Effects of Nitrogen Content on the Structure and Mechanical Properties of (Al0.5CrFeNiTi0.25)Nx High-Entropy Films by Reactive Sputtering
Next Article in Journal
An Information-Theoretic Framework for Evaluating Edge Bundling Visualization
Next Article in Special Issue
Tensile Behavior and Evolution of the Phases in the Al10Co25Cr8Fe15Ni36Ti6 Compositionally Complex/High Entropy Alloy
Previous Article in Journal
Examining the Schelling Model Simulation through an Estimation of Its Entropy
Previous Article in Special Issue
Microstructure and Mechanical Properties of Particulate Reinforced NbMoCrTiAl High Entropy Based Composite
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of Nitrogen Content on the Structure and Mechanical Properties of (Al0.5CrFeNiTi0.25)Nx High-Entropy Films by Reactive Sputtering

1
State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083, China
2
College of Physics and Energy, Shenzhen University, Shenzhen 518060, China
3
Department of Physics, School of Science, Hebei University of Science and Technology, Shijiazhuang 050000, China
*
Author to whom correspondence should be addressed.
Entropy 2018, 20(9), 624; https://doi.org/10.3390/e20090624
Submission received: 9 July 2018 / Revised: 10 August 2018 / Accepted: 19 August 2018 / Published: 21 August 2018
(This article belongs to the Special Issue New Advances in High-Entropy Alloys)

Abstract

:
In this study, (Al0.5CrFeNiTi0.25)Nx high-entropy films are prepared by a reactive direct current (DC) magnetron sputtering at different N2 flow rates on silicon wafers. It is found that the structure of (Al0.5CrFeNiTi0.25)Nx high-entropy films is amorphous, with x = 0. It transforms from amorphous to a face-centered-cubic (FCC) structure with the increase of nitrogen content, while the bulk Al0.5CrFeNiTi0.25 counterpart prepared by casting features a body-centered-cubic (BCC) phase structure. The phase formation can be explained by the atomic size difference (δ). Lacking nitrogen, δ is approximately 6.4% for the five metal elements, which is relatively large and might form a BCC or ordered-BCC structure, while the metallic elements in this alloy system all have a trend to form nitrides like TiN, CrN, AlN, and FeN. Therefore, nitride components are becoming very similar in size and structure and solve each other easily, thus, an FCC (Al-Cr-Fe-Ni-Ti)N solid solution forms. The calculated value of δ is approximately 23% for this multicomponent nitride solid solution. The (Al0.5CrFeNiTi0.25)Nx films achieve a pronounced hardness and a Young’s modulus of 21.45 GPa and 253.8 GPa, respectively, which is obviously much higher than that of the as-cast Al0.5CrFeNiTi0.25 bulk alloys.

Graphical Abstract

1. Introduction

High-entropy films (HEFs) are a brand-new type of alloy film, which has been developed recently based on the design concept of high-entropy alloys (HEAs) [1]. HEFs can be defined as multiple-component films with high-entropy mixing. Generally, the HEAs are composed of multi-principal-elements (at least five elements with five at a % ≤ each element content ≤ 35 at %) [2,3]. HEAs feature higher mixing entropy than traditional alloys and tend to form disorder face-centered cubic (FCC) and/or body-centered cubic (BCC) phase structures rather than ordered intermetallic compounds [4,5,6]. Due to severe lattice distortion and solid solution strengthening, attributable to the multi-components, the HEAs show many excellent mechanical properties, such as high-strength, good ductility, and high-wear and corrosion resistances [1]. Based on a similar scientific concept, HEFs have been designed and investigated gradually and show a great potential for application in the coating industry [7,8,9,10,11,12]. To date, many excellent properties of HEFs have been discovered and studied, such as high-wear resistance [13,14], high-corrosion resistance [15,16,17], diffusion-barriers effects [18,19,20], solar-thermal-conversion effects [10,21], plastic-deformation characteristics [22,23], thermal stabilities [7,24,25], and soft magnetic properties [26]. However, there are few theories that can explain the mechanism of the phase formation of the HEFs.
The phase formation and mechanical properties of (Al0.5CrFeNiTi0.25)Nx high-entropy thin films with different N2 flow rates are studied in this paper. The phase structures and mechanical properties of AlxCrFeNiTi0.25 (x: molar ratio, x = 0, 0.25, 0.5, 0.75, and 1.0) bulks have previously been studied systematically [27]. Herein, the optimal composition of AlxCrFeNiTi0.25 (x = 0.5) alloy is selected as a magnetron-sputtering target to explore the phase formation mechanism and mechanical properties of high-entropy thin films. Significantly, the phase structures of high-entropy thin films transform from amorphous to FCC with the increase of nitrogen content, while the bulk Al0.5CrFeNiTi0.25 alloy attains BCC phase structure. Phase formation mechanism is explored from both theoretical calculations and experiments. Concerning high entropy thin films, the ability for solid solution structure formation is first discussed from the atom radius difference (δ). This study can help to provide new insights into understanding the phase formation mechanism of multi-component alloy thin film solids with small atoms such as nitrogen.

