Electrodeposition Parameters Research Articles

Electrochemical Deposition of Silver Nanoparticle Assemblies on Carbon Ultramicroelectrode Arrays.

Silver nanoparticle (AgNP) assemblies combined with electrode surfaces have a myriad of applications in electrochemical energy storage and conversion devices, (bio)sensor development, and electrocatalysis. Among various nanoparticle synthesis methods, electrochemical deposition is advantageous due to its ability to control experimental parameters, enabling the formation of low-nanoscale (<10 nm) particles with narrow size distributions. Herein, we report the electrodeposition of AgNPs on a unique electrode platform based on carbon ultramicroelectrode arrays (CUAs), exploring several experimental variables including potential, time, and silver ion concentration. Extensive scanning electron microscopy analysis revealed that more reductive deposition potentials resulted in higher counts of smaller-sized AgNPs. While previous studies have employed planar, macro-sized electrodes with millimolar silver ion concentrations and minute-long times for AgNP electrodeposition, our results demonstrate that lower Ag+ concentrations (50-100 µM) and shorter deposition times (15-30 s) are sufficient for successful AgNP formation on CUAs. These findings are attributed to enhanced mass transfer from the radial diffusion of the array-based CUAs. The quantity of deposited Ag was determined to be 1100 ± 200 nmol cm-2, consistent with AgNP-modified CUA electrocatalytic activity for hydrogen peroxide reduction. This study emphasizes the importance of carefully considering AgNP electrodeposition parameters on unconventional electrode surfaces.

Damage-free non-mechanical transfer strategy for highly transparent, stretchable embedded metallic micromesh electrodes

Stretchable, flexible, transparent electrodes garner significant research interest as indispensable components of flexible optoelectronic devices. However, frequent mechanical transfers during processing pose a considerable challenge in preparing electrodes of scalable size with superior performance and intact structure. Herein, we present a stretchable embedded metallic micromesh (SEMM) electrode with high optoelectronic and robust mechanical properties. The SEMM electrode is fabricated via a damage-free non-mechanical transfer strategy with the assistance of a bifunctional metal transition layer that serves as both a seed layer during electrodeposition and a sacrificial layer during stripping of the electrode. Consequently, the SEMM electrode features a scalable size and an intact structure. By optimizing the electrodeposition parameters, the SEMM achieves high optical transmittance (∼83 %) and low sheet resistance (0.22 Ω sq−1), with a figure of merit reaching 8600–53 times greater than that of commercial polyethylene terephthalate-indium tin oxide (PET-ITO). Furthermore, the SEMM exhibits excellent mechanical stability, enduring up to 60 % of tensile strain and maintaining almost constant normalized resistance after 20,000 bending cycles. Based on the SEMM, a transparent film heater yields rapid response time, low operating voltage, and fast defogging capability. This non-mechanical transfer strategy offers a compelling approach for enhancing the structural integrity and scalability of stretchable embedded transparent electrodes.

Optimization of pulse electrodeposition parameters for enhanced resistance to corrosion and hydrogen permeation of zinc coatings

Corrosion and hydrogen permeation resistance of pulse electrodeposited Zn coatings were correlated with coating micro-texture and strain. The maximum and minimum corrosion resistance were noted for D6F75 (duty cycle 60; frequency 75 Hz) and D8F25 (duty cycle 80; frequency 25 Hz), respectively. The D6F75 coating exhibited a higher fraction of low-energy low-angle grain boundaries (LAGBs) and a preferred texture of (31¯2¯1) whereas the D8F25 coating exhibited comparatively low LAGBs fractions and(21¯1¯0) orientation. High resistance to hydrogen permeation exhibited by the D6F75 coating was attributed to hydrogen trapping within the coating, which reduced the micro-strain within the coating and diminished the hydrogen concentration gradient, thereby promoting greater surface recombination.

