Metal Corrosion Research Articles

Crystallographic Reorientation Induced by Gradient Solid-Electrolyte Interphase for Highly Stable Zinc Anode.

Oriented zinc (Zn) electrodeposition is critical for the long-term performance of aqueous Zn metal batteries. However, the intricate interfacial reactions between the Zn anode and electrolytes hinder a comprehensive understanding of Zn metal deposition. Here, the reaction pathways of Zn deposition and report the preferential formation of Zn single-crystalline nuclei followed by dense Zn(002) deposition is elucidated, which is induced by a gradient solid-electrolyte interphase (SEI). The gradient SEI composed of abundant B-O and C species facilitates faster Zn2+ nucleation rate and smaller nucleus size, promoting the formation of Zn single-crystalline nuclei. Additionally, the homogeneity and mechanical stability of SEI ensure the crystallographic reorientation of Zn anodes from Zn(101) to (002) planes, efficiently inhibiting dendrite growth and metal corrosion during the Zn2+ stripping/plating process. These advantages significantly enhance the stability of the Zn anode, as demonstrated by the prolonged cycling lifespan of symmetric Zn batteries and exceptional reversibility (>99.5%) over 5000 cycles in Zn//Cu asymmetric batteries. Notably, this strategy also enables the stable operation of anode-free Zn//I2 batteries with a long lifespan of 3000 cycles. This work advances the understanding of Zn electrochemical behaviors, encompassing Zn nucleation, growth, and Zn2+ stripping/plating.

Unveiling the Potential of Ultraviolet Fluorescence Imaging as a Versatile Inspection Tool: Insights from Extensive Photovoltaic Module Inspections in Multi‐MWp Photovoltaic Power Stations

UV fluorescence imaging (UVF) has the potential to grow into a powerful, informative, and economically attractive inspection method for photovoltaic (PV) power stations. UVF demonstrates the ability to indicate differences in polymer types and degradation states in backsheets and encapsulation materials of PV modules. The data acquisition rate of UVF measurements is 10 to 15 times higher than that achieved by state‐of‐the‐art near‐infrared spectroscopy, enabling the mapping of the bill of materials (BoMs) and degradation state for every module in large PV arrays. Combinations of UVF with vibrational spectroscopies allow the polymer BoMs to be recognized and correlated with aging phenomena such as metal corrosion or potential induced degradation. UVF imaging can also be used for conventional visualization of nonmaterial‐related anomalies, such as hot cells or cell cracks. The low purchase cost of the equipment makes UVF an affordable and high‐throughput diagnostic method yielding comprehensive information that would otherwise only be accessible by combining several slower and more laborious methods. Automated UVF image analysis and refinements of correlations between different BoMs and UVF pattern geometry can further unlock the potential of UVF as a straightforward tool accessible to all stakeholders and promote proactive strategies for the optimization of the reliability and performance of PV power stations.

Study of Global Seawater Corrosivity Classification Based on Marine Environmental Factors Data

ABSTRACTTo evaluate the global seawater corrosivity and ensure the service safety of marine equipment, the methods of seawater corrosivity classification, which contained the standard metal corrosion rates method and the environmental factors evaluation method, are proposed and then applied to the seawater corrosivity classification in typical China seas. By comparing the results from both methods, the feasibility of the environmental factors evaluation method based on the grey relational model is verified. Furthermore, with the collection and processing of typical seawater factors data of global ocean, the corrosivity of global seawater is classified into six grades with the corrosion test data of carbon steel as baseline, and its distribution in different months is visualized by means of ArcGIS technology. The results show that the sea areas with high corrosivity are mainly located at equatorial and tropical sea areas, and for carbon steel, seawater temperature was the main influence on seawater corrosivity.

A novel corrosion inhibitor for copper in sulfuric acid media: Complexation of iodide ions with Benincasa Hispida leaf extract

In the context of green and low-carbon development, the rapid development of industry brings the problem of metal corrosion costs increase, metal corrosion protection methods are of great concern. Extracts from Benincasa hispida leaves (BHLE), which were obtained through pressurised liquid extraction, were employed as a inhibitor for copper corrosion in 0.5 M H2SO4. Their composition and anti-corrosion properties were subsequently analyzed and evaluated. The electrochemical analysis results indicated that BHLE functions as a cathodic-type corrosion inhibitor. The anti-corrosion performance intensifies with the increase in concentration but diminishes gradually as the temperature rises, when the concentration of BHLE is 400 mg/L, the corrosion inhibition efficiency can reach 91.82 %, when the concentration of added potassium iodide reaches 16 mg/L the slow-release efficiency of the compounded corrosion inhibitor reaches 96.92 %. The addition of I− strengthens the inhibition efficiency through the adsorption form dominated by competitive adsorption. The adsorption of BHLE onto the surface of copper follows the Langmuir monolayer adsorption model.

