Surface Protection Research Articles

Construction of Sulfone‐Based Polymer Electrolyte Interface Enables the High Cyclic Stability of 4.6 V LiCoO2 Cathode by In Situ Polymerization

AbstractLithium cobalt oxide (LiCoO2) is considered an indispensable cathode material in the realm of consumer electronic batteries due to its high volumetric energy density. However, at a charging cut‐off voltage as high as 4.6 V, significant interfacial side reactions between LiCoO2 and the electrolyte occur, which adversely impact the battery's cycle performance. The surface‐related issues of LiCoO2 at high charge voltages not only constrain its utilization in conventional lithium‐ion batteries with liquid electrolytes but also limit its application in solid‐state batteries. Although traditional coating methods using inert inorganic compounds can partially alleviate this issue, their point‐like coatings fail to completely prevent the surface of LiCoO2 from direct contact with the electrolyte. The exploration of novel surface protection strategies for LiCoO2 remains imperative to address the associated challenges. Herein, introducing a sulfone‐based polymer electrolyte interface is proposed on the surface of LiCoO2 using methyl vinyl sulfone (MVS) through in situ polymerization. Remarkably, LiCoO2 with sulfone‐based polymer electrolyte interface exhibits a capacity retention rate of 83% after 500 cycles when employing a carbonate electrolyte without additives at a charge cut‐off voltage of 4.6 V. Furthermore, the LiCoO2 and polymer electrolyte interface exhibits exceptional cycle stability when paired with polyether solid electrolytes that do not possess high voltage tolerance. Moreover, the incorporation of a polymer electrolyte interface not only enhances the cycle stability of LiCoO2 but also improves its thermal stability. This work presents novel research perspectives for exploring high‐voltage stable LiCoO2.

Microstructure and properties of novel nano-lamellar Al27Nb18(CrZr0.5)xTi55−1.5x eutectic high-entropy alloy coatings on Ti-6Al-4V alloy

The serious wear damage caused by low surface hardness and poor wear resistance of titanium alloy severely limits its further application in engineering field. In this work, novel eutectic high entropy alloys (EHEAs) were designed by means of infinite solution strategy combined with mechanical assistance to explore the application of EHEAs in the field of surface protection coating. Three types of EHEA coatings were achieved through the adjustment of the Cr and Zr element proportions on Ti-6Al-4V alloy by laser cladding. The microstructure was eutectic structure composed of Laves and BCC/B2 phases with superlattice structure. A significant presence of stacking faults, Lomer-Cottrell locks and other defects is observed within the BCC/B2 phase, which contributes to the enhancement of both microhardness and nano-hardness. Al27Cr25Ti18Nb18Zr12 coating showed excellent wear resistance and minimal volume loss, which are 0.340 (65.38 % of the substrate) and 6.71 × 10−5 mm3/N·m (16.89 % of the substrate). Notably, the three alloys exhibit interesting selective corrosion behavior, which is mitigated by the presence of a nano-lamellar eutectic structure that limits pitting propagation.

Ionic Liquids as Extreme Pressure Additives for Bearing Steel Applications

The protection of steel surfaces from wear under extreme pressure conditions is of major importance in several industries as it provides better performance and longer life of machinery. The motivation for this work was to study the lubrication of steel by ionic liquids (ILs), which have recently emerged as greener alternatives to commercial lubricants and additives. Three ILs based on sulfur-containing anions, used as 2-wt% additives in polyethylene glycol base oil (MW 200; PEG 200), were tested in the lubrication of ASTM 52100 bearing steel contacts in extreme pressure conditions (under mixed lubrication with a Hertzian pressure of 1.12 GPa) using a mini traction machine (MTM). Due to the poor resistance to corrosion of bearing steel, a semi-ester of succinic acid derivative corrosion inhibitor (Lanxess RC 4801) was added to the mixtures at a 1 wt% concentration. The ILs 1-hexyl-methylimidazolium trifluoromethanesulfonate ([C6mim][TfO]) and 1-hexyl-4-picolinium trifluoromethanesulfonate ([C6-4-pic][TfO]) revealed promising results in terms of surface protection of bearing steel. In contrast, 4-picolinium hydrogen sulfate ([4-picH][HSO4]) as 2-wt% additive to PEG 200 + 1% RC 4801 did not show any improvement in wear performance compared to neat PEG 200 + 1% RC 4801. PEG 200 + 2% [C6mim][TfO] + 1%RC 4801 allowed for a decrease in wear up to ~ 76% and PEG 200 + 2% [C6-4-pic][TfO] + 1%RC 4801 up to ~ 46% when compared with neat PEG 200 + 1% RC 4801. Optical microscopy images suggest the formation of an adsorbed layer, which was further supported by chemical analysis via x-ray photoelectron spectroscopy (XPS) data for [C6mim][TfO].Graphical abstract

