Chemical short-range order controls deformation pathways in a complex concentrated alloy
Angelo F. Andreoli, Gabriela B. Ribeiro, Guilherme C. Stumpf, Maria F. L. Valverde, Gustavo Bertoli, Vinícius P. Bacurau, David D. S. Silva, Pedro H. F. Oliveira, Eric M. Mazzer, Mamta Silwal, Garritt J. Tucker, Rodrigo Freitas, Martin Sahlberg, Daniel Miracle, Francisco G. Coury
Abstract
Chemical short-range order (CSRO) is an intrinsic feature of complex concentrated alloys (CCAs), yet its influence on deformation mechanisms is controversial because of the inconclusive state of concurrent CSRO quantification during deformation. Here, we provide experimental evidence that CSRO acts as an intrinsic thermodynamic state variable governing stacking-fault energetics and deformation pathways in a Co30Cr40Ni30 alloy. By comparing quenched (CSRO-lean) and aged (CSRO-enriched) conditions with equivalent grain structure and phase constitution, we isolate the influence of atomic-scale chemical ordering on mechanical behavior. Calorimetry confirms reversible CSRO formation, while synchrotron X-ray diffraction and electron microscopy reveal that CSRO suppresses deformation-induced fcc-hcp martensitic transformation at both room and cryogenic temperatures. Despite differences in transformation dynamics, the macroscopic tensile response is still broadly similar. Atomistic simulations show that CSRO increases both stable and unstable stacking-fault energies, raising the energetic barrier for partial-dislocation activity and stabilizing the fcc lattice against transformation. Together, the experimental and computational results establish CSRO as an added degree of freedom for tuning stacking-fault energetics and controlling deformation pathways in complex concentrated alloys.
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