Microstructure and Mechanical Behavior of High-Entropy Alloys
- First Online:
- Cite this article as:
- Licavoli, J.J., Gao, M.C., Sears, J.S. et al. J. of Materi Eng and Perform (2015) 24: 3685. doi:10.1007/s11665-015-1679-7
- 3.5k Downloads
High-entropy alloys (HEAs) have generated interest in recent years due to their unique positioning within the alloy world. By incorporating a number of elements in high proportion, usually of equal atomic percent, they have high configurational entropy, and thus, they hold the promise of interesting and useful properties such as enhanced strength and alloy stability. The present study investigates the mechanical behavior, fracture characteristics, and microstructure of two single-phase FCC HEAs CoCrFeNi and CoCrFeNiMn with some detailed attention given to melting, homogenization, and thermo-mechanical processing. Ingots approaching 8 kg in mass were made by vacuum induction melting to avoid the extrinsic factors inherent to small-scale laboratory button samples. A computationally based homogenization heat treatment was given to both alloys in order to eliminate any solidification segregation. The alloys were then fabricated in the usual way (forging, followed by hot rolling) with typical thermo-mechanical processing parameters employed. Transmission electron microscopy was subsequently used to assess the single-phase nature of the alloys prior to mechanical testing. Tensile specimens (ASTM E8) were prepared with tensile mechanical properties obtained from room temperature through 800 °C. Material from the gage section of selected tensile specimens was extracted to document room and elevated temperature deformation within the HEAs. Fracture surfaces were also examined to note fracture failure modes. The tensile behavior and selected tensile properties were compared with results in the literature for similar alloys.
KeywordsdeformationFCC crystal structurefracturehigh-entropy alloysmicrostructuretensile properties
Consider the design of an entirely new alloy. The first design input is always the desired properties defined by the target application. One may then go on to choose the crystal structure (e.g., FCC, BCC, etc.) that will impart the desired properties. The alloy may also be solid solution or precipitation strengthened in which case compatible elemental additions and their effects can then be considered. For example, if a FCC solid solution strengthened alloy is the goal, per the Hume-Rothery rules, a list might be made of elements having a stable FCC matrix—Al, Ni, Cu, etc., as well as a list of elements that form FCC phase at some temperature (Fe, Co, etc.). However, this list may be misleading. For example, adding Al (FCC) to Fe stabilizes the BCC phase, while adding Mn (BCC) to Fe stabilizes the FCC phase. Thus, a more sophisticated approach is required such as the well-known CALPHAD method. The successful use of this method is highly dependent on the availability of accurate thermodynamic databases and must be coupled with experimental validation.
The application of the CALPHAD method in alloy design has led to significant departures from conventional compositions; but for both practical and historical reasons, most alloys are designed around one principal element. The supposition is that the principal element’s native structure will dominate the characteristics of the alloy leading to similar performance. Additional elements are then added to modify some combination of physical and/or mechanical properties relevant to the alloy’s intended application. This may include phase stability, solid solution strengthening, and secondary phase formation. In this manner, classes of alloys have been developed around iron, aluminum, titanium, and nickel. While the number of commercially relevant alloys developed in this manner is large, designing an alloy around one element is restrictive. One rapidly expanding field of research is focused on designing alloys with multiple principle elements typically in equi-molar, or near equi-molar, concentrations (Ref 1, 2). These alloys have been designated high-entropy alloys (HEAs) (Ref 3).
