Surface Functionalization Research Articles

Porous activated carbon integrated carbon nitride nanosheets as functionalized separators for the efficient polysulfide entrapment in Li[sbnd]S batteries

Electrification of vehicles, hybrid aircraft and the advancement of portable electronics are exacting the deployment of high energy-dense batteries. The high theoretical capacity of sulfur (1675 mAh g−1), cost-effectiveness and environmental benignity of the lithium‑sulfur batteries (LSBs) are propitious for electrochemical energy storage beyond Li-ion battery technology. In this work, we described a simple, scalable preparation and electrochemical performance of porous activated carbon (PC)-infused graphitic carbon nitride (GCN) nanosheets with various ratios (PC@GCN 11, PC@GCN 12 and PC@GCN 21) as a polysulfide anchoring functionalized separator for LSBs. The high specific area (822 m2/g), hetero porosity, conductive carbon framework, surface functionalities and enriched N-doping of the PC@GCN synergistically induce mitigation of polysulfides via chemical and physical adsorption pathways in LSBs. The PC@GCN 21 modified separator demonstrates a high initial discharge capacity of 1389 mAh g−1 at a 0.1C rate and exhibits better capacity retention over 500 cycles at a 1C rate (655 mAh g−1) with sulfur loading of 3.8 mg/cm2 accompanied by high coulombic efficiency (94 %). The assembled cell with high S-loading (5.12 mg/cm2) shows a high initial discharge capacity of 712 mAh g−1 at 0.1C rate conditions. High Li-ion transference number (0.714), stable shuttle current, minimal coulombic efficiency loss (0.84 %), low shuttle factor and negligible self-discharge behaviour support the superior performance of the PC@GCN 21 coated cells. This report demonstrates that combining the high surface area, non-polar porous carbon with polar graphitic carbon nitride is a practical approach for designing metal-free functionalized separators for energy-dense LSBs.

Short DNAzymes for Efficient Catalysis of "Click" Reactions in Solution and on Surface.

We have systematically investigated and found surprising superior catalytic activities of very short DNAzymes for copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC), both in solution and on surface. As a key reaction of the "click chemistry" class, CuAAC is a highly efficient and specific covalent conjugation tool with demonstrated applications in organic synthesis, bioconjugation, and surface functionalization; however, it requires the presence of the Cu(I) catalyst, which is an unstable species in aqueous solutions. We show here that one ultrashort, 14-nucleotide-truncated fragment of an earlier in vitro selected DNAzyme (CLICK-17) shows a striking and superior catalytic activity toward the in trans CuAAC reaction in solution and on surface in the presence of either Cu(I) or Cu(II), at significantly lowered concentrations. These results obviate the need for long-sequence DNAzymes, selected out of the homogeneous solution phase, for application in complex surface environments.

Surface-engineered caterpillar-like silica nanocomposites for enhanced interparticle friction and interlock in shear thickening suspension

This study presents a novel method for fabricating surface-engineered caterpillar-like silica nanocomposites by combining rod-like nanorods with spherical nanoparticles to control aspect ratios and surface functionalization. This unique design facilitates functional assembly at the nanoscale. Additionally, we developed an innovative composite by encapsulating polyurethane elastomers within shear thickening fluid (STF)-impregnated Kevlar, significantly enhancing the flexibility and durability of the resulting STF/Kevlar/PU composite. Microstructural and chemical modifications were characterized, and detailed rheological analysis revealed a 165 % increase in viscosity and a substantial rise in storage modulus from 91.56 to 18,640 Pa, indicating improved surface morphology and roughness. These enhancements promoted stronger interparticle friction and rotational motion during flow. Impact resistance tests further demonstrated a 314 % increase in peak impact force, driven by frictional interactions between the dispersed caterpillar-like particles. The results confirmed that surface roughness and adhesive forces play a critical role in activating stress-dependent frictional contacts, a key mechanism behind the improved performance. These findings highlight the potential of these composites for mitigating penetration injuries and offer precise control over the shear-thickening transition in engineering applications, making them promising candidates for lightweight protective materials.

