In-situ investigation of atmospheric corrosion behavior of bronze under thin electrolyte layers using electrochemical technique

The atmospheric corrosion behavior of bronze under thin electrolyte layer （TEL） with different thicknesses was monitored using cathodic polarization curves, open circuit potential （OCP） and electrochemical impedance spectroscopy （EIS）. Cathodic polarization result indicates that the cathodic limiting current density increases with decreasing the TEL thickness. EIS result shows that the corrosion rate increases with decreasing the TEL thickness at the initial stage because the corrosion is dominated by the cathodic process, whereas after long immersion time, the corrosion degree with the TEL thickness is in the sequence of 150 μm 〉 310 μm〉 10μm ≈ bulk solution 〉 57 μm. The measurements of OCP and EIS present in-situ electrochemical corrosion information and their results are in good agreement with that of physical characterizations.

Corrosion Measurements of Reinforcing Steel by Different Electrochemical Techniques

Electrochemical techniques of the corrosion measurements of reinforcing steeI in concrete have been evaluated. These techniques include half-cell potential measurements, impressed voltage method, impressed current method and potentiostatic polarization technique. The results of corrosion behaviour of the steel in both 5%NaCl and 5%MgSO4 show that each electrochemical technique provides some information about the condition of the steel bar or the corrosivity of the environment being evaluated, yet none provides a complete data regarding the corrosion resistance of reinforcing steel in aggressive media

Measurement of Concentration Distribution of Electrogenerated Etchant Using an Electrochemical Probe Technique

An electrochemical probe measurement system for detecting an electrogenerated etchant in solution is developed.Concentration distribution of electrogenerated etchant bromine as close as 8 micrometer to the surface of macrodisk is studied quantitatively.

Study of Corrosion Resistance of Laser Welded Au-Pd-Ag-In Alloy Using Electrochemical Techniques

The aim of this work was to evaluate the corrosion resistance of AuPdAgIn alloy, submitted to laser beam welding, in 0.9% NaCl solution, using electrochemical techniques. Measures of the open circuit potential (OCP) versus time were applied to electrochemical experiments, as well as potentiodynamic direct scanning (PDS) and electrochemical impedance spectroscopy (EIS) on AuPdAgIn alloy, submitted to laser beam welding in 0.9% NaCl solution. Some differences observed in the microstructure can explain the results obtained for corrosion potential, Ecorr, and corrosion resistance, Rp. EIS spectra have been characterized by distorted capacitive components, presenting linear impedance at low frequencies, including a non-uniform diffusion. The area of the laser weld presented corrosion potential slightly superior when compared to the one of the base metal. The impedance results suggest the best resistant corrosion behavior for laser weld than base metal region. This welding process is a promising alternative to dental prostheses casting.

An overview of electrochemical,non-electrochemical and analytical approaches for studying corrosion in magnesium and its alloys

Corrosion is a pervasive phenomenon affecting materials across a multitude of scales,from the atomic to the macroscopic.This review paper presents a comprehensive examination of the methodologies employed in the analysis of magnesium corrosion,including electrochemical,non-electrochemical and analytical approaches,emphasizing the need for a diverse array of analytical tools to understand the complex interplay between corrosion,microstructure,and the dissolution mechanisms of magnesium alloys.The research showcases the utility of specific tools like SEM/EDS and SKPFM for targeted site analysis,while XPS and FTIR provide a broader perspective on specimen surfaces.The paper also discusses the value of in-situ analysis techniques,which allow for the real-time observation of corrosion processes,offering a dynamic view of the emergence and evolution of corrosion products.These in-situ methods stand in contrast to ex-situ analyses,which only permit post-experimental evaluation.By highlighting the capabilities of various analytical tools,from those that reveal surface layer details to those that probe deeper structures,and from those that detect primary elements to those that trace minute quantities of impurities,this study underscores the intricate nature of corrosion and the critical role of advanced analytical techniques in fostering a deeper understanding of material degradation.The findings advocate for the increased application of in-situ analysis in magnesium corrosion research,as it provides a more immediate and accurate depiction of corrosion dynamics,potentially leading to more effective corrosion prevention and control strategies.