Generally, HEAs are materials with at least five or more principal elements, and were so named because their mixing entropies in solution are much higher than alloys based on a single element. Some alloys with <5 principal elements have been regarded as HEAs, though these are sometimes referred to as “medium entropy” alloys. To be considered a principal element, a concentration of between 5 and 35 at.% is necessary (Ref 3, 4). Minor elements can also be included, typically at levels <5 at.%. The resultant HEA is defined by the “group” of principal elements from which it is composed rather than one single principal element as in traditional alloys. The defining characteristic of an HEA is stabilization of a high-entropy solid solution phase. This phase may either compose the entire microstructure or coexist with strengthening phases. The entropy stabilized solid solution inhibits potentially undesirable phases that can form when multiple elements exist together in high concentrations. More importantly, a highly disordered solid solution imparts appealing properties that are typically not observed in traditional alloys. For example, HEA properties may include high room temperature strength/hardness, good wear resistance, good high temperature strength, good structural stability, and good corrosion/oxidation resistance (Ref 1). While these properties appear promising, many studies were carried out utilizing small-scale melting techniques, and therefore, the observed properties may not translate directly upon scale up when the same compositions are produced via commercial methods.
The performance levels that may be achieved from an alloy are highly sensitive to processing history. Within the HEA literature, there have been limited investigations on the importance of melt processing, homogenization heat treatment, and thermo-mechanical processing. Kao et al. (Ref 5) studied the microstructure and mechanical properties of AlxCoCrFeNi in the as-cast, “homogenized” (so-called, since no criteria for the homogenization cycle used was given), and mechanically deformed states. Zhang et al. subsequently examined the effect of annealing on the microstructure and properties of CoCrFeNiCuAl (Ref 6) and CoCrFeNiTiAlx (Ref 7). Ng et al. used a series of thermo-mechanical treatments to study the stability of the solid solution phases in a high-entropy Al0.5CoCrCuFeNi and found that the solid solution phases were stable only at high temperatures >850 °C and at temperatures below 300 °C (Ref 8). Most HEA studies present properties for the material in the as-cast condition. In this state, the dendritic structures that result from non-consumable arc melting (i.e., button) dominate performance. Finally, many small-scale melts only allow for compression samples to be produced as opposed to ASTM standard size tensile specimens. The limited geometric sample size has forced comparisons between HEA compression tests and commercial alloy tensile tests which may be misrepresentative (Ref 9).
Non-consumable arc melting is useful for making small-scale trial heats of material for laboratory investigations. However, this approach has many technical issues that can potentially influence the characteristics of the resulting alloy. A close look at non-consumable arc melting is needed to understand these limitations. Consider a non-consumable arc melted ingot. Such ingots are produced in contact with a water-cooled copper hearth. The hearth cools the ingot such that it is never fully molten, and as such, this melting technique makes it highly improbable, if not impossible, to fully and completely mix the elemental constituents in the alloy. Differences in density and melting point of the elements tend to exacerbate this problem with high density, high melting point elements such as W, Ta, and Nb being particularly hard to incorporate into a non-consumable arc melted ingot.
A solidification artifact also arises from this approach. Typically, an ingot made in this way results in an erratic dendrite structure that forms during the solidification process. If the portion of the alloy ingot in contact with the copper hearth melts, it solidifies nearly instantaneously forming a “chill grain” region which is free of dendrites. Quite often, the bottom of the ingot is not completely melted and displays characteristics of a heat-affected zone found in weldments (which is effectively what a non-consumable arc melted ingot is). Meanwhile, those regions near the upper surface, and topmost sides, solidify into long columnar dendrite grains with orientations dependent on both hearth configuration (i.e., the direction of heat extraction) and melt practice (i.e., heat input). Furthermore, the inevitable shrink cavity is difficult to control and may, or may not, have connectivity to the surface. Thus, the structure of the ingot, and presumably the physical and mechanical properties are complex, difficult to describe, and vary throughout the ingot, as well as from ingot to ingot. As a result of these melt-solidification artifacts along with other considerations, non-consumable arc melting is not used to produce alloys on an industrial scale because they may produce non-representative and non-reproducible properties. The HEAs produced and reported herein were made by conventional vacuum induction melting (VIM), which is a commercial type process often used to produce industrial scale ingots.
The alloys investigated in this effort represent well-reported, single-phase HEAs of CoCrFeNi and CoCrFeMnNi. Previous results in the literature on similar HEAs (Ref 10-13) do not provide much information related to the effects of ingot size and thermo-mechanical processing on the chemistry, microstructure, and mechanical properties. This report focuses on NETL’s efforts to produce single-phase HEAs of kilogram size using commercial melting, thermo-mechanical processing, and heat treatment practices. The results of the melting campaign are provided through analysis of microstructure and mechanical behavior at various temperatures.