Carbon dot aggregates: a new strategy to promote corrosion inhibition performance of carbon dots

The corrosion of metal not only produces serious economic losses and environmental pollution but also threatens equipment safety. Carbon dots (CDs) exhibit outstanding inhibition properties to availably retard the corrosion of metal. However, the present CDs-based corrosion inhibitors still fail to fully exert the environmentally friendly and low-cost merits of CDs. To address this issue, CD aggregates (CDAs) prepared by low-cost and eco-friendly CDs are developed as novel corrosion inhibitors for the first time, and their corrosion inhibition mechanism is disclosed. Specifically, CDAs with excellent long-term dispersion stability are synthesized by solvothermal treatment of CDs formed by citric acid and urea. CDAs at only 200 mg/L provide a corrosion inhibition effect of 90.38% for Q235 carbon steel in 1 mol/L HCl solution, approximately 1.53 times higher than that of CDs (59.21%). Moreover, the corrosion inhibition mechanism of CDAs is proposed through the analysis of adsorption isotherm, examination of corrosion morphologies, and theoretical calculations. That is, CDAs physically and chemically adsorb on the carbon steel surface, mainly hindering its anodic reaction, thus retarding the corrosion of carbon steel. This research firstly verifies the corrosion inhibition potential of green and low-cost CDAs and provides a novel strategy to promote the corrosion inhibition performance of CDs, promoting the progress of aggregate-based corrosion inhibitors.

Illuminating bioprocess responses to metal-based nanoparticles addition along hydrogen and methane production pathways: A review.

Recent research has discussed the positive impacts of metal-based nanoparticles (NPs) on bioprocesses producing either hydrogen (H2) or methane (CH4). The enhancement has been explained by mechanisms such as direct interspecies electron transfer (DIET), metal corrosion, and dissimilatory reduction. Such interactions could induce further benefits, such as controlling oxidation-reduction potential (ORP), mitigating toxicants, promoting enzymatic activity, and altering the microbiome, which have not yet been comprehensively discussed. Factors like metal type, oxidation state, and size of NPs are crucial for their reactivity and corresponding responses. This review discusses how different redox potentials of metals can regulate metabolic pathways and how NPs and their reactive ions can eliminate toxicants (e.g., sulfate) and enhance the activity of intra- and extracellular enzymes. The enrichment of responsive microorganisms in correlation with NPs is further discussed. A better understanding of the multifaceted role of metal-based NPs can guide potential new incorporation strategies to improve bioprocesses.

Study on the mechanism of aluminum melt corrosion of Fe-SG series metals

This paper investigates the corrosion behavior of Fe-SG series metals with different graphite nodule counts to molten Al by using the ultrasonic vibration hot-dip aluminum experimental method. Fe-SG series metals to aluminum melt exhibited a much better corrosion resistance compared to H13 tool steel. As the graphite nodule count increases, the hot melting loss rate of Fe-SG series metals gradually decreases, indicating an improvement in corrosion resistance to aluminum melt. Scanning and EDS analysis of the samples after hot-dip aluminum testing revealed that the thickness of the product layer increased progressively with the extension of hot-dip aluminum time. Through the analysis of the structure and composition of the product layer, it was found that the corrosion products in H13 steel were composed of Fe2Al5 and FeAl3. In addition to the two phases, the product layer of the Fe-SG series metals also contained granularly distributed Fe-Al-Si intermetallic compounds within the Fe2Al5 phase. This resulted in a better corrosion resistance to aluminum melt.

Synthesis and Evaluation of New Type Plant Extraction Corrosion Inhibitor

The use of corrosion inhibitors in the development of oil and gas fields is an important means of effectively preventing metal corrosion, at present, the green growth of the oil and gas industry requires low-toxicity, low-residue, easy-to-post-treatment and other environmentally friendly corrosion inhibitors, however, most industrially used corrosion inhibitors such as mercury salts quaternary ammonium salts, and imidazolines are toxic to some degree. In this paper, a plant extract corrosion inhibitor was synthesized, firstly, the purple sweet potato extract was extracted by ethanol, and then the purple sweet potato extract and alkyl halide such as methane were used to produce the purple sweet potato corrosion inhibitor through condensation extraction and other processes, and the corrosion inhibitory performance of the inhibitor was evaluated by the loss-in-weight method, scanning electron microscopy, polarization curves, and impedance spectroscopy. The results show that there is a certain inhibition effect on N80 steel in the simulated stratum water environment, and the retardation rate can reach 91.38% in the gas phase, and the corrosion product morphology and chemical elements on the surface of N80 steel specimens were characterized by SEM, EDS, and it can be observed that a relatively dense protective film was formed after adding purple sweet potato corrosion inhibitor, and the corrosion inhibition rate can be known according to the weightlessness curve, Tafel curve and impedance curve. The corrosion inhibition rate increases with the increase of corrosion inhibitor concentration.

A high-performance boron nitride nanocomposite coating with enhanced anticorrosion and flame retardant properties for aerospace applications

The efficiency of impermeable, two-dimensional material-infused nanocomposites in preventing metal corrosion is becoming more widely acknowledged. The remarkable chemical and thermal durability of 3-(2-aminomethylamino)butyltrimethoxysilane (AMBMS)-functionalized hexagonal boron nitride (BN) sets it apart from others. This study looks into adding more graphitic carbon nitride (GCN) and functionalized BN to the polymer to make it more resistant to corrosion and fire. Electrochemical methods were used on aluminum substrates to evaluate the performance of the proposed polyurethane (PU)/functionalized BN/GCN coating in a 3.5 wt% NaCl solution. After 800 h of exposure, Electrochemical Impedance Spectroscopy (EIS) indicated a coating resistance of 1.15 × 109 Ω.cm2, indicating significant increases in corrosion resistance. The protection efficiency of the composite coating was calculated to be 99.9 %. Furthermore, the coating exhibited an angle of contact with water of 163°, indicating its exceptional water repellency. The PU/functionalized BN/GCN composite had a much lower peak heat release rate than pure PU, which means it is better at keeping flames from spreading. These enhancements contribute to improved safety in potential applications. This durability is particularly important for aerospace applications, where long-term performance is critical. In short, the addition of functionalized BN/GCN to PU coatings significantly enhances the material’s mechanical, flame retardant, and corrosion resistance qualities, making it ideal for use in harsh environments such as aerospace.

Trends of Benzotriazoles and Benzothiazoles in Australian Pooled Urine Samples from 2012 to 2023.

Benzotriazoles (BZTs) and benzothiazoles (BTs) are high-production-volume chemicals utilized in many different commercial products and industrial processes, such as metal corrosion inhibitors, vulcanization accelerators, plastic-associated UV stabilizers, and pharmaceutical precursors. This study assessed age, gender, and temporal trends of BZTs and BTs in deidentified surplus pathology urine samples, pooled and stratified by age, gender, and sample collection year from a general Australian population (168 pools representing 16,800 individuals). Tolyltriazole (TTri), 5,6-dimethyl-1H-benzotriazole (DMBZT), 1,3-benzothiazole (BTH), 2-hydroxybenzothiazole (2-OH-BTH), and 2-aminobenzothiazole (2-amino-BTH) were detected in >50% of the pools. TTri was frequently detected in pooled samples representing ≤45-year-olds (both genders). Concentrations of DMBZT, BTH (females), 2-OH-BTH, and 2-amino-BTH (females) increased with age significantly, with adults (>15 years old) showing higher levels than children (≤15 years old). Gender differences in DMBZT concentrations (females > males) were observed across all sampling years and only in some for TTri (males > females: >45 years old), BTH (females > males), and 2-amino-BTH (males > females). A temporal increase in BTH, 2-OH-BTH, and 2-amino-BTH levels within the studied period (2012-2023) has been observed. Our findings suggest ongoing exposure of the Australian general population to BZTs and BTs, highlighting age, gender, and temporal trends of these compounds as measured via their urinary concentrations.