Titanium surface functionalization via directed energy deposition of CuNiTi ternary alloy

Pure titanium is a soft material that tends to degrade quickly during service due to wear and microbiologically influenced corrosion. Therefore, current research aims at the deposition, microstructural characterization, and surface functionalization of the TiCuNi coatings on pure titanium substrate to improve its surface properties. Cu–Ni premixed elemental powders are deposited on the pure Ti by laser-directed energy deposition (LDED) using a novel method of extracting Ti from the substrate through melt pool convection. The single-track deposit geometry and integrity characterization using dilution percentage, heat-affected zone width (HAZ), and microhardness values show the sound metallurgical bonding with the substrate. The X-ray diffraction (XRD) pattern and microstructure image reveal the presence of NiTi binary (B2) and Ti2CuNi ternary (B19) hard phases and equiaxed dendritic morphology, respectively, demonstrating ternary alloy coating formation. The microhardness value of the coatings is thrice that of the substrate due to the presence of hard NiTi (B2) binary and Ti2CuNi (B19) ternary phases. The coating’s wear resistance is significantly (80%) higher than the substrate, owing to hard phases and Cu as a solid lubricant. The wear track consists of small grooves, adhered debris, and a smooth profile, mainly due to a significant reduction in adhesion and abrasion compared to the substrate. Moreover, the polarisation corrosion potential and current density are increased and decreased by 53% and 97%, respectively, displaying symbolic improvement in the corrosion resistance. Hence, this work has presented the LDED ability to enhance the pure Ti anti-wear and corrosion resistance properties by depositing CuNiTi ternary alloy coating for potential aerospace, marine, and biomedical applications.

Magnetically separable sorbent based on activated carbon derived from a new precursor Rhizoclonium hookeri for facile oil spill clean-up

A huge quantity of synthetic toxic materials ends-up in water bodies causing long-lasting environmental and economic impacts due to catastrophic oil spill. Exploring marine algae as sorbent materials for oil spill remediation is a relatively new area and holds great potential. Herein, macroalgae Rhizoclonium hookeri (RH) derived magnetically recoverable RH-activated carbon (RHAC@Fe3O4) composite has been proposed as an innovative and robust strategy for oil spill clean-up. The application of RHAC@Fe3O4 composite was investigated for oil removal by varying time (10–60 min), dosage (0.2–1 g) and temperature (20, 30, 40 °C) to ascertain its optimal performance using both unused and used motor oil. Characterization studies showed that KOH activation resulted in developing pore structure and surface functionalities in the algal biochar. The percentage of oil uptake from simulated oil spill was over 90 % in 30 min at room temperature using 0.8 g composite. Moreover, Fe3O4 loading onto carbon material allowed magnetic separation as a convenient alternative to filtration for the recovery of oil laden composite. Apart from superior oil removal ability, synthesized composite demonstrated robust performance up to four cycles in synthetic sea water matrices. Comparative study revealed better oil sequestration efficiency of RHAC@Fe3O4 (93 %) as compared to its precursors, i.e. algal biochar (71 %) and AC (88 %). Based on these findings, it is advocated that designed RHAC@Fe3O4 composite being eco-friendly, economical and readily recoverable with enhanced oil uptake ability could potentially be an innovative platform for oil spill clean-up applications.

Highly efficient electrosynthesis of hydrogen peroxide through reversible transformation between catechol and o-benzoquinone on polydopamine modified carbon black

Carbon-based materials are more promising catalysts for H2O2 electrochemical production. However, the common method for modifying carbon-based materials is surface functionalization with harsh and uncontrollable reaction conditions, hindering the precise regulation of the active sites. Herein, we proposed a carbon-based material modified by polydopamine (CB-PDA) that was easily prepared and used in air diffusion electrode system for H2O2 production. The rapid and reversible transformation between catechol and o-benzoquinone on PDA could improve the H2O2 selectivity from 75.5 % to 97.0 % during the electrocatalytic process. The detection of adsorbed *HOOH and *OOH in oxygen reduction reaction proved the preference of CB-PDA for the two-electron pathway. The H2O2 formation rate constant of CB-PDA increased significantly from 25.85 to 60.82 mM h−1. The highest cumulative H2O2 concentration could reach 10200 mg L−1 in 9 h. Long-term operation tests proved the good operational stability. Furthermore, this system was cost-effective without additional aeration energy consumption and could achieve rapid disinfection in 10 min, which would have great potential to be used in environmental remediation.