2. Materials and Methods

The (Al0.5CrFeNiTi0.25)Nx films were deposited on p-type Si (100) wafers by a direct current (DC) magnetron sputtering using non-equal atomic ratio Al0.5CrFeNiTi0.25 targets of Φ 60 mm in diameter and 2 mm in thickness. The alloy target was prepared by arc-melting and the smelting was repeated at least five times to ensure uniform mixing of components. Prior to deposition, the Si substrates were cleaned sequentially and rinsed by acetone, alcohol, and distilled water in an ultrasonic bath. Pre-sputtering was an effective way to remove oxide or contaminants on the surface of the target. When the base pressure held at 2.0 × 10−4 Pa, high purity argon was injected into the vacuum chamber and the target was cleaned by argon ion bombardment for 15 min at a power of 100 W. The deposition of the (Al0.5CrFeNiTi0.25)Nx films were carried out in an Ar + N2 mixed atmosphere under a DC power of 100 W with a working pressure of 0.5 Pa. The schematic diagram of reactive sputtering is shown in Figure 1. The metal atoms escaped the surface of the target due to the bombardment of high energy particles. Due to the nitrogen atmosphere, different metal atoms reacted with N-atoms and were deposited on the substrates in the end. During the deposition, the total flow rate of Ar + N2 was maintained at 30 standard cubic centimeters per minute (sccm) and the ratio was N2/(Ar + N2) and RN2 was controlled at 0, 10%, 20%, 30%, 40%, and 50%, respectively. The work distance between the substrate and the target was 60 mm and the deposition time was maintained at 60 min. No external heating or bias was used on the substrate during the deposition process.
The crystal structures of (Al0.5CrFeNiTi0.25)Nx films were analyzed by a glancing-incidence (1°) X-ray diffractometer (XRD, BRUKERD8 Discover, Bruker, Karlsruhe, Germany) using the Cu Kα radiation at a scanning rate of 4°/min. The scanning step was 0.02° with a scanning range of 20°–90°. The morphology studies and thickness measurements were carried out using field-emission scanning electron microscopy (SEM, Auriga Field Emission Scanning Electron Microscope, Carl Zeiss, Jena, Germany) equipped with an Energy Dispersive X-ray Spectrometer (EDX) operated at 10 kV. The surface roughness of the coatings were measured by an atomic force microscope (AFM, Veeco DI-3100, Bruker, Beijing, China). The hardness and modulus of the as-deposited films were tested at five points for each sample with a nano-indenter using a Berkovich triangular pyramid indenter. The distance between each indentation was 50 μm. The Poisson’s ratio and Elastic modulus of the indenter tip were 0.07 and 1.141 × 106 MPa, respectively. Micrographs of indentations were tested by a laser scanning confocal microscope (LSCM, OLS-4100, Olympus, Tokyo, Japan).

3. Results and Discussion

3.1. Phase Structures

3.1.1. Phase Formation Mechanism Analysis

The XRD patterns of (Al0.5CrFeNiTi0.25)Nx films deposited at different RN2 are evaluated in Figure 2. An amorphous structure was observed with x = 0. As the N2 flow rate increased, the phase structures of (Al0.5CrFeNiTi0.25)Nx films showed a tendency to crystallize. Using XRD analysis, thin films displayed a simple FCC structure and the grains were nanoscale at about 20 nm. The bulk Al0.5CrFeNiTi0.25 alloys counterpart featured a BCC structure [27]. Due to the high-cooling rate, films were far from the equilibrium that could be achieved by bulk alloys, which led to the difference in structure even if they were the same system. Many similar results have been reported for other system film alloys [16,28,29,30,31]. While the metallic elements in this alloy system, which all had trends to form nitrides like TiN, CrN, AlN, and FeN, had results that showed only a simple FCC structure in an XRD pattern, rather than a various nitrides phase. It can be inferred that the solid solution occurred between nitrides in high-entropy thin films. Mutual dissolution between carbides and nitrides has been reported in many studies. Figure 3 shows the UC-ZrC0.81 pseudo-binary system that showed a miscibility relationship and the substitutional solid solution structure was formed with the carbides as solid solution units [32]. The nitrides also obtained similar results, such as Ti-Al-N, Cr-Al-N, Ti-Cr-N and Ti-Zr-N, Ti-Al-Si-N nitride films [33,34,35,36,37].
A previous study showed that FCC phases were found to have lower δ, whereas BCC phases showed higher δ [38]. Regarding (Al0.5CrFeNiTi0.25)Nx with x = 0, δ was approximately 6.4%, which was relatively large, and might form a BCC or ordered BCC structure. Metallic atoms solved each other and formed a BCC solid solution structure (Figure 4a). Accompanying the increase in nitrogen, nitrides formed in (Al0.5CrFeNiTi0.25)Nx and were similar in size and structure. The δ between nitrides was relatively small, thus an FCC structure might have formed. When RN2 was equal to 10% and 20%, a low concentration of nitrogen existed in the lattice. However, small amounts of nitrogen cannot facilitate lattice reconstruction. Thus, it still maintained an amorphous structure, however, with a higher nitrogen content, the formation of nitrides was promoted that efficiently improved the order of the lattice. The nitride components were becoming more similar in size and structure and solved each other easily, thus, an FCC (Al-Cr-Fe-Ni-Ti)Nx solid solution formed, which is shown in Figure 4b,c.
Figure 5 displays the distribution of component elements of (Al0.5CrFeNiTi0.25)Nx thin films deposited at RN2 = 50% through EDX, including surface, and line and point scanning. As presented in each element map in Figure 5a, the distribution of component elements was uniform, which indicates a segregate-free characteristic. The results of line and point scanning also reflected the same element distribution characteristics. The internal picture in Figure 5b is the composite surface-scanning of this region and segregate-free characteristics can be observed. Viewing the comparative analysis of the energy spectrum of Point A and Point B in Figure 5c, the distribution of elements was stable and had a slight fluctuation. Moreover, the lattice constant of the FCC solid solution structure was calculated by the Prague formula. The FCC solid solution structure with a lattice constant about 4.093 Å was completely different with nitrides such as TiN, CrN, and so on, which also confirmed the occurrence of a solid solution.

