Polarization Curves Research Articles

Green Film Forming Technology Based on Polydopamine Galvanized

At present, the mainstream passivation agent is chromate passivation agent, but it has the disadvantages of high toxicity and high price, so this project seeks to find a safer, cheap and green chromium-free passivation agent. Because dopamine and chitosan derivatives have certain corrosion inhibition properties on metals in acidic media, these polymer corrosion inhibitors can achieve high corrosion inhibition rates at high concentrations. Therefore, in this experiment, dopamine was added on the basis of sodium silicate, and the sample was passivated to explore the potential enhancement effect of dopamine on the passivated film performance. After the sample was treated, the impedance value could be fitted by electrochemical impedance spectroscopy and Zsimpwin software, and then the Tafel polarization curve was drawn. It was found that the addition of dopamine significantly improved the corrosion resistance of the passivated film. By promoting the positive shift of self-corrosion potential and greatly reducing the self-corrosion current density, the protective barrier effect of passivation film on metal matrix is effectively enhanced. Finally, the experiment successfully proved that the corrosion resistance of the passivation film after adding dopamine was better

Simultaneous optimization of electric production, azo dye, and yeast wastewater treatment in microbial fuel cell: Selection of the most suitable optimal conditions by PROMETHEE

Microbial fuel cell is a clean technology in which waste treatment and energy production continue simultaneously. Process performance depends on the independent variables and their interaction with each other specific to the waste to be treated. In this study, Microbial Fuel Cell (MFC), in which yeast production process wastewater is oxidized in the anolyte, and azo dye is reduced in the catholyte under abiotic conditions, was optimized using the Response Surface Methodology for maximum waste treatment and energy production. The independent variables were wastewater type, electrode array, and amount of sulfate-reducing inhibitor, while the dependent variables were azo dye removal, maximum power density, chemical oxygen demand (COD) removal, and coulomb efficiency. The effect of variables on all responses was determined using Analysis of Variance (ANOVA) and 3-dimensional (3D) graphs. The suitability of the models was tested by verification experiments under the determined optimum conditions (OPT 1, 2 and 3). Optimum experiments were ranked with the PROMETHEE approach according to azo dye removal (mg/L), maximum power density (mW/m2), COD removal (g/L), coulombic efficiency (%), and electrode cost (€/m2) criteria. The preference order of the optimum experiments was determined as OPT 1>OPT 2>OPT 3. With OPT 1, azo dye removal of 16.8 mg/L, maximum power density of 95.34 mW/m2, COD removal of 5.8 g/L and coulombic efficiency of 0.23 % were achieved. With a 1000 Ω external resistor, the maximum power density and coulombic efficiency increased to 147 mW/m2 and 1.5 %, respectively. In addition, the determined optimum experiments were examined using polarization curve and Electrochemical Impedance Spectroscopy.

Regulating hardness homogeneity and corrosion resistance of Al-Zn-Mg-Cu alloy via ECAP combined with inter-pass aging

The novel processing strategies of Equal Channel Angular Pressing (ECAP) combined with inter-pass aging was designed, and XRD, SEM, TEM, electrochemical testing, and hardness testing were used to evaluate the relationship between microstructure and performance of alloys in this work. The results indicate that the hardness uniformity of the circular cross-section perpendicular to the extrusion direction was improved by combining ECAP with inter-pass aging, resulting in a hardness inhomogeneity factor (∼0.030) that was lower than that achieved by peak aging and double-stage aging alloys. Polarization curves and electrochemical impedance spectra show that a more negative corrosion potential and a smaller corrosion current density were possessed by the alloy, with the maximum intergranular corrosion depth (IGC) being reduced to 38 μm. Microstructure observation indicates that the improvement in hardness uniformity is due to the uniformity of grain size and the improved distribution and size of the η’ phase, which is attributed to the interaction between the pinning and shear effects of precipitates and dislocations during deformation. The enhanced corrosion resistance was attributed to an orderly combination of deformation and aging that increases the grain boundary volume and disrupts the η phase continuity within grain boundaries.

