Electrolytic Method Research Articles

Effect of Chemical Polishing on the Formation of TiO2 Nanotube Arrays Using Ti Mesh as a Raw Material

As a unique form of TiO2, TiO2 nanotube arrays (TiO2NTAs) have been widely used. TiO2NTAs are usually prepared by Ti foil, with little research reporting its preparation by Ti mesh. In this paper, TiO2NTAs are prepared on a Ti mesh surface via an anodic oxidation method in the F-containing electrolyte. The optimal parameters for the synthesis of TiO2NTAs are as follows: the solvent is ethylene glycol and water; the electrolyte is NH4F (0.175 mol/L); the voltage is 20 V; and the anodic oxidation time is 40 min without chemical polishing. However, there is a strange phenomenon where the nanotube arrays grow only at the intersection of Ti wires, which may be caused by chemical polishing, and the other areas, where TiO2NTAs cannot be observed on the surface of Ti mesh, are covered by a dense TiO2 film. New impurities (the hydrate of TiO2 or other products) introduced by chemical polishing and attaching to the surface of the Ti mesh reduce the current of anodic oxidation and further inhibit the growth of TiO2 nanotubes. Hence, under laboratory conditions, for commercially well-preserved Ti mesh, there is no necessity for chemical polishing. The formation of TiO2NTAs includes growth and crystallization processes. For the growth process, F− ions corrode the dense TiO2 film on the surface of Ti mesh to form soluble complexes ([TiF6]2−), and the tiny pores remain on the surface of Ti mesh. Given the basic photoelectrochemical measurements, TiO2NTAs without chemical polishing have better properties.

Investigation of the influence of electrolytic milling machining parameters on the machining accuracy of thin-walled parts

Aircraft parts are often designed as thin-walled structures to reduce the weight of the aircraft. However, thin-walled structures are prone to deformation during the milling process, leading to a decrease in machining accuracy. To address this problem, a method combining milling and electrochemical machining, known as electrolytic milling, is proposed to minimize deformation and enhance the accuracy of thin-walled parts. The factors that affect the machining accuracy of electrolytic milling were analysed, and a model for predicting the thickness of the material removed was established. Electrolytic milling experiments were designed, and the model was solved. Based on the built model, the influences of feed rate, spindle speed, radial cutting depth, voltage and electrolyte concentration on material removal thickness were investigated. Compared with the milling method, the electrolytic milling method can improve the machining accuracy of thin-walled parts. Electrolytic milling experiments were conducted on box-shaped parts to verify the reliability of the proposed method.

Towards sustainable energy: a comprehensive review on hydrogen integration in renewable energy systems

As the world shifts towards sustainable energy sources, incorporating hydrogen into renewable energy systems emerges as a critical pathway. This thorough analysis delves deeply into the various facets of hydrogen integration, exploring its potential to revolutionize the energy landscape. Drawing upon recent advancements and research findings, the review examines the production, storage, and utilization of hydrogen within renewable energy frameworks. Key topics include electrolysis methods, storage technologies, and diverse applications spanning transportation, residential sectors, and industry. Furthermore, the review examines the obstacles and prospects linked with hydrogen integration, shedding light on policy frameworks, economic implications, and technological innovations driving its adoption. By offering insights into the multifaceted role of hydrogen, this review aims to inform researchers, stakeholders, and policymakers about the transformative potential of integrating green hydrogen into renewable energy systems for a sustainable future.

A Dual Effect Additive Modified Electrolyte Strategy to Improve the Electrochemical Performance of Zinc-Based Prussian Blue Analogs Energy Storage Device.

Prussian blue analogs (PBA) exhibit excellent potential for energy storage due to their unique three-dimensional open framework and abundant redox active sites. However, the dissolution of transition metal ions in water can compromise the structural integrity of PBAs, leading to significant issues such as low cycle life and capacity decay. To address these challenges, we proposed a dual-effect additive-modified electrolyte method to alleviate such issues, introducing sodium ferrocyanide (Na4Fe(CN)6) into aqueous alkaline electrolytes. It could not only capture Zn2+ dissolved on the surface of Na1.86Zn1.46[Fe(CN)6]0.87 (ZnHCF) electrode material during the cycling process but also conduct redox reactions on the electrode surface to provide additional capacitance. Through experiments and molecular simulation calculations, it showed that Na4Fe(CN)6 can restrict the movement of Zn dissolution into the electrolyte on the electrode surface. Based on this, an asymmetric supercapacitor based on ZnHCF//activated carbon was assembled with a modified electrolyte. The assembled supercapacitor displayed a specific capacitance of 1,329.65 mF cm-2, a power density of 2,900 mW cm-2, and an energy density of 388.28 mW h cm-2. This study provides a new idea for the design and construction of stable and efficient PBA energy storage materials by inhibiting the leaching of transition metals in PBA.