Biodegradation, Antibacterial Performance, and Cytocompatibility of a Novel ZK30-Cu-Mn Biomedical Alloy Produced by Selective Laser Melting.

In the present study, an antibacterial biomedical magnesium (Mg) alloy with a low biodegradation rate was designed, and ZK30-0.2Cu-xMn (x = 0, 0.4, 0.8, 1.2, and 1.6 wt%) was produced by selective laser melting, which is a widely applied laser powder bed fusion additive manufacturing technology. Alloying with Mn evidently influenced the grain size, hardness, and biodegradation behavior. On the other hand, increasing Mn content to 0.8 wt% resulted in a decrease of biodegradation rate which is attributed to the decreased grain size and relatively protective surface layer of manganese oxide. Higher Mn contents increased the biodegradation rate attributed to the presence of the Mn-rich particles. Taken together, ZK30-0.2Cu-0.8Mn exhibited the lowest biodegradation rate, strong antibacterial performance, and good cytocompatibility.

Recent Patents of Micro-arc Oxidation Technology

Abstract: Micro-arc oxidation (MAO) is a new surface treatment technology that can improve wear resistance, corrosion resistance, high voltage insulation, and other metal properties. Therefore, this technology is widely used in automobile manufacturing, aerospace, ship anti-corrosion, medical equipment, sewage treatment, and other fields. This paper reviews the representative patents of micro-arc oxidation technology at home and abroad. The micro-arc oxidation processing device, the process method of micro-arc oxidation processing, the power supply and electrical parameters of micro-arc oxidation, the preparation of electrolytes, and the methods of anticorrosion and protection of metal surface are analyzed. The development trend of micro-arc oxidation technology in the future is discussed. Micro-arc oxidation is a simple, green, and environment- friendly surface treatment technology, and there will be more patents in the field of micro- arc oxidation in the future.

Surface Modification of AM60 Mg-Al Alloy with Vanadium and V2O5 Sputtered Deposits: Activity in Marine Ambience

Vanadium (~450 nm) and V2O5 (~350 nm) were deposited by DC magnetron sputtering on an AM60 substrate to improve its degradation resistance in marine ambience. According to Raman and XPS analysis, the vanadium nanofilm mainly consists of amorphous V2O3, while V2O5 comprises two sheets of VO5 and VO4 units. After 30 days of immersion of the coated AM60 in a marine model solution (SME), the shift of the pH of the SME to more alkaline values was less pronounced for V2O5-AM60 because of the HCl acid formation during the partial dissolution of V2O5 in the presence of NaCl, and thus, a higher concentration of Mg2+ ions ~100 mg L-1 was released from the Mg (AM60) matrix. The lower concentration of ~40 mg L-1 from the V-AM60 surface was attributed to the possible intercalation of the released Mg ions (cations) into the conductive tunnels of V2O3 as the main component of the vanadium sputtered deposit. This oxide has been reported as a material for high-capacitive energy storage. In this way, the V-deposit provided longer partial protection for the AM60 surface (Mg matrix) from localized pitting attacks.

Effects of solar radiations on stratum corneum hydration: Part II, protective action of solar filters.

The skin surface lipids (SSLs) film, composed of sebum and keratinocyte membrane lipids, is crucial to the barrier function of the stratum corneum (SC). The first part of this study investigated the impact of solar radiation on the SC based on a novel hydration and dehydration approach using Raman spectroscopy. The SSLs were found to absorb solar light, and thus participate to the protection of the skin surface. However, the protective function of the SSLs may be limited and is dependent to the heterogenous distribution of SSLs over the body surface. To ensure comprehensive protection, synergistic measures such as the application of solar filters are necessary. In this second part of the study, we have evaluated the limits of the protection capacity of SSLs and explored the protective action of a solar filters on both SSLs composition and the water hydration and dehydration kinetics in the SC.

