Efficient synthesis of tungsten oxide hydrate-based nanocomposites for applications in bifunctional electrochromic-energy storage devices.

In this work, we realized the large-scale synthesis of WO3 · H2O nanoflakes (NFs), g-C3N4/WO3 · H2O nanocomposite (NC) and graphene (G)/WO3 · H2O NC via a sonochemical process with tungsten salt as the precursor, g-C3N4 or G sheets as the supports, and distilled water as the solvent. Both the g-C3N4/WO3 · H2O NC and G/WO3 · H2O NC exhibited much better electrochromic (EC) performance (higher coloration efficiencies and faster response times) than that of the WO3 · H2O NFs. Using the WO3 · H2O-based materials as electrode materials, EC batteries that integrate the energy storage and EC functions in one device have been assembled. The energy status of the EC batteries could be visually indicated by the reversible color variations. Compared with the plain WO3 · H2O-based EC batteries, the NC-based EC batteries possessed a lower color contrast between the charged and discharged conditions but much longer discharge durations. The EC batteries could be quickly charged in a few seconds by adding H2O2, and the charged batteries exhibited significantly-enhanced discharging durations in comparison with the initial ones. The g-C3N4/WO3 · H2O NC-EC batteries charged by a small amount of H2O2 could produce a long discharging duration up to 760 min.

MnO2/g-C3N4 nanocomposite with highly enhanced supercapacitor performance.

A novel sandwich-like MnO2/g-C3N4 nanocomposite (NC) based on the integration of high-density MnO2 nanorods (NRs) onto the surfaces of two-dimensional (2D) g-C3N4 sheets has been successfully fabricated through a facile soft chemical route at low temperature. The MnO2/g-C3N4 NC electrode enhanced the supercapacitor (SC) performance, benchmarked against both the bare MnO2 NRs electrode and the MnO2/graphene oxide (GO) NC electrode, exhibiting high specific capacitance of 211 F/g at a current density of 1 A/g, with good rate capacity and cycling stability. The sandwich-like hybrid structure, the unique 2D structure of the g-C3N4 sheets and the presence of nitrogen in the g-C3N4 all contributed to the promising SC performance of the MnO2/g-C3N4 NC. This work demonstrated the advantages of the g-C3N4 sheets over the commonly-used GO sheets in the design of novel hybrid composite for enhanced capacitance performance of MnO2-based electrochemical SCs, and the results could be extended to other electrode materials for SCs.

Increased secretion of bacterial pyomelanin caused by light accelerates corrosion of low alloy steel.

Microorganisms in the waterline zone can secrete pigments to avoid damage caused by ultraviolet radiation, some of which have corrosive effects. In this work, we found that the secretion of pyomelanin by P3 strain of Pseudoalteromonas lipolytica significantly increases under strong lighting conditions, accelerating the corrosion of the material. Molecular mechanisms indicate that strong light, as a stressful environmental factor, enhances the expression of melanin secretion-related genes to prevent bacteria from being damaged by ultraviolet radiation. Therefore, this work proposes a new corrosion mechanism in the waterline zone, pigment-producing microorganisms are also involved in the waterline corrosion process.

Artificially stacked atomic layers: toward new van der Waals solids.

Strong in-plane bonding and weak van der Waals interplanar interactions characterize a large number of layered materials, as epitomized by graphite. The advent of graphene (G), individual layers from graphite, and atomic layers isolated from a few other van der Waals bonded layered compounds has enabled the ability to pick, place, and stack atomic layers of arbitrary compositions and build unique layered materials, which would be otherwise impossible to synthesize via other known techniques. Here we demonstrate this concept for solids consisting of randomly stacked layers of graphene and hexagonal boron nitride (h-BN). Dispersions of exfoliated h-BN layers and graphene have been prepared by liquid phase exfoliation methods and mixed, in various concentrations, to create artificially stacked h-BN/G solids. These van der Waals stacked hybrid solid materials show interesting electrical, mechanical, and optical properties distinctly different from their starting parent layers. From extensive first principle calculations we identify (i) a novel approach to control the dipole at the h-BN/G interface by properly sandwiching or sliding layers of h-BN and graphene, and (ii) a way to inject carriers in graphene upon UV excitations of the Frenkell-like excitons of the h-BN layer(s). Our combined approach could be used to create artificial materials, made predominantly from inter planar van der Waals stacking of robust bond saturated atomic layers of different solids with vastly different properties.

Corrosion Behavior of Ni/NiCr/NiCrAlSi Composite Coating on Copper for Application as a Heat Exchanger in Sea Water.