Measurement of Pt consumption from Pt electrodes during water electrolysis using the quartz crystal microbalance (QCM) method: Effect of the water electrolysis method and the concentration of chloride ions in the aqueous solution

The consumption of the Pt electrocatalyst, which occurs when aqueous solution with neutral pH is electrolyzed with a Pt electrode to produce hydrogen or oxygen, was measured from the change in resonance frequency using the QCM method. First, it was found that the Pt consumption from the electrode during water electrolysis while applying a steady positive potential was very small, but it was almost proportional to the time the current was applied. Second, when electrolysis was performed by polarity reversal electrolysis of the anode and cathode periodically during electrolysis, the amount of Pt consumed increased in proportion to the number of polarity reversal was exchanged. The Pt consumption obtained by the QCM method was in close agreement with the value obtained by EDX method, proving the validity of the measurement method. The QCM measurement method was also proven to be a reliable method of measurement.

Technological Methods and Equipment for Plasma-Electrolytic Processing of Metals and Alloys

The proposed review presents the results of the analysis of the equipment and technological methods for implementing the plasma electrolytic chemical-thermal treatment and plasma electrolytic polishing. A group of methods based on the immersion of workpieces in an electrolyzer was considered, as well as a method of a local treatment by the jet feed of an electrolyte to the area of the surface being treated. The influence of the design and characteristics of the electrolyzer, the power source and the system for feeding the work-piece into the electrolyte on the specifics of plasma electrolytic treatment methods is shown. Technological methods improving the quality and productivity of treatment are considered. Limitations in the applicability of the existing equipment were revealed, and the prospects for the improvement in the field of development of equipment and technologies for plasma electrolytic treatment were determined.

Influence of Electrolyte Molarity and Applied Voltage on the Purification of Ferronickel by Electrolysis Method

The current advancements in the automotive industry highlight the critical need for electric vehicles, which require a reliable supply of nickel for battery production. A potential nickel source is Ferronickel's local content, which can be used as a secondary resource. However, research on converting smelted Ferronickel into electrolytic nickel is still limited. This study aims to examine the effects of electrolyte molarity and applied voltage during the electrolysis process for refining Ferronickel. The molarities of HCl employed in this research are 0.1, 0.25, 0.5, 0.75, and 1 M for 2 hours. Additionally, the molarities of HCl are set at 2, 3, and 4 M for 6 hours. Further experiments were performed using varying voltages of 1, 2, 4, 6, and 8 V while keeping the solution concentration constant at 1 M and maintaining an electrolysis duration of 2 hours. The electrolysis solution was subsequently analyzed using the AAS (atomic absorption spectrophotometry) test. The results indicated that higher molarity levels were associated with increased current, resulting in faster reaction rates and greater solubilization of nickel metal. The Ni concentration rose with higher molarity, increasing from 76.50 mg/L in .25 M HCl to 91.88 mg/L in 1 M HCl. In contrast, the Fe concentration remained nearly constant across various molarity levels, ranging from 11.81 mg/L in .25 M HCl to 11.95 mg/L in 1 M HCl, suggesting a minimal influence of molarity below 1 M. Fe exhibited a strong positive correlation with increasing electrolyte molarity, showing a significant rise in concentration from 49.06 g/L at 2 M to 90.17 g/L at 4 M. Ni showed a more modest response to elevated molarity, with concentrations increasing from 11.95 g/L at 2 M to 22.70 g/L at 4 M. The Ni concentration increased with the applied voltage up to 6 V, reaching 95.57 mg/L, but then decreased to 77.67 mg/L at 8 V, indicating that the optimum voltage is 6 V. The Fe concentration displayed slight fluctuations but remained relatively stable across different voltage levels, measuring 11.81 mg/L at 1 V and 12.28 mg/L at 8 V, indicating that the applied voltage does not significantly influence Fe concentration in the solution.