Modification as a Method for Regulation of Energy Characteristics and Functionalization of Solid Surfaces

Modification as a Method for Regulation of Energy Characteristics and Functionalization of Solid Surfaces

Preparation of spherical HMX@PDA-based PBX by co-axial droplet microfluidic technology: Enhancing the interfacial effect and safety performance of composite microspheres

Surface engineering plays a crucial role in improving the performance of high energy materials, and polydopamine (PDA) is widely used in the field of energetic materials for surface modification and functionalization. In order to obtain high-quality HMX@PDA-based PBX explosives with high sphericity and a narrow particle size distribution, composite microspheres were prepared using co-axial droplet microfluidic technology. The formation mechanism, thermal behavior, mechanical sensitivity, electrostatic spark sensitivity, compressive strength, and combustion performance of the microspheres were investigated. The results show that PDA can effectively enhance the interfacial interaction between the explosive particles and the binder under the synergistic effect of chemical bonds and the physical "mechanical interlocking" structure. Interface reinforcement causes the thermal decomposition temperature of the sample microspheres to move to a higher temperature, with the sensitivity to impact, friction, and electrostatic sparks (for S-1) increasing by 12.5%, 31.3%, and 81.5% respectively, and the compressive strength also increased by 30.7%, effectively enhancing the safety performance of the microspheres. Therefore, this study provides an effective and universal strategy for preparing high-quality functional explosives, and also provides some reference for the safe use of energetic materials in practical applications.

Surface Modification of Gold Nanorods: Multifunctional Strategies and Application Prospects.

Gold nanorods (AuNRs), as an important type of gold nanomaterials, have attracted much attention in the nano field. Compared with gold nanoparticls, AuNRs have broader application potential due to their tunable localized surface plasmon resonance properties and anisotropic shapes. Yet, conventional synthesis methods using surfactants have limited the use of AuNRs in a variety of fields such as biomedical applications, plasma-enhanced fluorescence, optics and optoelectronic devices. To solve this problem and improve the stability and biocompatibility of AuNRs, researchers in recent years have used surface modification and functionalization to modify AuNRs, among which the introduction of organic ligands to prepare organic/gold hybrid nanorods has become an effective strategy. Organic materials have better toughness and easy processing, and by introducing organic ligands into the surface of AuNRs, the molecular-level composite of organic and inorganic materials can be realized, thus obtaining hybrid nanorods with excellent properties. This paper reviews the research progress of hybrid nanocomposites, and introduces the synthesis methods of AuNRs and the development of surface ligand modification, then summaries the applications of a wide variety of ligands. Also, the advantages and disadvantages of different ligands and their roles in further self-assembly processes are discussed.

Novel Biomaterials Based Strategies for Neurodegeneration: Recent Advancements and Future Prospects.

Neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease, pose significant challenges for effective treatment due to the complex nature of the central nervous system and the limited delivery of therapeutic agents to the brain. Biomaterial-based drug delivery systems offer promising strategies to overcome these challenges and improve therapeutic outcomes. These systems utilize various biomaterials, such as nanoparticles, hydrogels, and implants, to deliver drugs, genes, or cells to the affected regions of the brain. They provide advantages such as targeted delivery, controlled release, and protection of therapeutic agents. This review examines the role of biomaterials in drug delivery for neurodegeneration, discussing different biomaterialbased approaches, including surface modification, encapsulation, and functionalization techniques. Furthermore, it explores the challenges, future perspectives, and potential impact of biomaterialbased drug delivery systems in the field of neurodegenerative diseases.

Green self-templated synthesis of P-doped mesoporous carbon from dual sodium salts with improved average pore size for capacitive deionization

Mesoporous carbon materials hold significant potential in capacitive deionization (CDI) technology owing to expansive accessible surface area, more adaptable pore structure, excellent conductivity properties and effective surface modification and functionalization. While templating is a common method for synthesizing mesoporous carbons, the commonly used hard and soft templating approaches among them suffer from the challenges of expensive precursors and templating agents, complex procedures, secondary contaminants and difficulties in template removal. In contrast, the self-templating method not only circumvents the traditional template removal or combustion steps but also eliminates the use of organic solvents and hazardous chemicals, thus minimizing environmental impact. In this paper, we have successfully synthesized phosphorus-doped mesoporous carbon with a large average pore size (paver) using a green and convenient self-templating method employing dual sodium salts of sodium alginate (SA) and sodium phytate (SP). Compared to single SA (6.76 nm) or SP (3.74 nm) self-templated carbonization, the average pore size of carbon materials obtained from dual self-templated carbonization with a proportional mixture (12.97 nm) is significantly improved. The larger average pore size provides a greater surface area for electrode-electrolyte interactions, allowing for easier access and faster diffusion of ions into the pores, thereby enhancing the electrochemical and capacitive deionization properties of the material. The resulting material demonstrates promising electrochemical and desalination performance as evidenced by possessing a specific capacitance of 175.8 A/g and an adsorption capacity of 19.65 mg/g, underlining its potential for application in capacitive deionization utilizing mesoporous carbon materials with large average pore size.

