Electrodeposition Of Nickel Research Articles

Investigation of the electrochemical conversion of brighteners during nickel electrodeposition, Part 1: chemical analysis by mass spectrometry

Investigation of the electrochemical conversion of brighteners during nickel electrodeposition, Part 1: chemical analysis by mass spectrometry

Electrochemistry of Nickelocene-Ferrocene Organometallic Complexes for Electrodeposition of Nickel–Iron–Based Nanostructured Film under Ambient Conditions for Oxygen Evolution Reaction

Electrochemistry of Nickelocene-Ferrocene Organometallic Complexes for Electrodeposition of Nickel–Iron–Based Nanostructured Film under Ambient Conditions for Oxygen Evolution Reaction

Electrolyte Solution Stirring Effect on Deposition Rate, Crystallographic Orientation, and Electrochemical Behaviour of Ni Film

Abstract Stirring the electrolyte meanwhile electrodeposition process is running may influence the properties of the forming films. In this work, the electrodeposition of copper (Cu) over aluminium (Al) alloy was performed. Subsequently, the electrodeposition of nickel (Ni) onto the formed Cu layer was conducted. In order to enhance the films properties, some various stirring speeds then are implied on the plating solution of the Ni electrodeposition process. The synthesized of Ni films were analysed by means of both X-ray diffraction (XRD) and a potentiostat equipment. The sample made shows different physical properties before and after electrodeposition based on sample weighed to examine the deposition rate. XRD patterns confirmed that all samples have a face-centered cubic (fcc) crystal structures with a space group of Fm-3m. Stirring speed play an important role of an inverse relationship with deposition rate, crystallite size, lattice strain, and corrosion rate. The sample that was made using the highest stirring speed yield a better corrosion resistance at around 0.239 mmpy due to less lattice strain.

The Multifaceted Role of Boric Acid in Nickel Electrodeposition and Electroforming

This study involved an investigation of the role of boric acid in nickel electroforming from sulfamate electrolytes, especially in relation to its ability to minimise interfacial pH changes during electrodeposition. Initial speciation calculations indicated that buffering by polyborate species and nickel-borate complexes are most likely responsible for this effect. However, the concentration of nickel-borate complexes was too low even at elevated pH to be a significant electroactive species. Polarisation and electrochemical quartz crystal microbalance measurements indicated that, in the absence of boric acid, electrodeposits typically contained Ni(OH)2, while boric acid additions resulted in pure Ni being deposited with a current efficiency approaching unity. Boric acid additions substantially modified the nickel and hydrogen partial currents, and influenced the overall current efficiency. Studies in nickel-free solutions indicated that boric acid adsorbs on the surface which explains the suppression of H2O reduction observed in the electroforming experiments. Collectively, solution buffering due to polyborate and nickel-borate species and inhibition of H2O reduction by adsorbed boric acid minimised interfacial pH changes and prevented the formation of nickel hydroxide.

Kinetics of Nucleation at the Electrodeposition of Zinc and Nickel from Ammonium Chloride Electrolytes

Kinetics of Nucleation at the Electrodeposition of Zinc and Nickel from Ammonium Chloride Electrolytes