Alloy Manufacture and Heat Treatment
Two alloys with nominal compositions CoCrFeNi (designated as HEA1) and CoCrFeMnNi (designated as HEA2) were melted using VIM. Each VIM furnace charge weighed approximately 7.8 kg and was composed of feedstock of commercial high purity pressed into compacts that would fit into the crucible. Some elements were introduced loosely in the crucible as they did not compact well (e.g., Mn). Nickel and cobalt additions were melt consolidated before being alloyed with the rest of the elements. A summary of the melt practice, homogenization heat treatment, and thermo-mechanical processing will not be given here. In depth discussion can be found in Ref 14.
Each constituent was placed in the crucible such that sequential melt-in of various materials occurred. Considerations for where each element was placed included its melting temperature, form, and degree of interaction with the electromagnetic field. Sequential melt-in is critical to avoid “bridge” formation during melting and to ensure the availability of proper clearance for further additions. The heats were poured into zirconia-coated graphite molds while under an argon partial pressure of 200 torr (0.26 atm). The mold cavity was a 75 mm-diameter cylinder with a funnel-shaped riser (i.e., hot top) to minimize pipe shrinkage.
After casting, the hot tops were cut from each ingot. A 2 mm-thick slice was then taken from the top of the ingot for chemical analysis. A Rigaku ZSX Primus II x-ray fluorescence (XRF) analyzer with NIST traceable standards and reported accuracies to 0.01 wt.% was used to carry out bulk chemical analysis. A LECO CS444LS was used to determine carbon and sulfur levels. Oxygen and nitrogen chemistries were determined with a LECO TC436AR. Both the carbon/sulfur and oxygen/nitrogen analyses were carried out using NIST certified standards with reported values accurate to 0.0002 wt.%.
Prior to fabrication (i.e., hot forging and rolling) and heat treatment, the ingot sidewalls were conditioned on a lathe to remove surface imperfections. Each ingot was then given a custom homogenization heat treatment calculated using a combination of CALPHAD estimations and kinetic modeling (Ref 15). The target of the homogenization routine was to reduce the residual chemical inhomogeneities across dendrite arms to within ±1% of the nominal chemistry. The calculated homogenization heat treatment used for both ingots was as follows: 1100 °C/1 h + 1180 °C/3 h + 1200 °C/5 h.
After homogenization, the ingots were placed within stainless steel foil pouches and heated to 800 °C for 3 h. This provided through thickness heating to the ingot for further hot work. Hot working consisted of upset forging, step flattening, and squaring each ingot into a roughly rectangular shape before hot rolling into plates. The final thickness of the hot worked plates was approximately 10 mm. Thermo-mechanical processing of the ingots from the original size produced in this study to this final shape was sufficient to achieve a fully wrought and equiaxed microstructure.
HEA1 and HEA2 were examined in the as-cast state, after homogenization, and after hot working using both optical and scanning electron microscopy (SEM). The top flat surface of the hot rolled plates was examined to assess residual grain elongation and directionality. A JEOL JSM 7000F SEM in both backscattered and secondary electron imaging mode was used for all SEM micrographs.
Approximately, 4 mm-thick slices of HEA1 and HEA2 from the homogenized ingots and hot worked plates were cut down into additional slices approximately 0.7 mm in thickness. Each slice was ground down to 220 μm, prior to punching out several 3 mm-diameter disks. The disks were ground and polished to a final thickness between 120 and 130 μm. The disks were electropolished using 100 mL of 60% perchloric acid in 900 mL methanol, at a temperature of −28 °C. An electropolishing potential of 18 V was established for HEA1, but there was more difficulty for HEA2. HEA2 had a tendency to etch over the range of voltages explored (17-25 V). The electrolyte used was perhaps not particularly well suited to HEA2, which contained much higher manganese levels when compared to HEA1. After inspecting the polished foils, several were ion milled with a Gatan Precision Ion Polishing System (PIPS). The goal of this was to increase the amount of electron-transparent material.
