Atomic Force Microscopy Research Articles

Environmentally Friendly MoS2-hBN Solid Lubricants: A Comprehensive Tribological Evaluation

Abstract MoS2-based solid lubricants have obtained significant attention and are extensively employed in the aerospace industry due to their desirable tribological performance. However, to enhance their performance in humid environments, MoS2 is often doped with Pb-based compounds. Considering the health and environmental concerns associated with Pb, it is necessary to develop eco-friendly alternatives. In this study, hexagonal boron nitride (hBN) has been used as a potential substitute for Pb-based dopants in MoS2-based solid lubricants and coatings with varying hBN contents (9.5, 11.5, 13.5, 15.5, and 17.5 wt%) were applied to stainless-steel substrates using a spray bonding technique. The friction and wear characteristics of the coatings were analyzed by using a ball-on-flat tribometer, employing constant load conditions. Subsequently, ex situ analysis techniques such as scanning electron microscopy, Raman spectroscopy, and atomic force microscopy were used to characterize the coatings. The results showed that the coating with a lower hBN concentration presented improved tribological properties, which was correlated with the development of an effective MoS2-based transfer/tribo-film. This suggests that optimizing hBN content is crucial for enhancing the lubrication performance.

Low thickness effect on the properties of Mn-doped ZnO thin films synthesized by sol-gel spin coating technique

In this study, 7% manganese-doped zinc oxide (MZO) thin films with varying low thicknesses were synthesized using the spin coating method. The structural, optical, and morphological properties of MZO films with different film thickness, were systematically investigated. The crystallite structure, superficial morphology, and optical characteristics were analyzed using X-ray diffraction (XRD), atomic force microscopy (AFM), scanning electron microscopy (SEM), and ultraviolet–visible spectroscopy (UV-Vis). Structural analysis confirmed that all films exhibit a hexagonal wurtzite phase with a pronounced peak along the c-axis, and slight variation in low thickness significantly affected the structural parameters. The surface morphology demonstrated good uniformity, characterized by rounded grain shapes in the plane, while surface roughness was found to be increased with increasing film thickness. Optical analysis revealed that as the number of coatings increased, both transmittance and band gap energy decreased, accompanied by a redshift in the absorption edge across all samples. This behavior is attributed to light scattering, as well as an increase in the refractive index and dielectric function with visible light energy, influenced by the number of layers and corresponding crystallite size.

Studying the structure and function of nucleosomes by atomic force microscopy

Chromatin is an epigenetic platform for the implementation of DNA-dependent processes. The nucleosome, as the basic level of chromatin compaction, largely determines its properties and structure. When studying the structure and functions of nucleosomes, physicochemical tools are actively used, such as magnetic and optical “tweezers,” “DNA curtains,” nuclear magnetic resonance, X-ray diffraction analysis and cryoelectron microscopy, as well as optical methods based on FRET. Despite the fact that these approaches make it possible to determine a wide range of structural and functional characteristics of chromatin and nucleosomes with high spatial and temporal resolution, atomic-force microscopy (AFM) complements the capabilities of these methods. This review presents the results of structural studies of nucleosomes in view of the development of the AFM method. The capabilities of AFM are considered in the context of the use of other physicochemical approaches.

One‐step synthesis of GO/AgNPs nanocomposite for diverse antimicrobial applications

AbstractDue to its diverse application potential, graphene oxide and silver nanoparticles (GO/AgNPs) nanocomposite material is currently under active research and scrutiny by scientists. This research synthesized the nanocomposite based on GO and AgNPs using a one‐step method with ascorbic acid's environment‐friendly reducing agent. Results indicated that the generated AgNPs, with a mean size of 20.3 nm, were deposited evenly upon the GO sheets' surface despite the absence of a stabilizer. The structural and chemical characteristics of GO/AgNP nanocomposites were studied using X‐ray diffraction, field‐emission scanning electron microscopy, atomic force microscopy, photoluminescence, and Raman analyses. The nanocomposites' antibacterial efficacy was tested with Escherichia coli (Gram‐negative) and Staphylococcus aureus (Gram‐positive). At a focus of 16 µg/L, the GO/AgNPs sample exhibited a width of inhibition zones (ZOI) of about 10 mm in diameter, larger than that of the AgNPs sample at a threefold higher concentration. These results show that the synthesized GO/AgNPs nanocomposite maintains and enhances its antimicrobial activity. Therefore, it holds promise as a safe and cost‐effective material resource for biomedicine or environmental treatment purposes.

