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Abstract (English):
The article shows that the hardness of most stainless steels is 2-3 times less than high-entropy coatings, which shows the prospect of their use as parts of various industrial structures. Microhardness of metallic glasses, which have a defect-free base, and do not differ from high-entropy coatings. An equation is obtained in the article, which shows that the destruction of the coating should be determined by the surface energy of the coating. It linearly depends on the hardness of the alloy and the destruction of the coating should decrease with decreasing surface energy without changing the mechanical properties of high-entropy coatings. Its decrease is also associated with the formation of nanostructures and the size dependence of the surface energy.

Keywords:
microhardness, high-entropy coating, steel, surface energy, destruction of the coating, nanostructure
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Introduction

In high-entropy alloys, as a result of the effect of intense mixing, the entropy contribution increases, which stabilizes the formation of a solid solution with a simple structure [1-3]. Based on Boltzmann's hypothesis on the relationship between entropy and system complexity, the configurational change in entropy ΔSconf during the formation of a solid solution of n elements with equiatomic content can be calculated using the following formula:

                                                                    (1)

where R is the universal gas constant, n is the number of mixing elements.

At n = 5, ΔSconf = 1.61R approaches the value of the melting entropy of most intermetallics (about 2R). However, it was later shown that a high entropy of mixing is not a necessary condition for the formation of a single-phase solid solution, but the very term for the name of such an alloy remains in use. We have also investigated high-entropy alloys and coatings obtained by mechanical alloying and magnetron sputtering of targets [4-7].

 

Purpose of the studylet us experimentally investigate the microhardness of high-entropy coatings and propose a model that will allow us to explain the observed effects within the framework of the energy theory..

Materials and methods

High-entropy (HEА) coatings of the following composition were used as objects of research: TiNiZrCuCr, CrFeNiTiZrCu, TiFeCuAlSn, AlCrNiTiZrCu, PbCrNiTiZrCu, CrNiTiZrAlCu, made by mechanical alloying [8]. Moreover, after annealing in a vacuum chamber, the samples became nanostructured. In fig. 1a shows, as an example, the samples under study, in Fig. 1b their SEM image, and in Fig. 1c diagram of the formation of nanostructured coatings [9].

 

а)

b)

 

 

с)

 

Figure 1 - Sputtered samples (a), REM samples (b), formation

nanostructured coatings [9].

The roughness of the coating as an example, measured on a JSPM-5400 atomic force microscope (AFM) manufactured by JEOL, is also negligible (Figure 2) [10].

а)

 

 

b)

 

Figure 1 - Sputtered samples (a), REM samples (b), formation

nanostructured coatings [9].

 

The roughness of the coating as an example, measured on a JSPM-5400 atomic force microscope (AFM) manufactured by JEOL, is also negligible (Figure 2) [10].

Figure 3 - Microhardness tester HVC-1000A

To determine the specific surface energy (surface tension) σ, we used the method described by us in [11]. The first method provides for the measurement of surface tension by determining the dependence of the microhardness on the thickness of the deposited coating. The dependence of the microhardness of the deposited coating on its thickness is described by the formula:

                                                  ,                                          (2)

where μ is the microhardness of the deposited coating; μ0 - "thick" sample; h is the thickness of the deposited coating. The parameter d is related to the surface tension σ by the formula:

                                                     ,                                            (3)

where σ is the surface tension of a massive sample; υ is the volume of one mole; R is the gas constant; T is the temperature.

                                   а)                                                 b)

Figure 4 - Dependence of microhardness on the thickness (a) and inverse thickness (b) of the CrFeNiTiZrCu coating on steel 20X13 [11]

As an example, consider the determination of the surface tension of the CrFeNiTiZrCu coating on steel 20X13. The results are shown in Figure 4. In the coordinates μ/μ0 ~ 1/h, the experimental curve is straightened in accordance with formula (2), giving the value h = 1.3 μm. For the CrFeNiTiZrCu coating on 20X13 steel, the surface tension obtained is σ = 1.409 J/m2. This value confirms the wear resistance of the CrFeNiTiZrCu coating on steel 20X13.

Results and discussion

Using the above methods, a table of experimental values can be given.

Table 1 shows that pentaatomic alloys have high hardness, surface energy ranges from 1 to 1.2 J/m2. Hexaatomic alloys have slightly less hardness. Let us compare the hardness of stainless steels [12] with the hardness of high-entropy coatings from Table 1.

Table 1 - Experimental properties of high-entropy coatings (HEА) and metallic glasses (MS) [13]

HEА

μ, HV

σ, J/m2

МS

μ, HV

CrTiNiZrCu

890

1.149

Fe78Mo2B20

1015

TiFeCuAlSn

700

1.192

Fe40Ni40P14B6

640

CrFeNiTiZrCu

740

1.409

Fe78P13C7

760

AlCrNiTiZrCu

585

1.644

Fe78Si10B12

890

PbCrNiTiZrCu

560

1.387

Ni75Si8B17

860

CrNiTiZrAlCu

530

1.152

Co75Si15B10

910

 

Table 2 - Hardness of stainless steels [12]

Steel

μ, HV

Steel

μ, HV

12X13

121-187

08X17T

372

40X13

143-229

10X17H13M2T

200

08X18H10

170

12X18H10T

179

 

The hardness of most stainless steels is 2-3 times less than high-entropy coatings, which shows the prospect of their use as parts of various industrial structures. For comparison, Table 1 shows the microhardness of metallic glasses, which have a defect-free base and do not differ much from high-entropy coatings [13]. What is the reason for this difference?

