Abstract

The martensitic and magnetic transformations, as well as the mechanical properties, of Ni₂MnAl alloys in as-cast (AC) and heat-treated (HT) conditions were investigated. Magnetic-field-induced strain was evaluated via magnetostriction, with reversible strains of 0.14% and 0.2% achieved in the martensitic phase at 2 K for the AC and HT alloys, respectively. Transformation temperatures and Curie temperatures were determined under constant applied magnetic field, revealing that γ-phase inclusions in the AC microstructure suppress antiferromagnetic domain response, yielding a lower magnetization (∼8.4 emu g⁻¹) compared to the HT alloy (∼13.4 emu g⁻¹). Both alloys exhibited hysteretic behavior in the martensitic state and a linear, paramagnetic response in the austenitic state. Mechanical testing showed predominantly brittle fracture in the AC alloy, while the HT alloy displayed a yield point and Lüders band behavior, indicating limited ductility. Ultimate tensile strength, yield strength, fracture strain, and hardness were quantified for both conditions, demonstrating the combined influence of microstructure, magnetic response, and mechanical behavior. These results highlight Ni₂MnAl as a promising candidate for magnetic-field-controlled shape memory applications, with tunable mechanical and functional properties via heat treatment.

Department(s)

Materials Science and Engineering

Publication Status

Open Access

Comments

U.S. Department of Energy, Grant DE-NA0002839

Keywords and Phrases

Magnetic field-induced strain; Magnetic reorientation; Magnetic shape memory alloy; Magnetic transformation; Martensitic transformation

International Standard Serial Number (ISSN)

2949-8228

Document Type

Article - Journal

Document Version

Final Version

File Type

text

Language(s)

English

Rights

© 2026 Elsevier, All rights reserved.

Creative Commons Licensing

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.

Publication Date

01 Jul 2026

Available for download on Wednesday, July 01, 2026

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