Experimental study on degradation of proton exchange membrane fuel cells for eco-friendly heavy equipment

Proton Exchange Membrane Fuel Cells(PEMFC) are considered the main power source for eco-friendly mobility. The degradation of PEMFCs in eco-friendly heavy equipment is analyzed. The target heavy equipment is 4.5 tons track loader of Doosan Bobcat. The complex movement of heavy equipment causes extreme dynamic load cycling in the powertrain. An electrochemical analysis of its Membrane Electrode Assembly(MEA) is conducted to clarify its degradation feature in this work. Dynamic load cycles are obtained from field tests using earth-moving machinery. A 2000 h durability test for a PEMFC single cell is conducted using the obtained dynamic load cycles. According to polarization curve analysis, the maximum power decreases from 19.95 to 13.82 W. This is mainly caused by the degradation of the catalytic activity of the Pt catalyst layer, as confirmed by cyclic voltammetry(CV). The electrochemical surface area(ECSA) decreases by 70 %.

Redox-mediated synthesis of Cu2O/CuO/Mn3O4/C quaternary nanocomposites as an efficient electrode material for oxygen reduction reaction and supercapacitor application

Earth-abundant transition metal oxides (TMOs) hold significant promise as electroactive materials in various electrochemical energy conversion and storage applications, offering economic and environmental advantages over their less abundant counterparts. In this work, a simple and cost-effective redox-mediated reaction strategy under hydrothermal conditions has been adopted to synthesize the quaternary nanocomposites Cu2O/CuO/Mn3O4/C with variable amounts of carbon. The synthesized nanocomposites have been characterized using various analysis techniques, including powder X-ray diffraction (PXRD), field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and Brunauer–Emmett–Teller (BET). The synthesized COM5 nanocomposite (Cu2O/CuO/Mn3O4/C-50), when used as an electrocatalyst for the oxygen reduction reaction (ORR), demonstrates a good limiting current density (JL), half-wave potential (E1/2), and onset potential (Eonset) of −5.50 mA/cm2, 0.75 V, and 0.95 V, respectively, as per the polarization curve. The COM5 nanocomposite exhibits a four-electron transfer mechanism, calculated using the Koutecky-Levich (K-L) equation. In an O2-saturated 0.1M KOH solution, the COM5 nanocomposite has shown a superior relative current durability of 84.46% over 14,000 s compared to the commercially available 10 wt% Pt/C, indicating its potential application in the ORR. However, for supercapacitor applications, the COM3 nanocomposite (Cu2O/CuO/Mn3O4/C-20) as active electrode material in galvanic charge-discharge (GCD) study shows superior performance (201 F/g at 1 A/g) compared to the COM2 nanocomposite (117 F/g at 1 A/g) in neutral aqueous electrolyte, possibly due to the lower charge transfer resistance (Rct) of 24.04 Ω compared to COM2 (34.63 Ω). In two-electrode studies, the COM3 nanocomposite exhibits a good energy density of 24.19 Wh/kg at 1 A/g and a 4.7 kW/kg power density at 5 A/g. Additionally, the COM3 nanocomposite shows excellent long-term durability (74% capacitance retention) at the current density of 5 A/g for 8000 cycles. The electrochemical findings indicate that the COM3 nanocomposite stands out as a superior electrode material for supercapacitors, while the COM5 nanocomposite proves to be an effective electrocatalyst for the oxygen reduction reaction.

Effects of Incorporating TiO2 Aggregates on the Growth, Anticorrosion, and Antibacterial Properties of Electrodeposited Multifunctional Coatings Based on Sn-Ni Materials

Multifunctional coatings based on Sn-Ni materials with and without titanium oxide nanoparticles (TiO2NPs) incorporation were prepared using the electrochemical deposition technique at 70 °C. TiO2NPs were dispersed in the electrolyte bath, and their influence on the surface texture, crystalline phase, and properties was investigated. Various techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray microanalysis (EDX) were used to characterize the prepared coatings. The formation mechanism of the deposited coatings has been demonstrated to be consistent with the electrochemical behavior of instantaneous growth, and the three-dimensional growth is controlled by diffusion phenomena. The anticorrosion effectiveness of the coatings was assessed using potentiodynamic polarization curves and electrochemical impedance spectroscopy in an artificial sweat medium, while the bactericidal activity of the composite coatings (the ability to induce cell death) was evaluated in accordance with the ISO 27447:2019 test. The influence of TiO2NPs at a low concentration of 1 g/L on the composition, structure, and properties of the deposited coatings was demonstrated. Particular attention was paid to the relationship between the anticorrosive and bactericidal properties of the coatings and their structure composition and wetting properties. The synergistic effect of chemical composition and surface-wetting properties has been demonstrated to enhance the anticorrosive and bactericidal properties of the prepared coatings.

