Size-dependent structure and magnetocaloric properties of Fe-based glass-forming alloy powders
Source abstract
Abstract
We investigated the influence of particle size on the microstructure and magnetocaloric effect of Fe-based alloy powders (11 μm to 100 μm in diameter). The degree of structure order varies with the powder size. The 11 μm to 18 μm powders show the largest peak magnetic entropy change (MEC). Increasing the degree of structure order tends to decrease the maximum MEC. Nevertheless, enhancement of refrigerant capacity and MEC (above 70 K) is achieved when the crystalline phase content is ∼50% (above 75 μm) in the 75 μm to 100 μm powders. Exponent n of the field dependence of MEC increases with the decrease in powder size above 22.5 K. The size dependence of the structure and properties is associated with the fact that a larger particle has a slower cooling rate and takes a longer time to form medium-to-long range ordered structures.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Magnetic and transport properties of perovskites and related materials · Metallic Glasses and Amorphous Alloys · Thermal Expansion and Ionic Conductivity
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Tongji University 1 School of Materials Science and Engineering, , Shanghai 201804, China
Chongqing Normal University 2 Chongqing Key Laboratory of Photo-Electric Functional Materials, College of Physics and Electronic Engineering, , Chongqing 401331, China
Shanghai University 3 Laboratory for Microstructures, , Shanghai 200444, China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Shanghai
References (29)
Show source-provided references
1. Phys.Rev.Lett. · 1997 · 78 · 449410.1103/PhysRevLett.78.4494 ↗
2. Nature · 2002 · 415 · 15010.1038/415150a ↗
3. Phys. Rev. B · 2001 · 64 · 01240910.1103/PhysRevB.64.012409 ↗
4. Rep.Prog.Phys. · 2005 · 68 · 147910.1088/0034-4885/68/6/R04 ↗
5. J. Alloys Compd. · 2006 · 408 · 116510.1016/j.jallcom.2004.12.112 ↗
6. Adv Mater · 2009 · 21 · 1
7. Phys. Rev. B · 2005 · 72 · 09443510.1103/PhysRevB.72.094435 ↗
8. Appl. Phys. Lett. · 2006 · 88 · 08191410.1063/1.2338770 ↗
9. Luo · Appl. Phys. Lett. · 2007 · 90 · 21190310.1063/1.2741120 ↗
10. J. Magn. Magn.Mater · 2010 · 322 · 229810.1016/j.jmmm.2010.02.029 ↗
11. J. Appl. Phys. · 2014 · 115 · 22390410.1063/1.4882735 ↗
12. J. Non-Cryst. Solids · 2013 · 359 · 110.1016/j.jnoncrysol.2012.09.020 ↗
13. Acta Mater. · 2013 · 61 · 128410.1016/j.actamat.2012.11.006 ↗
14. Appl. Phys. Lett. · 2009 · 94 · 11250710.1063/1.3097237 ↗
15. Appl. Phys. Lett. · 2006 · 88 · 04250510.1063/1.2167803 ↗
16. Appl. Phys. Lett. · 2010 · 96 · 18250610.1063/1.3427439 ↗
17. J. Appl. Phys. · 2006 · 100 · 08390310.1063/1.2358311 ↗
18. Appl. Phys. Lett. · 2011 · 98 · 19250310.1063/1.3589353 ↗
19. Appl. Phys. Lett. · 2009 · 95 · 26250110.1063/1.3276558 ↗
20. J. Magn. Magn. Mater. · 2006 · 300 · e38510.1016/j.jmmm.2005.10.125 ↗
21. J. Non-Cryst. Solids · 2015 · 425 · 11410.1016/j.jnoncrysol.2015.06.002 ↗
22. J. Appl. Phys. · 2007 · 101 · 09C50310.1063/1.2709409 ↗
23. J. Alloys Compd. · 2014 · 615 · 25510.1016/j.jallcom.2014.06.162 ↗
24. J. Alloy. Compd. · 2010 · 495 · 20910.1016/j.jallcom.2010.01.125 ↗
25. J. Alloys Compd. · 2010 · 496 · 710.1016/j.jallcom.2009.12.029 ↗
26. Appl. Phys. Lett. · 2012 · 101 · 10240710.1063/1.4751038 ↗
27. Appl. Phys. Lett. · 2014 · 104 · 21240110.1063/1.4879544 ↗
28. J. Appl. Phys. · 1984 · 55 · 433410.1063/1.333046 ↗
29. Acta Mater. · 2007 · 55 · 29510.1016/j.actamat.2006.08.028 ↗