Microstructural Regulation of Co TCPP by Acetylene Black: Enhanced Electrochemical Performance for Wearable Supercapacitors

Abstract With the rapid development of wearable devices, flexible supercapacitors have become an important energy storage prototype due to their inherent flexibility and high power density. Two-dimensional metal-organic framework (2D MOF) nanosheets are widely used in energy storage systems due to their structural tunability and anisotropy. However, their high surface energy tends to lead to aggregation, which results in poor dispersion and rheology of formulated inks and inhomogeneity of printed electrodes. Existing methods involve surface modulation by capped organic ligands, yet ignore the inherent conductivity and stability of MOFs. To overcome the low conductivity and aggregation problems of 2D MOFs, we adopted a novel approach combining mechanical intercalation and surface functionalization of cobalt-based porphyrin frameworks (Co TCPP) with acetylene black (AB). The unique microstructure of the composite material leads to favorable changes in the electronic properties of AB, which reduces the overall internal resistance and promotes rapid charge transfer. For this purpose, we have prepared micro-supercapacitors (MSCs) using dispensing printing technology. This integrated material has excellent mechanical flexibility and maintains 92% specific capacitance even under extreme bending and torsion. This study highlights the potential of integrating 2D MOFs with carbon-based materials (e.g., acetylene black) for a variety of applications in wearable electronics, and provides a guiding scheme for future micro-modulation of 2D MOFs using conductive materials.

Superhydrophobic FeNi3/Al2O3 multifunctional hybrid Janus particles for the catalytic degradation of azo dye, oil/water separation and microplastics removal

Emerging pollutants are causing global health and environmental challenges, necessitating the advancement of methodologies for their efficient removal. In this study, we present the efficacy of superhydrophobic FeNi3/Al2O3 Janus particles in the removal of oils and microplastics from water, combined with the degradation of azo dyes, leveraging their surface properties. Field Emission Scanning Electron Microscopy (FESEM) and Energy Dispersive X-ray Spectroscopy (EDS) revealed the morphology and elemental composition of these particles, which were further complemented by X-ray diffraction (XRD) for phase identification. After surface functionalization of the FeNi3/Al2O3 Janus particles with lauric acid, they exhibited superhydrophobicity (152 ± 1°) and superoleophilicity (0°). High-resolution X-ray photoelectron spectroscopy (HR-XPS) showed that the alumina face was modified with lauric acid, while the intermetallic face remained as FeNi3. Significantly, the alumina face demonstrated 99 % efficiency in separating oils and microplastics, while the FeNi3 face facilitated the complete degradation (100 %) of methyl red within three minutes, as shown by ultraviolet-visible spectrophotometry. These results highlight the multifunctional properties of superhydrophobic FeNi3/Al2O3 Janus particles in removing and degrading various pollutants.

Folic acid and ferritin functionalized reduced Iron-based metal-organic frameworks for anticancer therapy

Anticancer chemotherapies damage normal tissues and various drug carriers are under consideration to address this issue. Metal-organic frameworks (MOFs) are promising due to their drug-carrying capacity and tunable properties and target-inspired surface functionalization magnify their potential. In this study, we aim to investigate the anticancer activity of reduced iron-based MOFs (FeMOFs) functionalized with ferritin and folic acid and loaded with doxorubicin. Successful synthesis and functionalization are confirmed by Electron microscopes, Fourier transform infrared spectroscopy and X-ray diffraction. Anticancer activity is evaluated in different tumor cell lines at various doses. Results indicate that the folic acid functionalized MOF (FADMOF) showed maximum anticancer potential, leaving only 6 % of 4 T1 cells alive at the highest dose. While Ferritin and combo MOFs followed closely followed, and empty MOFs (RMOF) lagged. Further, in HeLa cells, the plain MOF (RMOF) shows best cytotoxicity reducing cell viability to a mere 30 % at the highest dose. Similarly, in MCF7 cells, the plain MOF (RMOF) shows best cytotoxicity reducing cell viability to a mere 25 % at the highest dose in a dose-dependent manner. Taken together, this study shows that functionalized MOFs have promising anticancer potential across various cancer cell lines. However, loading with Doxorubicin reduces their cytotoxicity.