3.1.2. Solid Solution Formation Ability

Regarding high-entropy alloys, the solid-solution formation ability was estimated by the value of Ω and δ [39], which were defined as follows:
Ω = T m Δ S m i x | Δ H m i x |
δ = i = 1 n c i ( 1 r i / r ¯ ) 2
where Tm was the melting temperature of the n-elements alloy, ∆Smix was the mixing-entropy of an n-element system, ∆Hmix was the mixing-enthalpy of an n-element system, ci was the atomic percentage of the component, ri was the atomic radius, and r ¯ = i = 1 n c i r i was the average atomic radius. Reviewing the previous study, it was concluded that the region where solid-solution structures were formed was in the range of 1.1 to 229.8 for Ω and 0.8% to 6.6% for δ. The radius of component elements in (Al0.5CrFeNiTi0.25)Nx are shown in Table 1, and the specific Ω and δ values of (Al0.5CrFeNiTi0.25)Nx at different N2 flow rates are shown in Table 2.
Concerning (Al-Cr-Fe-Ni-Ti)Nx, the δ was described as a function of nitrogen content, as shown in Figure 6a. The analytical curve was calculated based on the atomic ratio of the target, which was the theoretical value. While different deposition yields of component elements can cause fluctuations in the atomic ratio, the experimental values were well matched with theoretical values, as shown by the star points in Figure 6a. To clearly distinguish different phase regions of film alloys in this study, the nitrogen content was also described as a function of δ in Figure 6b. Regarding Al0.5CrFeNiTi0.25, δ was about 6.4% located in the SSS zone in Figure 6b, and the BCC solid solution phase structure was stable. When increasing the nitrogen content, the FCC structure formed in the (Al0.5CrFeNiTi0.25)Nx system. The calculated value of δ was about 23% for that FCC structure. When the nitrogen content was low, the amorphous structure was stable and located in the middle region.

3.2. Deposition Rates

Figure 7 presents the deposition rate of (Al0.5CrFeNiTi0.25)Nx as a function of RN2 and the exact value of thickness is shown in the internal table. Following the addition of nitrogen, the deposition rate of films was significantly reduced by about 30%. During the deposition, the total flow rate of Ar + N2 was maintained at 30 sccm. Thus, the density of argon decreased gradually with the increase of N2 flow rate and resulted in a lower efficiency of argon-ion bombardment of the target. Under higher RN2, the deposition rate continued to slow and maintain a lower sputtering yield. Added to the effect caused by low argon gas density, the ceramicization of the target surface was also an important factor. This was mainly due to the N-containing layer that formed on the target surface, which reduced the conductivity of the target and resulted in a low sputtering yield. This phenomena was “target poisoning” [40,41].

3.3. Surface Morphologies

The AFM images and SEM micrographs of the (Al0.5CrFeNiTi0.25)Nx films at different RN2 are shown in Figure 8. Initially, a very dense and smooth surface with low surface roughness was obtained. Looking at SEM micrographs, it was observed that a small amount of nanostructure precipitation occurred as the RN2 increased to 10%. When the N2 flow rate increased, the number and particle size of the nanostructures were increased significantly. Viewing the AFM images, many needle nanostructures were also observed in the high-entropy thin films. Additionally, the roughness of films was measured by AFM. The value of Ra gradually became larger and the exact value of surface roughness at different RN2 is shown in Table 2. The heights of the needle structure in all the HEFs were less than 60 nm, which was consistent with the results since the as-deposited HEFs were smooth and homogeneous, as shown in SEM micrographs.
The surface nanostructures displayed by AFM images were different from each other and the size of the needle structures became larger with the increase of RN2. These nano-scaled needle structures were related to the structure zone models, which had a great impact on the microstructural evolution of thin film. Initially, as RN2 was low, the growth of the HEFs effect by nitrogen ions was limited. The nucleation barrier was generally expected to be small, which contributed to the formation of randomly oriented islands for films deposited on the silicon substrates without substrate heating. Accompanying the increase of RN2, a strong driving force was obtained, which facilitated the surface atom diffusion and grain boundary motion. To achieve a stable state, the overall surface and interface energy were minimized through forming the new islands. Islands with lower energy consumed the others. Thus, the roughness of the HEFs increased gradually with the increase of RN2.