Effect of Rapid Quenching on Microstructures and Electrochemical Performances of La_2Mg(Ni_(0.85)Co_(0.15))_9M_(0.1)(M=B, Cr) Hydrogen Storage Alloys

The La-Mg-Ni-system （PuNi3-type） La2Mg （Ni0.85 Co0.15 ）9M0.1 （ M = B, Cr） hydrogen storage etectrode alloys were prepared by casting and rapid quenching. The electrochemical performances and microstructures of the as-cast and quenched alloys were determined and measured. The effects of rapid quenching on the microstructures and electrochemical properties of the alloys were investigated in detail. The obtained results show that the alloys are composed of the （La, Mg） Ni3 phase （PuNi3-type structure） and the LaNi5 phase, as well as the small amount of the LaNi2 phase. A trace of the Ni2B phase exists in the as-cast alloy containing boron, and the Ni2B phase in the alloy nearly disappears after rapid quenching. The relative amount of each phase in the alloys depends on the quenching rate. The rapid quenching technique can greatly improve the electrochemical performance of the alloy, and the effect of rapid quenching on the activation performances of the alloys is minor. Rapid quenching enhances the cycle stability of the alloy, and the cycle life of the alloy increases with the increase of the quenching rate.

Decoding lithium batteries through advanced in situ characterization techniques

Given the energy demands of the electromobility market,the energy density and safety of lithium batteries(LBs)need to be improved,whereas its cost needs to be decreased.For the enhanced performance and decreased cost,more suitable electrode and electrolyte materials should be developed based on the improved understanding of the degradation mechanisms and structure–performance correlation in the LB system.Thus,various in situ characterization technologies have been developed during the past decades,providing abundant guidelines on the design of electrode and electrolyte materials.Here we first review the progress of in situ characterization of LBs and emphasize the feature of the multi-model coupling of different characterization techniques.Then,we systematically discuss how in situ characterization technologies reveal the electrochemical processes and fundamental mechanisms of different electrode systems based on representative electrode materials and electrolyte components.Finally,we discuss the current challenges,future opportunities,and possible directions to promote in situ characterization technologies for further improvement of the battery performance.

Electrochemical deposition of Mg(OH)_(2)/GO composite films for corrosion protection of magnesium alloys

Mg(OH)_(2)/graphene oxide(GO)composite film was electrochemical deposited on AZ91D magnesium alloys at constant potential.The characteristics of the Mg(OH)_(2)/GO composite film were investigated by scanning electron microscope(SEM),energy-dispersive X-ray spectrometry(EDS),X-ray diffractometer(XRD)and Raman spectroscopy.It was shown that the flaky GO randomly distributed in the composite film.Compared with the Mg(OH)_(2)film,the Mg(OH)_(2)/GO composite film exhibited more uniform and compact structure.Potentiodynamic polarization tests revealed that the Mg(OH)_(2)/GO composite film could significantly improve the corrosion resistance of Mg(OH)_(2)film with an obvious positive shift of corrosion potential by 0.19 V and a dramatic reduction of corrosion current density by more than one order of magnitude.

Electrochemical hydrogen storage performance of AB_(5-)CoB composites synthesized by a simple mixing method

AB5 （MlNi4.0Al0.3Cu0.5Zn0.2） alloy and CoB alloy were prepared by arc melting. AB5-CoB composites were synthesized by simple mixing of AB5 alloy powders and CoB alloy powders, and their electrochemical hydrogen storage properties were studied as negative electrodes in KOH aqueous solution. The maximum discharge capacity of the AB5-CoB（50%） composite （the content of CoB in the composite is 50 wt.%） reached 365.3 mAh.g^-1. After 100 charge-discharge cycles, the discharge capacity of the AB5-CoB（50%） composite was still much higher than that of the AB5 alloy. The high rate discharge capability （HRD） and potentiodynamic polarization were also tested.

Combined electronic/atomic level computational, surface(SEM/EDS),chemical and electrochemical studies of the mild steel surface by quinoxalines derivatives anti-corrosion properties in 1 mol·L^(-1) HCl solution

This work is devoted to the study of the inhibition of corrosion of mild steel(MS)in molar hydrochloric acid(1 mol·L-1 HCl)by two named quinoxaline derivatives namely,2-(2,4-dichlorophenyl)-1,4-dihydroquinoxaline(HQ)and 2-(2,4-dichlorophenyl)-6-methyl-1,4-dihydroquinoxaline(CQ).The inhibitory efficacy of HQ and CQ compounds is first evaluated using the gravimetric method and using electrochemical techniques(stationary and transient techniques).The results showed that our compounds are efficient corrosion inhibitors and the inhibition rates(ηEIS%)reached up to 91%and 94.2%at 10-3 mol·L-1 for HQ and CQ,respectively.The mentioned molecules are classified as mixed-type inhibitors.The adsorption of these inhibitors on the surface of steel in hydrochloric HCl 1 mol·L-1 medium obeys the Langmuir adsorption isotherm.The results of the scanning electron microscope(SEM)showed the formation of a protective film on the surface of the steel in the presence of the inhibitors studied.Elementary analysis is obtained by energy dispersive X-ray spectroscopy(EDS).The inhibition property was further elucidated by theoretical approaches such as:Density Functional Theory(DFT),quantum chemical descriptors(QCD),local reactive indices,solvent effect,theoretical complexation,Molecular Dynamic(MD)simulation,effect of temperature on adsorption energy(Eads),Radial Distribution Function(RDF),and Mean Square Displacement(MSD).The results of these approaches support the experimental results.