Functionalization of boron nitride with poly(catechol-polyamine) and bis(γ-triethoxysilylpropyl)tetrasulfide for preparing epoxy nanocomposites with enhanced thermal conductivity

Hexagonal boron nitride (hBN) has garnered significant interest as inorganic thermally conductive material in electronic packaging due to its high-efficiency thermal management capability and electrical insulation properties. However, the relatively inert chemical environment of the BN surface hinders phonon transfer at the interface. Additionally, the high content of inorganic components in the matrix leads to the deterioration of the composite’s mechanical properties. In this research, h-BN surface is modified using poly(catechol-polyamine) (PCPA) and bis (γ-triethoxysi-lylpropyl)tetrasulphide (Si69) (denoted as BN-PCPA-Si69). The noncovalent PCPA modification protects the endothermic properties of BN, Si69 provides covalent bonding between thermally conductive fillers and bisphenol A-type epoxy resin (Ep), and the interfacial compatibility between BN and epoxy resin is improved. The heat conductivity of final BN/Ep composite achieved 0.817 W/(m·K) containing 30 wt% BN. Correspondingly, the heat conductivity of the composite (mBN/Ep) achieved 0.881 W/(m·K) containing 30 wt% BN-PCPA-Si69. Compared to pure epoxy resin (0.200 W/(m·K), the thermal conductivity (TC) of the mBN/Ep composite increased by 364% while maintaining good electrical insulation properties. The proposed BN surface functionalization approach has potential applications in fields such as microelectronic packaging, where materials need to balance high thermal conductivity and electrical insulation.

Hierarchically ordered porous carbon crystals for nanoconfined and sustainable fenton oxidation of water pollutants

In this work, we developed a hierarchically multi-faceted ordered porous carbon crystal (HOPC) for generating a favorable chemical microenvironment to intensify both Fe3+ binding and H2O2 utilization efficiency. The confined pore space and surface functionality enable •OH and micropollutants to be concentrated in the pores, thus significantly accelerating pollutant degradation kinetics (0.034 min−1) with reduced chemical consumption (0.081 mM H2O2). Theoretical calculations and in-situ characterizations reveal that both CO and pyrrolic N act as active sites bridging Fe3+, facilitating the transfer of outermost e− from the p-orbital of active sites (O and N) to the d-orbital of iron, effectively reducing Fe3+ to Fe2+ and enhancing the open-circuit potential of HOPC-Fe3+ complexes, as well as facilitating e− extraction from H2O2. For the first time, H2O2 was unveiled to be both an electron donor and acceptor to cooperate with the iron redox cycle for sustainable •OH generation toward fast pollutant decontamination.

Tannic Acid Carbon Dots with Both Antimicrobial Activity and Selectivity for Fe3+ Detection

AbstractIn the field of antimicrobial nanomaterials, biomass‐derived carbon quantum dots have attracted great attention from contemporary researchers due to their unique physicochemical properties and favorable biosafety. In this study, novel carbon quantum dots (CQDs) were synthesized from tannic acid by a one‐step hydrothermal method. The polymeric CQDs have good surface functionality and hydrophilicity with a large number of hydroxyl, carboxyl and amino functional groups. Antimicrobial experiments showed that CQDs had a good inhibitory effect on Gram‐negative Escherichia coli and Gram‐positive Staphylococcus aureus, as well as the drug‐resistant bacterium methicillin‐resistant Staphylococcus aureus. Scanning electron microscopy showed that the morphology of S.aureus cells treated with CQDs became shrivelled and irregular, the surface of E.coli cells protruded to form irregular vesicles, and the whole became shriveled up, whereas MRSA cells appeared to be depressed in the middle, and there was a residue of adherent CQDs on the cell surface. In addition, CQDs exhibit selective fluorescence bursting behavior for ferric ions and can be used as fluorescent probes for rapid, sensitive and selective detection of Fe3+. Therefore, CQDs not only possess good bacteriostatic properties, but also serve as fluorescent sensors for the detection of Fe3+. It can be used as a potential sensing array for selective detection of iron ions and bacterial abatement from contaminated water.