3.4. Mechanical Properties

Figure 9a displays the hardness and Young’s modulus of (Al0.5CrFeNiTi0.25)Nx films as a function of the N2 flow rate. Through the increase of the nitrogen content, the hardness and Young’s modulus of the films showed a significant upward trend. The high-entropy thin films showed the highest hardness and Young’s modulus at 21.78 GPa and 253.8 GPa, respectively. Compared with the bulk Al0.5CrFeNiTi0.25 alloys (the value of hardness was about 6 GPa), the hardness of the (Al0.5CrFeNiTi0.25)Nx HEFs was improved significantly. Considering the load-depth curves of Figure 9b, the manifest and precise change of the hardness and Young’s modulus of the HEFs was obtained. When the probe depressed into the same depth, a larger force was required with the increase of the RN2. This was attributed to the fact that solid solution significantly increased the hardness. It is well known that solid solution strengthening increases the yield strength of the material by increasing the stress τ to move dislocations [42]:
Δ τ = G b ε 3 / 2 c
where c was the concentration of the solute atoms, G was the shear modulus, b was the magnitude of the Burger’s vector, and ε is the lattice strain due to the solute. While increasing the N2 flow rates, the parameters c and ε were increased correspondingly, which resulted in a higher τ value. Thus, the effect of solid-solution strengthening was enhanced gradually with the increase of RN2. When the RN2 = 40% and 50%, the nitrogen content in films increased slowly. The difference in nitrogen content was only 2.66%, as shown in Table 2. The mechanical properties of the HEFs became stable.

4. Discussion

It is well known that the solid solutions can be divided into three types: Substitutional solid solutions; interstitial solid solutions; and vacancy solid solutions. Hume–Rothery rules are a set of basic rules that describe the formation of substitutional and interstitial solid solutions. Regarding a substitutional solid solution, the atomic radius of the solute and solvent atoms must differ by no more than 15%, while solute atoms should have a radius no larger than 59% of the radius of the solvent atoms for an interstitial solid solution [43]. However, the non-metallic elements, such as H, B, C, and N, having a very small atomic radius can form compounds with metal elements. When the ratio of a non-metal atom radius to a metal atom radius (Rx/RM) is less than 0.59, the compounds have a simple structure such as M4X, M2X, MX, MX2, which is called an interstitial phase. When Rx/RM > 0.59, the compounds have a complex structure such as Fe3C, thus, there is a interstitial compound [44]. Regarding (Al0.5CrFeNiTi0.25)Nx, the metallic elements all satisfy the formation rule for an interstitial phase and different nitrides with simple structures can be formed. The metallic elements will tend to be ionic and the ionic radius might well reflect the actual particle. Since most of the elements in this alloy system are transitional metals, their ionic radii are very close to each other. Nitride components are becoming more similar in size and structure and solve each other easily. Thus, the FCC structured phase is formed in (Al0.5CrFeNiTi0.25)Nx.
The correlation between the composition, processing, microstructures, and the properties of high-entropy thin films can be summarized systematically and is shown in Figure 10. First, the films are prepared by a magnetron sputtering technique and different N2 flow rates are selected to adjust the composition as well as to change the microstructures. This finds that the nitrogen content in the thin films increases gradually with the increase of the nitrogen content and the structure of films transform from amorphous to FCC. Second, it is further found that the mechanical properties (hardness/Young’s modulus) of the high-entropy crystalline films are much better than the high-entropy amorphous films. All told, there is an increasing trend of hardness with higher nitrogen for the high-entropy thin films. Third, due to the difference in the preparation process, the phase structure and the properties of the films are different from the bulk samples, although they are in the same composition system. This study can help enrich the cognition between composition processing, microstructures, and the properties for high-entropy materials, especially for high-entropy thin films.

5. Conclusions

The (Al0.5CrFeNiTi0.25)Nx high-entropy thin films were deposited on silicon wafers through magnetron sputtering without substrate bias and heating. It was found that the phase structures of the HEFs transformed from an amorphous to an FCC structure with the increase in nitrogen content—the formation of a nitride solid solution was the main reason. Using the XRD analysis, the grain size was nanoscale at about 20 nm. The formation ability of the solid solution phase for the Al-Cr-Fe-Ni-Ti-N system film alloys was discussed regarding δ. When the value of δ was higher than 23%, the solid solution structures were stable in (Al0.5CrFeNiTi0.25)Nx thin films. The (Al0.5CrFeNiTi0.25)Nx HEFs deposited at RN2 = 40% and 50% yielded a maximum hardness and modulus of 21.78 GPa and 253.8 GPa, respectively, which is much higher than the as-cast Al0.5CrFeNiTi0.25 bulk alloys. The enhancement in hardness was mainly attributed to solid-solution strengthening and the lattice distortion. Additionally, smaller grain-size was a beneficial factor for increasing hardness.