This study introduces a novel Ni/NiCr/NiCrAlSi composite coating to enhance the corrosion resistance of copper, particularly for its use in marine heat exchangers. Utilizing characterization techniques such as scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), potentiodynamic polarization, and electrochemical impedance spectroscopy (EIS), the paper investigates the coating's composition, structure, and corrosion resistance in 3.5 wt.% NaCl aqueous solutions. A significant focus is placed on the role of aluminum within the NiCrAlSi layer, examining its influence on the coating's structure and corrosion behavior. The results indicate that the NiCrAlSi layer with an aluminum content of 5.49 at.% exhibits the most improved corrosion resistance, characterized by the highest corrosion potential and a corrosion current density that is more than one order of magnitude lower compared to the Ni/NiCr coating. The effectiveness of this composite coating is attributed to its multilayer structure and the synergistic effect of alloying elements Cr, Al, and Si, which collectively inhibit corrosive medium penetration. These insights present the Ni/NiCr/NiCrAlSi coating as a promising candidate for copper protection in sea water environments, merging enhanced durability with cost-effectiveness.

Anti-Fouling and Anti-Biofilm Performance of Self-Polishing Waterborne Polyurethane with Gemini Quaternary Ammonium Salts.

Biofilms are known to be difficult to eradicate and control, complicating human infections and marine biofouling. In this study, self-polishing and anti-fouling waterborne polyurethane coatings synthesized from gemini quaternary ammonium salts (GQAS), polyethylene glycol (PEG), and polycaprolactone diol (PCL) demonstrate excellent antibiofilm efficacy. Their anti-fouling and anti-biofilm performance was confirmed by a culture-based method in broth media, with the biofilm formation factor against Gram-positive (S. aureus) and Gram-negative bacterial strains (E. coli) for 2 days. The results indicate that polyurethane coatings have excellent anti-biofilm activity when the content of GQAS reached 8.5 wt% against S. aureus, and 15.8 wt% against E. coli. The resulting waterborne polyurethane coatings demonstrate both hydrolytic and enzymatic degradation, and the surface erosion enzymatic degradation mechanism enables them with good self-polishing capability. The extracts cyto-toxicity of these polyurethane coatings and degradation liquids was also systematically studied; they could be degraded to non-toxic or low toxic compositions. This study shows the possibility to achieve potent self-polishing and anti-biofilm efficacy by integrating antibacterial GQAS, PEG, and PCL into waterborne polyurethane coatings.

Highly Orientated Sericite Nanosheets in Epoxy Coating for Excellent Corrosion Protection of AZ31B Mg Alloy.

The growing demands for material longevity in marine environments necessitate the development of highly efficient, low-cost, and durable corrosion-protective coatings. Although magnesium alloys are widely used in the automotive and aerospace industries, severe corrosion issues still hinder their long-term service in naval architecture. In the present work, an epoxy composite coating containing sericite nanosheets is prepared on the AZ31B Mg alloy using a one-step electrophoretic deposition method to improve corrosion resistance. Due to the polyetherimide (PEI) modification, positively charged sericite nanosheets can be highly orientated in an epoxy coating under the influence of an electric field. The sericite-incorporated epoxy coating prepared in the emulsion with 4 wt.% sericite exhibits the highest corrosion resistance, with its corrosion current density being 6 orders of magnitude lower than that of the substrate. Electrochemical measurements and immersion tests showed that the highly orientated sericite nanosheets in the epoxy coating have an excellent barrier effect against corrosive media, thus significantly improving the long-term anti-corrosion performance of the epoxy coating. This work provides new insight into the design of lamellar filler/epoxy coatings with superior anticorrosion performance and shows promise in the corrosion protection of magnesium alloys.

Prolonging the duration of preventing bacterial adhesion of nanosilver-containing polymer films through hydrophobicity.

A superhydrophobic coating composed of silver nanoparticles was developed on copper from fluorinated multilayered polyelectrolyte films to examine its performance in preventing microbial adhesion. Antibacterial and antibiofouling experiments for this novel coating were conducted with SRB. From the disk diffusion tests (for 48 h), it was found that, compared to the traditional coating composed of nanosilver, this novel coating significantly improved antibacterial performance and long-term effectiveness. The oxidation states of the immobilized silver in polyelectrolyte multilayer films were investigated with X-ray photoelectron spectroscopy (XPS), and the stability of the immobilized silver was evaluated through a leaching test. It was found that if silver was exposed to aqueous environments some ionic silver species would be produced and released. The ion release kinetics showed that the duration of sustained release of antibacterial Ag ions from the novel coatings was prolonged, which was why they had more long-term antibacterial performance.

FeS2 Nanoparticles Encapsulated in S/N Co-Doped Carbon Nanofibers With a Three-Dimensional Multi-Channel Structure for Lithium-Ion Batteries.