Gold nanoparticles decoration of zinc oxide nanowalls on flexible substrates

Metal oxide nanostructures decorated with noble metal nanoparticles are hybrid structures with a special interface that combines the unique properties of those two materials. Noble metal nanoparticles exhibit useful catalytic properties, and they can be functionalized with biomaterials. In this work, we use gold nanoparticles that can be functionalized using thiolated molecules bound to the metal surface. Zinc oxide nano-walls (NWs) are a high surface-to-volume ratio wide-bandgap semiconductor nanostructures that, due to their biocompatibility and non-toxicity characteristics, can be used in biosensing applications that involve contact with tissues and cells. ZnO nano-walls can be deposited from aqueous solutions at low temperatures, both on rigid and flexible substrates, using a simple and low-cost process that can be upscaled to high-volume production. In this work, we study the nucleation and growth of the ZnO nano-walls and we describe the gold nanoparticles decoration at three different schemes of surface functionalization. Among these schemes, we found that the process where ZnO nano-walls were deposited on polyimide substrates followed by activation using a self-assembled monolayer, resulted in a decoration with uniform size and distribution of gold nano-particles. That process was studied as a function of the growth temperature, solution concentration, and time. The morphology of the ZnO nano-walls was studied by Scanning Electron microscope imaging and the crystal structure was studied by X-ray diffraction.

Graphene/polyaniline waterborne composite coatings for metallic bipolar plates

Waterborne composite coatings were formulated for protection of metallic bipolar plates. The challenges lied in two aspects, one was the confliction between high electrical conductivity and good corrosion protection properties; the other was the water dispersibility of the constituent phases. Water-solubility of polyaniline (PANI) were controlled by adding polystyrene sulfonic acid during the polymerization of aniline. Graphene was functionalized by p-aminobenzoic acid and p-phenylenediamine to enhance the compatibility with PANI, while keeping the electrical conductivity of graphene at around 169 S/cm. Upon in-situ polymerization of the functionalized graphene/PANI composites, the electrical conductivity varied significantly from 41 S/cm to 91 S/cm with the surface functionality of graphene. The composite coatings were prepared thereafter with functionalized graphene/PANI/carbon black on the surface of 316 L stainless steel by centrifugal spraying coating. The interfacial contact resistance of the coatings reached 4 mΩ·cm2, comparable to Au coatings, but the corrosion current density was 4.37 μA/cm2 due to the existence of the hydrophilic groups in waterborne coatings, like amino groups and sulfonic acid groups. A post-treatment was carried out to consume some of the amino groups, so that the corrosion current density was decreased to 0.88 μA/cm2.

Surface functionalization of XC18 steel using a new transition metal complex for remarkable corrosion performance: Empirical and theoretical studies

Synthesis of transition metal complexes (TMC) having specific characteristics is advantageous for combining their organic and inorganic properties, to help prevent metals from corrosion. In this study, the corrosion inhibition behavior of [N, N’-bis(salicylidene)-2,2-dimethyl-1,3-propanediaminato] copper (II) (CuL) on the surface of XC18 steel surface immersed in 1.0 M HCl was investigated. The thermodynamic and kinetic corrosion parameters were determined using the mass loss (ML) and electrochemical measurement methods. CuL exhibited a good corrosion inhibition efficiency of 96.72 %. The adsorption behavior of CuL followed the Langmuir isotherm model, indicating both physical and chemical interactions. Morphological structural analysis demonstrated that CuL formed a protective film between the surface of XC18 steel and the corrosives elements, thus confirming its adsorption onto XC18 steel surface. Theoretical calculations were consistent with the experimental findings, thereby confirming that the adsorption of CuL onto the steel surface comprises both physisorption and chemisorption processes. These calculations elucidate the specific bonding nature and emphasize the significant inter- and intra-molecular interactions that enhance the stability and adsorption capability of the CuL inhibitor. The successful formation of a protective layer on the surface of XC18 steel using a TMC signifies exciting prospects for the development of advanced materials with diverse applications.