Enhance Hydrogen Production from Water Using 532 Lasers

ABSTRACT: hydrogen production via water electrolysis under the influence of laser sounds fascinating with its unique properties, was particularly effective in promoting hydrogen production. The mechanism by which the laser promotes hydrogen production The electrolytic cell used in this work contains 270 ml of distilled water stimulated with different amounts of alcohol (2 ml - 4 ml - 6 ml - 8 ml - 10 ml). This chamber consists of two vertically oriented cylinders. Inside each cylinder there are graphite electrodes, each measuring 10 x 5 x 7 mm3, connected to the positive and negative terminals of a direct current power source, in addition to using a green laser source (532). An efficiency study was conducted using a green laser with a wavelength of 532 nanometers as an optical light source for water analysis through electrolysis. Results were obtained using both the standard electrolysis method and with the green laser source (532 nm). In the case of standard electrolysis, we obtained (When adding 5 ml of cohol, we get 6.63 hydrogen ), while (Adding 10 ml of ill we get 7.44 of hydrogen ) was obtained when using the laser source. The results indicate that using the laser source enhances hydrogen production significantly compared to standard electrolysis, demonstrating the laser's high effectiveness in electrolysis due to its non-absorptive property in water. This could have significant implications for renewable energy and hydrogen fuel production.

APPLICATION OF ELECTROLYTIC PLASMA HARDENING FOR IMPROVING THE PROPERTIES OF MACHINE PARTS MADE OF STEEL 45

This study examined the effect of electrolytic plasma hardening (EPH) on the properties of 45-grade steel, which can serve as an alternative to traditional heat treatment methods used before the release of finished products. The results of the experiments showed that the mechanical and operational properties of 45-grade steel significantly improved after the application of EPH. Steel 45, widely used in mechanical engineering and agricultural machinery production due to its strength characteristics and durability, demonstrated a significant increase in performance after treatment. It was observed that the properties of 45- grade steel improved considerably after applying electrolytic plasma hardening methods, with the hardness of the samples increasing by 3.1-3.62 times, and wear resistance improving by 7 times. Moreover, the study highlighted the economic efficiency of the proposed treatment method, showing that the introduction of EPH can lead to a significant reduction in material costs, extended product life, and improved environmental performance by reducing energy consumption and emissions. The use of a non-toxic 20% sodium carbonate solution in EPH contributed to the uniform distribution of electric current in the cell and allowed for achieving optimal cooling rates of the sample.

Phosphate Ion-Selective Electrode Based on Electrochemically Modified Iron.

The significance of the detection of phosphate ions is immense in the realms of chemistry, biology, medicine, environment, and industry. The detection of phosphate ions is currently mainly reliant on blue molybdenum colorimetry, which is accurate but requires sample pretreatment, intricate operation, and a high price tag. Consequently, it is essential to create a sensor with superior efficiency, precision, straightforward functioning, and instantaneous online detection. This study has designed and created an electrochemical modification based on an iron metal electrode for this purpose. Cyclic voltammetry was used to initially ascertain the potential (-0.57 V) necessary for constant potential electrolysis. Employing a constant potential electrolysis method, the iron oxide and its phosphate were modified onto the surface of the iron electrode to enable reaction with phosphate ions. Scanning electron microscopy and energy dispersive X-ray spectroscopy were used to characterize and analyze the morphology and elemental composition of Fe-PME, elucidating how it responds to phosphate ionation. The two-electrode system was then utilized for the evaluation of the phosphate ion response of Fe-PME at pH 4. Fe-PME's response to phosphate ions is demonstrated by the results, ranging from 10-5 to 0.1 M and with a slope of -52.8 mV dec-1. Fe-PME exhibited satisfactory results when compared to the conventional blue colorimetry of molybdenum.

Neuroelectrophysiology-compatible electrolytic lesioning.

Lesion studies have historically been instrumental for establishing causal connections between brain and behavior. They stand to provide additional insight if integrated with multielectrode techniques common in systems neuroscience. Here, we present and test a platform for creating electrolytic lesions through chronically implanted, intracortical multielectrode probes without compromising the ability to acquire neuroelectrophysiology. A custom-built current source provides stable current and allows for controlled, repeatable lesions in awake-behaving animals. Performance of this novel lesioning technique was validated using histology from ex vivo and in vivo testing, current and voltage traces from the device, and measurements of spiking activity before and after lesioning. This electrolytic lesioning method avoids disruptive procedures, provides millimeter precision over the extent and submillimeter precision over the location of the injury, and permits electrophysiological recording of single-unit activity from the remaining neuronal population after lesioning. This technique can be used in many areas of cortex, in several species, and theoretically with any multielectrode probe. The low-cost, external lesioning device can also easily be adopted into an existing electrophysiology recording setup. This technique is expected to enable future causal investigations of the recorded neuronal population's role in neuronal circuit function, while simultaneously providing new insight into local reorganization after neuron loss.

