Electrochemical anodic oxidation assisted fabrication of memristors

Owing to the advantages of simple structure,low power consumption and high-density integration,memristors or memristive devices are attracting increasing attention in the fields such as next generation non-volatile memories,neuromorphic computation and data encryption.However,the deposition of memristive films often requires expensive equipment,strict vacuum conditions,high energy consumption,and extended processing times.In contrast,electrochemical anodizing can produce metal oxide films quickly(e.g.10 s) under ambient conditions.By means of the anodizing technique,oxide films,oxide nanotubes,nanowires and nanodots can be fabricated to prepare memristors.Oxide film thickness,nanostructures,defect concentrations,etc,can be varied to regulate device performances by adjusting oxidation parameters such as voltage,current and time.Thus memristors fabricated by the anodic oxidation technique can achieve high device consistency,low variation,and ultrahigh yield rate.This article provides a comprehensive review of the research progress in the field of anodic oxidation assisted fabrication of memristors.Firstly,the principle of anodic oxidation is introduced;then,different types of memristors produced by anodic oxidation and their applications are presented;finally,features and challenges of anodic oxidation for memristor production are elaborated.

Phenol degradation by anodic oxidation on boron-doped diamond electrode combining TiO_2 Photocatalysis

Boron-doped diamond （BDD） electrocatalysis is combined with photocatalysis using titanium dioxide （TiO2） as a catalyst to improve pollutant-oxidation efficiency. Phenol solution is chosen as model wastewater. Different methods involving BDD and/or TiO2 during the degradation processes are compared. Parameters such as the currency density and initial concentration are varied in order to determine their effects on the oxidation process. Moreover, the degradation kinetics of phenol is experimentally studied. The results reveal the superiority of series combination of BDD and TiO2, especially the treatment process of electrocatalysis and succedent photocatalysis, and the optimum working currency density for electrocatalysis is 25.48 mA/cm2. The removal rate decreases with the increase in the initial phenol concentration and the degradation reaction follows quasi-first-order kinetics equation.

Effect of intermetallic phases on the anodic oxidation and corrosion of 5A06 aluminum alloy

Intermetallic phases were found to influence the anodic oxidation and corrosion behavior of 5A06 aluminum alloy. Scattered in- termetallic particles were examined by scanning electron microscopy （SEM） and energy dispersive spectroscopy （EDS） after pretreatment. The anodic film was investigated by transmission electron microscopy （TEM）, and its corrosion resistance was analyzed by electrochemical impedance spectroscopy （EIS） and Tafel polarization in NaC1 solution. The results show that the size of A1-Fe-Mg-Mn particles gradually decreases with the iron content. During anodizing, these intermetallic particles are gradually dissolved, leading to the complex porosity in the anodic film beneath the particles. After anodizing, the residual particles are mainly silicon-containing phases, which are embedded in the an- odic film. Electrochemical measurements indicate that the porous anodic film layer is easily penetrated, and the barrier plays a dominant role in the overall protection. Meanwhile, self-healing behavior is observed during the long immersion time.

Photocatalytic activity of porous TiO_2 films prepared by anodic oxidation

Anatase titanium dioxide is an active photocatalyst, however, it is difficult to be immobilized on the substrate. The crystalline TiO2 porous film was prepared directly on the surface of pure titanium by anodic oxidation. The film was then used for photocatalysis via the methyl orange degradation method. The effects of anodization voltage, pH value, TiO2 film area and degradation time on the photocatalyst were investigated respectively by UV-visible spectrum. It was indicated that the TiO2 film prepared by anodic oxidation at 140 V had the best photocatalysis capability and the degradation of methyl orange was accelerated with acid addition.

Electrochemical incineration of dimethyl phthalate by anodic oxidation with boron-doped diamond electrode

The anodic oxidation of aqueous solutions containing dimethyl phthalate （DMP） up to 125 mg/L with sodium sulfate （Na2SO4） as supporting electrolyte within the pH range 2.0-10.0 was studied using a one-compartment batch reactor employing a boron-doped diamond （BDD） as anode. Electrolyses were carded out at constant current density （1.5-4.5 mA/cm^2）. Complete mineralization was always achieved owing to the great concentration of hydroxyl radical （-OH） generated at the BDD surface. The effects of pH, apparent current density and initial DMP concentration on the degradation rate of DMP, the specific charge required for its total mineralization and mineralization current efficiency were investigated systematically. The mineralization rate of DMP was found to be pH-independent and to increase with increasing applied current density. Results indicated that this electrochemical process was subjected, at least partially, to the mass transfer of organics onto the BDD surface. Kinetic analysis of the temporal change of DMP concentration during electrolysis determined by High Performance Liquid Chromatography （HPLC） revealed that DMP decay under all tested conditions followed a pseudo first-order reaction. Aromatic intermediates and generated carboxylic acids were identified by Gas Chromatography- Mass Spectrometry （GC-MS） and a general pathway for the electrochemical incineration of DMP on BDD was proposed.