Effect of CTAB on the aggregation properties of Congo Red organized in layer-by-layer electrostatic self-assembled film: a spectroscopic and Atomic force microscopy study

Effect of CTAB on the aggregation properties of Congo Red organized in layer-by-layer electrostatic self-assembled film: a spectroscopic and Atomic force microscopy study

Synthesis of Trisiloxane with the Dioxaborolane Group as a Cathode Film-Forming Electrolyte Additive for High-Temperature LiMn2O4/Li4Ti5O12 Batteries.

LiMn2O4 batteries have been widely applied as various portable electronic devices and electric vehicles owing to the merits of low cost, high operating voltage, excellent rate capability, and environmental friendliness. However, the poor performance at elevated temperatures remains a serious technical challenge in terms of commercial application purposes. A borate-containing trisiloxane compound of TSMBO is designed and synthesized as a cathode film-forming electrolyte additive to improve the electrochemical performances of LiMn2O4/Li4Ti5O12 batteries, especially at high temperatures of 55 °C. Atomic force microscopy measurement confirms that the trisiloxane moiety in TSMBO can construct a cathode electrolyte interface (CEI) with higher mechanical strength and better flatness compared to the disiloxane moiety in the TSMBO analogue with a similar chemical structure. The robust CEI film on the surface of the LiMn2O4 cathode and the inhibited hydrolysis of LiPF6 in the electrolyte significantly suppress the dissolution of Mn from the LiMn2O4 cathode and maintain the structural integrity of the LiMn2O4 lattice over cycling. Thus, the LiMn2O4/Li4Ti5O12 coin cell using the TSMBO-containing electrolyte with an optimized addition level of 0.5 wt % exhibits a higher capacity retention of 49.3% compared with 34.3% for the baseline electrolyte after 300 cycles under 1C rate at 55 °C. The LiMn2O4/Li4Ti5O12 pouch cell tests show excellent high-temperature and cycling performance at 55 °C and a higher capacity retention of 90.4% after 500 cycles at 2C compared to 79.7% for that with the baseline electrolyte after 430 cycles at 2C. This work demonstrates that TSMBO is a promising electrolyte additive for practical use to improve the cycling stability of LiMn2O4/Li4Ti5O12 batteries at elevated temperatures.

Utilizing collagen-coated hydrogels with defined stiffness as calibration standards for AFM experiments on soft biological materials: the case of lung cells and tissue

Abstract Atomic Force Microscopy (AFM) is crucial in mechanobiology for high-resolution imaging and nanomechanical measurements of biological samples, providing insights into their mechanical properties. However, AFM faces challenges such as tip damage and cantilever selection errors, impacting measurement accuracy. This study proposes a methodology using collagen-coated hydrogels with predefined stiffness for calibrating AFM measurements on soft biological materials. By facilitating appropriate cantilever selection, assessing systematic errors, and evaluating tip damage, this approach ensures reliable Young’s modulus measurements. The proof of concept with human lung cells and tissue specimens demonstrates improved accuracy and reliability of AFM-based nanomechanical characterizations, essential for understanding cellular mechanics and disease progression.

Myrrh Oleo‐Gum Resin as a Functional Additive in Pectin and κ‐Carrageenan Composite Films for Food Packaging

ABSTRACTMyrrh oleo‐gum‐resin (MOGR) is a natural substance that has a rich history of medicinal use due to its anti‐inflammatory, antimicrobial, and antioxidant properties. The present study reports on the fabrication and assessment of pectin and K‐carrageenan composite films infused with varying proportions (0.3%, 0.5%, and 0.7%) of MOGR. Morphological analysis of the film samples was conducted using Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM). The results indicated that the introduction of MOGR led to a notable increase in surface roughness. The SEM micrographs of the films showed that the MOGR addition had an important effect on the microstructure of the film. The surface hydrophobicity of the MOGR‐loaded films increased, as confirmed by the rise in the contact angle. Moreover, there was an increase in the thickness (0.062 ± 0.004–0.095 ± 0.006 mm) and opacity (1.24 ± 0.07–9.41 ± 0.24) of the films with the addition of MOGR; however, tensile strength (7.30 ± 0.50–4.92 ± 0.34 MPa), elongation at break (32.41% ± 1.0%–29.70% ± 0.24%), and barrier properties decreased. Additionally, a rise in MOGR concentration corresponded to a rise in overall color difference ΔE (0.77 ± 0.03–5.09 ± 0.49) of the films. Notably, the incorporation of MOGR led to an increase in the antioxidant activity of the composite films, indicating potential applications in functional packaging materials.

On the mechanism for work function change of gold electrodes by ultrathin polyethyleneimine (PEI) films: Effect of molecular order.

Polyethyleneimine (PEI) is a widely used cationic polyelectrolyte. In organic electronics, it is a universal surface modifier for shifting the electrode work function (Φ) and improving charge injection into electronic devices. This effect may depend on the conformation and dipolar order of the PEI ultrathin film, but their detailed experimental evaluation has not yet been reported. Thus, we used sum-frequency generation (SFG) spectroscopy to probe the net orientation of polar groups of PEI films on glass and gold. The films were fabricated by spin-coating from alcoholic solutions or by dip-coating from aqueous solutions of various pH values, with both branched (b-PEI) and linear (l-PEI) structures. The obtained SFG spectra and atomic force microscopy (AFM) images indicated that the conformational ordering of the PEI layers increases over the period of 14 days after fabrication, being slightly more pronounced for l-PEI vs b-PEI, and for dip-coating vs spin coating fabrication. Furthermore, both the pH of the dip-coating solutions and the substrate nature influence the final morphology and order of the adsorbed films. On glass, they are optimized at an intermediate pH 5, while on gold, the greatest homogeneity is observed at pH 2 and the largest dipolar order is observed at pH 10. The pH dependence of changes in the work function of gold by PEI (|ΔΦ|) suggests that the electronic contribution is dominant. Nevertheless, the evolution of the PEI dipolar ordering was accompanied by small variations of |ΔΦ|, suggesting that it does have a significant contribution, especially at conditions for which the electronic contribution is reduced.

Antimicrobial, Synergistic, and Antibiofilm Activity of Sildenafil Against Pseudomonas aeruginosa: Preliminary Studies

The present study tested sildenafil citrate as an example of pharmacological repositioning against the opportunistic pathogen Pseudomonas aeruginosa, known for its potent biofilm formation. We evaluated its antimicrobial, synergistic, and antibiofilm effects using broth microdilution, checkerboard assays, and atomic force microscopy techniques. Sildenafil citrate showed antimicrobial activity, effectively inhibiting bacterial growth at minimum inhibitory concentrations ranging from 3.12 to 6.25 mg/mL and minimum bactericidal concentrations between 3.12 and 25 mg/mL. When combined with reference antimicrobial agents—cefepime, imipenem, cilastatin, and polymyxin—sildenafil citrate had a synergistic effect. It also effectively inhibited and eradicated biofilms, reducing total biomass by 87.1% for inhibition and 83.8% for eradication. Atomic force microscopy confirmed the efficacy of sildenafil citrate in destroying and inhibiting biofilms, decreasing the overall amplitude of the biofilm. Consequently, sildenafil citrate appears to be a promising candidate for combination with commercial antimicrobial drugs to prevent and treat P. aeruginosa infections.

Electrochemical Deterioration of a Gold Thin Film in Bicarbonate Solution: Correlative Optical, Nano-Mechanical, and Chemical Considerations.

The electrochemical dissolution of metals in liquid electrolytes is of great concern for various electrochemical technologies. However, it is also the focus for boosting metal recovery processes, e.g., from electronic wastes, one of which is the extraction of gold (Au) using eco-friendly electrolytes. To shed more light on the possibility and improvement of such metal leaching, this work presents the investigation of electrochemical deterioration of a Au nanofilm coated on a silicon (Si) support─ubiquitous materials in electronic components─in aqueous potassium bicarbonate (KHCO3) electrolyte, a solution widely used in food products. In addition to the time-dependent in situ Raman spectra revealing the reduced reflectivity of Au associated with its molecular degradation, the significant role of the electric double layer (EDL) at the metal/electrolyte interface is also indicated. Analyzing surface adhesion maps and force-distance spectra acquired using atomic force microscopy and spectroscopy (AFM/AFS), metal degradation is related to nanoscale worm-shaped reconstructed surface features that act as local sites of reduced refractive index. Complemented by the non-negligible fraction of K observed on the treated Au surfaces using scanning electron microscopy and energy dispersive spectroscopy (SEM/EDS), an electrochemical framework of metal degradation is proposed, depicting the electric-field-induced transport of K+ and H+ ions toward the Au surface regardless of bias polarity and implying the formation of ternary gold hydrides. The consideration of faradic current in the EDL circuit also suggests the occurrence of ternary gold oxides. Such determination is reinforced by the attributability of the polar and electrostatic characteristics of the worm-like features to residual negatively charged anionic clusters of the hydrides and the oxides. The analysis process and the new understanding of metal degradation provide a potential route for inspecting other metal/solution systems.

Effect of Molybdenum Concentration and Deposition Temperature on the Structure and Tribological Properties of the Diamond-like Carbon Films

Two series of non-hydrogenated diamond-like carbon (DLC) films and molybdenum doped diamond-like carbon (Mo-DLC) films were grown on the silicon substrate using direct current magnetron sputtering. The influence of molybdenum doping (between 6.3 and 11.9 at.% of Mo), as well as the deposited temperature (between 185 and 235 °C) on the surface morphology, elemental composition, bonding microstructure, friction force, and nanohardness of the films, were characterized by atomic force microscopy (AFM), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and a nanoindenter. It was found that the increase in the metal dopant concentration led to a higher metallicity and graphitization of the DLC films. The surface roughness and sp3/sp2 ratio were obtained as a function of the Mo concentration and formation temperature. The nanohardness of DLC films was improved by up to 75% with the addition of Mo. Meanwhile, the reduction in the deposition temperature decreased the nanohardness of the DLC films. The friction coefficient of the DLC films was slightly reduced with addition of the molybdenum.

Fabrication of an Antibacterial/Anticoagulant Dual-Functional Surface for Left Ventricular Assist Devices via Mussel-Inspired Polydopamine Chemistry.

Infections and thrombosis remain unsolved problems for implanted cardiovascular devices, such as left ventricular assist devices. Hence, the development of surfaces with improved blood compatibility and antimicrobial properties is imperative to reduce complications after artificial heart implantation. In this work, we report a novel approach to fabricate multifunctional surfaces for left ventricular transplanted ventricular assist devices (LVADs) by immobilizing nitric oxide (NO) generation catalysts and heparin and reducing silver nanoparticles in situ. The general view, structure, and chemical compositions of the pure/modified surfaces were characterized using digital imaging, scanning electron microscope (SEM), atomic force microscope (AFM), water contact angle (WCA), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma (ICP). All of the results demonstrated that the AgNPs and heparin were successfully immobilized on the surface. The Cu ions and NO release experimental results showed that the immobilized copper ions could catalyze the production of NO from S-nitrosothiols within the biological system. Meanwhile, due to the synergistic anticoagulant effect of NO and surface-immobilized heparin, the fabricated modified surfaces exhibited antiplatelet adhesion activities and good hemocompatibility. Finally, the antimicrobial activity of the samples was evaluated by Escherichia coli and Staphylococcus aureus, and cytocompatibility was measured using human umbilical vein endothelial cells (HUVECs). The results demonstrated that silver nanoparticles (AgNPs) immobilized by surface reduction reaction did not cause any significant inhibition of cell proliferation while providing stable and effective antimicrobial properties. We envision that this simple surface modification strategy with bifunctional activities of antimicrobial and anticoagulant will find widespread use in clinically used indwelling left ventricular assist devices.

PVDF‐based nanocomposite coatings with superhydrophobic and antibacterial properties on stainless steel surfaces

AbstractIn this study, using a spray‐coating technique, stainless steel surfaces were coated with polyvinylidene fluoride (PVDF) and carbon soot nanoparticles. We imparted various surface properties onto the coatings' surfaces by varying the nanoparticle content and the preparation method. The main aim was to develop antibacterial surfaces by inducing superhydrophobic properties in stainless steel surfaces. In a one‐step preparation method, 5% and 10% of nanoparticles were insufficient to achieve superhydrophobicity, whereas 20% significantly increased the water contact angle to 153°. Morphological evaluations revealed the formation of a nano‐scale structure, which also led to a staggering antibacterial rate of 99.5% against Listeria monocytogenes. Using a two‐step preparation, soot nanoparticles were localized at the coating's top layer, which led to superhydrophobicity at a lower nanoparticle content (10%). However, the bacterial adhesion study showed a lower antibacterial rate (~93%). The difference in bacterial adhesion results was explained by various roughness structures according to the atomic force microscopy results. The developed system has a promising potential to be used as self‐cleaning and antibacterial coatings in the medical and food industries.Highlights Stainless steel surfaces were coated with PVDF and carbon soot nanoparticles Imparted various surface properties onto the coatings' surfaces Developed antibacterial surfaces by inducing superhydrophobic properties Using a two‐step, soot nanoparticles were localized at the coating's top layer Bacterial adhesion study showed a lower antibacterial rate (~93%).

Room-temperature selective cyclodehydrogenation on Au(111) via radical addition of open-shell resonance structures

Cyclodehydrogenation is an important ring-formation reaction that can directly produce planar-conjugated carbon-based nanomaterials from nonplanar molecules. However, inherently high C–H bond energy necessitates a high temperature during dehydrogenation, and the ubiquity of C − H bonds in molecules and small differences in their bond energies hinder the selectivity of dehydrogenation. Here, we report a room-temperature cyclodehydrogenation reaction on Au(111) via radical addition of open-shell resonance structures and demonstrate that radical addition significantly decreases cyclodehydrogenation temperature and further improves the chemoselectivity of dehydrogenation. Using scanning tunneling microscopy and non-contact atomic force microscopy, we visualize the cascade reaction process involved in cyclodehydrogenation and determine atomic structures and molecular orbitals of the planar acetylene-linked oxa-nanographene products. The nonplanar intermediates observed during progression annealing, combined with density functional theory calculations, suggest that room-temperature cyclodehydrogenation involves the formation of transient radicals, intramolecular radical addition, and hydrogen elimination; and that the high chemoselectivity of cyclodehydrogenation arises from the reversibility and different thermodynamics of radical addition step.

Varying the Core Topology in All-Glycidol Hyperbranched Polyglycerols: Synthesis and Physical Characterization.

In the present study, low molecular weight cyclic polyglycidol is used as a macroinitiator for hypergrafting glycidol and producing cyclic graft hyperbranched polyglycerol (cPG-g-hbPG) in the molecular weight range of 103-106gmol-1. Linear graft hyperbranched polyglycerol (linPG-g-hbPG) and hyperbranched polyglycerol (hbPG) are prepared as reference samples. This creates a family of hbPG structures with cyclic, linear, and star cores, allowing to evaluate their properties in solution and in bulk. The morphology study of the high molecular weight structures using atomic force microscopy revealed a spherical shape for cPG-g-hbPG and hbPG, and a cylindrical shape for linPG-g-hbPG in the nanometric range. Small angle X-ray scattering confirmed the compact particle-like structure of this family of hbPG architectures. Interestingly, the glass transition temperature showed a structure dependence, with cPG-g-hbPG having the highest values and hbPG having the lowest values for the same molecular weight. This study is a step forward in the generation of water-soluble polymers with tailored structure and functionality for advanced applications.

Anomalous Nernst Effect-Based Near-Field Imaging of Magnetic Nanostructures.

The anomalous Nernst effect (ANE) gives rise to an electrical response transverse to magnetization and an applied temperature gradient in a magnetic metal. A nanoscale temperature gradient can be generated by the use of a laser beam applied to the apex of an atomic force microscope tip, thereby allowing for spatially resolved ANE measurements beyond the optical diffraction limit. Such a method has been previously used to map in-plane magnetized magnetic textures. However, the spatial distribution of the out-of-plane temperature gradient, which is needed to fully interpret such ANE-based imaging, was not studied. We therefore use a well-known magnetic texture, a magnetic vortex core, to demonstrate the reliability of the ANE method for imaging of magnetic domains with nanoscale resolution. Moreover, since the ANE signal is directly proportional to the temperature gradient, we can also consider the inverse problem and deduce information about the nanoscale temperature distribution. Our results together with finite element modeling indicate that besides the out-of-plane temperature gradients there are even larger in-plane temperature gradients. Thus, we extend the ANE imaging to study the out-of-plane magnetization in a racetrack nanowire by detecting the ANE signal generated by in-plane temperature gradients. In all cases, a spatial resolution of ≈70 nm is obtained. These results are significant for the rapidly growing field of thermoelectric imaging of antiferromagnetic spintronic device structures.