Rational design of bismuth-based catalysts for electrochemical CO_(2) reduction

Sustainable conversion of carbon dioxide(CO_(2))to high value-added chemicals and fuels is a promising solution to solve the problem of excessive CO_(2) emissions and alleviate the shortage of fossil fuels,maintaining the balance of the carbon cycle in nature.The development of catalytic system is of great significance to improve the efficiency and selectivity for electrochemical CO_(2) conversion.In particular,bismuth(Bi)based catalysts are the most promising candidates,while confronting challenges.This review aims to elucidate the fundamental issues of efficient and stable Bi-based catalysts,constructing a bridge between the category,synthesis approach and electrochemical performance.In this review,the categories of Bi-based catalysts are firstly introduced,such as metals,alloys,single atoms,compounds and composites.Followed by the statement of the reliable and versatile synthetic approaches,the representative optimization strategies,such as morphology manipulation,defect engineering,component and heterostructure regulation,have been highlighted in the discussion,paving in-depth insight upon the design principles,reaction activity,selectivity and stability.Afterward,in situ characterization techniques will be discussed to illustrate the mechanisms of electrochemical CO_(2) conversion.In the end,the challenges and perspectives are also provided,promoting a systematic understanding in terms of the bottleneck and opportunities in the field of electrochemical CO_(2) conversion.

Electrochemical and Theoretical Studies of 1-Alkyl-2-substituted Benzimidazoles as Corrosion Inhibitors for Carbon Steel Surface in HCl Medium

The inhibition efficiencies of newly synthesized four 1-alkyl-2-substituted benzimidazole compounds（a^d） have been studied for the corrosion of carbon steel in 1.0 M HCl by using potentiodynamic polarization measurement. The four inhibitors act as mixed-type inhibitors,which mainly inhibit cathodes. The inhibition efficiency of these compounds enhanced when the concentration of the inhibitors increased. A theoretical study of the corrosion inhibition efficiency of these compounds was carried out by using the B3 LYP level with the 6-31＋G＊ basis set. Considering the solvent effect,the IEFPCM model was selected. Furthermore,the adsorption energies of the inhibitors with the iron（001） surface were studied by using molecular dynamic（MD） simulations. The theoretical results show that these inhibitors all exhibit several adsorption active-centers. Meanwhile,the MD simulations indicate that the adsorption occurs mostly through benzene ring and the lone pair electrons of the nitro atoms. These results demonstrated that the theoretical studies and MD simulations are reliable and promising methods for analyzing the inhibition efficiency of organic inhibitors.

Development and Electrochemical Testing of Novel Bipolar Nickel Metal Hydride Batteries

Some aspects in the designt and development of bipolar Ni/MH battery are presented. After optimizing sealing technique and modifying capacity ratio of two adjacent electrodes in one sub-cell, some bipolar Ni/MH stacks with 6 sub-cells have been assembled and investigated. Electrochemical testing results show the bipolar battery has excellent high rate discharge capability and fast recharge ability, artd satisfactory charging efficiency in different states of charge. Moreover, the hattery also displays good stability under pulse cycles in simulating hybrid vehicle working oonditions.

Electrochemical biosensors represent promising detection tools in medicalfield

In recent years,there has been a growing demand for rapid detection methods,leading to the proliferation of biosensors,particularly electrochemical biosensors,which have garnered substantial attention from researchers.The fusion of biosensors with advanced electrochemical sensing technology has given rise to a diverse array of electrochemical biosensors characterized by their rapid detection capabilities and heightened sensitivity.Consequently,an imperative exists to comprehensively recapitulate recent advances in electrochemical biosensors,especially within the realm of clinical medicine.This review aims to elucidate the applications of electrochemical biosensors and delineate future development prospects,facilitating a more profound comprehension and further progression of thisfield.Specifically,we will examine the utilization of electrochemical biosensors in clinical medicine,encompassing their roles in point-of-care testing,disease diagnosis,and therapeutic monitoring.Moreover,we will spotlight emerging trends and prospective innovations,such as the evolution of nanostructured sensors and portable devices.By providing a comprehensive overview of the advances and potential applications of electrochemical biosensors in clinical medicine,this review will significantly contribute to the advancement of thisfield and serve as a catalyst for further research into innovative detection tools.