Author Contributions

X.-H.Y. finished the preparation of high-entropy thin films. X.-H.Y. and W.-B.L. together carried out analyzing and writing. K.Z. provided equipment. Y.Z. offered the theoretical guidance.

Funding

Y. Z. would like to thank the financial supports from the National Science Foundation of China (NSFC, Granted Nos. 51471025 and 51671020). W.-B.L. gratefully acknowledges the financial support from the Natural Science Foundation of Shenzhen University (Grant No. 2017069) and the Shenzhen Basic Research Project JCYJ20170302142339007, and the Youth Innovation Talent Project of Guangdong Province (Grant No. 2017KQNCX175), and the National Natural Science Foundation of China (Grant No. 51801128).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Zhang, Y.; Zuo, T.T.; Tang, Z.; Gao, M.C.; Dahmen, K.A.; Liaw, P.K.; Lu, Z.P. Microstructures and properties of high-entropy alloys. Prog. Mater. Sci. 2014, 61, 1–93. [Google Scholar] [CrossRef]
  2. Yeh, J.W.; Chen, S.K.; Lin, S.J.; Gan, J.Y.; Chin, T.S.; Shun, T.T.; Tsau, C.H.; Chang, S.Y. Nanostructured High-Entropy Alloys with Multiple Principal Elements: Novel Alloy Design Concepts and Outcomes. Adv. Eng. Mater. 2004, 6, 299–303. [Google Scholar] [CrossRef]
  3. Zhang, W.; Liaw, P.K.; Zhang, Y. Science and technology in high-entropy alloys. Sci. China Mater. 2018, 61, 2–22. [Google Scholar] [CrossRef] [Green Version]
  4. Ma, D.; Grabowski, B.; Körmann, F.; Neugebauer, J.; Raabe, D. Ab initio thermodynamics of the CoCrFeMnNi high entropy alloy: Importance of entropy contributions beyond the configurational one. Acta Mater. 2015, 100, 90–97. [Google Scholar] [CrossRef]
  5. Wu, Y.D.; Cai, Y.H.; Chen, X.H.; Wang, T.; Si, J.J.; Wang, L.; Wang, Y.D.; Hui, X.D. Phase composition and solid solution strengthening effect in TiZrNbMoV high-entropy alloys. Mater. Des. 2015, 83, 651–660. [Google Scholar] [CrossRef]
  6. Zhang, Y.; Zhou, Y.J.; Lin, J.P.; Chen, G.L.; Liaw, P.K. Solid-Solution Phase Formation Rules for Multi-component Alloys. Adv. Eng. Mater. 2010, 10, 534–538. [Google Scholar] [CrossRef]
  7. Hsieh, M.H.; Tsai, M.H.; Shen, W.J.; Yeh, J.W. Structure and properties of two Al–Cr–Nb–Si–Ti high-entropy nitride coatings. Surf. Coat. Technol. 2013, 221, 118–123. [Google Scholar] [CrossRef]
  8. Huang, P.K.; Yeh, J.W. Effects of substrate temperature and post-annealing on microstructure and properties of (AlCrNbSiTiV)N coatings. Thin Solid Films 2009, 518, 180–184. [Google Scholar] [CrossRef]
  9. Liu, L.; Zhu, J.B.; Hou, C.; Li, J.C.; Jiang, Q. Dense and smooth amorphous films of multicomponent FeCoNiCuVZrAl high-entropy alloy deposited by direct current magnetron sputtering. Mater. Des. 2013, 46, 675–679. [Google Scholar] [CrossRef]
  10. Sheng, W.; Yang, X.; Wang, C.; Zhang, Y. Nano-Crystallization of High-Entropy Amorphous NbTiAlSiWxNy Films Prepared by Magnetron Sputtering. Entropy 2016, 18, 226. [Google Scholar] [CrossRef]
  11. Gao, L.; Song, J.; Jiao, Z.; Liao, W.; Luan, J.; Surjadi, J.U.; Li, J.; Zhang, H.; Sun, D.; Liu, C.T. High-Entropy Alloy (HEA)-Coated Nanolattice Structures and Their Mechanical Properties. Adv. Eng. Mater. 2017, 20. [Google Scholar] [CrossRef]
  12. Liao, W.; Lan, S.; Gao, L.; Zhang, H.; Xu, S.; Song, J.; Wang, X.; Lu, Y. Nanocrystalline high-entropy alloy (CoCrFeNiAl 0.3) thin-film coating by magnetron sputtering. Thin Solid Films 2017, 638, 383–388. [Google Scholar] [CrossRef]
  13. Lin, D.; Zhang, N.; He, B.; Zhang, G.; Zhang, Y.; Li, D. Tribological properties of FeCoCrNiAlB x high-entropy alloys coating prepared by laser cladding. J. Iron Steel Res. Int. 2017, 24, 184–189. [Google Scholar] [CrossRef]
  14. Pogrebnjak, A.; Yakushchenko, I.; Bagdasaryan, A.; Bondar, O.; Krause-Rehberg, R.; Abadias, G.; Chartier, P.; Oyoshi, K.; Takeda, Y.; Beresnev, V. Microstructure, physical and chemical properties of nanostructured (Ti–Hf–Zr–V–Nb) N coatings under different deposition conditions. Mater. Chem. Phys. 2014, 147, 1079–1091. [Google Scholar] [CrossRef]
  15. Ye, Q.; Feng, K.; Li, Z.; Lu, F.; Li, R.; Huang, J.; Wu, Y. Microstructure and corrosion properties of CrMnFeCoNi high entropy alloy coating. Appl. Surf. Sci. 2016, 396, 1420–1426. [Google Scholar] [CrossRef]
  16. Hsueh, H.T.; Shen, W.J.; Tsai, M.H.; Yeh, J.W. Effect of nitrogen content and substrate bias on mechanical and corrosion properties of high-entropy films (AlCrSiTiZr)100−xNx. Surf. Coat. Technol. 2012, 206, 4106–4112. [Google Scholar] [CrossRef]
  17. Shon, Y.; Joshi, S.S.; Katakam, S.; Rajamure, R.S.; Dahotre, N.B. Laser additive synthesis of high entropy alloy coating on aluminum: Corrosion behavior. Mater. Lett. 2015, 142, 122–125. [Google Scholar] [CrossRef]
