Pressure-stabilized dual-BCC polymorphism in a rhenium-based high-entropy alloy

Accessing metastable structural states in high-entropy alloys (HEAs) offers a promising route to tailor material properties, yet the use of high pressure to engineer such states remains underexplored. Here, we report the pressure-driven synthesis of a unique metastable dual-BCC microstructure in a near-equimolar ReNbTiZrHf alloy. Starting from an ambient two-phase mixture of hexagonal (C14-derived) and body-centered cubic (BCC) phases, compression induces a selective, diffusionless transformation of the hexagonal constituent into a second, crystallographically distinct BCC polymorph, while the original BCC phase remains stable. Upon decompression, the pressure-induced BCC phase is kinetically trapped, yielding a dual-BCC state that is inaccessible via conventional thermal processing. The pressure-stabilized BCC polymorph is Re-enriched and inherits the exceptional stiffness of its hexagonal parent (bulk modulus <a:math xmlns:a="http://www.w3.org/1998/Math/MathML"> <a:mrow> <a:mo>∼</a:mo> <a:mn>290</a:mn> </a:mrow> </a:math> GPa), creating a composite microstructure with pronounced elastic and mechanical contrast relative to the softer original BCC matrix <b:math xmlns:b="http://www.w3.org/1998/Math/MathML"> <b:mrow> <b:mo>(</b:mo> <b:mo>∼</b:mo> <b:mn>180</b:mn> <b:mo> </b:mo> <b:mi>GPa</b:mi> <b:mo>)</b:mo> </b:mrow> </b:math> . These findings demonstrate that pressure can effectively navigate the flat free-energy landscapes of chemically complex alloys, establishing a robust pathway for polymorph engineering and metastable phase design in refractory HEAs.