Assembly and electrochemical testing of renewable carbon-based anodes in SIBs:A practical guide

Sodium-ion batteries(SIBs)are considered as a promising candidate to replace lithium-ion batteries(LIBs)in large-scale energy storage applications.Abundant sodium resources and similar working principles make this technology attractive to be implemented in the near future.However,the development of high-performance carbon anodes is a focal point to the upcoming success of SIBs in terms of power density,cycling stability,and lifespan.Fundamental knowledge in electrochemical and physicochemical techniques is required to properly evaluate the anode performance and move it in the right direction.This review aims at providing a comprehensive guideline to help researchers from different backgrounds(e.g.,nanomaterials and thermochemistry)to delve into this topic.The main components,lab configurations,procedures,and working principles of SIBs are summarized.Moreover,a detailed description of the most used electrochemical and physicochemical techniques to characterize electrochemically active materials is provided.

Electrochemical Corrosion Behavior of Aluminum in Perchloric Acid

The effects of acetate, citrate, benzoate, tetra-ethylammonium iodide (TEA) and 1,4,8,11 tetra-azacyclo-tetradecane (cyclam) on the corrosion behavior of aluminum in 1 M HClO4 at 40°C were studied by potentiodynamic polarization technique. Acetate, citrate, and benzoate inhibited the corrosion of aluminum and shifted the breakdown potential to positive direction. Cyclam was investigated as a macrocyclic organic inhibitor to the acid corrosion of aluminum. The addition of cyclam to the corroding medium showed a pronounced effect on the anodic but not on the cathodic part of the polarization curve. The addition of TEA to the medium enhanced the corrosion rate and shifted the breakdown potential to more negative value as the concentration increased. The results were discussed on the basis of the adsorption mechanism and the nature of the adsorbed species.

Synthesis, Spectral and Electrochemical Studies of Complex of Uranium(IV) with Pyridine-3-Carboxylic Acid

The investigation of complexation of uranium with biological active ligands is vital for understanding uranium speciation in biosystems. A number of studies have been undertaken for investigating the complexation of uranium in its (VI) oxidation states but similar investigations pertaining to the interaction of uranium, in lower oxidation states, with biological ligands is scarce. The aim of the work is to bridge this gap and studies have been carried out to determine the coordination pattern of pyridine-3-carboxylic acid with uranium(IV). Semi-micro analysis, spectro-analytical techniques, magnetic susceptibility and cyclic voltammetry have been employed for the characterization of the synthesized complex.

Insight into the Electrochemical Behaviors of NCM811|SiO-Gr Pouch Battery through Thickness Variation

LiNi0.8Co0.1Mn0.1O2(NCM811)|SiOx-graphite(SiO-Gr.)battery chemistry is of intensive attention because its achievable practical energy density is approaching impressively 300 Wh Kg^(-1).However,it still suffers rapid capacity fades during repeated cycles,both chemical,electrochemical and mechanical irreversibility contribute.A comprehensive understanding behind the fading behavior of the cell chemistry is required before fully realize the benefits of this chemistry.Herein,the in-situ thickness variation is introduced as a diagnostic technique and is performed on 5-55 Ah NCM811|SiO-Gr cells.With the help of Li reference electrode and in-situ X-ray diffraction device,the correspondence between thickness variation and the electrode potential is carefully investigated.Firstly,the NCM811|SiO-Gr cell is characterized with the maximum cell thickness at around 80%state-of-charge(SOC)in the discharge process,rather than at 100%SOC.Secondly,the electrochemical behaviors during rate charge/discharge are diagnosed,and a Li platting signal is resolved from thickness variation profile at 2C.This work confirms that the thickness monitoring is a nondestructive and informative complement to conventional diagnostic techniques for failure analysis of pouch cells.

Controlled Growth of Well-Aligned Carbon Nanotubes, Electrochemical Modification and Electrodeposition of Multiple Shapes of Gold Nanostructures

An efficient method has been developed to synthesize well-aligned multi-walled carbon nanotubes (MWCNTs) on a conductive Ta substrate by chemical vapour deposition (CVD). Free-standing MWCNTs arrays were functionalized through electrochemical oxidation with the formation of hydroxyl and carboxyl functional groups. Using a new oven drying technique, we demonstrate that the unidirectionally aligned and laterally spaced geometry of the CNT arrays can be retained after being subjected to each step of electrochemical modification. Samples were analyzed by using a field emission scanning electron microscope (SEM), transmission electron microscope (TEM), Fourier transformed infrared (FTIR) and Raman spectroscopy. Useful electrochemical methods for the synthesis of various gold nanostructures onto the aligned MWCNTs were then presented for the first time. The results demonstrated that flowerlike nanoparticle arrays, nanosheets and nanoflowers were obtained on the aligned CNTs under different experimental conditions. These kinds of aligned-CNT/Au nanostructures hybrid materials introduced by these efficient and simple electrochemical methods could lead to development of a new generation device for ultrasensitive catalytic and biological application.