TY - JOUR
T1 - Tailoring martensitic transformation for strength-ductility synergy in Co36.8Ni39.2Al24 hypereutectic medium-entropy alloy
AU - Liu, Haoxiang
AU - He, Yixuan
AU - Yao, Dongrui
AU - Zeng, Shiyan
AU - Li, Xiahe
AU - Zhang, Haoran
AU - Jiao, Zhichao
AU - Liu, Xudong
AU - Wang, Haifeng
N1 - Publisher Copyright:
© 2026
PY - 2026/11/20
Y1 - 2026/11/20
N2 - Tailoring the deformation-induced martensitic transformation (DIMT) presents an effective strategy to overcome the strength-ductility trade-off in high-entropy alloys. The characteristics of precipitates play a critical role in governing DIMT behavior. In this study, a Co36.8Ni39.2Al24 hypereutectic medium-entropy alloy (HMEA) with a high fraction of primary B2 phase was selected to elucidate the contribution of DIMT. The precipitation behavior and the impact on mechanical properties in the Co36.8Ni39.2Al24 HMEA were investigated through isothermal annealing at 650–950 °C. Annealing at temperatures above 650 °C fully reverted pre-existing martensite within the B2 matrix. Specifically, annealing at 800 °C produced a high density of nanoscale, ordered L12 precipitates with Kurdjumov-Sachs (K-S) orientation relationship with the B2 matrix, while higher temperatures led to coarsened, disordered face-centered cubic (FCC) precipitates with a loss of the K-S relationship. The 800 °C-annealed sample exhibited an optimal strength-ductility synergy, which originated from both the complete elimination of pre-existing martensite and the presence of low-misfit L12 precipitates that effectively retarded DIMT kinetics, thereby sustaining a high work-hardening rate. In contrast, the high-misfit FCC precipitates formed at 950 °C acted as high-strain nucleation sites, accelerating DIMT and leading to rapid transformation saturation, which weakened the transformation-induced plasticity (TRIP) effect. This work provides fundamental insight into precipitate-mediated control of DIMT and proposes a practical strategy for designing TRIP-assisted high-performance high-entropy alloys.
AB - Tailoring the deformation-induced martensitic transformation (DIMT) presents an effective strategy to overcome the strength-ductility trade-off in high-entropy alloys. The characteristics of precipitates play a critical role in governing DIMT behavior. In this study, a Co36.8Ni39.2Al24 hypereutectic medium-entropy alloy (HMEA) with a high fraction of primary B2 phase was selected to elucidate the contribution of DIMT. The precipitation behavior and the impact on mechanical properties in the Co36.8Ni39.2Al24 HMEA were investigated through isothermal annealing at 650–950 °C. Annealing at temperatures above 650 °C fully reverted pre-existing martensite within the B2 matrix. Specifically, annealing at 800 °C produced a high density of nanoscale, ordered L12 precipitates with Kurdjumov-Sachs (K-S) orientation relationship with the B2 matrix, while higher temperatures led to coarsened, disordered face-centered cubic (FCC) precipitates with a loss of the K-S relationship. The 800 °C-annealed sample exhibited an optimal strength-ductility synergy, which originated from both the complete elimination of pre-existing martensite and the presence of low-misfit L12 precipitates that effectively retarded DIMT kinetics, thereby sustaining a high work-hardening rate. In contrast, the high-misfit FCC precipitates formed at 950 °C acted as high-strain nucleation sites, accelerating DIMT and leading to rapid transformation saturation, which weakened the transformation-induced plasticity (TRIP) effect. This work provides fundamental insight into precipitate-mediated control of DIMT and proposes a practical strategy for designing TRIP-assisted high-performance high-entropy alloys.
KW - High-entropy alloy
KW - Martensitic transformation kinetics
KW - Precipitates
KW - Trip effect
UR - https://www.scopus.com/pages/publications/105033023624
U2 - 10.1016/j.jmst.2026.02.029
DO - 10.1016/j.jmst.2026.02.029
M3 - 文章
AN - SCOPUS:105033023624
SN - 1005-0302
VL - 272
SP - 128
EP - 141
JO - Journal of Materials Science and Technology
JF - Journal of Materials Science and Technology
ER -