journal article·2020-01-01Open access

Phase transformation and enhanced coercivity in B-N-doped MnAl nanocrystalline bulk alloys prepared by high pressure torsion

Ping-Zhan Si, Chul-Jin Choi, Jihoon Park, Hong-Liang Ge, Juan Du

AIP Advances· Volume 10· Issue 1

Abstract

High coercivity B-N-doped MnAl alloys were prepared by the traditional induction melting, high temperature homogenization, water-quenching, post-annealing, and severe plastic deformation process. The massive phase transformation of the ε→τ in the B-N-doped ε-MnAl occurs at the temperatures above 680 K and accomplishes at 760 K, both of which are slightly higher than those of the ε-MnAl without elemental doping. The Currie point of the B-N-doped τ-MnAl is measured to be 620 K, which is lower than that of the doping-free τ-MnAl. High-pressure torsion was employed to decrease the crystal size and increase the coercivity of samples. A coercivity up to 0.54 T was achieved in the B/N doped MnAl bulk sample after severe plastic deformation under 6 GPa. The aging processing on the severely deformed samples enhances the remanent magnetization significantly and decreases the coercivity slightly. Our work shows that the high-pressure torsion process is effective in developing coercivity in MnAl-based bulk magnet.
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Research context

OpenAlex topics: Magnetic Properties of Alloys · Magnetic properties of thin films · Magnetic and transport properties of perovskites and related materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Materials and Chemistry, China Jiliang University 1 , Hangzhou 310018, China

Powder & Ceramic Division, Korea Institute of Materials Science 2 , Changwon 51508, R. Korea

College of Materials Science and Engineering, Shanghai University 3 , Shanghai 200444, China

Funding

National Research Foundation of Korea · Foundation for Innovative Research Groups of the National Natural Science Foundation of China

References (20)

Show source-provided references
1. Acta Mater. · 2018 · 158 · 11810.1016/j.actamat.2018.07.049 ↗
2. Acta Mater. · 2018 · 157 · 4210.1016/j.actamat.2018.07.010 ↗
3. Materials · 2017 · 10 · 101610.3390/ma10091016 ↗
4. J. Appl. Phys. · 2015 · 118 · 03390510.1063/1.4927289 ↗
5. J. Magn. Magn. Mater. · 2019 · 483 · 16410.1016/j.jmmm.2019.03.103 ↗
6. AIP Adv. · 2016 · 6 · 05600910.1063/1.4943242 ↗
7. J. Magn. Magn. Mater. · 2007 · 308 · 21410.1016/j.jmmm.2006.05.032 ↗
8. 10.1002/pssb.20190035610.1002/pssb.201900356 ↗
9. Acta Mater. · 2017 · 128 · 16010.1016/j.actamat.2017.02.011 ↗
10. J. Magn. Magn. Mater. · 2019 · 474 · 59110.1016/j.jmmm.2018.11.006 ↗
11. AIP Adv. · 2018 · 8 · 05621610.1063/1.5007176 ↗
12. J. Appl. Phys. · 1986 · 59 · 382410.1063/1.336723 ↗
13. J. Phys.: Condens. Matter · 2014 · 26 · 06421110.1088/0953-8984/26/6/064211 ↗
14. J. Japan Inst. Metals and Mater. · 1964 · 28 · 48310.2320/jinstmet1952.28.8_483 ↗
15. Metals · 2014 · 4 · 2010.3390/met4010020 ↗
16. IEEE Trans. Mag. · 1977 · 13 · 132810.1109/TMAG.1977.1059574 ↗
17. J. Alloys Compd. · 2016 · 675 · 16310.1016/j.jallcom.2016.03.098 ↗
18. AIP Adv. · 2017 · 7 · 05621310.1063/1.4974277 ↗
19. J. Solid State Chem. · 2016 · 237 · 30010.1016/j.jssc.2016.02.031 ↗
20. Mater. Sci. & Eng. A · 2016 · 652 · 32510.1016/j.msea.2015.11.074 ↗