Efficient Metal Corrosion Area Detection Model Combining Convolution and Transformer

In the context of rapid industrialization, efficiently detecting metal corrosion areas has become a critical task in preventing material damage. Unlike conventional semantic segmentation targets, metal corrosion characteristics vary significantly in color, texture, and size. Traditional image segmentation methods need improvement in scenarios involving occlusions, shadows, and defects. This paper proposes a convolution and sequence encoding combined network, MCD-Net, for metal corrosion area segmentation. First, a visual Transformer sequence encoder is introduced into the convolutional encoder–decoder network to enhance global information processing capabilities and establish long-range feature dependencies. A feature fusion method based on an attention module is proposed to enhance the model’s ability to recognize corrosion boundaries, thereby enhancing segmentation accuracy and model robustness. Finally, in the model’s decoding stage, a score-based multi-scale feature enhancement method is employed to emphasize significant features in the corrosion areas. Experimental results indicate that this method attained an F1 score of 84.53% on a public corrosion dataset, demonstrating the model’s deeper understanding and reasoning capabilities for shadow and defect features, as well as excellent noise resistance performance.

Correlation between Voltammetry of Immobilized Particles and Mott-Schottky analysis of metal corrosion patinas.

The conjoint application of the voltammetry of immobilized particles (VIMP) methodology and the Mott-Schottky analysis (MS) of impedance data to studying metal corrosion patinas is described. The study is applied to copper and bronze objects exploiting the semiconducting character of cuprite and other copper corrosion products. A simplified theoretical modeling of MS analysis at microparticulate deposits extracted from metal corrosion layers attached to graphite electrodes is provided. The proposed model compensates for the disturbing effect of the regions of the basal electrode directly exposed to the electrolyte. Alternative models accounting for the variation of the density of charge carriers with depth are tested as well as the correlation between VIMP and MS data with reasonably satisfactory results.

Revealing the Reaction Pathway of Anodic Hydrogen Evolution at Magnesium Surfaces in Aqueous Electrolytes.

Aqueous metal corrosion is a major economic concern in modern society. A phenomenon that has puzzled generations of scientists in this field is the so-called anomalous hydrogen evolution: the violent dissolution of magnesium under electron-deficient (anodic) conditions, accompanied by strong hydrogen evolution and a key mechanism hampering Mg technology. Experimental studies have indicated the presence of univalent Mg+ in solution, but these findings have been largely ignored because they defy our common chemical understanding and evaded direct experimental observation. Using recent advances in the ab initio description of solid-liquid electrochemical interfaces under controlled potential conditions, we describe the full reaction path of Mg atom dissolution from a kinked Mg surface under anodic conditions. Our study reveals the formation of a solvated [Mg2+(OH)-]+ ion complex, challenging the conventional assumption of Mg2+ ion formation. This insight provides an intuitive explanation for the postulated presence of (Coulombically) univalent Mg+ ions, and the absence of protective oxide/hydroxide layers normally formed under anodic/oxidizing conditions. The discovery of this unexpected and unconventional reaction mechanism is crucial for identifying new strategies for corrosion prevention and can be transferred to other metals.

Performance of carbon felt as cathodes in magnesium corrosion method to recover phosphate from swine wastewater

With the large-scale development of the livestock and poultry breeding industries, swine wastewater with high nitrogen and phosphorus concentrations has become an urgent problem. Given the continuous demand for phosphorus resources in industrial production, the study of phosphate recovery in phosphorus-rich wastewater is of great value for the sustainable utilization of phosphorus resources and for alleviating the eutrophication of aquatic ecosystems. In this study, a magnesium metal corrosion method was used to recover phosphorus resources from swine wastewater using carbon felt as the cathode instead of traditional cathode materials such as graphite and titanium plates. The effects of different cathode materials on the corrosion potential of magnesium metal plates were compared, and the effects of carbon felt as a cathode plate on the removal rate and pH of phosphate from wastewater were discussed. Additionally, the economic feasibility of phosphate recovery from swine wastewater was evaluated. The experimental results showed that the effect of carbon felt on the corrosion potential of the magnesium metal plate was more evident than that of the graphite and titanium plates (Ecorr = −1.74676). When carbon felt was used as the cathode plate, the most energy-saving reaction conditions were as follows: reaction time T = 30 min, ratio of wastewater volume to plate area V: S = 500 cm3:50 cm2, aeration rate Re = 8 L/min, stirring rate r = 400 rpm, phosphate recovery rate = 92.3%, and pH = 8.83. The economic feasibility assessment shows that the proposed method is $2.047 g-1 PO4-P without considering the reuse of carbon felt. Carbon felt has good stability and can be recycled eight times or more, and the proposed method achieves a more efficient phosphate recovery rate at a relatively low cost.