Preparation and crystalline phase of a TiO_2 porous film by anodic oxidation

Anatase titanium dioxide is an active photocatalyst, but it is difficult to immobilize on the substrate. A crystalline TiO2 porous film was prepared directly on the surface of pure titanium by anodic oxidation in this work. Constant voltage and constant current anodic oxidation were adopted with sulphuric acid used as the electrolyte, pure titanium as the anode and copper as the cathode. The morphology and structure of the porous film on the substrate were analyzed with the aid of Field Emission Scanning Electron Microscopy （FESEM） and X-ray Diffraction （XRD）. The effects of the parameters of anodic oxidation （such as voltage, the concentration of sulphuric acid, anodization time and current density） on the aperture and the crystalline phase of the TiO2 porous film were systematically investigated. The results indicate that the increase of current density facilitates the augment of the aperture and the generation of anatase and mille. In addition, the forming mechanism of anatase and mille TiO2 porous films was discussed.

A Study on the Relationship between Anodic Oxidation and the Thermal Load on the Aluminum Alloy Piston of a Gasoline Engine

In order to analyze the influence of the anodizing process on the thermal load of an aluminum alloy piston,dedicated temperature tests have been carried out using the Hardness Plug method and the results for the anodized piston have been compared with those obtained separately for an original aluminum piston.In addition,numerical simulations have been conducted to analyze the temperature field and thermal stress distribution.Simulations and experiments show that the maximum temperature of the anodized piston is 16.36%and 5.4%smaller than that of the original piston under the condition of maximum torque and maximum power,respectively.The thermal stress of the temperature field of both pistons is within 50 Mpa,which meets the strength requirements of the material at high temperature.However,the area with significant thermal stress of the anodized piston is significantly smaller than that of the original piston.Combined with the fatigue analysis data,it can be seen that the safety factor of the anodized piston greater than 1.8 is 99.13%.Therefore,adopting the anodizing process not only reduces the piston thermal load,but also helps to extend its life and improve its reliability.

Evolution of insoluble eutectic Si particles in anodic oxidation films during adipic–sulfuric acid anodizing processes of ZL114A aluminum alloys

The effects of insoluble eutectic Si particles on the growth of anodic oxide films on ZL114A aluminum alloy substrates were in- vestigated by optical microscopy （OM） and scanning electron microscopy （SEM）. The anodic oxidation was performed at 25℃ and a con- stant voltage of 15 V in a solution containing 50 g/L sulfuric acid and 10 g/L adipic acid. The thickness of the formed anodic oxidation film was approximately 7.13 μm. The interpore distance and the diameters of the major pores in the porous layer of the film were within the ap- proximate ranges of 10~20 nm and 5-10 nm, respectively. Insoluble eutectic Si particles strongly influenced the morphology of the anodic oxidation films. The anodic oxidation films exhibited minimal defects and a uniform thickness on the ZL114A substrates; in contrast, when the front of the oxide oxidation films encountered eutectic Si particles, defects such as pits and non-uniform thickness were observed, and pits were observed in the films.

Calcination/acid-activation treatment of an anodic oxidation TiO_2/Ti film catalyst

The aim of this work was to investigate the effects of calcination/acid-activation on the composition, structure, and photocatalytic （PC） reduction property of an anodic oxidation TiO2/Ti film catalyst. The surface morphology and phase composition were examined by scanning electron microscopy and X-ray diffraction. The catalytic property of the film catalysts was evaluated through the removal rate of potassium chromate during the PC reduction process. The results showed that the film catalysts were composed of anatase and rutile TiO2 with a micro-porous surface structure. The calcination treatment increased the content of TiO2 in the film, changed the relative ratio of anatase and rutile TiO2, and decreased the size of the micro pores of the film catalysts. The removal rate of potassium chromate was related to the technique parameters of calcination/acid-activation treatment. When the anodic oxidation TiO2/Ti film catalyst was calcined at 873 K for 30 min and then acid-activated in the concentrated H2SO4 for 60 min, it presented the highest catalytic property, with the removal rate of potassium chromate of 96.3% during the PC reduction process under the experimental conditions.

MESO-SUBSTITUTION REACTION OF ZINC OCTAETHYLPORPHYRIN VIA ANODIC OXIDATION

meso-Nitration,chlorination and acetoxylation of ZnOEP via anodic oxidation are reported to proceed via EE'C,ECE and EE'C mechanism respectively.

