic capability.Inspec keywords: catalysts, nanofabrication, nanocomposites, dyes, nanoparticles, reduction (chemical), copper, graphene compoundsOther keywords: phytosynthesis, organic dyes, reusable nanocatalyst, Euphorbia cheiradenia Boiss extract, 4‐nitrophenol, nanoparticles, graphene oxide, nanocomposites, methylene blue, methyl orange, congo red, sodium borohydride, catalytic capability, Cu‐CO     

Sulfur‐Modified Graphitic Carbon Nitride Nanostructures as an Efficient Electrocatalyst for Water Oxidation

There is an urgent need to develop metal‐free, low cost, durable, and highly efficient catalysts for industrially important oxygen evolution reactions. Inspired by natural geodes, unique melamine nanogeodes are successfully synthesized using hydrothermal process. Sulfur‐modified graphitic carbon nitride (S‐modified g‐CN _x ) electrocatalysts are obtained by annealing these melamine nanogeodes in situ with sulfur. The sulfur modification in the g‐CN _x structure leads to excellent oxygen evolution reaction activity by lowering the overpotential. Compared with the previously reported nonmetallic systems and well‐established metallic catalysts, the S‐modified g‐CN _x nanostructures show superior performance, requiring a lower overpotential (290 mV) to achieve a current density of 10 mA cm^?2 and a Tafel slope of 120 mV dec^?1 with long‐term durability of 91.2% retention for 18 h. These inexpensive, environmentally friendly, and easy‐to‐synthesize catalysts with extraordinary performance will have a high impact in the field of oxygen evolution reaction electrocatalysis.