Ion milling of metal samples is usually avoided due to damage that accumulates in surfaces exposed to highly energized argon ion beams. In order to minimize this effect, a relatively low operating potential (3 kV) was employed. Despite careful operation, some damage was expected, and may present as “black speckled contrast” in bright-field images. The surface damage effect provides additional spots in some of the zone axis diffraction patterns which were accounted for when conducting analyses.
The HEA1 and HEA2 10 mm-thick rolled plates were sectioned into approximately 10 mm × 10 mm rectangular cross-section bars that were 76 mm long. These rectangular bars were subsequently machined into 76 mm-long cylindrical tensile specimens, employing L = 4D geometry for the gage section [per ASTM E8 (Ref 16)] with a reduced section length of 30 mm and a gage length equal to 25.4 mm (6.35 mm gage diameter). Tensile tests were performed according to ASTM E8 (Ref 16) with initial crosshead displacement rate of 0.127 mm/min (i.e., an initial strain rate of 8.33 × 10−5/s for a 25.4 mm gage length). The extensometer recorded the tensile strain through 0.012 at which point it was removed. Once the extensometer was removed, the crosshead displacement rate was increased to 1.27 mm/min for the remainder of the tensile test (i.e., new strain rate equal to 8.33 × 10−4/s). Elongation measurements determined from the recorded crosshead displacement were then verified by measuring the true tensile specimen displacement between gage marks on the reduced section (i.e., gage marks used for elevated temperature extensometer placement). The diameter at the point of fracture in the gage length of the tensile specimen was also measured in order to determine the reduction in area. For elevated temperature testing, the specimen was brought up to the test temperature slowly over several hours so as not to overshoot the desired test temperature. Once the tensile specimen reached the desired test temperature, it was held at that temperature for a minimum of 20 min before initiation of the test.
Ingot Structure, Alloy Chemistry, Manufacture, and Heat Treatment
Design (upper) and measured (lower) compositions of HEA1 and HEA2
SEM of HEA1 and HEA2 in the as-cast condition showed a dendritic structure typically seen in castings (Ref 14). The x-ray maps of the constituent elements illustrated how Co, Cr, and Fe partition to the dendrite core, while Mn and Ni partition to the interdendritic region (Ref 14). In order to reduce segregation, homogenization of the as-cast structures of HEA1 and HEA2 was performed using NETL’s computational approach (Ref 15). Doing so greatly reduced the chemical inhomogeneity due to solidification segregation (Ref 14).
After the homogenization heat treatment step, the ingots were thermo-mechanically processed. During and after the hot working step, HEA1 and HEA2 showed no signs of surface or edge defects. The hot working temperature of 800 °C was selected as a compromise to allow both alloys to be forged simultaneously while enhancing grain refinement. The hot working temperature was 0.6 and 0.7 of the computed homologous temperature for HEA1 and HEA2, respectively. Careful attention to grain refinement during hot working was important as neither alloy contained secondary phases to inhibit grain growth.
The overall structure of the wrought alloys contained a mixture of equiaxed and residual wrought grains (Ref 14). Several elongated second phase particles were also evident and were investigated via SEM along with other microstructural characteristics. SEM backscattered electron imaging indicated that aside from the elongated secondary phase, neither alloy contained additional anomalous phases (Ref 14). The grains were also moderately twinned (common for FCC crystal structure materials). The elongated secondary phases were rich in Mn and S and are likely MnS particles. These particles likely formed during casting did not dissolve below the 800 °C hot working temperature, and subsequently elongated during hot rolling operations.