Electrochemical synthesis, physical properties and corrosion behavior of electropolymerized polyaniline films developed on 316L stainless steel

AbstractPolyaniline (PANI) films may be developed on metallic substrates by a variety of electrochemical techniques. In the present work, PANI films were electrodeposited on AISI 316L stainless steel substrates by cyclic voltammetry (CV), chronoamperometry (CA), and chronopotentiometry (CP) with the objective of comparing the efficacy of each method, based on the integrity of the developed films. Cyclic voltammetry and anodic polarization were used to determine optimal electrodeposition parameters for the development PANI films using the CA and CP methods. The structure and morphology of the coatings were characterized by scanning electron microscopy, energy‐dispersive x‐ray spectroscopy, Fourier‐transform infrared spectroscopy, and ultraviolet–visible spectroscopy. Among the evaluated techniques, CV led to the formation PANI films with the best homogeneity as well as the lowest number of defects, such as cracks or pores. Subsequently, the corrosion resistance of AISI 316L steels with and without PANI was compared in a physiological saline solution (0.9% NaCl). Potentiodynamic polarization tests indicated that the PANI‐coated samples exhibited lower corrosion current density values (0.012 vs. 0.018 μA/cm2) and lower passive current density values (0.04 vs. 0.06 μA/cm2) in comparison to the bare AISI 316L steel. Additionally, long‐term monitoring by electrochemical impedance spectroscopy revealed that PANI films consistently exhibited superior polarization resistance up to 32 days of exposure in the 0.9%NaCl solution (233,000 vs. 207,000 Ωcm2).

Pulse-constructed energy–saving PbO2 electrode for copper electrowinning

Energy-saving PbO2 exhibit significant application potential in the non-ferrous metal electrowinning industry. By optimizing the deposition time, heteropolar spacing, nitric acid concentration, pulse current density and pulse frequency, the optimum conditions for deposition of PbO2 electrode were obtained. Meanwhile, the effects of electrodeposition parameters on the electrochemical performance, phase structure and morphology of β-PbO2 were systematically evaluated. The mechanism of action of pulse and direct current deposition was proposed. The simulated copper electrowinning experiment shows that an improved current efficiency (91.6 %) was achieved and the low energy consumption (1855.1 kW⋅h/t) for copper production per ton was significantly reduced. Compared with the electrode prepared by direct current deposition, the current efficiency of copper is increased by 4.3 % and the energy consumption is reduced by 198.6 kWh/t. Additionally, the PbO2 electrode produced by the optimized pulse deposition process exhibits excellent stability, which service-time is increased by approximately 99.4 %. This research offers insights for developing energy-efficient and long-lived electrode materials.

Electrodeposition and Optimisation of Amorphous NixSy Catalyst for Hydrogen Evolution Reaction in Alkaline Environment.

Anion exchange membrane (AEM) water electrolysers have shown their potential in green hydrogen production. One of the crucial tasks is to discover novel cost-effective and sustainable electrocatalyst materials. In this study, a low-cost Ni-S-based catalyst for hydrogen evolution reaction was prepared via a simple electrodeposition process from a modified Watts bath recipe. Physical characterisation methods suggest this deposit film to be amorphous. Optimisation of the electrodeposition parameters of the NixSy catalyst was carried out using a rotating disk electrode setup. The optimised catalyst exhibited excellent catalytical performance in 1 M KOH on a microelectrode, with overpotentials of 41 mV, 111 mV and 202 mV at 10, 100 and 1000 mA cm-2 with Tafel slope of 67.9 mV dec-1 recorded at 333 K. Long-term testing of the catalyst demonstrated steady performance over a 24 h period on microelectrode at 100 mA cm-2 with only 71 mV and 37 mV overpotential increase at 293 K and 333 K respectively. Full cell testing with the optimised NixSy as cathode and NiFe(OH)2 as anode showed 1.88 V after 1 h electrolysis at 500 mA cm-2 in 1 M KOH under 333 K with FAA-3-30 membrane.

Multiscale textured solar absorber coatings for next-generation concentrating solar power

A high-temperature stable solar absorber is crucial for next-generation (Gen3) concentrating solar power (CSP) plants, to enable high temperature operation, maximize power generation efficiency, and thereby reduce the levelized cost of energy. This study presents novel, fractal-textured solar absorber coatings whose multiscale feature scales effectively match the visible region of the solar spectrum, leading to superb absorptive properties. Single and bimetallic oxide coatings of copper, cobalt and manganese were prepared on Inconel 625 substrates using electrodeposition. The effect of electrodeposition parameters and annealing temperature are systematically studied to optimize the morphology and properties of the oxide coatings. Multiscale textured bimetallic coatings of copper manganese oxide and copper cobalt oxide demonstrate a superior absorptance of 0.985, a remarkably low emittance <0.45 and an exceptional optical efficiency of ∼96 % under Gen3 CSP operating conditions, surpassing previously reported values in the literature by about 5 %. Durability tests confirmed the coatings’ steadfast endurance of mechanical and environmental stress, making them suitable for long-term application in harsh CSP environments.

Evaluation of electrodeposition synthesis of gold nanodendrite on screen-printed carbon electrode for nonenzymatic ascorbic acid sensor

Gold nanodendrite (AuND) is a type of gold nanoparticles with dendritic or branching structures that offers advantages such as large surface area and high conductivity to improve electrocatalytic performance of electrochemical sensors. AuND structures can be synthesized using electrodeposition method utilizing cysteine as growth directing agent. This method can simultaneously synthesize and integrate the gold nanostructures on the surface of the electrode. We conducted a comprehensive study on the synthesis of AuND on screen-printed carbon electrode (SPCE)-based working electrode, focusing on the optimization of electrodeposition parameters, such as applied potential, precursor solution concentration, and deposition time. The measured surface oxide reduction peak current and electrochemical surface area from cyclic voltammogram were used as the optimization indicators. We confirmed the growth of dendritic gold nanostructures across the carbon electrode surface based on FESEM, EDS, and XRD characterizations. We applied the SPCE/AuND electrode as a nonenzymatic sensor on ascorbic acid (AA) and obtained detection limit of 16.8 μM, quantification limit of 51.0 μM, sensitivity of 0.0629 μA μM−1, and linear range of 180–2700 μM (R2 value = 0.9909). Selectivity test of this electrode against several interferences, such as uric acid, dopamine, glucose, and urea, also shows good response in AA detection.

Enhanced electrocatalytic activity of Ni-Mn-Co-Fe alloys for efficient hydrogen and oxygen evolution reactions: A study on the effects of electrodeposition parameters

The synthesis of high-performance and cost-effective electrocatalysts for water splitting and fuel cell processes is crucial for hydrogen energy production and is considered one of the most significant challenges. This work produced a Ni‒Mn‒Co‒Fe electrocatalyst for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) via electrodeposition, which is a highly efficient and cost-effective method for synthesizing electrodes. The operating deposition parameters for Ni-Mn-Co-Fe were investigated, including the bath composition; scan rates of 5, 10, and 50 mV/s; pH values of 1.5, 3.5, and 7.5; bath temperatures of 25, 40, and 60 °C; and applied potentials ranging from −0.5 to −1.4 V vs. Ag/AgCl. The electrocatalytic activity of the electrocatalyst was evaluated at various temperatures and KOH concentrations. Linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS) were employed to estimate the electrocatalytic activity. The electrocatalytic performance of various electrodes for the HER and OER in alkaline environments, including Ni, Ni‒Mn, Ni‒Co, Ni‒Mn‒Co, Ni‒Mn‒Fe, and Ni‒Mn‒Co‒Fe, was examined. The results indicate that the Ni‒Mn‒Co‒Fe electrode required overpotentials of 436 mV and 447 mV to achieve a current density of 100 mA/cm2 for the HER and OER, respectively, demonstrating outstanding electrocatalytic activity. Moreover, after 20 h of electrolysis at a current density of 100 mA/cm2, the overpotential changes were minimal (less than 4 %), indicating exceptional electrochemical stability. As a bifunctional electrode in the overall water-splitting system, a cell voltage of 1.57 V vs. RHE is required to deliver a current of 10 mA/cm2.

Fabrication of Three-Dimensional Dendritic Ag Nanostructures: A SERS Substrate for Non-Invasive Detection.

This paper discusses the fabrication of three-dimensional dendritic Ag nanostructures, showcasing pronounced Localized Surface Plasmon Resonance (LSPR) effects. These nanostructures, employed in surface-enhanced Raman scattering (SERS), function as sensors for lactic acid in artificial sweat. The dendritic structures of the silver nanoparticles (AgNPs) create an effective SERS substrate, with additional hotspots at branch junctures enhancing LSPR. We achieve differential LSPR effects by varying the distribution and spacing of branches and the overall morphology. Adjustments to electrodeposition parameters, such as current and plating solution protective agents on an anodized aluminum oxide (AAO) base, allow for precise control over LSPR intensities. By pre-depositing AgNPs, the electron transmission paths during electrodeposition are modified, which leads to optimized dendritic morphology and enhanced LSPR effects. Parameter optimization produces elongated rods with main and secondary branches, covered with uniformly sized, densely packed, non-overlapping spherical AgNPs. This configuration enhances the LSPR effect by generating additional hotspots beyond the branch tips. Fine-tuning the electrodeposition parameters improved the AgNPs' morphology, achieving uniform particle distribution and optimal spacing. Compared to non-SERS substrates, our structure amplified the Raman signal for lactic acid detection by five orders of magnitude. This method can effectively tailor SERS substrates for specific analytes and laser-based detection.

A study of tin electrodeposition from ethaline: The electrode material effect

AbstractThis article studies the influence of electrode material on tin (Sn) electrodeposition from deep eutectic solvent. The Sn electrodeposition from ethaline‐based electrolyte onto glassy carbon (GC) and Pt substrates has been studied using cyclic voltammetry and chronoamperometry. The patterns and parameters of Sn nucleation and growth processes have been determined by means of Scharifker and Hills and Scharifker–Mostany models. Results show that Sn nucleation onto GCE follows instantaneous 3D nucleation, while in the case of PtE, it is controlled by adsorption, instantaneous 3D nucleation, and residual water reduction. The growth mechanism is diffusion‐controlled for both electrodes. The parameters of Sn electrodeposition onto GCE and PtE such as diffusion coefficient (D), nucleation rate (A), and active site density of Sn nuclei (No) are evaluated. The results showed that A and No increase linearly as the deposition potential is displaced towards more electronegative values while D is almost unchanged, regardless of the involved working electrode. The morphology and the structure of the electrodeposited Sn are also discussed based on scanning electron microscopy, X‐ray diffraction, and energy‐dispersive X‐ray spectroscopy investigations.

Flotation-assisted electrodeposition process to recover copper from waste printed circuit boards

Electrodeposition is an attractive method to recover copper from waste printed circuit boards (WPCBs), which preferably requires metal-rich concentrate as raw material. In this study, a metal-rich route for WPCBs was established to assist copper electrodeposition by using flotation method. Different from aqueous disperse medium in conventional flotation, we proposed ethanol as a disperse medium to improve dispersivity and sustainability. An H-type electrolytic cell with a cation exchange membrane was used to electrolyze copper in metal-rich concentrate at the anode and recover pure copper on the cathode. The experiments were conducted to investigate the effect of grade on the proportion of metal-rich concentrate after flotation and the electrodeposition rate of copper, and the key factors (solid-to-liquid ratio and applied voltage) affecting copper electrodeposition were evaluated. The results show that the flotation with ethanol can greatly enrich copper, and the copper content in metal-rich concentrate can be increased by 182.3 %, with a copper recovery rate of 85.1 %. Increasing the solid-to-liquid ratio and applied voltage can increase the deposition rate of copper, but affects the stability of electrodeposition. The optimized electrodeposition parameters are: electrolyte temperature of 50℃, solid-to-liquid ratio of 25 g/L, and applied voltage of 10 V. The purity of copper in electrodeposits can reach over 99 %.

(Invited) The Influence of the Magnetic Field on Ni Thin Film Electrodeposition as an Electrocatalytically Active Material for Hydrogen Evolution Reaction

Ni thin film were synthesized through the electrodeposition method from three different electrolytes. Furthermore, they were assessed as electrocatalyst for hydrogen evolution reaction (HER) in 1 M NaOH. Herein, various electrodeposition parameters such as pH of the electrolytes, deposition potential, temperature, and the influence of the magnetic field were measured. We made a comparison between the different morphologies and different characteristics depending on the thin film electrodeposition process parameters. Moreover, we have studied the wettability changes of material in dependence from to the composition of the electrolyte and the applied external magnetic field. The deposition process was accomplished by using chronoamperometry technique. The measuring scanning electron microscope, and X-Ray diffraction were used to characterize the surface morphology and the crystalline structures of the fabricated films.

(Battery Student Slam 8 Award Winner) Evaluating Electrodeposited Tin and Antimony-Based Anodes for Sodium-Ion Batteries

The widescale adaption of intermittent renewable energy sources, such as wind and solar, must be accompanied by a grid storage network to store energy when it is abundant and redistribute it as needed for on-demand use. Short-term storage in the form of rechargeable batteries is an attractive avenue for meeting these storage needs. The dominant technology in today’s market, the lithium-ion battery (LIB), is cost-prohibitive due to the need for rare-earth materials. Using the same working principle as LIBs, sodium-ion batteries (NIBs) utilize earth-abundant, low-cost sodium compounds instead of lithium compounds. Tin (Sn) and antimony (Sb) alone are promising anode materials for sodium-ion batteries with high theoretical capacities (847 and 660 mAh/g for Sn and Sb with Na, respectively) relative to current LIB anode chemistry (372 mAh/g) [1,2]. When combined, SnSb has shown to have increased stability relative to Sn or Sb alone [3]. Here, we synthesized Sn-Sb thin films with varied Sn and Sb atomic ratios by co-electrodeposition from a deep eutectic solvent by modifying solution stoichiometry and electrodeposition parameters. Using a combination of X-ray photoelectron spectroscopy (XPS), X-ray diffraction, and energy dispersive X-ray spectroscopy (EDS), phases and compositions of Sn-Sb synthesized by electrodeposition were identified. Once synthesized, we sought to determine the influence of morphology, surface chemistry, and composition on the capacity retention and rate capabilities of Sn and Sb-based anodes in NIBs. An optimized electrode composition was identified using a carbonate-based electrolyte, which resulted in stable capacity retention cycling at a rate of C/2 for 270 cycles.[1] W. T. Jing, C. C. Yang, and Q. Jiang, Journal of Materials Chemistry A, 8, 2913–2933 (2020).[2] S. Megahed and B. Scrosati, Journal of Power Sources, 51, 79–104 (1994).[3] W. P. Kalisvaart, H. Xie, B. C. Olsen, E. J. Luber, and J. M. Buriak, ACS Applied Energy Materials, 2, 5133–5139 (2019).

Electrodeposition of Copper-Silver Alloys from Aqueous Solutions: A Prospective Process for Miscellaneous Usages

The electrodeposition of copper (Cu), silver (Ag), and their alloys has been a subject of interest since the 19th century. Primarily due to their exceptional features such as good mechanical hardness and electrical conductivity, high resistance to corrosion, and electromigration, Cu–Ag electrodeposits continue to be investigated and developed to improve their properties for different applications. This paper reviews the state of the art in the field of electroplated Cu–Ag alloys in an aqueous solution, with particular emphasis on the observed properties and variety of electrochemical processes used to produce high-quality materials. Moreover, this review paper focuses on the experimental conditions employed for Cu–Ag electrodeposition, intending to understand the basis and manipulate the processes to obtain coatings with superior characteristics and for attractive usage. Finally, the most trending applications of these coatings are discussed depending on different parameters of electrodeposition to provide prospects for potential research.

The transition of strain rate sensitivity induced by Fe solutes in electrodeposited nanocrystalline Ni–Fe alloy

A face-centered cubic nanocrystalline (NC) Ni–Fe alloy was fabricated by adjusting electrodeposition parameter. By evaluating the hardness of NC Ni–Fe via nanoindentation at the selected strain rates from 0.005 s−1 to 0.2 s−1, a transitional point of strain rate sensitivity index (m) was exhibited, contrary to the constant value that reported in other works. Based on X-ray diffraction and transmission electron microscopy analysis, which evidenced the apparent lattice expansion as much more Fe solutes dissolved in intragrain rather than grain boundary (GB), we attributed the unexpected enhancement of m value at lower strain rates to pronounced GB-mediated plasticity facilitated by residual dislocations near GBs, whilst the lower m value at higher strain rates mainly to the intragranular dislocation motions. This work contributes directly to understanding the profound effect of alloying on the mechanical behaviors of NC materials.

Effects of substrate materials and electrodeposition parameters on hydrogen evolution reaction of Ni–Cu–Fe coatings

In this study, the effects of substrate materials and electrodeposition parameters on the hydrogen evolution reaction (HER) of Ni–Cu–Fe coatings were studied. For this purpose, different materials, including carbon steel (CS), stainless steel 304 (SS), and pure commercial graphite (G) were used as substrates, while the coating process was done in both modes of constant current density (CC) and variable current density, the latter to produce a functionally-graded (FG) coating. Microstructural investigations were done by using scanning electron microscopy, while the HER behavior was analyzed by electrochemical tests, including cyclic voltammetry (CV), linear scanning voltammetry (LSV), and electrochemical impedance (EIS) measurements. The morphology of the produced Ni–Cu–Fe coatings was completely affected by the coating parameters in the deposition bath and the type of substrates. In samples with micro/nano-cone morphology, deposited at a constant current density of 2.5 A/dm2, better HER behavior was obtained due to the highly effective surface and easier separation of hydrogen bubbles. Besides, the best electrocatalytic activity and the lowest overpotential (110 mV at 10 mA/cm2 in CC mode) were related to the samples coated on G. The proper selection of the substrate material plays an important role in improving the electrocatalytic behavior of composite coatings.

Influence of electrodeposition parameters on the fabrication of Ni–Co/SiC + TiN composite films through pulse current electrodeposition

In this investigation, pulsed current electro-deposition (PCE) was used to prefabricate Ni–Co/SiC + TiN composite coatings (NCSTCCs) on mild steel surfaces. The research focused on the influence of two electrodeposition parameters, pulse frequency (PF) and duty cycle (DC), on NCSTCF features including microscopic surface morphology, crystal orientation, grain size, microhardness, SiC and TiN nanoparticles (NPs), deposition quantity, and corrosion resistance properties. The results indicated that NCSTCCs produced under a 10% DC showed minimal SiC and TiN contents with a percent volume of just 5.6 v/v% and 5.4 v/v% respectively under the fixed condition of 60 Hz PF. However, the three-dimensional surface diagram indicated that the Ni–Co/SiC + TiN composite film deposited at 50% DC and 10 Hz PF displayed the highest SiC and TiN contents (11.6 v/v% and 11.7 v/v%) among all the films. Furthermore, NCSTCCs deposited under 50% DC and 10 Hz PF had peak microhardness at 667.4 kg/mm2, while the composite film achieved a microhardness of 514.1 kg/mm2 when prepared using 10% DC and 60 Hz PF. Moreover, when the DC and PF were at 50% and 10 Hz respectively, the Ni–Co/SiC + TiN composite film presented the maximum charge transfer resistance (4915.7–4927.2 Ω·cm2), indicating an excellent corrosion resistance.

Analysis of the influence of local electrodeposition conditions on the accuracy of electrochemical 3D-printing

Problem. Additive manufacturing of metal parts by local electrodeposition is a new promising area with several unique features. The use of electrolysis makes it possible to manufacture metal parts at room temperature with high accuracy and low energy consumption. The accuracy and speed of electrochemical 3D printing are inversely related, and therefore it is important to find optimal electrodeposition conditions at maximum speed without degrading accuracy. The aim of the study. The purpose of this work was to analyse the influence of electrodeposition parameters (electrode distance, electrical conductivity and electrolyte polarization) on the accuracy of metal deposit formation in a computer model and to conduct experimental verification of optimal conditions for electroforming a real object from copper sulphate electrolyte. Methodology of implementation. To achieve the goals of the study, computer simulation of the electrochemical deposition process in the COMSOL Multiphysics software and electrochemical measurements of the characteristics of copper sulphate electrolytes were used. Research results. Computer simulation established optimal conditions: the distance between the edge of the capillary and the surface on which deposition occurs is not more than 0.5 mm, the electrolyte in which the inverse slope of the cathode polarization curve is not lower than 2000 mA/(V×cm2) and the electrical conductivity is not higher than 0.02 S/сm. The influence of the electrolyte composition on the inverse polarization of the cathode process and its electrical conductivity was investigated. The optimal composition of the electrolyte was selected, containing 200 g/L CuSO4, 60 g/L H2SO4, 0.2 g/L KCl and RUBIN T-200 additive. In the selected electrolyte, the value of the inverse slope of the cathode polarization curve is 2120 mA/(V×cm2). Verification of the process of local electrodeposition in the selected electrolyte during the electroformation of a cylindrical object with a diameter of 4 mm and a height of 100 μm was carried out. It was determined that no more than 5 % of metal was deposited outside the capillary of the working electrode. Conclusions. The results of the work can be used to create an electrochemical 3D printing system. Further research should be aimed at approbation of the obtained parameters of local electrodeposition in an installation that simulates the operation of a 3D printer and establish the accuracy and speed of printing of a three-dimensional object. Key words: additive manufacturing, electrical conductivity, electrolyte composition, polarization, local electrodeposition.

Electrodeposition of Tin and Antimony-Based Anode Materials for Sodium-Ion Batteries

Tin antimonide (SnSb) is a promising alloying anode for sodium-ion batteries due to its high theoretical capacity and relative stability. The material is popular in the battery field, but, to our knowledge, few studies have been conducted on the influence of altering Sn and Sb stoichiometry on anode capacity retention and efficiency over time. Here, Sn-Sb electrodes were synthesized with compositional control by optimizing electrodeposition parameters and stoichiometry in solution and the alloys were cycled in sodium-ion half-cells to investigate the effects of stoichiometry on both performance and electrochemical phenomena. Higher concentrations of antimony deposited into the films were found to best maintain specific capacity over 270 cycles in the tin-antimony alloys, with each cell showing a slow, gradual decrease in capacity. We identified that a 1:3 ratio of Sn:Sb retained a specific capacity of 486 mAh g−1 after 270 cycles, highlighting a need to explore this material further. These results demonstrate how control over stoichiometry in Sn-Sb electrodes is a viable method for tuning performance.