Engineering bioactive MWCNT-reinforced hydroxyapatite coatings on Ti29Nb5Zr alloy by plasma electrolytic oxidation method: A comprehensive approach to dental implant surface optimization

Titanium-niobium-zirconium (TiNbZr) alloys represent a promising class of newly developed titanium-based biomaterials, engineered to exhibit superior properties for biomedical applications. This study investigates the influence of hydroxylated multi-walled carbon nanotubes (MWCNTs) on the surface properties of hydroxyapatite coatings prepared by the plasma electrolytic oxidation (PEO) method for implant applications. The optimal concentration of MWCNTs in the PEO coating was determined based on the superior surface, electrochemical, and biological properties obtained. The incorporation of MWCNTs led to an enhancement in surface roughness from Ra 0.06 ± 0.02 to Ra 0.618 ± 0.03 µm, improved wettability with a decrease in contact angle from 63.03° ± 1.1–28.29° ± 0.07, and a reduction in elastic modulus from 77.20 ± 2.26 GPa to 54.50 ± 2.22 GPa. Furthermore, electrochemical corrosion resistance analysis revealed an increase in inner passivation resistance up to 2.24 × 10 ×7 Ω.cm2 with the addition of MWCNTs. Antibacterial activity analysis demonstrated that the optimal concentration of MWCNTs resulted in a 3.1-fold and 2.7-fold reduction in E. coli and S. aureus bacteria, respectively, compared to uncoated samples. Cell viability against MC3T3-E1 cells showed a 25 % higher viability with MWCNTs than uncoated substrates.

Multi-Dimensional Modelling of Bioinspired Flow Channels Based on Plant Leaves for PEM Electrolyser

The Polymer Electrolyte Membrane Water Electrolyser (PEMWE) has gained significant interest among various electrolysis methods due to its ability to produce highly purified, compressed hydrogen. The spatial configuration of bipolar plates and their flow channel patterns play a critical role in the efficiency and longevity of the PEM water electrolyser. Optimally designed flow channels ensure uniform pressure and velocity distribution across the stack, enabling high-pressure operation and facilitating high current densities. This study uses flow channel geometry inspired by authentic vine leaf patterns found in biomass, based on various plant leaves, including Soybean, Victoria Amazonica, Water Lily, Nelumbo Nucifera, Kiwi, and Acalypha Hispida leaves, as a novel channel pattern to design a PEM bipolar plate with a circular cross-section area of 13.85 cm2. The proposed bipolar design is further analysed with COMSOL Multiphysics to integrate the conservation of mass and momentum, molecular diffusion (Maxwell–Stefan), charge transfer equations, and other fabrication factors into a cohesive single-domain model. The simulation results showed that the novel designs have the most uniform velocity profile, lower pressure drop, superior pressure distribution, and heightened mixture homogeneity compared to the traditional serpentine models.

Аспекты безопасного использования современных дезинфицирующих средств на молочных предприятиях

The article analyzes the main aspects of safe application of chemical disinfectants widely used at dairy enterprises. Effective disinfection at dairy enterprises is directly related to the production of high-quality, safe and competitive food products. When selecting a disinfectant for use at a dairy enterprise, a comprehensive evaluation is necessary not only for effectiveness, but also a multilateral consideration of its safe use. Increasing requirements to ecologization of milk processing enterprises dictate the search for new combinations of functional components in the formulations of chemical sanitizers. The article shows the necessity of consideration of adhesion properties of disinfectants, their corrosive activity and indifference to various materials used at food processing enterprises. It is suggested to control working chloroactive disinfectant solutions, first of all, obtained by electrolysis method, not only by the content of active chlorine, but also by the value of redox potential. The relevance of research aimed at studying the inhibitory properties of active substances and residual quantities of disinfectants on starter microflora and the importance of a systematic approach to the integrated assessment of all elements of safe use of disinfectants at dairy enterprises is formulated. Keywords: disinfectants, toxicity and hazard, effect on human body, environmental safety, redox potential, corrosivity, chemical contamination, inhibition.

