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Reasons for the superior mechanical properties of medium-entropy CrCoNi compared to high-entropy CrMnFeCoNi

Acta Materialia · 2017 · Vol. 128 · pp. 292–303
Guillaume LaplancheAleksander KostkaC. ReinhartJ. HunfeldGunther EggelerE.P. George

Abstract

The tensile properties of CrCoNi, a medium-entropy alloy, have been shown to be significantly better than those of CrMnFeCoNi, a high-entropy alloy. To understand the deformation mechanisms responsible for its superiority, tensile tests were performed on CrCoNi at liquid nitrogen temperature (77 K) and room temperature (293 K) and interrupted at different strains. Microstructural analyses by transmission electron microscopy showed that, during the early stage of plasticity, deformation occurs by the glide of 1/2<110> dislocations dissociated into 1/6<112> Shockley partials on {111} planes, similar to the behavior of CrMnFeCoNi. Measurements of the partial separations yielded a stacking fault energy of 22 ± 4 mJ m−2, which is ∼25% lower than that of CrMnFeCoNi. With increasing strain, nanotwinning appears as an additional deformation mechanism in CrCoNi. The critical resolved shear stress for twinning in CrCoNi with 16 μm grain size is 260 ± 30 MPa, roughly independent of temperature, and comparable to that of CrMnFeCoNi having similar grain size. However, the yield strength and work hardening rate of CrCoNi are higher than those of CrMnFeCoNi. Consequently, the twinning stress is reached earlier (at lower strains) in CrCoNi. This in turn results in an extended strain range where nanotwinning can provide high, steady work hardening, leading to the superior mechanical properties (ultimate strength, ductility, and toughness) of medium-entropy CrCoNi compared to high-entropy CrMnFeCoNi.

High Entropy Alloys StudiesAdditive Manufacturing Materials and ProcessesHigh-Temperature Coating BehaviorsMaterials scienceCrystal twinningStacking-fault energyWork hardeningStrain hardening exponentComposite materialUltimate tensile strengthAlloyMetallurgyDeformation mechanism

Funding

  • Deutsche Forschungsgemeinschaft
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