Pyrite (FeS2) is one of the potential candidates for advanced rechargeable Li-ion batteries (LIBs) owing to its inherent capacity (849 mAh g-1), environmental friendliness, and abundant natural resources. However, the volume expansion of FeS2 and the dissolution of polysulfide in the electrochemical reaction severely limit its application in the field of energy conversion and storage. Herein, FeS2 nanoparticles are encapsulated in S/N co-doped three-dimensional multi-channel structural carbon nanofibers (FeS2@CNFs) through the electrospinning method. As a cathode material for LIBs, FeS2@CNFs demonstrated excellent rate property and cyclic stability. The 3FeS2@CNFs (weight ratio of FeS2 is 30%) present the initial capacity of 1,336.7 mAh g-1 and the remaining 856.5 mAh g-1 at 0.02A g-1 after 100 circles. The favorable electrochemical properties have confirmed that carbon nanofibers can enhance the electroconductivity of electrodes, reduce the volume collapse of FeS2, and remit the dissolution of polysulfide during the Li+ ions insertion/de-insertion process. In addition, co-doped S/N can supply abundant active sites for electrochemical reactions, providing enough space for Li+ ion storage. The results indicate that 3FeS2@CNFs is a cathode with a developmental prospect for LIBs.

Design of Multi-Functional Superhydrophobic Coating via Bacterium-Induced Hierarchically Structured Minerals on Steel Surface.

The fabrication of an eco-friendly, multi-functional, and mechanically robust superhydrophobic coating using a simple method has many practical applications. Here, inspired by shell nacre, the micro- or nano-scale surface roughness that is necessary for superhydrophobic coatings was formed via Bacillus subtilis-induced mineralization. The biomineralized film coated with hexadecyltrimethoxysilane (HDTMS) exhibited superhydrophobicity with water contact angles of 156°. The biomimetic HDTMS/calcite-coating showed excellent self-cleaning, anti-icing, and anti-corrosion performances. Furthermore, mechanically robust superhydrophobicity could be realized by hierarchically structured biomineralized surfaces at two different length scales, with a nano-structure roughness to provide water repellency and a micro-structure roughness to provide durability. Our design strategy may guide the development of "green" superhydrophobic coatings that need to retain effective multi-functional abilities in harsh marine environments.

Properties and Corrosion Resistance Mechanism of a Self-Healing Propane-1,2,3-Triol-Loaded Polysulfone Microcapsule Coating Loaded with Epoxy Resin.

Propane-1,2,3-triol-loaded polysulfone (PSF) microcapsules were prepared by the solvent evaporation method. The particle size of the microcapsules is about 140 µm. The shell wall thickness is about 17 µm approximately. The microcapsules have high thermal stability and antiwear performance. The self-healing coating was prepared by adding the prepared capsule into the epoxy resin coating. After electrochemical and corrosion immersion experiments, the resistance modulus of the coating added to the microcapsules was higher than the others in a 3.5 wt % NaCl corrosion solution, and it had the lowest corrosion current density, so the self-healing microcapsule coatings showed excellent healing ability and corrosion inhibition function for microcracks. This was attributed to the formation of a hydrophobic film after propane-1,2,3-triol was released from the damaged microcapsules.

Solvothermal synthesis of Ce-doped tungsten oxide nanostructures as visible-light-driven photocatalysts.

Cerium (Ce)-doped tungsten oxide nanostructures have been generated by using a simple solvothermal method with cerium chloride salts and tungsten hexachloride as precursors. The as-synthesized samples were characterized by electron microscopy, x-ray diffraction and x-ray photoelectron spectrometry. The photocatalytic activities of the samples were evaluated by degradation of methyl orange in an aqueous solution under visible light irradiation. Results showed that the as-synthesized samples underwent morphological evolution with decreasing W/Ce molar ratio, from one-dimensional bundled nanowires through straighter, shorter and thicker bundled nanorods to two-dimensional bundled blocks, then to a mixture of bundled nanorods and agglomerated nanoparticles, and finally to particle agglomerates. The Ce-doped tungsten oxides exhibited better photocatalytic activities than that of the undoped tungsten oxide. The cerium-doped tungsten oxide bundled blocks synthesized with a W/Ce molar ratio of 15:1 possessed the most effective photocatalytic activity among the tested samples. These novel nanomaterials may find potential applications as visible-light-driven photocatalysts.

Tetra-kis[(4-meth-oxy-carbon-yl)anilinium] hexa-chloridostannate(IV) dichloride.

The asymmetric unit of the title compound, (C(8)H(10)NO(2))(4)[SnCl(6)]Cl(2), contains two (4-meth-oxy-carbon-yl)anilinium cations, one chloride anion and one half of a hexa-chlorido-stannate(IV) dianion situated on a twofold rotation axis. All aminium H atoms are involved in N-H⋯Cl hydrogen bonding, which consolidate the crystal packing along with weak C-H⋯O inter-actions.

2-Amino-terephthalic acid-4,4'-bipyridine (1/1).