Surface Modification of Chromium–Nickel Steel by Electrolytic Plasma Nitriding Method

Electrolytic plasma nitriding is an attractive chemical heat treatment used to improve the surface properties of steel by implementing nitrogen saturation. This method is widely applied to steel and iron-based alloys operating under various operating conditions. In this work, using liquid-phase plasma nitriding technology, a nitrided layer was obtained on the surface of 40CrNi steel in electrolytes of different concentrations. The microstructure and phase composition of the nitrided layer were investigated and analyzed using scanning electron microscopy (SEM) and X-ray diffraction (XRD), and we performed Vickers hardness and wear resistance tests using the ball-on-disc method. The microhardness and wear resistance of nitrided 40CrNi steel were significantly improved due to the lubricating properties of the ε-Fe2N phase formed on its surface.

Study on separation and purification of titanium alloys (TC4-6Al-4V) by molten salt electrolysis

With the widespread expansion of titanium applications and its significant increase in usage, the issue of recycling titanium resources after consumption has emerged. Focusing on titanium alloys with high usage, such as TC4 (Ti-6Al-4V), this article proposes a titanium separation and recovery method based on molten salt electrolysis. This method thoroughly analyzes the characteristics of elements in TC4 and electrochemical principles, ensuring that vanadium in the TC4 alloy does not undergo electrochemical dissolution when the electrolysis potential is below 0.3 V vs Pt. Subsequently, through electrochemical analysis, it was discovered that the precipitation of aluminum ions is influenced by concentration. Therefore, by controlling the concentration of aluminum in the eutectic molten salt, such as increasing the electrolyte concentration and shortening the electrolysis time, the precipitation of aluminum can be effectively avoided. Under the experimental conditions mentioned above, vanadium elements deposit at the bottom of the crucible in the form of anode slime, while aluminum dissolves and remains in the electrolyte. Meanwhile, titanium ions in the cathode region undergo electron reduction and deposit in the cathode area in the form of titanium, thus achieving precise separation of alloy elements. Experimental verification shows that the purity of the obtained titanium reaches 99.17 atomic percent. Therefore, this molten salt electrolysis method, which combines the physical properties of alloy elements with electrochemical principles, not only provides a new perspective for the separation and recovery of titanium and other critical metals, but also offers new research directions for the recovery technology of other alloy elements.

A dual functional Co3O4 thin film with remarkable electrochromic and energy storage performance in the electrolytes of choline chloride and urea

The electrolyte layer plays an important role in ion transport in electrochromic devices, and the optimized preparation of efficient electrolytes can positively affect the conduction process on the electrode surface and at the electrode-electrolyte interface.In this study, we start from a green perspective while improving the performance. Combined with typical eutectic solvents: choline chloride and urea materials. A suitable ratio favorable for the reaction of Co3O4 film is explored and combined with sodium hydroxide, a traditional electrolyte, to enhance the electrochromic performance.The electrochromic and electrochemical properties of Co3O4 films prepared via the sol-gel method in the novel electrolyte were then evaluated. The results show that the performance has been greatly improved, the transmittance rate is 2.5 times higher than the original, the coloration efficiency is 5.8 times higher than the original, and it is more stable and has higher charging and discharging efficiency. This presents a promising avenue for the advancement of oxide films as bifunctional materials for electrochromism and energy storage. The newly developed electrolyte may prove beneficial in enhancing the performance and stability of electrochromic devices through the use of alkaline electrolytes.