Gluconate solutions for nickel electrodeposition and nickel electroless plating

Nickel electroplating has found a wide range of industrial applications as a technique for creating protective and decorative coatings of metallic and non-metallic surfaces, protecting materials against corrosion at elevated temperatures in both alkaline environments and organic acid solutions, forming a sublayer for obtaining coatings of other metals on steel, enhancing the hardness and wear resistance of surfaces, as well as for improving solderability. Such coatings can be obtained from weakly acidic aqueous and weakly alkaline complex electrolytes. In this review, we analyze the available literature on complexation of nickel(+2) with D-gluconate ion CH2OH(CHOH)4COO‾, along with that on compositions and some technological characteristics of complex D-gluconate solutions for nickel electrodeposition and electroless plating. Thus, a corrosion-resistant smooth light-colored nickel coating, tightly adhered to a copper substrate, was obtained from an electrolyte with a pH level of 8, containing 53 g/dm3 of NiSO4 •6H2O, 44 g/dm3 of D-C6H11O7Na, 25 g/dm3 of H3BO3, 53 g/dm3 of (NH4)2SO4, and 0.5–3 g/dm3 of CO(NH2)2, at a temperature of 25 °C, a cathodic current density of 2.5 A/dm2 with a current efficiency of 96.4%. An electroless Ni-P(3–18 wt%) alloy coating on copper was obtained from a solution with a pH level of 9, containing 5–30 g/dm3 of NiSO4 •6H2O, 10–60 g/dm3 of D-C6H11O7Na, 5–40 g/dm3 of NaH2PO2 •H2O, 3 g/dm3 of HOOCCH2CH2COOH, 0.5 g/dm3 of CH3(CH2)11OSO3Na, 0.002 g/dm3 of Pb(CH3COO)2•3H2O, at a temperature of 90 °C and a deposition rate of up to 0.75 μm/min. The review also discusses methods for preparing D-gluconate electrolytes for nickel plating using sodium D-gluconate, D-glucono-1,5-lactone, and nickel D-gluconate. One advantage of D-gluconate nickel plating solutions consists in the absence of toxicity and low cost of D-gluconates.

Study of the influence of bath alkalinity on the nickel electrodeposition process in the presence of aspartic acid

Study of the influence of bath alkalinity on the nickel electrodeposition process in the presence of aspartic acid

Electrochemical Behaviour of Nickel(II)-Rhenium(VII) And Electrodeposition of Nickel-Rhenium Alloy from Choline Chloride - Urea Deep Eutectic Solvent

The electrochemical behaviour of nickel(II)-rhenium(VII) and the electrodeposition of nickel-rhenium alloy using choline chloride: 2 Urea deep eutectic solvent (Reline DES) is reported. Speciation of nickel(II)-rhenium(VII) in Reline DES was studied using UV -Visible spectroscopy. Cyclic voltammetry of Ni2+-ReO4 − in Reline indicates the simultaneous reduction of two metal ions at glassy carbon electrode controlled by non-reversible diffusion process. Chronoamperograms obtained for the reduction of Ni2+-ReO4 − suggests nucleation and three-dimensional growth of bimetallic phase on electrode surface followed progressive nucleation. Electrodeposition of nickel—rhenium alloy was carried out on copper substrates under galvanostatic and potentiostatic conditions. Smooth and uniform deposits were obtained by galvanostatic deposition. X-ray diffraction analysis of the deposit confirmed it to be nickel-rhenium alloy (at −1.2 V) in amorphous form which upon annealing at 1000 °C crystallizes into hexagonal phase with concurrent morphology change from spherical particles to irregular polygons.

Iron-promoted rapid self-reconstruction of nickel-based catalysts for efficient oxygen evolution

High-performance oxygen evolution reaction (OER) catalyst is critical for improving the water splitting efficiency. In this work, an efficient self-supported OER catalyst was prepared by electrodeposition of nickel–iron layered double hydroxide nanosheets on titanium mesh substrate (NiFe-LDH/Ti-mesh). This self-supporting design exposes abundant active sites. At 100 mA cm−2, the NiFe-LDH/Ti-mesh shows a low overpotential of 310 mV in 1.0 M KOH. When assembled into an anion exchange membrane water electrolyzer, it can run stably over 200 h. In-situ Raman reveals that the NiFe-LDH/Ti-mesh surface was reconstructed into NiFeOOH active species. In-situ infrared shows that the introduction of Fe promotes the evolution of oxygen intermediates. Theoretical calculations reveal a weakened binding strength of *OH and accelerated formation of *O in OER by the introduction of Fe. This study provides a facile approach for developing self-supported high-performance OER electrocatalyst, and advances the understanding on the origin of NiFe-based catalysts as well.