Aerophilic Surfaces for Sustained Corrosion Protection of Metals Underwater

AbstractCorrosion and biofouling are wetting‐related phenomena that limit the effective use of metals in aqueous media. Nonwettable surfaces can mitigate the adverse effects of wetting by minimizing contact with water. However, current achievements in this field fall short of meeting industrial requirements due to the short lifetime of plastrons. This study proposes a method to measure the protective sustainability of plastron. Superhydrophobic (SHS) and aerophilic (APhS) surfaces are constructed on lightweight aluminum and are initially analyzed by conventional goniometry, which show comparable values. However, the plastron that develops underwater is substantially different. While SHS exhibit unevenly broken plastron, APhS show uniform, continuous plastron. As an example of the sustained protective performance of plastron, the corrosion resistance of SHS and APhS is presented. Potentiodynamic polarization, impedance spectroscopy, and long‐term immersion in seawater show a drastic enhancement in corrosion resistance, exclusively for APhS. In fact, almost no electrochemical signals are measurable, and no pitting corrosion is observed after 415 days of immersion in seawater. Conversely, SHS show no noticeable improvement and corrode faster than bare Al due to plastron loss. Since goniometric measurements do not provide information on plastron, it is essential to analyze the plastron for any non‐wettable surface utilized underwater.

Study on microstructure and wear resistance of laser cladding TiAlZrVNiX high entropy alloy coating based on Laves phase modulation

The incorporation of Laves phase into HEAs coating represents a novel approach to enhance wear resistance, building upon the innovative background of titanium alloy surface protection. The TiAlZrVNiX (X = 1, 1.5, 2) HEAs coatings were prepared in this study using laser cladding advantages to achieve dependable wear-resistant coatings. The microstructure, phase composition, microhardness, and tribological properties of the HEA coatings were simultaneously investigated. TiAlZrVNiX coatings were composed of V-rich HCP solid solution phases, C14-Laves phases, and NiTi2 phases. The microhardness of the 1.5Ni coating measured 708.75HV0.3 and wear rate of 1.12 × 10−13m3N−1 m−1. The primary wear mechanism was abrasive wear, and it had been confirmed that the 1.5Ni coating exhibited best wear resistance. The Laves phase with high space utilization would produce precipitation strengthening and dispersion strengthening, effectively reducing the stress-induced microcrack diffusion. Additionally, the introduction of Ni elements induced the growth of the NiTi2 phase in order to enhance the strength while mitigating brittleness, thereby enhancing the wear resistance of the coatings.

Strategy for preparing nanocrystalline Ta-N gradient layer with enhanced mechanical and tribological performance via microwave plasma nitriding

Herein, microwave plasma nitriding (MPN) was employed to fabricate a nanocrystalline tantalum nitride (Ta–N) layer with enhanced mechanical and tribological performance. The results revealed that the nitrogen content in the Ta–N layer appeared as a gradient distribution, resulting in a component gradient structure comprising Ta2N, a solid solution of N in Ta and superlattice TaN0.04 from the top surface to the matrix, which was advantageous for relaxing the stress between the top Ta–N layer and the matrix. Nanocrystalline Ta–N layers (D(avg) = 45–55 nm) with dense and smooth surfaces were obtained at ≤950 °C, while grains grew and pores appeared on the surface of the Ta–N layers (D(avg) = 195–205 nm) at >950 °C. Consequently, the nanocrystalline Ta–N layer with gradient structure and desired thickness exhibited robust hardness and modulus of 26.89 and 247.64 GPa, respectively, which were considerably higher than those prepared by traditional gas/ion/liquid nitriding. The friction and wear test results showed that compared with pure Ta, the MPN-treated Ta matrix exhibited a shallower wear track, lower wear volume, and smaller superficial area, indicating that the Ta–N layer offered excellent surface protection for the matrix.