  18. Tsai, M.H.; Yeh, J.W.; Gan, J.Y. Diffusion barrier properties of AlMoNbSiTaTiVZr high-entropy alloy layer between copper and silicon. Thin Solid Films 2008, 516, 5527–5530. [Google Scholar] [CrossRef]
  19. Chang, S.Y.; Li, C.E.; Chiang, S.C.; Huang, Y.C. 4-nm thick multilayer structure of multi-component (AlCrRuTaTiZr)Nx as robust diffusion barrier for Cu interconnects. J. Alloys Compd. 2012, 515, 4–7. [Google Scholar] [CrossRef]
  20. Chang, S.Y.; Chen, D.S. 10-nm-thick quinary (AlCrTaTiZr)N film as effective diffusion barrier for Cu interconnects at 900 °C. Appl. Phys. Lett. 2009, 94, 222. [Google Scholar] [CrossRef]
  21. Sheng, W.J.; Yang, X.; Zhu, J.; Wang, C.; Zhang, Y. Amorphous phase stability of NbTiAlSiNX high-entropy films. Rare Metals 2017, 5, 1–8. [Google Scholar] [CrossRef]
  22. Feng, X.; Fu, W.; Zhang, J.; Zhao, J.; Li, J.; Wu, K.; Liu, G.; Sun, J. Effects of nanotwins on the mechanical properties of Alx CoCrFeNi high entropy alloy thin films. Scripta Mater. 2017, 139, 71–76. [Google Scholar] [CrossRef]
  23. Feng, X.B.; Zhang, J.Y.; Wang, Y.Q.; Hou, Z.Q.; Wu, K.; Liu, G.; Sun, J. Size effects on the mechanical properties of nanocrystalline NbMoTaW refractory high entropy alloy thin films. Int. J. Plasticity 2017, 95, 264–277. [Google Scholar] [CrossRef]
  24. Cheng, C.Y.; Yeh, J.W. High thermal stability of the amorphous structure of GexNbTaTiZr (x = 0.5, 1) high-entropy alloys. Mater. Lett. 2016, 181, 223–226. [Google Scholar] [CrossRef]
  25. Feng, X.; Tang, G.; Gu, L.; Ma, X.; Sun, M.; Wang, L. Preparation and characterization of TaNbTiW multi-element alloy films. Appl. Surf. Sci. 2012, 261, 447–453. [Google Scholar] [CrossRef]
  26. Lin, P.-C.; Cheng, C.-Y.; Yeh, J.-W.; Chin, T.-S. Soft Magnetic Properties of High-Entropy Fe-Co-Ni-Cr-Al-Si Thin Films. Entropy 2016, 18, 308. [Google Scholar] [CrossRef]
  27. Liu, S.; Gao, M.C.; Liaw, P.K.; Zhang, Y. Microstructures and mechanical properties of Alx CrFeNiTi 0.25 alloys. J. Alloys Compd. 2015, 619, 610–615. [Google Scholar] [CrossRef]
  28. Liang, S.C.; Tsai, D.C.; Chang, Z.C.; Sung, H.S.; Lin, Y.C.; Yeh, Y.J.; Deng, M.J.; Shieu, F.S. Structural and mechanical properties of multi-element (TiVCrZrHf)N coatings by reactive magnetron sputtering. Appl. Surf. Sci. 2011, 258, 399–403. [Google Scholar] [CrossRef]
  29. Lai, C.H.; Lin, S.J.; Yeh, J.W.; Chang, S.Y. Preparation and characterization of AlCrTaTiZr multi-element nitride coatings. Surf. Coat. Technol. 2006, 201, 3275–3280. [Google Scholar] [CrossRef]
  30. Lin, C.H.; Duh, J.G.; Yeh, J.W. Multi-component nitride coatings derived from Ti–Al–Cr–Si–V target in RF magnetron sputter. Surf. Coat. Technol. 2007, 201, 6304–6308. [Google Scholar] [CrossRef]
  31. Tsai, D.C.; Huang, Y.L.; Lin, S.R.; Liang, S.C.; Shieu, F.S. Effect of nitrogen flow ratios on the structure and mechanical properties of (TiVCrZrY)N coatings prepared by reactive magnetron sputtering. Appl. Surf. Sci. 2010, 257, 1361–1367. [Google Scholar] [CrossRef]
  32. Zhang, Y.; Lin, J.P.; Chen, G.L.; Yang, J.X.; Ren, Y.G.; Zhang, S.Z. Uranium carbide powder metallurgy. Powder Met. Technol. 1995, 4, 303–306. (In Chinese) [Google Scholar] [CrossRef]
  33. Zhou, M.; Makino, Y.; Nose, M.; Nogi, K. Phase transition and properties of Ti–Al–N thin films prepared by rf-plasma assisted magnetron sputtering. Thin Solid Films 1999, 339, 203–208. [Google Scholar] [CrossRef]
  34. Kimura, A.; Kawate, M.; Hasegawa, H.; Suzuki, T. Anisotropic lattice expansion and shrinkage of hexagonal TiAlN and CrAlN films. Surf. Coat. Technol. 2003, 169, 367–370. [Google Scholar] [CrossRef]
  35. Hörling, A.; Sjölén, J.; Willmann, H.; Larsson, T.; Odén, M.; Hultman, L. Thermal stability, microstructure and mechanical properties of Ti1−xZrxN thin films. Thin Solid Films. 2008, 516, 6421–6431. [Google Scholar] [CrossRef]
  36. Vetter, J.; Scholl, H.; Knotek, O. (TiCr) N coatings deposited by cathodic vacuum arc evaporation. Surf. Coat. Technol. 1995, 74, 286–291. [Google Scholar] [CrossRef]
  37. Carvalho, S.; Rebouta, L.; Ribeiro, E.; Vaz, F.; Denannot, M.; Pacaud, J.; Rivière, J.; Paumier, F.; Gaboriaud, R.; Alves, E. Microstructure of (Ti, Si, Al) N nanocomposite coatings. Surf. Coat. Technol. 2004, 177, 369–375. [Google Scholar] [CrossRef]
  38. Zhang, Y.; Lu, Z.P.; Ma, S.G.; Liaw, P.K.; Tang, Z.; Gao, M.C. Guidelines in predicting phase formation of high-entropy alloys. Mrs Commun. 2014, 4, 57–62. [Google Scholar] [CrossRef]
  39. Yang, X.; Zhang, Y. Prediction of high-entropy stabilized solid-solution in multi-component alloys. Mater. Chem. Phys. 2012, 132, 233–238. [Google Scholar] [CrossRef]
  40. Lu, C.Y.; Diyatmika, W.; Lou, B.S.; Lu, Y.C.; Duh, J.G.; Lee, J.W. Influences of target poisoning on the mechanical properties of TiCrBN thin films grown by a superimposed high power impulse and medium-frequency magnetron sputtering. Surf. Coat. Technol. 2017, 332, 86–95. [Google Scholar] [CrossRef]
  41. Arif, M.; Eisenmenger-Sittner, C. In situ assessment of target poisoning evolution in magnetron sputtering. Surf. Coat. Technol. 2017, 324, 345–352. [Google Scholar] [CrossRef]
  42. Pelleg, J. Mechanical Properties of Materials; Springer: New York, NY, USA, 2008; pp. 236–239. ISBN 978-94-007-4341-0.SG. [Google Scholar]
  43. Mizutani, U. The Hume-Rothery rules for structurally complex alloy phases. In Surface Properties and Engineering of Complex Intermetallics; World Scientific: Singapore, 2010; pp. 323–399. [Google Scholar] [CrossRef]
  44. Barrett, C.S. Structure of Metals; McGraw-Hill Book Company, Inc.: New York, NY, USA, 1943. [Google Scholar]
Figure 1. The schematic diagram of reactive sputtering.
Figure 1. The schematic diagram of reactive sputtering.
Entropy 20 00624 g001
Figure 2. X-ray patterns of the (Al0.5CrFeNiTi0.25)Nx films deposited at different RN2.
Figure 2. X-ray patterns of the (Al0.5CrFeNiTi0.25)Nx films deposited at different RN2.
Entropy 20 00624 g002
Figure 3. The UC-ZrC0.81 pseudo-binary phase diagram. Reproduced with the permission from Reference [34].
Figure 3. The UC-ZrC0.81 pseudo-binary phase diagram. Reproduced with the permission from Reference [34].
Entropy 20 00624 g003
Figure 4. Schematic of lattice structure. (a) Al0.5CrFeNiTi0.25 bulk; (b) (Al0.5CrFeNiTi0.25)Nx films; and (c) schematic diagram of high-entropy thin film formation.
Figure 4. Schematic of lattice structure. (a) Al0.5CrFeNiTi0.25 bulk; (b) (Al0.5CrFeNiTi0.25)Nx films; and (c) schematic diagram of high-entropy thin film formation.
Entropy 20 00624 g004
Figure 5. Energy dispersive X-ray spectroscopy of (Al0.5CrFeNiTi0.25)Nx high-entropy thin films deposited at RN2 = 50%: (a) face-scanning; (b) line-scanning; the insert picture is the composite surface scanning of this region; and (c) point-scanning.
Figure 5. Energy dispersive X-ray spectroscopy of (Al0.5CrFeNiTi0.25)Nx high-entropy thin films deposited at RN2 = 50%: (a) face-scanning; (b) line-scanning; the insert picture is the composite surface scanning of this region; and (c) point-scanning.
Entropy 20 00624 g005
Figure 6. (a) Analytical curve of δ as a function of nitrogen content in (Al0.5CrFeNiTi0.25)Nx and (b) analytical curve of nitrogen content as a function of δ in (Al0.5CrFeNiTi0.25)Nx films (12% according to Inoue Principle, 15% and 59% according to the Hume–Rothery Rule).
Figure 6. (a) Analytical curve of δ as a function of nitrogen content in (Al0.5CrFeNiTi0.25)Nx and (b) analytical curve of nitrogen content as a function of δ in (Al0.5CrFeNiTi0.25)Nx films (12% according to Inoue Principle, 15% and 59% according to the Hume–Rothery Rule).
Entropy 20 00624 g006
Figure 7. Deposition rates of (Al0.5CrFeNiTi0.25)Nx films at different RN2.
Figure 7. Deposition rates of (Al0.5CrFeNiTi0.25)Nx films at different RN2.
Entropy 20 00624 g007
Figure 8. AFM images and SEM micrographs of (Al0.5CrFeNiTi0.25)Nx films at different RN2.
Figure 8. AFM images and SEM micrographs of (Al0.5CrFeNiTi0.25)Nx films at different RN2.
Entropy 20 00624 g008
Figure 9. Mechanical properties of (Al0.5CrFeNiTi0.25)Nx films deposited at different RN2. (a) Hardness and modulus and (b) load-depth curve.
Figure 9. Mechanical properties of (Al0.5CrFeNiTi0.25)Nx films deposited at different RN2. (a) Hardness and modulus and (b) load-depth curve.
Entropy 20 00624 g009
Figure 10. Relationship between composition, processing, properties, and the structures of high-entropy films.
Figure 10. Relationship between composition, processing, properties, and the structures of high-entropy films.
Entropy 20 00624 g010
Table 1. The radius of component elelments in (Al0.5CrFeNiTi0.25)Nx films.
Table 1. The radius of component elelments in (Al0.5CrFeNiTi0.25)Nx films.
ElementNAlTiCrFeNi
Radius (nm)0.0710.14340.14450.12490.12410.1246
Table 2. The nitrogen content, Ω value, δ value, and the roughness of films at different RN2.
Table 2. The nitrogen content, Ω value, δ value, and the roughness of films at different RN2.
RN2 (%)01020304050
Nitrogen Content (at %)05.9410.9725.1029.5532.21
Ω1.601.310.440.230.200.19
δ6.39%13.14%16.43%22.97%24.45%25.21%
Ra (nm)1.3751.5743.7804.5424.4905.574

Share and Cite

MDPI and ACS Style

Zhang, Y.; Yan, X.-H.; Liao, W.-B.; Zhao, K. Effects of Nitrogen Content on the Structure and Mechanical Properties of (Al0.5CrFeNiTi0.25)Nx High-Entropy Films by Reactive Sputtering. Entropy 2018, 20, 624. https://doi.org/10.3390/e20090624

AMA Style

Zhang Y, Yan X-H, Liao W-B, Zhao K. Effects of Nitrogen Content on the Structure and Mechanical Properties of (Al0.5CrFeNiTi0.25)Nx High-Entropy Films by Reactive Sputtering. Entropy. 2018; 20(9):624. https://doi.org/10.3390/e20090624

Chicago/Turabian Style

Zhang, Yong, Xue-Hui Yan, Wei-Bing Liao, and Kun Zhao. 2018. "Effects of Nitrogen Content on the Structure and Mechanical Properties of (Al0.5CrFeNiTi0.25)Nx High-Entropy Films by Reactive Sputtering" Entropy 20, no. 9: 624. https://doi.org/10.3390/e20090624

APA Style

Zhang, Y., Yan, X. -H., Liao, W. -B., & Zhao, K. (2018). Effects of Nitrogen Content on the Structure and Mechanical Properties of (Al0.5CrFeNiTi0.25)Nx High-Entropy Films by Reactive Sputtering. Entropy, 20(9), 624. https://doi.org/10.3390/e20090624

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop