Nanocrystalline Structure Research Articles

Deposition-controlled phase separation in CuNb metallic alloys

Vapor co-deposited metal nanocomposites with immiscible components have shown to have several superior properties including mechanical performance, radiation tolerance, and enhanced functionalities. The morphology and structural design of these nanocomposites are important in determining the expression of these properties. The conditions used to deposit thin film nanocomposites are the governing factors in determining the final nanostructure. In this work, we link the effects of process gas pressure, substrate temperature, and sputtering target power on resultant Cu/Nb thin film nanostructures. We find that for films with equiatomic phase fractions of Cu and Nb, inhomogeneous precipitate segregation dominated the structure at lower substrate temperature depositions while higher temperatures distributed the Cu and Nb phases more uniformly. Increasing process gas pressure during deposition lead to a spatially homogeneous, nanocrystalline structure of Cu/Nb. In situ annealing of this sample shows that the phase separated morphology of the two immiscible materials depends on the initial composition. Finally, compositions of Cu and Nb that were highly disparate lead to interface segregation of the minority phase. The morphological evolution observed in the Cu/Nb system is compatible with modified structural zone models for immiscible thin film systems.

Design, characterization and green synthesis of samarium-decorated magnetic Fe3O4 nanoparticles: cytotoxicity and DNA binding studies

In this study, we have successfully synthesized magnetic Fe3O4 nanoparticles adorned with samarium (Sm-MNPs) utilizing ginger extract for the very first time. Furthermore, a comprehensive characterization of the nanoparticles along with an exploration of their physicochemical attributes was conducted. The biological functionalities of the synthesized nanoparticles were investigated through a thorough examination of their interaction with calf thymus DNA (ctDNA) using diverse spectroscopic techniques encompassing ultraviolet–visible (UV–Vis) and fluorescence spectroscopy at varying temperatures. Subsequently, we evaluated the cytotoxicity of the magnetic nanoparticles using a colorectal cancer cell model (HCT116 cells) and a tetrazolium colorimetric assay (MTT assay). The characterization of the ginger extract-coated magnetic nanoparticles (ginger-Sm-MNPs) revealed their superparamagnetic nature, nanocrystalline structure, spherical morphology, hydrodynamic size of 155 nm, and uniform distribution. The outcomes from UV–Vis and fluorescence spectroscopy affirmed the binding of ginger-Sm-MNPs with ctDNA. Additionally, the MTT assay demonstrated that the cytotoxicity of ginger-Sm-MNPs surpassed that of both magnetite nanoparticles and ginger extract. Notably, the inhibitory concentrations (IC50) for the green-synthesized nanoparticles after 24 and 48 h of incubation were determined as 198.1 and 135.8 μg/mL, respectively. In conclusion, our study findings suggest the potential utility of ginger-Sm-MNPs as a promising candidate for various biomedical applications. Communicated by Ramaswamy H. Sarma

Insight into nitriding behavior and corrosion mechanism in 17-4PH steel: The influence of nanocrystalline structure

In this study, the influence of nanocrystalline structure on the plasma nitriding (PN) behavior of 17-4PH steel and corresponding corrosion mechanisms under different treatments were systematically investigated. The results showed that nanocrystalline structures introduced by ultrasonic surface rolling process (USRP) would affect the nitrides morphology, composition and distribution via accelerating element diffusion. The fabricated nanocrystalline structures could enhance the corrosion resistance of original and plasma-nitrided 17-4PH steel, which was attributed to its various microstructures. Homogeneous microstructures suppressed or alleviated the formation of micro-galvanic couple in USRP-treated 17-4PH steel and USRP-15 + PN specimen.

Influence of Electron Beam Treatment on Structure and Phase Composition of TiB2–Ag Coating Deposited by Electrical Explosion Spraying

Due to many factors, the electrical explosion spraying process is not stable, which directly causes unstable coating quality and structure. Electron beam treatment may be used to improve the surface and modified structure of coatings sprayed by electrical explosions. In this study, a new TiB2–Ag metal matrix composite coating was deposited by electrical explosion spraying and modified by electron beam treatment. The prepared coatings were characterized by surface macro- and microanalysis, XDR, cross-section SEM, and TEM. The composition of the spray-coating phase differs from sample to sample. The electron beam treatment normalized the phase composition. Ag TiB2 B2O became the main phase in the modified coating. Increasing the pulse energy density and duration leads to a reduction in the low-melting Ag phase and the formation of copper contact phases due to heating and melting of the copper substrate by excess electron beam energy. The coating structure consists of a silver matrix and TiB2 inclusions. The electron beam treatment did not affect the structure; however, the microstructure of the coating transformed into a cellular crystallization structure. The silver matrix nanostructure was transformed into a nanocrystalline structure with an average crystal size ranging from tens to hundreds of nanometers.