Collaborative disposal of exhaust gas and waste wind turbine blades: Mechanical properties of recycled glass fibres and economic analysis

The accumulation of waste wind turbine blades poses significant environmental challenges. Pyrolysis offers an industrially viable solution for both disposal and the recycling of valuable glass fibers from these blades. Exhaust gas from industrials with waste heat can be utilized to reduce the process cost. However, for mixed atmosphere of exhaust gas containing both CO2 and O2, its influence on resin matrix decomposition characteristics and fiber mechanical properties are currently unclear. This work provided a solution collaborated with exhaust gas to disposal of waste wind turbine blades, in which operating parameters (atmosphere composition and process procedure) were optimized. Results showed that the early invention at pyrolysis with low concentration of O2 in exhaust gas played a major role in facilitating the formation of surface protection. Atmosphere during oxidation of pyrolytic residual carbon was crucial in maintaining fiber strength. At this stage, the interaction between CO2 (especially at 15% concentration) and O2 could mitigating fiber degradation through promoting the re-oxidization of Si dangling bonds and reducing water corrosion. However, stepwise processing of pyrolysis first and then oxidation under exhaust gas with O2 containing was not recommended due to its little cost-effectiveness. The single step disposal of wind turbine blades collaborated with coal-fired flue gas could increase the strength of recycled glass fiber by over 50% and reduced process costs by 34%.

Increased Cytotoxicity of Bimetallic Ultrasmall Silver-Platinum Nanoparticles (2 nm) on Cells and Bacteria in Comparison to Silver Nanoparticles of the Same Size.

Ultrasmall nanoparticles (diameter 2 nm) of silver, platinum, and bimetallic nanoparticles (molar ratio of Ag:Pt 0:100; 20:80; 50:50; 70:30; 100:0), stabilized by the thiolated ligand glutathione, were prepared and characterized by transmission electron microscopy, differential centrifugal sedimentation, X-ray photoelectron spectroscopy, small-angle X-ray scattering, X-ray powder diffraction, and NMR spectroscopy in aqueous dispersion. Gold nanoparticles of the same size were prepared as control. The particles were fluorescently labeled by conjugation of the dye AlexaFluor-647 via copper-catalyzed azide-alkyne cycloaddition after converting amine groups of glutathione into azide groups. All nanoparticles were well taken up by HeLa cells. The cytotoxicity was assessed with an MTT test on HeLa cells and minimal inhibitory concentration (MIC) tests on the bacteria Escherichia coli and Staphylococcus xylosus. Notably, bimetallic AgPt nanoparticles had a higher cytotoxicity against cells and bacteria than monometallic silver nanoparticles or a physical mixture of silver and platinum nanoparticles. However, the measured release of silver ions from monometallic and bimetallic silver nanoparticles in water was very low despite the ultrasmall size and the associated high specific surface area. This is probably due to the surface protection by a dense layer of thiolated ligand glutathione. Thus, the enhanced cytotoxicity of bimetallic AgPt nanoparticles is caused by the biological environment in cell culture media, together with a polarization of silver by platinum.

Trade-off between sulfidated zero-valent iron reactivity and air stability: Regulation of iron sulfides by ammonium dihydrogen phosphate

The reactivity and stability of zero-valent iron (ZVI) and sulfidated zero-valent iron (S-ZVI) are inherently contradictory. Iron sulfides (FeSX) on the S-ZVI surface play multiple roles, including electrostatic adsorption and catalyzing reduction. We proposed to balance the reactivity and air stability of S-ZVI by regulating FeSX. Benefiting from the superior coordination and accelerate electron transport capabilities of phosphate, herein, eco-friendly ammonium dihydrogen phosphate (ADP) was employed to synthesize N, P, and S-incorporated ZVI (NPS-ZVI) and regulate the FeSX. Raman, FTIR, XPS, and density functional theory (DFT) calculations were combined to reveal that HPO42- acts as the main P species on the Fe surface. The superior reactivity of NPS-ZVI was quantified by kobs, kSA, and kM of Cr(VI), which were 210.77, 27.44, and 211.17-fold than ZVI, respectively. NPS-ZVI demonstrated excellent reusability, with no risk of secondary pollution. Critically, NPS-ZVI could effectively maintain FeSX stability under the combination of diffusion limitation and surface protection mechanisms of ADP. The superior reactivity of NPS-ZVI was attributed to the fact that ADP maintains FeSX stability and accelerates electron transport. This study provides a novel strategy in balancing the reactivity and air stability of S-ZVI and offers theoretical support for material modification.

Nanoparticle-Mediated Mucosal Vaccination: Harnessing Nucleic Acids for Immune Enhancement.