The Effect of the Rare Earth Element Cerium on the Electrocrystallization and Microstructure of Nickel Electrodeposits in Industrial Electrolytes

To meet the industrial production needs for high-quality and precisely controllable structured high-end nickel foils, rare Earth compounds are added as additives in complex industrial electrolytes to improve the quality of the nickel deposition layer. This study investigates the effects of adding rare Earth compounds to the existing industrial production electrolytes (which already contain various organic and inorganic additives in a mixed acid solution) on the surface microstructure, cerium content, grain size, and crystal orientation of the nickel deposition layer. Using direct current electrodeposition, different concentrations of rare Earth compounds were added to the industrial electrolyte, and the cerium content, grain size, and crystal orientation were characterized. The results show that adding 0.8 g·l−1 CeCl3 accelerates the nucleation rate and shortens the nucleation relaxation time. The addition of rare Earth elements promotes multi-directional preferential growth, resulting in uniform and fine grain size, improved grain structure of the deposition layer, and reduced surface roughness of the nickel plating layer. Therefore, rare Earth elements can be used to regulate the structure, microstructure, and grain refinement of the nickel deposition layer without affecting its composition.

Eggshell derived hydroxyapatite reinforced nickel electrodeposition via post-supercritical-CO2 approach: Enhanced electrochemical corrosion resistance for seascape applications

The corrosion resistance of brass materials, commonly used in PCBs, MEMS, and the automobile industry, is significantly compromised in chlorine-containing environments prevalent in marine, chemical, and petroleum industries. To address this issue, we proposed the development of a nickel/hydroxyapatite (Ni/HAP) composite coating using a post-supercritical carbon dioxide (post-SC-CO2) approach, aiming to enhance corrosion resistance compared to conventional methods. The study evaluates the effectiveness of the post-SC-CO2 process against SC-CO2 and conventional electrodeposition techniques. The fabricated Ni/HAP coatings are examined through various physico-chemical characterizations to elucidate their surface morphology, phase purity, and chemical compositions. The surface morphology of Ni/HAP coating from post-SC-CO2 method features micro-cones, indicating SC-CO2 phenomena at atmospheric pressure. The electrochemical impedance spectroscopy analysis demonstrates that the conventionally electrodeposited Ni/HAP coating attains a corrosion resistance of 4.331 × 104 Ω cm2, 31.59 % enhancement in protection efficiency compared to a standalone Ni coating. In contrast, coatings fabricated using SC-CO2 and post-SC-CO2 methods exhibit corrosion protection efficiencies that are 92.97 % and 70.84 % higher, respectively, compared to the conventional electrodeposition technique. These findings highlight the superior performance of the post-SC-CO2 electrodeposition method in improving corrosion resistance, indicating its significant potential for industrial applications.

Influence of nicotinic acid additive on the electrodeposition of nickel from aqueous solution

In nickel-plating aqueous baths, both organic and inorganic additives are employed to enhance surface finish, reduce roughness, and achieve a uniform morphology of the coatings. This study investigates how four different concentrations of nicotinic acid (NA) additive, combined with a fixed concentration of boric acid, influence nickel electrodeposition in an aqueous solution, with minimal effect on the speciation of Ni(II) clusters. NA inhibits the Ni(II) reduction process even at a low concentration of 0.01 M, resulting in negligible changes in behavior compared to the additive-free environment. A higher concentration of 0.06 M NA is required to achieve a high-quality surface. The study demonstrates that the inclusion of NA significantly alters the electrochemical behavior relative to the additive-free regime. For instance, the use of both additive systems leads to coatings with relatively high microhardness and brighter, smoother deposits.