In situ characterization of thermomechanically loaded solution strengthened, nanocrystalline nickel alloys

Nanocrystalline (NC) Ni-40Cu and Ni-40Cu-0.6P (at.%) alloys were mechanically loaded in tension at ambient (23 °C) and elevated (150 °C) temperatures with the deformed nanostructure captured by in situ transmission electron microscopy coupled with digital image correlation for data mining high strain regions prior to catastrophic failure. The addition of the P provided grain boundary partitioning that stabilized the NC structure under both loading cases, which was not found to be the case for the binary alloy. While mechanical strength softening was observed in each of the alloys upon thermomechanical loading, the retention of strength was substantially higher in the ternary alloy than its binary counterpart. Digital image correlation was found to be a useful means for image mining to identify different regions where failure mechanisms were initiated. Intergranular failure was observed as the dominant failure mechanism in all specimens with the binary alloy revealing a coarser fracture profile as compared to a finer fracture profile in the ternary alloy. Atomistic simulations are used to understand P solute strengthening of the grain boundaries against this fracture failure mode.

Investigation of the Effect of Combined Photo- and Thermal Annealing on the Structure and Properties of Zinc Oxide Films for Flexible Electronics

In this work, the evolution of the structural electrophysical parameters of nanostructured zinc oxide films, the preparation of a sol-gel by thermal treatment and combined treatment, including thermal exposure and UV exposure, were studied. It has been established that the use of thermal treatment of films leads to the formation of large aggregates (20—30 µm), density to enlargement with the duration of processing, while the structure of the material at a low level of the hierarchy, determined by the sensitivity of the sensitivity to analysis, as well as the optical band gap is practically independent from processing time. This is probably due to the formation of nanoparticles of the material responsible for the properties associated with the accumulation of the sol prior to its formation on the substrates. The introduction of additional UV irradiation into the system leads to the destruction of aggregates formed during heart failure and the formation of X-ray amorphous ZnO particles during treatment for 90 minutes. Increasing the processing time of the issuance to "crosslinking" the selection, the number of sizes of single crystals and the simultaneous increase in the concentration of point defects, leading to a decrease in the optical revealed band gap. Thus, the combined UV and heat treatment of the film makes it possible, on the one hand, to form a material with a nanocrystalline structure, and, on the other hand, to control its defectiveness. These results are promising for application in the manufacture of thermoelectric batteries, gas, catalysts and photocatalysts.

Comparative evaluation of osseointegration of new percutaneous implants made of Ti Grade 4 ultrafine‑grained alloy

Introduction It has been shown that titanium implants with a structured surface provide an increased rate of osseointegration what makes their application quite promising.The purpose of this work was to conduct a comparative evaluation of the efficiency of osseointegration of new percutaneous implants for prosthetics made of ultrafine-grained Ti Grade 4 alloy.Materials and methods The study was carried out on 12 male rabbits of the Soviet Chinchilla breed. Six rabbits of the control group had implants made of Ti6Al4V powder using selective laser sintering technology that were osseointegrated into the tibia, 6 rabbits of the experimental group had implants made of Ti Grade 4 by equal channel angular pressing. The formation of the "bone-implant" block was examined 26 weeks after the implantation.Results Histologically, after 26 weeks of the experiment, porous changes, enlargement of the Haversian canals, and pronounced osteoclastic resorption were not detected in the animals of the experimental group throughout the stump in the compact plate. Around the implant, a bony case repeating the bone shape was formed, represented by lamellar bone tissue. Using X-ray electron probe microanalysis, it was found that in the substrate formed on the surface of the implant in rabbits of the experimental group, there was significantly more calcium in all areas over the implant relative to the animals of the control group. In the control group, relative to the experimental group, an increased level of C-reactive protein in blood serum was retained longer. Complications and significant clinical and laboratory abnormalities were not found in both groups during the entire experiment.Discussion Our data are consistent with the results of other experimental studies, which unambiguously noted that titanium implants with a structured surface show increased osseointegration characteristics in comparative studies relative to implants without modification of the structure of the material of the threaded surface. The absence of complications and undesirable reactions of the animal organism also indicates the acceptable safety of the tested products.Conclusion Osseointegration of a percutaneous implant that has a mixed nanocrystalline and ultrafine-grained structure was more effective than the reference implant. This makes the use of such implant promising for solving clinical problems in prosthetics.