Composition analysis comparison between the bulk (XRF) and local scale in the TEM
Tensile mechanical properties for HEA1 as function of temperature
0.2% YS, MPa
Tensile mechanical properties for HEA2 as function of temperature
0.2% YS, MPa
Ingot Structure, Alloy Chemistry, Manufacture, and Heat Treatment
Vacuum induction melt-produced ingots exhibit the classic grain morphology seen in many text books with a thin outer zone of chill grain, a columnar grained zone extending inward, and an equiaxed grained zone in the center. The machining and hot working techniques employed in the current study broke down this structure and refined it. HEA1 and HEA2 underwent reductions of approximately 88% during hot working from ingot form to a 10 mm-thick plate. The extent to which a material’s grain structure may be altered via hot work is limited by its initial and desired final geometries.
The homogenization heat treatment was quite effective in reducing segregation within the alloys. In order to achieve the ±1% chemistry variation target in a practical heat treat duration, a multi-step homogenization cycle was necessary. The first step in the homogenization cycle allowed elements enough time to diffuse in the segregated regions so that the melting point within the interdendritic regions increased. Subsequent homogenization cycle steps then utilized higher and higher temperatures, with corresponding increase of the soak time to achieve the homogenization target. As an example, a casting may be heated to within 50 °C of its incipient melt point (calculated based on chemistry of the interdendritic region). Kinetic models are then used to estimate the chemical change in the interdendritic region after a certain amount of time at the initial temperature. After the new chemistry is calculated, a new interdendritic liquidus can be determined and used to guide increases to the heat treatment temperature.
The amount of oxygen, nitrogen, carbon, and sulfur in both HEA1 and HEA2 was higher than desired. High-purity materials were used consistent with industry standards rather than ultra-high-purity laboratory grade materials. The interstitial elements were carried by the feed materials into the melt, and control of these elements is a day-to-day concern of many alloy producers. As such, some discussion is needed on the potential and observed impacts of these contaminants. The carbon and nitrogen might be anticipated to form carbides or carbo-nitrides (especially with Cr). Oxygen is expected to form various metal oxides. While neither carbides nor carbo-nitrides were observed, oxides were occasionally found (and were observed in both SEM and TEM investigations). The sulfur would be expected to form sulfides (especially with Mn) and many of these precipitates segregated to grain boundaries. Sulfur is the least desirable and most problematic. Suspected manganese sulfides were observed in both alloys via SEM and TEM. Fortunately, the presence of the sulfides did not influence the hot workability of these alloys, nor did they appear to have a significant effect on mechanical performance. Although it was not done in the current study, sulfur can be removed in the melt by reacting with elements such as yttrium (Ref 19).
The wrought microstructures of HEA1 and HEA2 revealed that the as-cast dendrite structure was fully refined with fine (<25 µm), equiaxed grains forming as a result of hot working. The fine grain size may be attributable both to the relatively low hot working temperature as well as sluggish diffusion observed in HEAs (Ref 1, 4). There were also, unfortunately, some residual areas that did not recrystallize as a result of the final 15 min hold within the 800 °C furnace. The residual worked areas (likely due to the same factors influencing grain size) are not generally desirable. A higher hot working temperature may be needed in order to prevent their formation. Post-work heat treatment is also an option; however, this was not used in the current study due to the unknown grain growth kinetics of both alloys.
Electron microscopy of HEA1 and HEA2, especially TEM, revealed that each was essentially single phase with oxide and sulfide inclusions. No secondary phases based on the HEA elements were observed at either the grain boundaries or twin boundaries. The combination of analytical techniques utilized showed that these alloys have a FCC matrix and the desired chemistry.
A number of individuals have looked at the single-phase HEAs described in this work in terms of processing, microstructure, and mechanical behavior (Ref 20-25). In particular, trying to compare the tensile mechanical properties of HEAs is difficult given the many ways the alloys have been manufactured (i.e., melting procedure, solidification route, heat treatments including homogenization approach, fabrication methodology). Complications invariably arise due to variations in grain size, the possibility of residual segregation (which may not have been characterized), leading to possible phase formation (intentional or otherwise), starting dislocation density, etc. Given these concerns, several papers have been published specifically on either the compressive or tensile properties of CoCrFeNi and CoCrFeNiMn (Ref 22-25).