The asymmetric unit of the title compound, C(10)H(8)N(2)·C(8)H(7)NO(4), contains two half-mol-ecules, which constitute a 1:1 co-crystal. The 2-amino-terephthalic acid mol-ecule is situated on an inversion center being disordered between two orientations in a 1:1 ratio. In the 4,4'-bipyridine mol-ecule, which is situated on a twofold rotational axis, the two pyridine rings form a dihedral angle of 37.5 (1)°. In the crystal, mol-ecules are held together via inter-molecular N-H⋯O and O-H⋯N hydrogen bonds. The crystal packing exhibits π-π inter-actions between the aromatic rings with a centroid-centroid distance of 3.722 (3) Å.

Bis[3-(meth-oxy-carbon-yl)anilinium] hexa-chloridostannate(IV).

In the title compound, (NH(3)C(6)H(4)CO(2)CH(3))(2)[SnCl(6)], the anions are situated on inversion centers so the asymmetric unit contains one cation and one half-anion. In the crystal, inter-molecular N-H⋯Cl and N-H⋯O hydrogen bonds link the cations and anions into layers parallel to the ac plane. The crystal packing exhibits voids of 37 Å(3).

Bis(4-acetyl-anilinium) hexa-chlorido-stannate(IV).

In the title compound, (C(8)H(10)NO)(2)[SnCl(6)], the Sn(IV) atom exists in an octa-hedral coordination environment. In the crystal, inter-molecular N-H⋯O and N-H⋯Cl hydrogen bonds link the cations and anions into a three-dimensional framework.

Study of pitting corrosion inhibition effect on aluminum alloy in seawater by biomineralized film.

Metallic materials can be easily corroded in marine environments, in which pitting corrosion is very common. In this study, we investigated the effect of Bacillus subtilis, isolated from the South China Sea on the corrosion behavior of 2A14 aluminum alloy in seawater. Surface analysis of the alloy in the presence of the bacteria was used to observe corrosion morphology and the corrosion products studied. Electrochemical method was used to analyze the corrosion susceptibility of the alloy in seawater in the presence of the bacteria. Surface analysis suggested that a protective film with CaMg(CO3)2 was gradually formed on the surface of the alloy in the presence of the bacteria. The electrochemical results showed that the radius of the impedance arc of the alloy immersed in seawater with bacteria increased gradually with time. The bacteria promoted the formation of the CaMg(CO3)2 film, which blocked seawater from the alloy and consequently, inhibited pitting corrosion.

Effect of Conducting Polyaniline/Graphene Nanosheet Content on the Corrosion Behavior of Zinc-Rich Epoxy Primers in 3.5% NaCl Solution.

The corrosion behavior of zinc-rich epoxy primers or paints (ZRPs) with different conducting polyaniline-grafted graphene (PANI/Gr) contents was investigated. Conductivity of the formed PANI/Gr nanosheets was significantly improved by employing the Gr as the inner template to synthesize the PANI. The protective properties and electrochemical behavior of coatings with artificial defects were investigated by monitoring the free corrosion potential versus time and by using localized electrochemical impedance spectroscopy (LEIS). A synergetic enhancement of the physical barrier role of the coating and the zinc sacrificial cathodic protection was achieved in the case of ZRP including PANI/Gr nanosheets. In addition, the ZRP mixed with the PANI/Gr at a content of 0.6% exhibited the best anticorrosion performance across the range of investigated PANI/Gr contents.

Bacillus subtilis Inhibits Vibrio natriegens-Induced Corrosion via Biomineralization in Seawater.

The marine bacterium, Vibrio natriegens, grows quickly in a marine environment and can significantly accelerate the corrosion of steel materials. Here, we present an approach to inhibit V. natriegens-induced corrosion by biomineralization. The corrosion of steel is mitigated in seawater via the formation of a biomineralized film induced by Bacillus subtilis. The film is composed of extracellular polymeric substances (EPS) and calcite, exhibiting stable anti-corrosion activity. The microbial diversity and medium chemistry tests demonstrated that the inhibition of V. natriegens growth by B. subtilis was essential for the formation of the biomineralized film.

catena-Poly[[bis-[(2-carboxy-benzoato-κO)silver(I)](Ag-Ag)]bis-(µ-isonicotinic acid-κN:O)].

The title compound, [Ag(C(8)H(5)O(4))(C(6)H(5)NO(2))](n), contains one Ag(I) atom, one phthalate ligand and one isonicotinic acid mol-ecule in the asymmetric unit. Each Ag atom is three-coordinated in a T-shaped geometry by two O atoms and one N atom from one phthalate ligand and two isonicotinic acid ligands. The isonicotinic acid ligand bridges two Ag atoms, forming a one-dimensional chain. Adjacent chains are linked by Ag-Ag inter-actions, leading to a double-chain. These double-chains are further linked via hydrogen bonds into a two-dimensional layer.