Catalytic Growth of High-Performance Graphite-like Carbon Films on a Nitrided Substrate: Experimental Study and First-Principles Calculations.

This study reports a novel process for the fabrication of high-performance graphite-like carbon (GLC) films on nitrided substrates through successive steps in a plasma nitriding system. Unlike films fabricated via conventional dual treatments (nitriding + film deposition), here-fabricated GLC films were grown on the surface of nitrided steel via a catalytic reaction. A transition zone having a nanocrystalline and amorphous structure was observed at the interface between the nitrided substrate and GLC films, which increased the durability of GLC films because this structure enhanced the adhesion of GLC films on the nitrided substrate, improving resistance to spallation and wear. Experimental study and first-principles calculations showed that the Fe3N phase had a stronger catalytic effect on GLC films than the Fe4N phase, and GLC films grown on the nitrided layer dominated by Fe3N were thicker with stronger adhesion and excellent frictional and wear properties compared with GLC films grown on the nitrided layer dominated by Fe4N because of the beneficial structure formed at the interface. This study reports a simple and inexpensive method to fabricate a dual layer containing high-performance GLC films via a catalytic growth and interface matching mechanism.

Controlled synthesis of efficient novel Cr0.2Co2.8O4–MoO3 nanocomposites for high-performance O2-evolution and methanol oxidation in alkaline medium

The world of electrochemical devices is constantly pushing the boundaries to what's possible, and nanocomposites are becoming crucial electrocatalysts for enhancing electrochemical performance. In this study, the affect in electrochemical behaviour on altering constituent amount in the electrocatalysts has been discussed. For this we synthesized a novel Cr0.2Co2.8O4–MoO3 nanocomposites with varying constituent proportional amount using simple low-temperature route. The formation and the physicochemical properties have been investigated by Fourier-transform infrared spectroscopy (FTIR), X-Ray diffraction analysis (XRD), X-ray photoelectron spectroscopy (XPS), Raman, Scanning electron microscopy (SEM)/energy dispersive X-ray spectroscopy (EDS) and Brunauer-Emmett-Teller (BET) techniques. The XRD and XPS patterns confirms the nano crystalline structures and compositional difference in metal cations distribution respectively. Results from Cyclic Voltammetry (CV), Tafel experiments, Chronoamperometry and Electrochemical impedance Spectroscopy (EIS) shows the ratio of Cr0.2Co2.8O4 to MoO3 strongly affects the catalytic performance in both oxygen evolution and methanol oxidation reactions. The observed enhancement in electrocatalytic activity can be ascribed to the combined impact of the two materials facilitating the electron transfer process by increasing the number of active sites and thereby. Amongst different synthesized electrocatalysts the one with 1:4 composition exhibited not only the highest Specific activity of 2.5 × 103 mA cm−2/g at 700 mV towards OER but also retains maximum current showing their highest stability.

Cross-sectional transmission electron microscopy studies of Si coated heat-treated stainless steel with improved optical absorption for solar thermal applications

Heat-treatment of stainless steel substrate is reported to improve absorptance due to an increase in roughness along with the formation of surface oxides. Depositing a thin Si layer on stainless steel prior to the heat-treatment results in the formation of islands of nano-micrometer sizes with gaps between them which helps in improving absorptance. Cross-sectional Transmission Electron Microscopy studies are required to understand the development of the surface structures and improved optical properties. The cross-sectional bright- and dark-field Transmission Electron Microscopy images showed the presence of a bright Si-rich region where small nanocrystalline islands were embedded. On top of this layer, larger nanocrystalline protrusions were observed. Energy Dispersive X-ray analysis and Selected Area Diffraction data showed that the substrate elements diffuse out through the Si layer forming smaller islands of various Fe-Cr-Mn-based silicides in the Si layer and islands of Fe, Cr, and Mn-based silicides and oxides at the surface. The High-Resolution Transmission Electron Microscopy images showed that the islands are nanocrystalline in nature and are embedded in a Si-rich amorphous region. The absence of O in the Si-rich layer in SAD data was observed. Also, from the top layer EDX data, Fe peak intensity was found to be higher than Cr peak intensity. These observations indicate that the presence of the Si layer helps in reducing the inward diffusion of O into the substrate, thus preventing internal oxidation. Also, this Si layer prevents the Cr from forming a continuous Cr oxide layer and instead forms mixed oxide/silicide islands which enhance optical properties. Similar studies in the heat-treated substrate without a Si layer showed the presence of sharp-angled nanocrystalline structures of Fe-Cr-based oxides and smooth-angled nanocrystalline structures of Fe-Mn-based oxides on the surface.

Resistance to Wear during Friction without Lubrication of Steel-Cast Iron Pairing with Nanocrystalline Structure-Reinforced Surface Layers

During the TDT of 41Cr4 steel specimens, a uniformly reinforced white layer with a nano-crystalline structure is formed in the surface layers. The wear resistance of sliding friction without the lubrication of a pair of steel 41Cr4—grey cast iron EN-GJL-200 (EN) under the face-to-face (“ring-ring”) scheme has been studied. It is revealed that when the sliding velocity changes from 0.25 m/s to 4 m/s and the unit load changes from 0.2 MPa to 1.0 MPa, a pair with a reinforced surface layer on 41Cr4 steel specimens and unreinforced specimens of EN-GJL-200 (EN) grey cast iron has a higher wear resistance than an unreinforced pair. The wear resistance increases for both reinforced and not reinforced specimens operating in a friction pair.

Degradation of methylene blue using Ca-doped LaMnO3 as a photocatalyst under visible light irradiation

Calcium doped lanthanum manganiteLa0.75Ca0.25MnO3 having Perovskite structure shows high degree of catalytic efficiency for the removal of Methylene Blue organic dye from its aqueous solution. The sample powder (LCMO) was prepared through sol–gel technique and was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Inductively coupled plasma- atomic emission spectroscopy (ICP-AES), Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDX) and UV–Vis spectroscopy (UV–Vis). The XRD data showed the formation of single crystalline phase. SEM images shows that the micro sized LCMO sample has nanocrystalline structure with average diameter of 1–5 µm. The ICP-AES and EDX data confirmed formation of required stoichiometric La1-xCaxMnO3 Oxide. On account of reduction of band gap energy by calcium doping, the Photocatalytic performance of the perovskites for photodegradation of Methylene Blue (MB) dye as an Organic water pollutant, was evaluated over visible light irradiation at constant dose for several hours, with a pH at 4,. The result showed the photocatalytic efficiency La0.75Ca0.25MnO3 nanocomposite was 68.52% of the initial dye concentration within 100 min illumination time. The linear increase of photodegradation rate was found in our sample as a function of time of irradiation. These findings shows convincingly that La1-xCaxMnO3 photocatalyst possess great promise for visible light driven photodegadation of MB dye. The reproducibility of the sample for degradation was studied.

Determination of DNA architecture of bacteria under various types of stress, methodological approaches, problems, and solutions.

Actively growing cells maintain a dynamic, far from equilibrium order through metabolism. Under starvation stress or under stress of exposure to the analog of the anabiosis autoinducer (4-hexylresorcinol), cells go into a dormant state (almost complete lack of metabolism) or even into a mummified state. In a dormant state, cells are forced to use the physical mechanisms of DNA protection. The architecture of DNA in the dormant and mummified state of cells was studied by x-ray diffraction of synchrotron radiation and transmission electron microscopy (TEM). Diffraction experiments indicate the appearance of an ordered organization of DNA. TEM made it possible to visualize the type of DNA ordering. Intracellular nanocrystalline, liquid-crystalline, and folded nucleosome-like structures of DNA have been found. The structure of DNA within a cell in an anabiotic dormant state and dormant state (starvation stress) coincides (forms nanocrystalline structures). Data suggest the universality of DNA condensation by a protein Dps for a dormant state, regardless of the type of stress. The mummified state is very different in structure from the dormant state (has no ordering within a cell). It turned out that it is possible to visualize DNA conformation in toroidal and liquid crystal structures in which there is either no or a very small amount of the Dps protein. Observation of the DNA conformation in nanocrystals and folded nucleosome-like structures so far has been inconclusive. The methodological advances described will facilitate high-resolution visualization of the DNA conformation in the near future.

Antipathogenic copper coatings: electrodeposition process and microstructure analysis

Copper coatings are an important group of decorative-protective materials characterised by high corrosion resistance, excellent thermal and electrical conductivity, which lately gained more significance due to their antimicrobial activity. The main aim of the presented research was to electrodeposit homogenous copper coatings from the non-cyanide electrolyte solution in galvanostatic conditions on steel (1.4024) and nickel (Ni201) substrates, commercially used for surgical instruments. The effect of substrate finishes used in the production line, by shot peening with glass balls, corundum treatment and brushing on the coatings surface formation, was investigated. The substrates’ and coatings’ microstructural properties were analyzed by scanning and transmission electron microscopy, atomic force microscopy, and X-ray diffraction analysis. The current efficiency of the copper reduction on nickel and steel substrates was found to be above 95%. The copper layers adhere to both substrates, except those deposited on a brushed surface. Regardless of the substrate used, they have a nanocrystalline structure with an average crystallite size of 30 nm. Moreover, the coating surface morphology, which affects the nature of interaction with microorganisms, was effectively modified by the appropriate substrate finishing without changing the electrodeposition conditions.

Effect of cold-drawn-induced amorphous phase on microstructure and pseudoelasticity properties of nanocrystalline NiTi alloys

Amorphous structures can be induced by cold deformation in the NiTi shape-memory alloys, which transform into nanocrystalline structures after annealing. In this study, the effect of cold-drawn-induced amorphous phase on the microstructure and pseudoelasticity properties of nanocrystalline NiTi alloys was investigated. Ni-49.2 at.%Ti alloy samples were subjected to different cold-drawn deformations. Transmission electron microscopy was used to investigate the microstructure of the samples. Three types of microstructures: twin-related lamellae, nanocrystalline, and amorphous, were observed in the cold-drawn samples. The amorphous volume fractions of the samples were determined using differential scanning calorimetry. The results suggested that the amorphous volume fraction increased with increasing cold-drawn deformation. The pseudoelasticity properties of the samples with different cold-drawn deformations were investigated using tensile tests. Notably, 59.05% cold-drawn deformation, which induced approximately 39.1% volume fraction of the amorphous phase, was the turning point in the performance of the NiTi alloy. The stress hysteresis and upper plateau stress increased with increasing cold-drawn deformation when the cold-drawn deformation was lesser than 59.04%. Furthermore, the difference in stress hysteresis and upper plateau stress was not significant when the cold-drawn deformation was greater than 59.04% because a complete nanocrystalline microstructure could be obtained after annealing when the volume fraction of the amorphous phase reached 39.1% in the NiTi alloy.

Structural, mechanical, and anticorrosive properties of (TiZrNbTa)Nx films

(TiZrNbTa)Nx films were fabricated at various nitrogen flow ratios (RN2) through reactive direct current magnetron co-sputtering. The structural, mechanical, and anticorrosive properties of the (TiZrNbTa)Nx films were explored. The metallic TiZrNbTa film formed a body-centered cubic phase, and the film (N05) deposited at RN2 = 5% exhibited a nanocrystalline structure consisting of close-packed hexagonal and face-centered cubic (FCC) phases. In contrast, the films prepared at RN2 > 10% demonstrated an FCC phase. The N05 film has hardness and elastic modulus of 23.5 and 220 GPa, respectively, the highest hardness and relatively lower elastic modules among the studied nitride films. Moreover, the N05 film has the highest polarization resistance of 198 kΩ·cm2 measured by the potentiodynamic polarization method. The chemical states of the (TiZrNbTa)Nx films were examined by X-ray photoelectron spectroscopy.

Dense nanocrystalline ReB2 bulk with ultrahigh hardness

Microcrystalline ReB2 with a high hardness of 48 GPa measured under a small load of 0.49 N has been reported as a superhard material. Nanocrystalline ReB2 is expected to achieve better mechanical properties than its microcrystalline counterparts. Here we report dense nanocrystalline ReB2 bulks synthesized by modified mechanical alloying and high-pressure sintering techniques. The modified mechanical alloying technique reduces the content of WC impurity from 7.75 wt% to 1.59 wt% in as-synthesized nanocrystalline ReB2 powders with an average grain size of 6.6 ± 2.0 nm. The extrinsic high-pressure (6 GPa) and the intrinsic nanocrystalline structure greatly promote the densification process of the ReB2 bulks during sintering. Our optimized nanocrystalline ReB2 bulk is ∼99% dense and with an average crystallite size of 40 nm, resulting in a high hardness of ∼33 GPa under a load of 9.8 N and indentation fracture toughness of ∼5 MPa m1/2. The high hardness can be ascribed to the synergistic effect of high density and nanocrystalline structure of ReB2 bulks. This work provides promising strategies to largely enhance the mechanical properties of different ceramics for practical applications.

Magneto-Optical Properties of Ni0.4Cu0.3Zn0.3Gd0.125Fe1.875O4 Nano Ferrite for Application of Soft Magnetic Material

Abstract: Ni0.4Cu0.3Zn0.3Gd0.125Fe1.875O4 spinel ferrite powder is successfully synthesized using sol-gel auto combustion technique. The structural, optical and magnetic properties investigated by using X-ray Diffractometer, FTIR Spectrometer, Scanning Electron Microscope and Vibrating Sample Magnetometer (VSM). XRD analysis confirmed that formation of Nano crystalline cubic spinel structure of the sample. The crystallite size of synthesized nanoparticles is about 29.45nm. The IR study support the confirmation spinel structure of Ni0.4Cu0.3Zn0.3Gd0.125Fe1.875O4 sample. Band gap energy Eg obtained using UV-Visible absorption data is about 2.4238 eV. The magnetic properties have been studied from VSM data shows that

Nanocrystallization of Cu46Zr33.5Hf13.5Al7 Metallic Glass

The recently discovered Cu46Zr33.5Hf13.5Al7 (at.%) bulk metallic glass (BMG) presents the highest glass-forming ability (GFA) among all known copper-based alloys, with a record-breaking critical casting thickness (or diameter) of 28.5 mm. At present, much remains to be explored about this new BMG that holds exceptional promise for engineering applications. Here, we report our study on the crystallization behavior of this new BMG, using isochronal and isothermal differential scanning calorimetry (DSC), X-ray diffraction (XRD), and transmission electron microscopy (TEM). With the calorimetric data, we determine the apparent activation energy of crystallization, the Avrami exponent, and the lower branch of the isothermal time–temperature–transformation (TTT) diagram. With XRD and TEM, we identify primary and secondary crystal phases utilizing samples crystallized to different degrees within the calorimeter. We also estimate the number density, nucleation rate, and growth rate of the primary crystals through TEM image analysis. Our results reveal that the crystallization in this BMG has a high activation energy of ≈360 kJ/mole and that the primary crystallization of this BMG produces a high number density (≈1021 m−3 at 475 °C) of slowly growing (growth rate < 0.5 nm/s at 475 °C) Cu10(Zr,Hf)7 nanocrystals dispersed in the glassy matrix, while the second crystallization event further produces a new phase, Cu(Zr,Hf)2. The results help us to understand the GFA and thermal stability of this new BMG and provide important guidance for its future engineering applications, including its usage as a precursor to glass–crystal composite or bulk nanocrystalline structures.

Features of Tribooxidation of the High-Entropy Coating (AlCrZrTiTa)N during Dry High-Speed Cutting

The high-entropy PVD coating (AlCrZrTiTa)N, characterized by its high hardness (50–60 GPa), elastic modulus above 300 MPa, and high heat resistance up to 1300 °C, is used for coating cutting tools operating under extreme metalworking conditions. The nanostructured monolayer 3 μm PVD coating was deposited on cutting plates in the hybrid arc deposition PVD coater. The coating had an amorphous nanocrystalline microstructure with a grain size of about 10–50 nm. The samples of SS 304 steel were investigated during dry high-speed (600 m/min) cutting. Raman spectroscopy was used to study the formation of tribooxides on the tool surface at the running-in stage of the cutting. After 130 m of cutting, Cr2O3 oxide appears on the wear surface while other elements are bound with N atoms. When the cutting length is increased to up to 260 m, oxide Al2O3 · ZrO2 (mullite) and amorphous oxides TaO2 and CrO2 are formed. The method EELFS made it possible to determine the amorphous nanocrystalline structure of triboceramics based on CrO2 and Al2O3 · ZrO2. The nearest atomic surrounding of Cr-Cr, O-O, and Cr-O and their subsequent comparison with the available literature data allow us to calculate the equilibrium lattice constants of the CrO2 unit cell, which are equal to (a, b) = 4.3754 Å and c = 0.5927. The triboceramic films on the base of non-equilibrium mullite Al2O3·ZrO2 have an amorphous structure. In the first coordination sphere, the interatomic distances of Zr-O and Al-O were 1.79 and 1.89 Å. An accelerated adaptive reaction to extreme external stimuli, at the very beginning of the running-in stage, is established. The tribological adaptability of the high-entropy ultra-fine amorphous nanocrystalline coating under extremely loaded dry high-speed cutting is based on non-equilibrium phenomena: the partial oxidation of fragments of the nitride and dynamic formation of protective tribooxides, which have a good thermal barrier and frictional properties. These factors interact synergistically and determine the life of the cutting tool.