Recent advancements in in vitro transcribed mRNA (IVT-mRNA) vaccine manufacturing have attracted considerable interest as advanced methods for combating viral infections. The respiratory mucosa is a primary target for pathogen attack, but traditional intramuscular vaccines are not effective in generating protective ion mucosal surfaces. Mucosal immunization can induce both systemic and mucosal immunity by effectively eliminating microorganisms before their growth and development. However, there are several biological and physical obstacles to the administration of genetic payloads, such as IVT-mRNA and DNA, to the pulmonary and nasal mucosa. Nucleic acid vaccine nanocarriers should effectively protect and load genetic payloads to overcome barriers i.e., biological and physical, at the mucosal sites. This may aid in the transfection of specific antigens, epithelial cells, and incorporation of adjuvants. In this review, we address strategies for delivering genetic payloads, such as nucleic acid vaccines, that have been studied in the past and their potential applications.

Revealing the nontrivial topological surface states of catalysts for effective photochemical carbon dioxide conversion

Topological semimetals with protected surface states mark a new paradigm of research beyond the early landmarks of band-structure engineering, allowing fabrication of efficient catalyst to harness the rich metallic surface states to activate specific chemical processes. Herein, we demonstrate a facile solid-phase method for in-situ doping of Ir at the Os sites in the Os3Sn7, an alloy with topological states, which significantly improves the photocatalytic performance for the reduction of CO2 to CO and CH4. Experimental evidence combined with theoretical calculations reveal that the nontrivial topological surface states greatly accelerate charge-separation/electron-enrichment and adsorption/activation of CO2 molecules, rendering highly efficient reaction channels to stimulate the formation of *COOH and *CO, as well CHO*. This work shows the promise of achieving high photocatalytic performances with synthesizing topological catalysts and provides hints on the design of novel topological catalysts with superior photoactivity towards the CO2 reduction reaction.

Personal Protective Equipment Use and Surface Contamination With Antineoplastic Drugs: The Impact of the COVID-19 Pandemic.

Surface contamination with antineoplastic drugs (ADs) is persistent. The use of personal protective equipment (PPE) is recommended to reduce exposure to ADs. This study explored the impact of the COVID-19 pandemic on nurses' PPE use and surface contamination with ADs. Demographic characteristics, PPE use, and associated factors were assessed on two inpatient oncology units where etoposide and cyclophosphamide were administered before (N = 26) and during the COVID-19 pandemic (N = 31). PPE use when handling contaminated excreta was significantly higher during the pandemic. Perceived risk of chemotherapy exposure was significantly associated with greater PPE use when handling AD-contaminated excreta, and conflict of interest was related to less PPE use during AD administration and handling of AD-contaminated excreta. During the pandemic, surface contamination with etoposide increased in shared areas and decreased in patient rooms.

Punica grantum peel extract decorated Al-MOF scaffold as Solid-State Sensor/Concentrator for the Sensing/Reduction of Cr(VI) and its extended utility as a corrosion inhibitor in Al-Air batteries

The growing presence of hexavalent chromium in environmental and industrial settings highlights the importance of developing an eco-benign platform for real-time in-situ sensing/screening and decontamination. This research presents a facile and portable solid-state optical sensor using waste Punica Granatum, i.e., pomegranate peel extract (PPE) adorn onto Aluminium-based Metal-Organic Frameworks (Al-MOFs) for the sensing of carcinogenic Cr(VI) and its decontamination to benign Cr(III). The sensor fabrication entails a hydrothermal synthesis to form Al-MOF scaffolds decorated with PPE through direct immobilization. Al-MOF exhibits a large surface area with well-defined pore channels that facilitate PPE’s voluminous/uniform anchoring in restricted orientations to serve as an ion-selective probe for specifically targeting ultra-trace Cr(VI). The surface/structural morphology and porosity of the Al-MOF-PPE material are characterized using scanning/transmission electron microscopy and BET/BJH analysis. The reduction of Cr(VI) by the Al-MOF-PPE is validated by electron spectroscopy for chemical analysis, corroborated by a conspicuous color transition from light yellow to dark brown. The efficient reduction of Cr(VI) by Al-MOF-PPE is achieved at pH 2–3, in the linear response range of 0.3–300 ppb and a detection limit of 0.23 ppb for Cr(VI). The sensory system prefers minimal PPE probe content (4 mg) and sensor dosage (5 mg) for ion-sensing and decontamination studies, highlighting its remarkable operational efficacy. Post Cr(VI) reduction, electrochemical studies confirm the utility of Al-MOF-PPE-Cr(III) as a corrosion inhibitor for metal surfaces. Tafel plots demonstrate that Al-MOF-PPE-Cr(III) exhibits cathodic and anodic inhibition characteristics, ensuring excellent surface protection for aluminum electrodes upto 220 min in Al-air batteries. The proposed Al-MOF-PPE offers dual functionality as a naked-eye platform for Cr(VI) decontamination, and the Al-MOF-PPE-Cr(III) material is an excellent corrosion inhibitor for energy storage devices.

Tunable Dual Self-Healing Composite Coatings with Self-Assembled Structures Regulated by Janus Nanoparticles.

The durability of concrete structures can be enhanced in a convenient and permanent manner through the surface protection of cementitious materials with composite polymer coatings. However, polymer coatings are susceptible to various mechanical and physical deterioration in complex and variable environments. In this paper, the theory of polymer microstructure regulation was employed to improve the sustainability of the protective performance of composite coatings. The self-assembled core-shell structure regulated by amphiphilic Janus nanoparticles is employed to modify the tunable polystyrene acrylate-polysiloxane self-healing coatings. The results demonstrate that the adhesion strength of the prepared self-assembled coating reached 3.7 MPa, which is sufficient to resist the damage to the microstructure of cementitious materials caused by physical erosion, seepage, and ionic corrosion. The self-healing coating, regulated by Janus particles, exhibited a residual creep of only 57.03% and a maximum loss angle tangent of 0.381. Furthermore, the material exhibited a superior shape memory function due to the presence of strong hydrogen bonding. The regulated self-healing coating repaired the polymer structural damage under mechanical and thermal deformation by bridging and filling effects. The coating demonstrated a tensile strength recovery of up to 71.23% in a wetted state, accompanied by a rapid restoration of its electrochemical properties and corrosion resistance. Furthermore, the self-healing emulsion penetrates the substrate defects and forms numerous polymer crystalline particles that effectively fill the microcracks.

Superhydrophobic Surfaces Prepared from Columnar Units by Convenient Electrodeposition with Excellent Mechanical Stability Impact and Corrosion Resistance.

Regular array structures prepared by laser processing and three-dimensional printing have promising applications in building stable superhydrophobic structures. However, the size of the materials processed by these two methods is affected by the size of the processing equipment, which prevents the processing of large-size materials. In this paper, a columnar unit consisting of a spherical structure with similar mechanical stability to the array structure is designed and prepared for metal surface protection. A convenient electrodeposition method was used to deposit a layer of columnar micron-sized copper consisting of spheres on the surface of a 6061 aluminum alloy. Subsequently, modified ZrO2 nanoparticles and polytetrafluoroethylene (PTFE) were sprayed on the surface to form a superhydrophobic surface with synergistic columnar units and ZrO2 (CAZ). The structure was tested and found to have excellent mechanical stability, maintaining the superhydrophobic properties of the surface even after 200 abrasion cycles of 1000-grit sandpaper under a 500 g load. Moreover, the vertical deformation of the CAZ sample under normal pressure was increased by a factor of 4 compared to the original substrate. Importantly, in subsequent corrosion resistance tests, the CAZ samples showed a two-order-of-magnitude improvement in self-corrosion current density and impedance modulus at low frequencies compared to the original substrate. This strategy is an effective method for preparing mechanically stable superhydrophobic structures that are low-cost and large enough to provide long-term protection for metal surfaces. It is particularly suitable for surface protection of instruments and automotive chassis armor.

Optimal lubricating protection and interfacial behavior for titanium alloy surface from phosphorus-based ionic liquids

The poor wear resistance of titanium alloy makes it challenging to develop high-performance lubricating materials. For the characteristic of highly designable structure, ionic liquids (ILs) are the potential lubricants with excellent physicochemical properties and lubricating performance. Herein, three protic phosphorus-based ionic liquids (PPILs) were designed and synthesized with the exploration of their interfacial lubrication behavior and interaction mechanism on the titanium substrate. The as-synthesized IL lubricants exhibit optimal tribological properties on steel-titanium friction pairs even at high load and temperature. The surface analysis showed that IL can form the lubricating protective film on the titanium-based metal surface, effectively reducing the adhesive wear. Combined with surface analysis techniques (SEM, XPS, FIB-TEM and TOF-SIMS), the lubrication mechanism was discussed systematically.