The influence of temperature and the magnetic field on Ni electrodeposition from citrate bath and its electrocatalytic performance towards hydrogen evolution reaction

The demand for energy surpasses the available supply, leading to various economic, social, and environmental consequences. Hydrogen is one of the most clean and renewable source for energy. Therefore, the electrocatalytic hydrogen evolution reaction (HER) presents a promising eco-friendly approach for generating sustainable hydrogen energy. However, in alkaline conditions, HER encounters slow kinetics due to challenges associated with hydrogen adsorption and hydrolysis. In this article, thin Ni films were synthesized using the electrodeposition technique from citrate electrolyte. Their suitability as electrocatalysts for the hydrogen evolution reaction (HER) in a 1 M NaOH solution was estimated. This research investigates how the uniform magnetic field and temperature affect the process of nickel electrodeposition from a citrate bath and its subsequent influence on surface morphology and catalytic properties for the hydrogen evolution reaction (HER). Additionally, alterations in surface material wettability were examined based on changing the temperature during using the magnetic field for the electrodeposition process and shows how this effect on the catalytic performance towards HER. The outputs show that using the magnetic field for fabrication of Ni thin films at room temperature enhances the surface morphology and its catalytic performance for HER. However, the study reveals that using the temperature for Ni electrodeposition improves its catalytic performance independently of the magnetic field, whereas combining temperature with the magnetic field for Ni thin film fabrication diminishes their catalytic performance for the hydrogen evolution reaction (HER). The nickel thin film produced at 25 °C under the influence of a magnetic field, whether parallel or perpendicular, demonstrates the lowest overpotential of − 268 mV to achieve a current density of 10 mA cm−2. Additionally, it exhibits the smallest Tafel slope values of 106 mV dec−1 and 128 mV dec−1 for the parallel (Bǁ) and perpendicular (BꞱ) directions, respectively. However, the magnetic field effect diminishes at elevated temperatures. Nickel thin films prepared at 35 °C under the influence of perpendicular (BꞱ) and parallel (Bǁ) directions exhibit higher overpotential values of − 314 mV and − 322 mV, respectively.

Role of Substrate on the Fractal Characteristics of Nanostructure Surfaces of Electrodeposited Nickel Thin Films

This study investigates the structure, morphological, and roughness properties of electrodeposited nickel thin films grown on different substrates, that is, silicon, copper, and gold. X‐ray diffraction analysis reveals that the Ni coatings exhibit a face‐centered‐cubic phase, regardless of the substrate used, although the texture is mainly influenced by the substrate. Atomic force microscopy images show that larger grains are obtained with gold substrates, while smaller ones are observed with copper and silicon substrates, in agreement with scanning electron microscopy. The results demonstrate that both topological and fractal characteristics of the Ni thin films are significantly influenced by the type of substrate. Statistical parameters are quantified to compare the surface morphology of the different samples. Fractal analysis reveals that the fractal dimensions of all surfaces range between 2 and 3, indicating self‐affinity. Fractal succolarity and lacunarity are measured to assess the penetration of a liquid into the surface and the distribution of gaps in the Ni film surfaces, respectively. Minkowski functionals are utilized for topological analysis to characterize the internal structure of the Ni thin films. The observed differences in roughness characteristics provide evidence that the type of substrate affects the nucleation and growth of surface features during electrodeposition.

Ultrasonic-assisted pulse electrodeposition process for producing nanocrystalline nickel films and their corrosion behavior: Competition between mass transport and nucleation

Ultrasonic-assisted pulse electrodeposition of nanocrystalline nickel (NC-Ni) coatings from Watts bath on copper substrate was investigated. Direct (DC), pulsed (PC), and pulse reversed (PRC) current electrodeposition techniques were employed to electrodeposit NC-Ni coatings in the absence and presence of ultrasound wave with a nominal power ranging from 95 W to 200 W and their surface morphology, hardness, and crystalline microstructure were compared. We observed that as the ultrasound power increases, the cathodic efficiency and the microhardness increase, whereas the crystallite size and surface roughness decrease for NC-Ni electrodeposited by the three techniques in the same way. However, the effect of pulse waveform is dominant. The finest crystallite size (24 nm) and highest hardness (585 HV) were achieved for NC Ni coatings PC electrodeposited using an ultrasound with 200 W nominal power. It is believed that the coating produced by PC and PRC techniques develops a preferential orientation in (111) and (100) planes, respectively. The application of ultrasound wave and increasing its nominal power changes the preferential orientation of all obtained coatings to (111) planes. The corrosion behavior of NC Ni coatings, as investigated by potentiodynamic polarization and electrochemical impedance spectroscopy in NaOH solution, demonstrates the effect of nanocrystalline on the passivation and corrosion resistance of NC-Ni coatings.