Poly(o-anisidine) and poly(o-anisidine-co-aniline) polymers synthesized on the ZnFeNi alloy coated steel surface

Abstract ZnFeNi alloy was synthesized on the carbon steel surface in a sulfate bath using the galvanostatic method at a constant current of 1.5 mA for 300 seconds. Poly(o-anisidine) homopolymer and poly(o-anisidine-co-aniline) copolymer were synthesized on the ZnFeNi coated electrode surface. Poly(o-anisidine) homopolymer was synthesized in 0.05 M o-anisidine+0.2 M sodium oxalate medium, and poly(o-anisidine-co-aniline) copolymer was synthesized in 0.05 M o-anisidine+0.05 M aniline+0.2 M sodium oxalate medium. Electrochemical synthesis was carried out by cyclic voltammetry technique. The synthesized materials were characterized by electrochemical impedance spectroscopy, linear sweep voltammetry, open circuit potential-time and anodic polarization curves. Open circuit potential-time curves showed that polymer coatings had higher open circuit potential. By linear sweep voltammetry measurements, it was determined that ZnFeNi alloys were present at the base of the polymer layers after polymer synthesis. It was understood from the anodic polarization curves that the polymer coated electrodes had lower current values ​​than the uncoated ZnFeNi coated electrode, and the poly(o-anisidine) coated electrode had lower current values ​​than the poly(o-anisidine-co-aniline) coated electrode. From electrochemical impedance spectroscopy measurements, it was determined that the polarization resistance of polymer-coated electrodes was higher than the polymer-free electrode during long periods of waiting in 3.5% corrosive solution. Among the polymer-coated electrodes, it was understood that the homopolymer poly(o-anisidine) showed better corrosion performance than the poly(o-anisidine-co-aniline) copolymer.

Synergistic inhibition effect of Chlorella sp. and benzotriazole on the corrosion of Q235 carbon steel in alkaline artificial seawater

The interaction of microalgae on the reinforced concrete with corrosion inhibitor is not well understood. Moreover, the inhibition role of microalgae on corrosion has been reported in recent years. In this study, the corrosion inhibition behavior of Q235 carbon steel (CS) due to the presence of Chlorella sp. and benzotriazole (BTA) in alkaline artificial seawater was investigated by means of weight loss, electrochemical measurements including open circuit potential, electrochemical impedance spectroscopy, and potentiodynamic polarization curves, and surface analysis including scanning electron microscopy, energy dispersion spectrometer, and X-ray photoelectron spectroscopy. The results of reduced corrosion rates in the algae-BTA system demonstrated that Chlorella sp. could facilitate the corrosion inhibition efficiency of BTA on the CS specimens. Moreover, polarization measurement showed the algae-BTA system had a mixed-type corrosion inhibition effect. The mechanisms of inhibition were proposed to be the precipitation of iron complexes such as Fe-BTA-EPS and Fe-BTA and iron compounds on the steel surface in the presence of the microalgae and BTA–. This study highlights the application of CS corrosion control by combining biological and chemical approaches that can be used for future research and practice, rather than purely chemical approaches.

Synthesis and Performance Evaluation of Multialkylated Aromatic Amide Oligomeric Surfactants as Corrosion Inhibitor/Drag Reducing Agents for Natural Gas Pipeline.