Also, another factor to keep in mind when comparing tensile data from the testing done in this research with other information found in the literature is the tensile specimen size difference. In research reported herein, ASTM E8 was adhered to for tensile specimen preparation, meaning that cylindrical tensile test specimens, >76 mm in length with a reduced gage section equivalent to 30 mm in length with 6.35 mm in diameter, were used. These specimens were extracted and machined from plate about 12 mm in thickness. As such they were considerably larger than those used in comparison studies found in the literature (Ref 22-25). Actual tensile testing was also performed according to ASTM E8, meaning after yield the crosshead displacement rate was increased for the remainder of the test (i.e., from 0.127 to 1.27 mm/min, corresponding to an effective strain rate increase from 8.33 × 10−5 to 8.33 × 10−4/s when using a 25.4 mm gage length extensometer).
Compression testing was performed in (Ref 24) using strain rates between 10−4 and 10−2/s at temperatures between 600 and 800 °C at 100 °C intervals. From the compression tests, yield stress and flow stress proved to be the most relevant for comparison purposes. While a direct comparison was impossible, the flow stress for “HEA2” type material was between 282 MPa (10−4/s) and 375 MPa (10−3/s) at 700 °C and 174 MPa (10−4/s) and 264 MPa (10−3/s) at 800 °C. At 700 °C, HEA2 had an approximate flow stress (UTS value) of 321 MPa. This falls within the values measured in Ref 24. At 800 °C, HEA2 had an approximate flow stress (UTS value) of 155 MPa, which was a bit lower than was observed in Ref 24 for compression. However, given the possible reasons for these differences as noted above, the magnitude similarity is surprisingly good.
Zaddach et al. (Ref 25) looked at HEA1- and HEA2-type chemistries and performed tensile tests at room temperature. The one major difference was that the tensile specimens were “annealed” for a period of time at either 1100 °C or 625/650 °C after thermo-mechanical processing (TMP) but prior to testing. The corresponding NETL material was also given a short duration post-TMP heat treatment during plate flattening process. For the NiFeCrCo material (corresponding to HEA1) annealed at 1100 °C, the room temperature tensile properties were 197 MPa (0.2% YS), 582 MPa (UTS), and 82% (Elongation). Conversely, when annealed at only 625 °C, the tensile properties for the NiFeCrCo material were 540 MPa (0.2% YS), 786 MPa (UTS), and 49% (Elongation). The amount of recovery in the material was more significant at the higher post-TMP process temperature. For HEA1, corresponding to NiFeCrCo, the measured tensile properties at room temperature [see Table 3] were 611 MPa (0.2% YS), 794 MPa (UTS), and 38% (Elongation), or slightly higher values in strength and a bit lower in ductility as measured by elongation at failure than observed in the Zaddach et al. research (Ref 25).
For HEA2-type material (i.e., NiFeCrCoMn), Zaddach et al. (Ref 25) measured tensile properties at room temperature to be (1) 135 MPa (0.2% YS), 497 MPa (UTS), and 55% (Elongation) for 1100 °C annealed material and (2) 660 MPa (0.2% YS), 851 MPa (UTS), and 25% (Elongation) for 650 °C annealed material. The tensile properties for HEA2 fell within this range at 538 MPa (0.2% YS), 725 MPa (UTS), and 40% (Elongation) [see Table 4]. The trend in strength and ductility was consistent between the two sets of materials even accounting for the discrepancies in the processing of materials for testing.
Typical minimum room temperature tensile properties for selected austenitic stainless steels 
0.2% YS, MPa
Ratio of YS to UTS for HEA1, HEA2, and 316 SS  as function of temperature
Test temperature, °C
The intriguing tensile performance of HEA1 and HEA2 is further revealed upon examination of their tensile curves (Fig. 3). Besides the high work hardening rate observed at most temperatures, the curve at 500 °C is a bit erratic. This behavior, i.e., serrations in the stress-stain curve at elevated temperatures, has been reported in other high-entropy alloy research (Ref 4). At room temperature, the stress-strain curves for HEA1 and HEA2 are representative of typical FCC materials, i.e., gradual increase in stress with increasing strain (i.e., work hardening) until maximum load is reached. As the temperature of the tensile test increases, the amount of work hardening decreases with the point of maximum load (corresponding to UTS) shifting to lower values of strain. At 800 °C, maximum load occurs shortly after yield with a more pronounced region of flow stress (i.e., minor variation in stress with increasing strain, and in this case it decreases slightly (from an engineering stress-strain perspective) with increasing strain until failure).
As stated before, serrated flow was observed during tensile tests at 500 °C. Serrated or “jerky” flow is a well-known phenomenon that has been extensively studied due to its negative effects on the surface of forged components. Serrated flow has several potential causes including formation of twins, stress-induced martensitic transformations, or interactions between solute atoms and dislocations (Ref 27-29). The latter of these mechanisms is often referred to as the Portevin-Le Chatelier effect. As the temperature of a tensile specimen is increased, solute atoms may achieve sufficient mobility to move to, and effectively pin, dislocations until the applied stress overcomes the pinning effect. The result is a marked decrease in measured stress as the material deforms rapidly until the process begins to repeat itself leading to the serrated pattern in the stress-strain curve. As the temperature of a sample is further increased, additional pathways for solute atom mobility may become available leading to less intense interactions between solute atoms and dislocations causing the Portevin-Le Chatelier effect to diminish. This behavior is observed in the current set of experiments with serrated flow becoming active at around 500 °C and vanishing at 600 °C. An additional characteristic of the Portevin-Le Chatelier effect is a minimum in ductility (Ref 28). In both the HEAs studied, there was a decrease in ductility as the serrated flow became active. For these reasons it is most likely that solute atoms are pinning dislocations in the alloys that were studied. This effect has also been well documented in several other investigations on similar HEA systems (Ref 4).
In HEAs, it is difficult to define which element is the solute, and therefore, there exists significant ambiguity as to which element is primarily responsible for dislocation pinning. On a practical note, the serrated flow deactivated well below temperatures that would be used in hot forming operations. This means that any surface imperfections related to the Portevin-Le Chatelier effect should not be an issue. If the HEAs under study were to be used at service temperatures between 500 and 600 °C, there are also means by which this effect can be minimized including introducing cold work to the material.
Several structural features are seen in Fig. 12. There are numerous twins seen throughout the image, but note those to the left of the figure. At this magnification, many of the twins have widths at least 100 nm in size. At room temperature, clusters of the twins had widths in the 20 to 50 nm range. Also, note the dark “spots” to the right. Upon detailed inspection, these spots were actually Cr-rich precipitates with carbon also found in the XEDS spectra. At this juncture, they were assumed to be carbides. (Note from Table 1 that HEA1 had approximately 0.04 wt.% carbon.)
Not surprisingly, HEA1, i.e., 500 °C tensile-tested sample, exhibits a microstructure that includes some components of the room temperature tested samples. There is twinning, but not so much fine twinning as was seen in the room temperature sample. There is a high dislocation content, showing the same cellular type structure around dislocation-free regions as was observed in the room temperature sample. Some fine structures, believed to be micro-twins, were also observed (again, similar to the room temperature sample). These fine structures do not appear to be an additional phase as there was no XEDS or diffraction evidence. Weak beam, dark-field (WBDF) imaging was attempted, although working at preferred systematic diffraction conditions was out of the question due to the grain size, twinning, dislocation strain effects, etc. The empirical WBDF images that include bright contrast for dislocations against a dark background for the matrix material also include numerous fringes. Hopefully, these are evidence of stacking faults associated with the dislocation structure, not just the result of a poorly selected (multi-beam) diffraction condition.