One-step controlled electrodeposition nickel sulfides heterointerfaces favoring the desorption of hydroxyl groups for efficient hydrogen generation

One-step controlled electrodeposition nickel sulfides heterointerfaces favoring the desorption of hydroxyl groups for efficient hydrogen generation

Correction to “Potential Oscillations during Cobalt–Nickel Electrodeposition in the Presence of Butynediol”

Correction to “Potential Oscillations during Cobalt–Nickel Electrodeposition in the Presence of Butynediol”

Effect of 2-Mercapto-1-methylimidazole on the Electrodeposition of Nickel on an Ordered Au(111) Electrode.

A nickel film electroplated onto a metal substrate can be used as a catalyst for water splitting and a magnetic material for spin valves. Although the nucleation and growth of Ni on Au(111) have already been examined with in situ scanning tunneling microscopy (STM), the current study provides new insights of the structure of the first layer of Ni on an ordered Au(111) electrode in 0.1 M KSO4 + 1 mM H2SO4 + 10 mM NiSO4 (pH 3). Prolonged STM scanning of the Ni monolayer on a Au(111) electrode revealed interfacial mixing to produce a surface alloy, initially assuming segregated Ni domains and later transforming them to a homogeneous Ni/Au phase. The formation of the Ni/Au(111) surface alloy affected the structure of the subsequent bulk Ni deposition. The inclusion of 2-mercapto-1-methylimidazole (MMI) in the deposition bath incurred Ni deposition at a less negative potential and a faster rate, resulting in an overall 5.3 times more Ni deposited on the Au electrode in potentiodynamic experiments. MMI molecules were adsorbed on the Ni deposit to prevent Ni dissolution in the Au(111) electrode. MMI could catalyze the presumed rate-determining step from Ni2+ to Ni+ en route to the metallic Ni. The resultant Ni film with MMI had a 3D texture without a preferred crystal orientation on the Au electrode, as opposed to a layer type growth of Ni on Au(111) without MMI.

Electrochemical analysis of the corrosion resistance of annealed steel with nickel coating in marine environment simulations: chronoamperometric and voltametric study

This study conducts a comprehensive investigation into the corrosion resistance of annealed steel wire, commonly used in marine construction, emphasizing its importance for the material's durability and functionality in such applications. An innovative approach was implemented by applying a Nickel (II) Chloride Hexahydrate coating through electrodeposition. This process was meticulously adjusted, varying critical parameters such as exposure time and electrical potential. To mimic marine corrosive conditions, a Sodium Chloride solution was used, allowing for a detailed comparative analysis between coated and uncoated samples. The evaluation was based on rigorous quantitative measurements of the wire's surface state and corrosion potential, using TAFEL curves for precise interpretation. The findings empirically demonstrated that the coating significantly enhances corrosion resistance, markedly outperforming untreated steel. These results reinforce the proposition of nickel electrodeposition as an effective and viable strategy for corrosion protection in marine industrial applications.

Facilitating electroless metalization of blind holes in glass substrates by electrochemical discharge-assisted surface roughening

This study introduces a novel approach involving the utilization of electrochemical discharges (ECD) to roughen a glass substrate to enhance the electroless metalization within blind holes. An array of 6 × 6 microholes was machined in a glass substrate using room-temperature-based Ultrasonic machining (USM) followed by electroless nickel and copper electrodeposition. Oxidation of the electroless seed layer obstructing the conductive pathway during electrodeposition and constraints to the flow of electroless solution into microholes resulted in unfilled vias. Roughening of the glass surface with ECD enabled the deposition of a thicker electroless seed layer and also infiltrated electroless solution into microholes through a network of valleys and channels generated on the top surface. A continuous electroless seed layer deposition was demonstrated in a blind via with an aspect ratio (AR) of nearly 1.5.