Science Letters:Anodic oxidation of salicylic acid at Ta/BDD electrode

Boron-doped diamond （BDD） film electrodes using Ta as substrates were employed for anodic oxidation of salicylic acid （SA）. The effects of operational variables including initial concentration, current density, temperature and pH were examined. The results showed that BDD films deposited on the Ta substrates had high electrocatalytic activity for SA degradation. There was little effect ofpH on SA degradation. The current efficiency （CE） ,aas fbund to be dependent mainly on the initial SA concentration, current density and temperature. Chemical oxygen demand （COD） was reduced from 830 mg/L to 42 mg/L under a current density of200A/m^2 at 30℃.

Improving electrochemical properties of carbon paper as negative electrode for vanadium redox battery by anodic oxidation

Anodic oxidation with different electrolyte was employed to improve the electrochemical properties of carbon paper as negative electrode for vanadium redox battery(VRB).The treated carbon paper exhibits enhanced electrochemical activity for V^2+/V^3+redox reaction.The sample(CP-NH3)treated in NH3 solution demonstrates superior performance in comparison with the sample(CP-NaOH)treated in NaOH solution.X-ray photoelectron spectroscopy results show that oxygen-and nitrogen-containing functional groups have been introduced on CP-NH3 surface by the treatment,and Raman spectra confirm the increased surface defect of CP-NH3.Energy storage performance of cell was evaluated by charge/discharge measurement by using CP-NH3.Usage of CP-NH3 can greatly improve the cell performance with energy efficiency increase of 4.8%at 60 mA/cm^2.The excellent performance of CP-NH3 mainly results from introduction of functional groups as active sites and improved wetting properties.This work reveals that anodic oxidation is a clean,simple,and efficient method for boosting the performance of carbon paper as negative electrode for VRB.

Synthesis of Micron-sized Hexagonal and Flowerlike Nanostructures of Lead Oxide (PbO_2) by Anodic Oxidation of Lead

Micron sized hexagon- and flower-like nanostructures of lead oxide（α-PbO2） have been synthesized by very simple and cost effective route of anodic oxidation of lead sheet. These structures were easily obtained by the simple variation of applied voltage from 2-6 V between the electrodes. Lead sheet was used as an anode and platinum sheet served as a cathode. Anodic oxidation at 2 V resulted in the variable edge sized（1-2 μm） hexagon-like structures in the electrolyte. When the applied potential was increased to 4 V a structure of distorted hexagons consisting of some flower-like structures were obtained. Further increment of potential up to 6 V resulted in flower like structures of α-PbO2 having six petals. The diameter of the flower-like structures was 200-500 nm and the size of a petal was 100-200 nm.

Application of Anodic Oxidation with Graphite Electrodes in Pretreated Leachates

Currently, landfills are the main method used for the final disposal of urban solid waste. The degradation processes that waste goes through in these sites, alongside rainwater that percolates through them, generate highly polluting liquids (leachate). In the treatment of leachate, advanced oxidation processes (AOP) can significantly reduce the concentrations of different pollutants. Due to the high documented potential around AOPs, in this study, the effectiveness of anodic oxidation in the removal of the remaining organic load in leachates pretreated in a biological system was evaluated. Graphite electrodes were used as anode and cathode. The efficiency of anodic oxidation, in terms of the removal of chemical oxygen demand (COD) and color, was evaluated under different current densities (7, 12, 17 and 22 mA/cm2) and pH values (3, 4.5 and 6). Under the best conditions found (22 mA/cm2 and pH of 6) and with an oxidation time of 5 hours, a maximum removal of 68% in COD and 91% in color was achieved, which represented a quality in the final effluent of 271 mg/L and 151 Pt-Co in COD and color, respectively. Therefore, considering that graphite is an economic and widely available material, the results obtained show anodic oxidation, with the use of graphite electrodes, as a technically viable alternative as a final purification stage for pretreated leachates.

Influence of oxidation heat on hard anodic film of aluminum alloy

The special experimental device and sulfuric acid electrolyte were adopted to study the influence of anodic oxidation heat on hard anodic film for 2024 aluminum alloy. Compared with the oxidation heat transferred to the electrolyte through anodic film, the heat transferred to the coolant through aluminum substrate is more beneficial to the growth of anodic film. The film forming speed, film thickness, density and hardness are significantly increased as the degree of undercooling of the coolant increases. The degree of undercooling of the coolant, which is necessary for the growth of anodic film, is related to the degree of undercooling of the electrolyte, thickness of aluminum substrate, thickness of anodic film, natural parameters of bubble covering and current density. The microstructure and performance of the oxidation film could be controlled by the temperature of the coolant.