Synergistic Cationic Shielding and Anionic Chemistry of Potassium Hydrogen Phthalate for Ultrastable Zn─I2 Full Batteries.

Electrolyte additives are investigated to resolve dendrite growth, hydrogen evolution reaction, and corrosion of Zn metal. In particular, the electrostatic shielding cationic strategy is considered an effective method to regulate deposition morphology. However, it is very difficult for such a simple cationic modification to avoid competitive hydrogen evolution reactions, corrosion, and interfacial pH fluctuations. Herein, multifunctional additives of potassium hydrogen phthalate (KHP) based on the synergistic design of cationic shielding and anionic chemistry for ultrastable Zn||I2 full batteries are demonstrated. K cations, acting as electrostatic shielding cations, constructed the smooth deposition morphology. HP anions can enter the first solvation shell of Zn2+ for the reduced activities of H2O, while they remain in the primary solvation shell and are finally involved in the formation of SEI, thus accelerating the charge transfer kinetics. Furthermore, by in situ monitoring the near-surface pH of the Zn electrode, the KHP additives can effectively inhibit the accumulation of OH- and the formation of by-products. Consequently, the symmetric cells achieve a high stripping-plating reversibility of over 4500 and 2600 h at 1.0 and 5mA cm-2, respectively. The Zn||I2 full cells deliver an ultralong term stability of over 1400 cycles with a high-capacity retention of 78.5%.

Proteomics and EPS Compositional Analysis Reveals Desulfovibrio bisertensis SY-1 Induced Corrosion on Q235 Steel by Biofilm Formation

Microorganisms that exist in the seawater form microbial biofilms on materials used in marine construction, especially on metal surfaces submerged in seawater, where they form biofilms and cause severe corrosion. Biofilms are mainly composed of bacteria and their secreted polymeric substances. In order to understand how biofilms promote metal corrosion, planktonic and biofilm cells of Desulfovibrio bizertensis SY-1 (D. bizertensis) from Q235 steel were collected and analyzed as to their intracellular proteome and extracellular polymeric substances (EPS). The intracellular proteome analysis showed that the cellular proteins were strongly regulated in biofilm cells compared to planktonic cells, e.g., along with flagellar proteins, signaling-related proteins were significantly increased, whereas energy production and conversion proteins and DNA replication proteins were significantly regulated. The up-and-down regulation of proteins revealed that biofilm formation by bacteria on metal surfaces is affected by flagellar and signaling proteins. A significant decrease in DNA replication proteins indicated that DNA is no longer replicated and transcribed in mature biofilms, thus reducing energy consumption. Quantitative analysis and lectin staining of the biofilm on the metal’s surface revealed that the bacteria secreted a substantial amount of EPS when they began to attach to the surface, and proteins dominated the main components of EPS. Further, the infrared analysis showed that the secondary structure of the proteins in the EPS of the biofilm was mainly dominated by β-sheet and 3-turn helix, which may help to enhance the adhesion of EPS. The functional groups of EPS analyzed using XPS showed that the C element of EPS in the biofilm mainly existed in the form of combinations with N. Furthermore, the hydroxyl structure in the EPS extracted from the biofilm had a stronger hydrogen bonding effect, which could maintain the stability of the EPS structure and biofilm. The study results revealed that D. bizertensis regulates the metabolic pathways and their secreted EPS structure to affect biofilm formation and cause metal corrosion, which has a certain reference significance for the study of the microbially influenced corrosion (MIC) mechanism.