Drag reducing agents (DRAs) including amphiphiles and polymers can enhance energy efficiency and transmission volume in natural gas pipelines. However, the correlation between DRA molecular structure and drag reduction efficiency remains unclear. In this paper, the multialkylated aromatic amides (MAA) oligomeric surfactants with different numbers of amide group/n-dodecane chain (from 1 to 3) were first synthesized and characterized. Then, the potential efficiency of MAA as the corrosion inhibitors (CIs)/DRAs for natural gas pipelines was investigated by interfacial activity analysis, film-forming property test, electrochemical polarization curve measurement, and in-door loop test. The results showed that the molecular structure is the key factor influencing the performance of MAA. By increasing the number of amide group/n-dodecane chains, the interfacial activity of MAA improves greatly, thus outstandingly affecting the film-forming property of the MAA on the carbon steel sheet. For MAA-1, the formed film is too thin to cover the surface roughness, and then the corrosion inhibiting (78.64%)/drag reducing (0-2%) rates are the lowest. For MAA-3, the formed film is the thickest and smooth, thus imparting the largest corrosion inhibiting (93.88%)/drag reducing (10-14%) rates to MAA-3. For MAA-2, the formed film is thicker but not smooth, and the corrosion inhibiting (89.88%)/drag reducing (4-6%) rates are intermediate. We speculate that the structure of the MAA greatly influences the adsorption and self-assembly of MAA on the inner pipe wall and then generates different performances. This work is helpful for guiding the development of natural gas DRAs with high efficiency.

Thermal fluctuations on the corrosion behaviour of 17-4PH stainless steel alloys fabricated via material extrusion additive manufacturing technique

Herein, the influence of fluctuating thermal conditions on the corrosion behaviour of 17-4PH stainless steel alloys manufactured via fused filament fabrication is reported. The printed samples were sintered and then exposed to different temperature-fluctuating conditions to simulate the application environment of such alloys. The first set of samples (A) was studied as-sintered, the second set of samples (B) was aged at 480°C for 3 h followed by quenching in water, the third set (C) was exposed to conditions of B followed by aging at 360°C for 3 h and quenching in water and the final set of samples (D) was exposed to conditions of C followed by aging at 200°C for 3 h, quenching in water, aging at 400°C for 3 h, and finally quenching in water. The surface roughness evolved with the temperature conditions. The optical microscopy revealed that sample B had a fine and homogenous distribution of precipitates. Sample B had the highest microhardness values followed by C, D, and A in that order. XRD analysis revealed the presence of retained FCC austenitic phases within the microstructure whose peaks became stronger with the increased thermal fluctuations. The potentiodynamic polarisation studies revealed a distinct linear Tafel region on the cathodic region and a dual-slope inflection point on the anodic region of the polarisation curves. Sample D exhibited the highest corrosion rate whereas sample B revealed the lowest. As such, exposing fused filament fabricated 17-4 PH SS to fluctuating temperature conditions leads to degradation of mechanical strength and corrosion resistance.

Study on corrosion behavior and first-principle analysis of M50 steel in lubricating oil contaminated by salt water

The corrosive wear of M50 steel in lubricating oil contaminated with saline is a form of wear that often occurs within the main shaft bearings of aviation engines carried by aircraft working at sea. In the present paper, the corrosion behavior of M50 steel in lubricating oil contaminated with saline was studied. The open-circuit potential, polarization curve and impedance spectrum were analyzed by rotating electrochemical corrosion wear test. A three-layer interface microscopic molecular model was established with Materials Studio to simulate the dynamic corrosion evolution process of M50 steel self-matching pairs and the adsorption energy was calculated. The results show that the corrosion type is pitting corrosion. With the increase of saline concentration, the corrosion area becomes wider and shallower, and the size of the pitting core gradually decreases. The weight loss of M50 steel increases over time, but the trend slows down, which is also shown in the MS simulation results. Electrochemical tests show that the tribocorrosion of M50 steel is related to load, speed. As the load increases, the corrosion rate decreases. And, as the speed increases, the corrosion rate increases. This has practical significance for extending the understanding of tribocorrosion of M50 steel in marine atmospheric environments.

Electrolytic Plasma Nitriding of Medium-Carbon Steel 45 for Performance Enhancement

This article analyzes the effect of electrolytic plasma nitriding on the performance of medium-carbon steel 45 under increased mechanical loads and in aggressive environments. Nitrided samples in carbamide electrolytes, both with and without the addition of ammonium nitrate, were compared to the initial material. SEM with EDX and XRD analysis was used to examine the microstructure and phase composition of nitrided samples. Wear resistance was studied using the ‘ball-on-disk’ method and Vickers microhardness testing, while corrosion resistance was studied using potentiodynamic polarization curves. The study results show that the sample without ammonium nitrate demonstrated better mechanical and corrosion properties due to a more homogeneous and denser nitride layer, approximately 10 µm thick, containing phases FeN and Fe4N. Its wear resistance doubled compared to that of the initial sample. The sample treated in an electrolyte with the addition of ammonium nitrate demonstrated a higher current density (2.8672 × 10−5 A/cm2) and a lower corrosion potential (−0.565 V) compared to the initial sample (i_corr = 1.8971 × 10⁻5 A/cm2, E_corr = −0.480 V) and the sample without ammonium nitrate (i_corr = 1.7315 × 10−5 A/cm2, E_corr = −0.376 V). This is due to the formation of an uneven nitride layer and the presence of microcracks on the surface.

Improved wear and corrosion resistance of magnesium AZ80 alloy prepared by laser surface remelting

Laser surface remelting (LSR) is a laser-based surface treatment method. In the LSR process, microstructural defects such as cracks and porosity are suppressed in addition to grain refinement, and the mechanical properties are improved. The present research investigated the effects of LSR parameters on the microstructure, wear, and corrosion behavior of Mg AZ80 alloy. The results showed that in LSR, the coarse-grained (29.8 μm) structure of AZ80 was transformed into a fine-grained structure (3.1 μm) with no microstructural defects. The evaporation of Mg during LSR and the formation of Al-rich and Mg-poor phases are the most important challenges in the surface treatment of AZ80. This limitation was solved by optimizing the LSR parameters, which included a gas flow rate of 2 L min−1, pulse duration of 3 ms, scanning speed of 3 mm s−1, pulse frequency of 8 Hz, and heat input of 64 J mm−1. The prevention of Mg evaporation was associated with the elimination of porosity and cracks, reducing of the solidification range, and uniform distribution of β-Mg17Al12 precipitation phases in α-Mg refined grains. The tribological behavior of the laser-treated region showed that the COF, depth of the wear scar, wear rate, and wear volume loss were reduced by 18%, 48%, 37%, and 66%, respectively, compared to AZ80. This result is attributed to the refinement of α-Mg grains and the uniform distribution of β-Mg17Al12 in the laser-treated region. The results of the polarization curves of the corrosion test in 3.5 wt% NaCl solution showed that the optimal laser-treated region with the lowest corrosion current density (34.68 × 10−6 μA.cm−2) and highest self-corrosion potential (1.425 V) exhibited the highest corrosion resistance. A slight change in the breakdown potential current slope in the laser-treated region indicates the formation of a protective film on the surface after the completion of LSR, which increases corrosion resistance.

NiMOF-Derived MoSe2/NiSe Hollow Nanoflower Structures as Electrocatalysts for Hydrogen Evolution Reaction in Alkaline Medium.

Metal-organic frameworks (MOFs) are crystalline porous materials for storage and energy conversion applications with three-dimensional pore structure, high porosity, and specific surface area, which are widely utilized in electrocatalysis. Herein, MoSe2/NiSe composites were synthesized by selenization reaction using NiMOF as the precursor. The composites were hollow nanoflower structures with a synergistic effect between MoSe2 and NiSe to promote rapid electron transfer, which exhibited good hydrogen evolution reaction performance in an alkaline medium. At a current density of 10 mA/cm2, the HER overpotential reaches 80 mV, the Tafel slope is 33.86 mV/dec, and the material has good stability, with polarization curves remaining essentially unchanged after 3000 cycles. These results indicate that the method has a promising application in the preparation of efficient and sustainable catalysts for hydrogen production in alkaline medium.

Modeling of Catalyst Degradation in Polymer Electrolyte Membrane Fuel Cells Applied to Three‐Dimensional Computational Fluid Dynamics Simulation

ABSTRACTIn a polymer electrolyte membrane (PEM) fuel cell, the following degradation mechanisms are associated with the catalyst particles and their support: carbon support corrosion triggered by carbon and platinum oxidation, platinum dissolution with redeposition, and particle detachment with agglomeration. In this work, an electrochemical model for those degradation effects is presented as well as its coupling with a three‐dimensional computational fluid dynamics PEM fuel cell performance model. The overall model is used to calculate polarization curves and current density distributions of a PEM fuel cell in a fresh and aged state as well as the degradation process during an accelerated stress test with 30 000 voltage cycles. The obtained simulation results are compared to measurements on a three‐serpentine channel PEM fuel cell with an active area of 25 cm2 under various temperatures and humidities. The experimental data are obtained with a segmented test cell using respective degradation protocols and test conditions proposed by the United States Department of Energy. In addition to the temperature and humidity changes, the influence of geometry and material parameters on the degree of degradation and the resulting fuel cell performance is explored in detail.

Potentiodynamic Polarization Study of PH3 Electrochemical Oxidation

ABSTRACTIn this study, the electrochemical behaviour of phosphine in sulphuric acid solutions on the surface of various electrode materials was conducted by voltammetric investigations. The effects of electrode materials such as lead, copper, and platinum electrodes on the PH3 anodic oxidation were investigated. Polarization curves were recorded by saturating the sulphuric acid solution with phosphine. The results received show that the electrochemical oxidation of phosphine on the lead electrode is accompanied by an oxygen evolution potential and, on the copper electrode, copper (II) ions show catalytic effects. The maximum anodic oxidation of phosphine on a platinum electrode was observed at the potential range of 0.8–1.0 V, and in the presence of copper (II) ions on the polarogram a maximum of phosphine oxidation is recorded at a potential of approximately 0.1–0.2 V.

Green Hydrogen Synthesis from Human Urine as Sustainable Bioenergy Resources

With the earths cry for help as pollution rate increases, researchers are faced with a common task of tackling pollution resulting from dependence on fossil fuel as well as delivering sustainable energy. Renewable energy resources such as solar, wind, hydro to mention a few are currently finding applications within the world energy mix but some limitations which range from meteorology of locations to expected maximum energy output attainable. Hydrogen, the most abundant element in the world stand chance of abating this problem. However conventional method of its producing, poses severe treat to the atmospheric environment with the release of oxides of carbon hence, referred as blue hydrogen. Contrarily, green hydrogen from human urine stands a more sustainable and environmentally friendly energy resource. This study was aimed to empirically model the synthesis of green hydrogen from urea in human urine by an electrolytic process. The synthesized hydrogen was characterized on physiochemical properties of conductivity, turbidity, pH, specific gravity and colour, while the precursor urine characterized on gender, exposure duration and storage temperature. The synthesis process was modelled using Microsoft excel solver for the overall cell energy or polarization curve model, the Faraday’s efficiency model and gas purity model at electrolyte concentrations of 25 wt./wt., 30 wt./wt. and 35 wt./wt. of potassium oxide (buffer} to urea over a five-temperature interval range of 45 to 85 oC. Findings revealed that the gas produced was 99.88% hydrogen at the cathode. Also, hydrogen produced increased with increase in electrolyte concentration and moderate temperature with optimal conditions at 35 w/w electrolyte concentration and 65 oC. However, the minimum cell voltage was 2.06 V at 85 oC and 35 w/w electrolyte concentration. With an exception of the Faraday’s efficiency model at 30 wt./wt. electrolyte concentration across the system’s operating temperature range yielding an R2 value of 0.711, all the models yielded coefficient of determination values in the range of 0.96 and 0.99, indicating good fit for the alkaline urine electrolysis for green hydrogen synthesis from human urine.

Electroanalytical Studies on Codeposition of Cobalt with Ruthenium from Acid Chloride Baths

The aim of this study was to systematically analyze the influence of potential and the Co(II)–Ru(III) molar ratio on the electrochemical behavior of the Co–Ru system during codeposition from acidic chloride electrolytes. The equilibrium speciation of the baths was investigated spectrophotometrically and compared with theoretical calculations based on the stability constants of Co(II) and Ru(III) complexes. The codeposition of the metals was characterized using electroanalytical methods, including cyclic voltammetry, chronoamperometry, and anodic stripping linear voltammetry. The alloys obtained at different potentials were analyzed for their elemental composition (EDS, mapping), phase composition (XRD), and surface morphology (SEM). The morphology and composition of the alloys were mainly dependent on the deposition potential, which controlled the cobalt incorporation. Ruthenium–rich alloys were produced at potentials of −0.6 V and −0.7 V (vs. SCE). In these conditions, cobalt anomalously codeposited due to the formation of the CoOH+ intermediate, triggered by the intense hydrogen evolution on the ruthenium sublayer. Bulk cobalt electrodeposition began at a potential of around −0.8 V, resulting in the formation of cobalt-rich alloys. The early stages of the electrodeposition were investigated using different nucleation models. A transition from 2D progressive nucleation to 3D instantaneous nucleation at around −0.8 V was identified as being caused by cobalt incorporation. This was well correlated with electroanalytical data, partial polarization curves of alloy deposition, elemental mapping analysis, and the structure of the deposits.

Photocatalytic fuel cell based on dual Z-scheme heterojunction photoanode InVO4/g-C3N4/Bi2WO6/Ti for efficient Rhodamine B degradation and power generation

Finding suitable semiconductor materials to construct efficient photoanode is the key to improve PFC performance. In this paper, InVO4/g-C3N4/Bi2WO6/Ti composite photoanode was prepared and assembled with Cu cathode to construct PFC for rhodamine B (RhB) degradation and power generation. The InVO4/g-C3N4/Bi2WO6/Ti photoanode was characterized by XRD, FT-IR, XPS, SEM, TEM, EDS and DRS. The electrochemical properties of the PFC including polarization curves, power density, transient photocurrent, LSV and CV curves were analyzed to explore its power generation and electron transfer mechanism. The results showed that the ternary composite photoanode had stronger light absorption, smaller Eg (1.96 eV) and Rct (0.71 Ω), and higher photocurrent current density (0.16 mA cm−2) than binary and single composite photoanodes, indicating that it had higher utilization rate of excitation light energy and carrier mobility. The RhB degradation rate, Pmax, Jsc and Voc of PFC were 93.1 % (90 min), 18.02 µW cm−2, 0.223 mA cm−2 and 0.44 V, respectively. Further mechanistic studies show that the PFC has good photoexcited carrier separation and strong redox capacity due to double Z-scheme heterojunction between Bi2WO6 and InVO4 and between Bi2WO6 and g-C3N4, so as to generate more O2− and h+ to degrade RhB through N-deethylation, dealkylation and ring opening reactions. This study provides a practical approach for the development of high-efficiency double Z-scheme composite photoanode.

Cellulose acetate-based polymer electrolyte for energy storage application with the influence of BaTiO3 nanofillers on the electrochemical properties: A progression in biopolymer-EDLC technology

The bio-based solid polymer electrolyte serves as a promising choice for the next generation of energy storage devices to meet the requirement of green chemistry. In the current research, a green plasticized magnesium ion-conducting biopolymer electrolyte was developed using simple solution casting method for Electric Double Layer Capacitors (EDLC) applications. The biopolymer Cellulose Acetate (CA) as the host polymer, with varying concentrations of BaTiO3 as the nanofiller, Mg(CF3SO3)2 as the ionic dopant, and PEG as the plasticizer. A 2 wt% addition of BaTiO3 to the biopolymer electrolyte exhibits maximum conductivity measuring 2.4 × 10−3 S/cm. Linear Sweep Voltammetry (LSV) analysis demonstrates maximum stability voltage of 3.51 V. The ionic transference number (tion) and (tMg2+) were determined to be 0.99 and 0.41 respectively. The fabricated EDLC device with the same electrolyte showed polarisation curve without any noticeable peaks in the Cyclic Voltammetry (CV) plot, indicating no redox reactions occurring at the electrode-electrolyte interface. Galvanostatic Charge Discharge (GCD) results showed excellent coulombic efficiency, stability and Energy Density and Power Density performance over 2000 cycles. The incorporation of BaTiO3 into biopolymer membranes presents a viable approach towards sustainable energy storage solutions by enhancing the energy storage capacity of EDLC devices.