A kind of double-sided porous anodic alumina membrane fabricated with the three-step anodic oxidation method

The porous anodic alumina membranes （PAAMs） have been successfully used as templates for the fabrication of functional nano-materials due to their outstanding regularity and physicochemical properties. In this paper, a transparent double-sided anodic alumina membrane with ultra-thin aluminum substrate was fabricated with the three-step anodic oxidation method in the oxalic acid electrolyte. The characters such as the top-surface morphology, membrane thickness, and depth of nanopores of this three-layer （A1203-A1-A1203） sandwiched nano-structure were controllable through regulating the main anodic oxidation conditions, e.g., anodic oxidation time of various steps, coating remove process. The experiments data revealed that the aluminum substrate is exponential declined with the oxidation time when it was approximately reduced by a few micrometers. This new double-sided anodic alumina membrane can be used as the high-quality functional field emission materials and templates.

Nickel-free sealing technology for anodic oxidation film of aluminum alloy at room temperature

Different additives were added into the potassium fluorozirconate solution to prepare different nickelfree sealing reagents,with which the anodic oxidation film of aluminum alloy was sealed at room temperature.The phosphor chromic acid weight loss method was used to evaluate the sealing effects.Using electron scanning microscopy(SEM),the surface and cross-sectional micromorphologies of the anodic oxidation films sealed by different fluorozirconate sealants were observed.The position and state of zirconium element distribution in the film hole were investigated by the further quantitative and distribution analysis of Zr element.This study provides an experimental evidence for the theoretical studies of fluorozirconate-sealed anodic oxidation films.It is shown that the fluorozirconate has good sealing effects and has a wide prospect for sealing the aluminum alloy samples.Its products were highly corrosion resistant,and were filled in the openings of the micropores in the oxide film.

A green and efficient access to aryl nitriles via an electrochemical anodic oxidation

The nitrile functionality is a key building block in synthetic chemistry, and has wide applications in pharmaceuticals. However, traditional methodologies for the synthesis of nitriles are limited to harsh reaction conditions. Herein, we report a new and efficient access to aryl nitriles by an electrochemical synthesis. Compared with the conventional synthetic methods, this electrochemical synthesis is more environmentally friendly and easier to handle.

Improvement in antibacterial ability and cell cytotoxicity of Ti-Cu alloy by anodic oxidation

Ti-Cu alloy has potential to be used in plastic surgery and dental implants due to its strong antibacterialproperties,high strength and good corrosion resistance.In this paper,Ti-5Cu was anodic-oxidized to enhance the surface compatibility.The influence of the oxidation on the corrosion resistance,antibacterial properties and biological properties was investigated.X-ray diffraction(XRD)and X-ray photoelectron spectroscopy(XPS)results showed that a double-layer oxide coating with dense inner layer and porous outside layer was formed on Ti-Cu sample.The oxide coating consisted mainly of TiO2,CuzO and small amount of CuO,improved the corrosion resistance of Ti-Cu alloy by one order of magnitude due to the formation of the dense oxide inner layer,but high Cu ion release was detected.The plate count results showed that the antibac-terial activity of Ti-Cu sample was improved to≥99%due to the comprehensive function of CuO and Cu_(2)O in the coating and Cu^(2+)release.Cell test results showed that thecoating exhibited good cell compatibility,the porous sur-face structure improved the adhesion of cells,and Cu ion release promoted the cell proliferation.

Anodic oxidation of azo dye C.I. Acid Red 73 by the yttrium-doped Ti/SnO2-Sb electrodes

This work was conducted to study the ability of anodic oxidation of azo dye C.I. Acid Red 73 （ART3） using the yttrium-doped Ti/SnO2-Sb electrodes. The effects of Sb doping level, yttrium doping level, thermal decomposition temperature and cycle times of dip-coating thermal decomposition on the properties of the electrodes were investigated. The results showed that the excellent electrochemical activity of Ti/SnO2-Sb-Y electrode can be achieved at a 7：1 molar ratio of Sn：Sb and thermal decomposition temperature of 550~C. Moreover when the cycle times of dip-coating and thermal decomposition were up to 10 times, the performance of the electrode tends to be stable. The Ti/SnO2-Sb electrodes doped with yttrium （0.5 tool-%） showed the most excellent electrochemical activity. In addition, the influences of operating variables, including current density, initial pH, dye concentration and support electrolyte, on the colour removal, chemical oxygen demand （COD） removal and current efficiency were also investigated. Our results confirmed that the current efficiency increased with the concentrations of dye and sodium chloride. Moreover, increasing the current density and the initial pH would reduce the current efficiency.