Optical and surface properties of Schiff base ligands and Cu(II) and Co(II) complexes

Objectives. To study the transition of electrons in 1,2-phenyl(4’-carboxy)benzylidene Schiff base ligand and transition metal ions, optical properties, as well as the surface chemistry of supported transition metals using diffuse reflectance spectroscopy (DRS); to study the roughness and morphology of the Schiff base ligand and its complexes using atomic force microscopy (AFM).Methods. DRS, AFM, and Fourier-transform infrared spectroscopy instruments were used to identify electron transitions, optical properties, and surface morphology in Schiff base ligands and their complexes.Results. The DRS revealed the d–d transitions and charge transfer shifts of all compounds, and helped identify the structure of the ligand. One of the optical properties studied was the energy gap calculation of the ligand and its complexes. The copper complex exhibited more semiconducting behavior with surface morphology properties such as surface roughness parameters lower than those of the ligand and the cobalt complex. This can be attributed to the smaller size of the copper atom, as well as lower electron transitions compared to the cobalt complex and the square planar bonding shape.Conclusions. In Schiff base ligands, the reflectance spectrum bands reveal three electron transitions: n→π*, π→π*, and σ→σ* transitions. In cobalt complexes, four transitions are indicated: 4A2(F)→4T1(F), 4A2(F)→4T1(P), charge transfer bands, and tetrahedral geometry. Copper complexes exhibit three transitions: 2B1g→2A1g, 2B1g→2Eg, and charge transfer bands, with a square planar geometry for their structure. The energy gap calculations were 2.42, 2.29, and 2.30 eV, respectively. In the case of the SH ligands, copper complexes, and cobalt complexes, all compounds exhibited semiconductor properties. However, the complexes displayed increased conductivity due to the influence of the metal and coordination structure.

Effect of substrate rotation on the growth behavior and topography of the [formula omitted] film deposited over a large area using DC magnetron sputtering with a rectangular target: Simulation approach and experiment

It is often challenging to achieve a uniform film with the necessary surface properties when using deposition techniques. If the film is not uniformly deposited or lacks suitable surface roughness, it may not meet performance standards. To understand and control the factors controlling the deposition process, this paper presents a simulation approach to predict the growth behavior of a Ti-film deposited on substrates during the bombardment of the target with argon ions at low pressure. The simulation of the deposition process consists of several Monte Carlo simulations, which include predicting the source of the atoms flow from the target surface and tracing its trajectories through the vacuum chamber until it falls or reaches the surface of the substrates, then predicting the thickness distribution and topography of film. After conducting a comparison between simulation predictions and experimental data, it was found that the measurements obtained using the Profilometer, Scanning Electron Microscope, and Atomic Force Microscopy were relatively close. The results indicate that substrate rotation during deposition leads to a thinner film that is more uniform and less rough, it was also found that the coefficient of variation in the film thickness distribution was improved from 3.96% in the case of a non-rotating substrate to 0.33% in the case of a rotating substrate. The proposed approach can be used to improve the design of magnetron sputtering systems and to provide theoretical guidance for optimizing the thickness distribution and topographical characteristics of the performance specifications of high-quality film without economic constraints.

The Effect of DLC Surface Coatings on Microabrasive Wear of Ti-22Nb-6Zr Obtained by Powder Metallurgy

Titanium alloys have a high cost of production and exhibit low resistance to abrasive wear. The objective of this work was to carry out diamond-like carbon (DLC) coating, with dissimilar thicknesses, on Ti-22Nb-6Zr titanium alloys produced by powder metallurgy, and to evaluate its microabrasive wear resistance. The samples were compacted, cold pressed, and sintered, producing substrates for coating. The DLC coatings were carried out by PECVD (plasma-enhanced chemical vapor deposition). Free sphere microabrasive wear tests were performed using alumina (Al2O3) abrasive suspension. The DLC-coated samples were characterized by scanning electron microscopy (SEM), Vickers microhardness, coatings adhesion tests, confocal laser microscopy, atomic force microscopy (AFM), and Raman spectroscopy. The coatings did not show peeling-off or delamination in adhesion tests. The PECVD deposition was effective, producing sp2 and sp3 mixed carbon compounds characteristic of diamond-like carbon. The coatings provided good structural quality, homogeneity in surface roughness, excellent coating-to-substrate adhesion, and good tribological performance in microabrasive wear tests. The low wear coefficients obtained in this work demonstrate the excellent potential of DLC coatings to improve the tribological behavior of biocompatible titanium alloy parts (Ti-22Nb-6Zr) produced with a low modulus of elasticity (closer to the bone) and with near net shape, given by powder metallurgy processing.