We will consider the question of the response of a subsystem of n electrons in high-entropy alloys to an external action during friction from the standpoint of nonequilibrium statistical thermodynamics. The electrons in the alloy will be considered as a system of non-interacting particles immersed in a thermostat. The thermostat is a metal alloy minus n "free" electrons. Quantum transitions during friction, caused by the interaction of a system of electrons with a thermostat, will be dissipative (with probability P), in contrast to the interaction during friction (with probability F). Dissipative processes lead to the fact that the secondary field (system response) is always less than the primary one, which causes the formation of heat during friction.

We will assume that the electron subsystem exchanges only energy with the thermostat during friction. Then the corresponding ensemble of particles will be canonical. In this case, the expression for the statistical entropy is:

                                                                  (2)

where fi is the distribution function; k is Boltzmann's constant.

Differentiating (2) in time and transforming, we get:

                          (3)

where Pij is the probability of transition from the initial i (with energy Ei) to the state j excited by friction (with energy Ej). For dissipative processes, the principle of detailed balance has the form:

                                                                                 (4)

where gi, gj are statistical weights for the levels Ei and Ej. Then (4) takes the form:

                                        (5)

Canonical distribution function:

where the statistical sum:

                                                                   

where G is the Gibbs potential (free energy) of the thermostat + electron system.

We assume that the non-configurational part of the Gibbs potential linearly depends on the concentration of n electrons:

                                         (6)

where h(n)= ω(n)×e-G/kT; ω(n) - statistical weight.

After cumbersome but simple calculations, it is easy to show that the function h(n) is a Gaussian distribution about a value with low variance, i.e.:

                                                   (7)

Substituting (7) into (6), we have:

                                                        (8)

To estimate the sum in (8), we replace it by the integral:

                                  (9)

Then (8) takes the form:

                                               (10)

Taking the logarithm of (10), we get:

                                                                                  (11)

where  is the part of the total Gibbs potential associated with the electron concentration. From the estimate of the first logarithmic term it follows:

                            (12)

Approximating the logarithm in the first term on the right-hand side of (12) by the first term of its expansion in a series, and expressing the second term in terms of the Gibbs potential of the thermostat Gf, we obtain:

                                             (13)

Substituting (13) into (11) and neglecting the 1/2 term in comparison with , we obtain:

                                           (14)

As above, assuming that the thermodynamic potential  depends on the equilibrium number of electrons Gf in a linear manner, i.e:

                                                        (15)

where G0 is the thermodynamic potential of the thermostat, we find:

                                                        (16)

With the help of (16), the expression for Z is transformed to the form:

                                                         (17)

Substituting (17) into (5), we find:

                   (18)

Neglecting small terms and replacing the sum by an integral in (18) (which is true for the continuous spectrum of electron energies in the alloy), we obtain:

                                                         (19)

where ΔS is the change in entropy in the dissipative process; Em is the average value of the energy of the ground state of electrons during friction; Δt is the time of movement during friction.

The response function of the thermostat + electrons system is:

,                   (20)

where F is the probability of a quantum transition inducing a secondary field of electrons, and F = 1/τ is the "radiative" lifetime of the electron system in an excited state during friction.

From (20), we obtained the following formula for the destruction efficiency Ώ = η of a metal coating:

                                                (21)

Equation (21) describes the destruction of the coating η proportional to k - the Boltzmann constant, the change in entropy ΔS and the time of motion during friction Δt, the work of friction forces Em = A = σ S, the concentration of electrons n near the Fermi level, surface energy σ, contact area S and vice versa is proportional to the relaxation time τ and the Gibbs energy G0 of the thermostat.

For high-entropy coatings G0 = H-TS + PV → S ~ 2R and the destruction of the coating should decrease. The surface energy σ linearly depends on the hardness of the alloy: σ = α μ, α = const, and the destruction of the coating should decrease with a decrease in the surface energy.

Its decrease is also associated with the formation of nanostructures and the dependence of the surface energy σ according to A.I. Rusanov. [15]: σ = К r → 0 at r → 0 (see Figure 1c).

Conclusion

The method of mechanical alloying for obtaining high-entropy coatings is much cheaper than the method of metallurgy, which produces cast high-entropy ingots. The hardness of high-entropy coatings is 2-3 times higher than the hardness of stainless steels, but it turns out to be similar to the hardness of metal glasses, which are also quite difficult to obtain.

We have shown experimentally and theoretically that the destruction of high-entropy coatings is mainly determined by the surface energy, which is proportional to the hardness of the coating. The surface energy for the coating decreases due to its nanostructural state, without significantly changing its physical properties. The destruction of high-entropy coatings is also reduced due to an increase in the entropy of the coating.

Thanks

The work was carried out under the program of the Ministry of Education and Science of the Republic of Kazakhstan. Grants No. 0118RK000063 and No. F.0781.

References

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