For the bands of dislocations, it is hard to determine if they are entirely due to tensile deformation or have begun to reorganize into a lower energy structure (e.g., a subgrain boundary) due to the test temperature and duration of the tensile test at 800 °C. Other images showed nice dislocation structures that could be due to either.
Compared to the HEA-1 sample that was tensile tested at room temperature, this sample exhibits considerably less fine twinning. However, some twinning is present. Grain boundaries are much more readily observed and a few Cr-rich precipitates (probably carbide) were found. The dislocation density was quite high across most of the sampled area, although a few grains were observed that appeared to be anomalously low in this regard, showing very few dislocations despite tilting through a fairly wide range of orientations. There is some evidence for deformation bands. Dislocations were resolved relatively easily (whereas with the room temperature and 500 °C samples, dislocations were unresolved due to their extremely high density and associated strain fields). Part of the reason for this is the test temperature which allows greater dislocation mobility, not only glide but climb. At least for HEA1, the test duration at 800 °C was much longer than at 500 °C. (Note from Table 3 that elongation at 800 °C was 64% compared to 26% at 500 °C, resulting in a longer time at a higher temperature for HEA1. Although TEM of HEA2 has not been completed, it is expected that for tests through 500 °C feature development will be much the same. Given the shorter duration test at 800 °C for HEA2, much of what has been seen in HEA1 at 800 °C may not occur to the same extent as in HEA2.)
Tramp contaminant elements such as O, N, C, and S were observed to come from high purity but conventional quality feed stocks. These impurities formed various precipitate phases including suspected Mn-S, Cr-based carbides, and oxides of Al and Si.
Grain refinement of both alloys was successful due to combined thermo-mechanical processing, i.e., hot forging followed by hot rolling.
Previous efforts on HEA alloys do not specify or validate the level of homogenization in the HEA (Ref 20-25). This work differs in that it presents a validation of a homogenization treatment that reduced segregation to 1% of nominal chemistry for each element through the use of a computationally based algorithm (Ref 15).
The microstructures of HEA1 and HEA2 are single phase with precipitates due to impurities from the starting feed stock. However, with the exception of second phases formed by the impurity elements, no second phases (other than these) were observed even at the TEM level.
The general characteristics of tensile mechanical behavior are similar to that of 300-series austenitic stainless steels, in that these alloys (i.e., single-phase FCC matrix) undergo extensive work hardening during tensile deformation. The yield stress and tensile strength of HEA1 and HEA2 are, in general, consistent with what others have observed for these HEA compositions (Ref 22-25). More importantly, the HEAs studied herein tend to have tensile strength equivalent to, or greater than, typical of 300-series austenitic stainless steels. HEA1 and HEA2 also have higher yield stress than does 316SS but this may be a result of thermo-mechanical processing approach. As a consequence, the ductility is lower. Also, there is a decrease in ductility to a minimum for these HEAs, which while similar, for example, to 316SS is a bit deeper and occurs at higher temperatures.
Serrated flow (Portevin-Le Chatelier effect) was observed in both HEA1 and HEA2 at 500 °C. This behavior has been seen by others researching HEAs (Ref 30).
The main goal of this research was to produce single-phase HEAs using more commercial type melting practice. This has been accomplished. However, significant problems remain when considering other possible HEA combinations where differences in the melting range of the elements might prove challenging using large-scale commercial melting technologies.
Another significant problem in HEA manufacture has centered upon eliminating segregation in the consolidated alloy. This is more problematic in that segregation mainly arises from the way in which the material is produced (i.e., the melt-solidification route), and as such, such melting practice may limit the extent to which the residual segregation can be reduced. Significant segregation with associated phase formation can complicate material characterization and interpretation of mechanical properties (with reproducibility of microstructures also a problem).
This work was funded by the Cross-Cutting Technologies Program at the National Energy Technology Laboratory (NETL)—Strategic Center for Coal, managed by Robert Romanosky (Technology Manager) and Charles Miller (Technology Monitor). The Research was executed through NETL’s Office of Research and Development’s Innovative Process Technologies (IPT) Field Work Proposal.
This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof.