High-Performance Anisotropic Nanocomposites with a Novel Core/shell Microstructure
Source abstract
Abstract
Anisotropic nanostructures of magnetically hard and soft materials are fascinating for exploring next-generation ultrastrong permanent magnets with less expensive rare-earth elements. It is a big challenge fabricating high-performance nanocomposites due to the difficulty in controlling the grain size of the soft phase. Here, surfactant-assisted low-temperature chemical coating (LTCC) is adopted to fabricate SmCo5@FeCo nanocomposites. A uniform coating layer of the soft phase ranging from 5 to 15 nm FeCo particles is obtained. Both high coercivity Hc of 17.2 kOe and high energy product (BH)max of 29.4 MGOe in the optimal anisotropic SmCo5@FeCo nanocomposites with 15 wt % soft phase coating had been successfully fabricated, which has an enhancement of 31% compared with that of the uncoated single SmCo5 phase. The excellent performance is ascribed to nanosized grains of both soft and hard phases and a high remanence ratio Mr/Ms of 0.976. These results made a big step toward synthesizing a stronger bulk nanocomposite system.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Magnetic Properties of Alloys · Magnetic and transport properties of perovskites and related materials · Hydrogen Storage and Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Materials, Shanghai University, Shanghai 200444, P. R. China
School of Materials Science and Engineering, China Jiliang University, Hangzhou 310018, P. R. China
Ningbo Institute of Material Technology & Engineering, Chinese Academy of Sciences, Ningbo 315201, P. R. China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Zhejiang Province
References (32)
Show source-provided references
1. 10.1109/20.10293110.1109/20.102931 ↗
2. 10.1103/physrevb.48.1581210.1103/physrevb.48.15812 ↗
3. 10.1016/j.eng.2018.11.03410.1016/j.eng.2018.11.034 ↗
4. 10.1038/420374a10.1038/420374a ↗
5. 10.1021/acs.nanolett.6b0221010.1021/acs.nanolett.6b02210 ↗
6. 10.1088/1674-1056/27/11/11750210.1088/1674-1056/27/11/117502 ↗
7. 10.1016/j.jmst.2019.04.04110.1016/j.jmst.2019.04.041 ↗
8. 10.1016/j.jmst.2021.01.08310.1016/j.jmst.2021.01.083 ↗
9. 10.1002/adma.20160643010.1002/adma.201606430 ↗
10. 10.1109/tmag.2005.85495210.1109/tmag.2005.854952 ↗
11. 10.1109/tmag.2012.219564610.1109/tmag.2012.2195646 ↗
12. 10.1002/adma.20120232810.1002/adma.201202328 ↗
13. 10.1063/1.365603810.1063/1.3656038 ↗
14. 10.1063/1.297368810.1063/1.2973688 ↗
15. 10.1007/s40195-017-0631-210.1007/s40195-017-0631-2 ↗
16. 10.1016/j.jmst.2020.09.05210.1016/j.jmst.2020.09.052 ↗
17. 10.1021/nl403043d10.1021/nl403043d ↗
18. 10.1021/acs.nanolett.7b0259310.1021/acs.nanolett.7b02593 ↗
19. 10.1016/s1574-9304(05)80077-x10.1016/s1574-9304(05)80077-x ↗
20. 10.1063/1.335839010.1063/1.3358390 ↗
21. 10.1039/c9nr06653e10.1039/c9nr06653e ↗
22. 10.1002/ange.20190776310.1002/ange.201907763 ↗
23. 10.3934/matersci.2015.3.29410.3934/matersci.2015.3.294 ↗
24. 10.1016/j.jallcom.2014.12.02610.1016/j.jallcom.2014.12.026 ↗
25. 10.1016/0304-8853(94)00876-010.1016/0304-8853(94)00876-0 ↗
26. 10.1039/c3nr33602f10.1039/c3nr33602f ↗
27. 10.1038/nature0120810.1038/nature01208 ↗
28. 10.1103/physrevb.58.1207110.1103/physrevb.58.12071 ↗
29. 10.1088/0957-4484/18/46/46570110.1088/0957-4484/18/46/465701 ↗
30. 10.1016/j.physleta.2020.12695410.1016/j.physleta.2020.126954 ↗
31. 10.1007/s00396-020-04724-210.1007/s00396-020-04724-2 ↗
32. 10.1063/1.150486910.1063/1.1504869 ↗