Neutron phase filtering for separating phase- and attenuation signal in aluminium and anodic aluminium oxide

Neutron imaging has gained significant importance as a material characterisation technique and is particularly useful to visualise hydrogenous materials in objects opaque to other radiations. Fields of application include investigations of hydrogen in metals as well as metal corrosion, thanks to the fact that neutrons can penetrate metals better than e.g. X-rays and are highly sensitive to hydrogen. However, at interfaces refraction effects sometimes obscure the attenuation image, which is used for hydrogen quantification. Refraction, a differential phase effect, diverts the neutron beam away from the interface in the image leading to intensity gain and intensity loss regions, which are superimposed to the attenuation image, thus obscuring the interface region and hindering quantitative analyses of e.g. hydrogen content in the vicinity of the interface. For corresponding effects in X-ray imaging, a phase filter approach was developed and is generally based on transport-of-intensity considerations. Here, we compare such an approach, that has been adapted to neutrons, with another simulation-based assessment using the ray-tracing software McStas. The latter appears superior and promising for future extensions which enable fitting forward models via simulations in order to separate phase and attenuation effects and thus pave the way for overcoming quantitative limitations at refracting interfaces.

Effect of Heat Treatment on Corrosion Behavior of S275 Mild Steel Using Accelerated DC Voltage, LPR, and EIS

AbstractThis study used an external DC voltage of 1.5 V to accelerate corrosion in heat-treated S275 mild steel samples at different time intervals. LPR and EIS were used to study the corrosion behavior of original and quenched steel samples. There was only a negligible difference in the corrosion rate (CR) for the original and the quenched samples up to 30 min of voltage application in a 3.5% NaCl electrolyte media. When the exposure time increased to 60 min, the original sample showed seven times higher CR than the quenched samples. The pits on the surface of the original samples acted as cathodes, enhancing the reaction rate on the surface and increasing its CR dramatically. This led to bimodal corrosion, where the first part is led by concentration and diffusion; while, the second part is led by localized corrosion. The smaller pits on the original surface samples served as cathodic reaction centers, exacerbating corrosion. The corrosion rate of the original samples ranged from 0.8 to 7.8 mmpy; whereas, the corrosion rate of the quenched samples remained consistently around 0.8 mmpy. This trend can be observed in long-term corrosion in different metals. The uniformly oriented martensitic microstructure and the quenched samples’ small grain size prevented the enhanced ion penetration due to applied voltage. This study analyses the long-term stability of structural steel samples in marine environments by accelerating the corrosion rate by an applied external DC voltage.

Quantitative Advantages of Corrosion Sensing Using Fluorescence, Microscopy, and Single-Molecule Detection.

The corrosion of metals and alloys is a fundamental issue in modern society. Understanding the mechanisms that cause and prevent corrosion is integral to saving millions of dollars each year and to ensure the safe use of infrastructure subject to the hazardous degrading effects of corrosion. Despite this, corrosion detection techniques have lacked precise, quantitative information, with industries taking a top-down, macroscale approach to analyzing corrosion with tests that span months to years and yield qualitative information. Fluorescence, a well-established optical method, can fill the niche of early-stage, quantitative corrosion detection and can be employed for both bulk and localized testing over time. The latter, fluorescence microscopy, can be pushed to greater levels of detail with single-molecule microscopy, achieving nanometer spatial and subsecond temporal resolutions of corrosion that allow for the extraction of dynamic information and kinetics. This review will present how fluorescence microscopy can provide researchers with a molecular view into the chemical mechanisms of corrosion at interfaces and allow for faster, quantitative studies of how to detect and prevent corrosion.

Enhanced photocathodic protection performance of TiO2/SnO2/CdIn2S4 composites for 304 stainless steel in marine environments

In humid and saline environments, metal corrosion leads to significant economic losses, necessitating enhanced anti-corrosion methods. This study aims to enhance the photocathodic protection (PCP) performance of TiO2 nanotubes (NTs) by incorporating SnO2 quantum dots (QDs) and CdIn2S4 nanoflowers (NFs). TiO2 NTs were fabricated on titanium substrates via anodization, followed by successive deposition of SnO2 QDs and CdIn2S4 NFs using immersion and hydrothermal methods. The composite materials were characterized using SEM, TEM, XRD, and XPS. The PCP performance was evaluated through electrochemical tests on 304 stainless steel (304ss). The TiO2/SnO2/CdIn2S4 (T/S/C) composite exhibited a photocurrent density seven times that of pure TiO2 NTs, indicating significantly enhanced separation ability. The composite also demonstrated a notable open-circuit potential (OCP) of −1045 mV vs. SCE. Furthermore, T/S/C could provide delayed protection for up to 10 h in the dark, indicating its electron storage capability. The T/S/C composite material enhances the corrosion resistance of 304ss, offering a promising approach for practical anti-corrosion applications.