Recovery of Zinc and Rhenium for the Production of Zinc Perrhenates

This study outlines findings from an investigation into the development of a hydrometallurgical process for manufacturing various forms of zinc perrhenate, entirely from waste from recycling and from the Zn–Pb industry. Scraps of Re-bearing Ni-based superalloys and acidic waste, circulating zinc solutions generated during the production of Zn by the electrolytic method and which contain >45 g/dm3 of Zn, Na, Mn, and Mg, were used in the research. In the publication, the conditions for the production of three types of zinc perrhenate, i.e., Zn(ReO4)2·4H2O, Zn(ReO4)2, and Zn(ReO4)2·2H2O, are presented. As a result of the analysis of the obtained results, it was concluded that to obtain the above-mentioned forms of zinc perrhenate, zinc carbonate can be used, precipitated from acidic, waste, and multi-component solutions after their prior neutralization to pH 4.0 and partial purification from Mn, Mg, and Na using metallurgical zinc oxide. Zinc carbonate should be precipitated using Na2CO3 at pH 6.3 and subsequently purified from other impurities, i.e., Mg, Na, and Mn, using aqueous ammonia solutions. As a result, zinc carbonate was obtained, which was used in a reaction with an aqueous solution of HReO4 to produce zinc perrhenate. The precipitated forms of Zn(ReO4)2 were obtained by appropriately drying the crude and hydrated Zn(ReO4)2 to obtain its tetrahydrate, dihydrate, and anhydrous forms, respectively, using drying temperatures of 55, 135, and 185 °C. The developed technology has been submitted for a patent and is an example of a technology founded on the principles of sustainable development, with a particular emphasis on the minimalization of loss of rhenium and zinc at all stages of its realization.

Zero-Gap Liquid Alkaline Water Electrolyzers: Challenges in Benchmarking and Directions for Development

Green hydrogen is expected to play a central role in the replacement of fossil energy sources, especially in difficult to decarbonize sectors of the economy. Currently, low temperature methods of electrolysis are the only commercially realized sources of green hydrogen. Liquid alkaline water electrolysis (LAWE) is the most widely utilized method of electrolysis, with a 100-year history of use. Given this lengthy history one could be forgiven for assuming that there is little development left. However, standard LAWE materials and cell designs do not achieve the production, efficiencies, and durability necessary to meet the anticipated demand for green hydrogen.To spur development in this neglected area of hydrogen production, the US Department of Energy, Hydrogen and Fuel Cell Technology Office (DOE-HFTO) added LAWE to its Hydrogen from Next-generation Electrolyzers of Water (H2NEW) Consortium. One of the main tasks for this part of the consortium is to benchmark and validate materials and cell components for LAWE. This includes the development of lab-scale cell hardware and test protocols that can be widely disseminated in the research community. The result of this work will be the development of the methods and materials necessary to achieve robust and reproducible datasets for the improvement of catalysts, separators, cell architecture and operation.We will present the status of the benchmarking effort. This will include a description and explanation of a lab-scale LAWE test station, electrolyte handling, and hydrogen safety. The requirements for the safe operation of an electolyzer using high concentration alkaline electrolytes differs significantly from more typical proton exchange, or anion exchange membrane systems. We will also discuss common sources of error that can significantly influence cell performance and result in poor reproducibility. Acknowledgement:This research is supported by the U.S. Department of Energy (DOE) Hydrogen and Fuel Cell Technologies Office through the Hydrogen from Next-generation Electrolyzers of Water (H2NEW) consortium.

Syntheses of Ni-Based Layered-Double Hydroxide Materials Via Liquid Phase Deposition Method for Alkaline Water Electrolysis

For the sustainable society, hydrogen production has received much attention during decades. The alkaline water electrolysis process has been recognized as one of the important processes for hydrogen products. For the achievements of an effective water electrolysis system, the decrease of the overpotential on the oxygen evolution reaction (OER), which is the four-electron and proton transfer process. These complex 4-electron sluggish processes lead to the large energy losses in the whole water electrolysis. Although the noble catalysts such as IrO2 or RuO2 exhibit high OER activity, their large-scale applications are limited due to cost problem. From this point of view, the low-cost transition metal materials, especially Ni-based catalysts, have been extensively studied. And also, it has been reported that the well-defined layered double hydroxide (LDH) structures can promote water oxidation through the interlayer anion effects. Despite this fact, the specific procedures for the preparation of Ni-based LDH structures have not been well established. Therefore, in this study, we have investigated the preparation of Ni-based LDH structures in the aqueous solution at room temperature, the so-called liquid phased deposition (LPD) method.Through the LPD method, we have synthesized various types of Ni-based LDH structures. As an example, the Ni-Al LDH structures were synthesized on the conductive substrate. It was found that our synthesized Ni-Al LDH exhibited relatively high OER activity and durability against electrochemical potential cycling [1]. In addition, the dependencies of the OER activity on the interlayer anion species were clearly demonstrated. In addition, the other types of Ni alloy LDHs were also prepared and their OER activity was investigated. Through the electrochemical measurements, we have confirmed the advantages of our materials prepared by LPD methods as an anode for alkaline water electrolysis.