Nickel-induced magnetic behaviour of nano-structured α-Fe2O3, synthesised by facile wet chemical route
Source abstract
Abstract
We report the synthesis of pristine and nickel containing iron oxide (α-Fe2O3) nanocrystallites by facile environmentally benign wet chemical process. The magnetic behaviour of the samples has been found to change progressively with nickel content. The Mössbauer spectra revealed the precipitation of secondary phase of nickel ferrite (NiFe2O4) at ∼2 wt% nickel contents. The transmission electron micrographs together with asymmetric magnetic hysteresis loop have confirmed the formation of core–shell structure. The Morin temperature of nanostructured α-Fe2O3 as estimated by superconducting quantum interference device has been found to be 257, 245, 247 and 242 K at nickel content of 0, 1, 2 and 4 wt%, respectively. The similar trends of increase/decrease in Morin temperature have been noticed by Mössbauer analysis. Furthermore, below Morin temperature, the temperature range of coexisted antiferromagnetic and ferromagnetic states has been found to increase with increase in nickel content.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Iron oxide chemistry and applications · Magnetic Properties and Synthesis of Ferrites · Magnetic properties of thin films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics, National Institute of Technology Kurukshetra, Haryana, India
Department of Physical Technologies, University of Applied Sciences and Art, Göttingen, Germany
Department of Experimental Physics, Faculty of Science, Regional Centre of Advanced Technologies and Materials, Palacky University, Olomouc, Czech Republic
Funding
CSIR · Ministry of Education, Youth and Sports of the Czech Republic
References (29)
Show source-provided references
1. 10.1021/jp063390610.1021/jp0633906 ↗
2. 10.1007/s11356-012-0842-z10.1007/s11356-012-0842-z ↗
3. 10.1016/j.cej.2013.09.08910.1016/j.cej.2013.09.089 ↗
4. 10.1038/ncomms254710.1038/ncomms2547 ↗
5. 10.1039/c3ra42214c10.1039/c3ra42214c ↗
6. 10.1039/c2dt11822j10.1039/c2dt11822j ↗
7. 10.1088/0022-3727/42/24/24540510.1088/0022-3727/42/24/245405 ↗
8. 10.1088/1674-4926/32/1/01300110.1088/1674-4926/32/1/013001 ↗
9. 10.1039/C3CE41994K10.1039/C3CE41994K ↗
10. 10.1007/s10973-016-5969-610.1007/s10973-016-5969-6 ↗
11. 10.1186/1556-276X-8-21310.1186/1556-276X-8-213 ↗
12. 10.1126/science.121561410.1126/science.1215614 ↗
13. 10.1002/pssa.221041023210.1002/pssa.2210410232 ↗
14. 10.1016/j.tsf.2007.05.02010.1016/j.tsf.2007.05.020 ↗
15. 10.1002/pssb.20145118310.1002/pssb.201451183 ↗
16. 10.1166/jnn.2012.653310.1166/jnn.2012.6533 ↗
17. 10.1063/1.475947410.1063/1.4759474 ↗
18. 10.1016/j.apsusc.2013.08.02210.1016/j.apsusc.2013.08.022 ↗
19. 10.1016/j.apsusc.2014.12.09810.1016/j.apsusc.2014.12.098 ↗
20. 10.1016/j.apsusc.2011.05.09110.1016/j.apsusc.2011.05.091 ↗
21. 10.1016/j.apsusc.2014.08.19310.1016/j.apsusc.2014.08.193 ↗
22. 10.1016/j.apsusc.2015.06.05310.1016/j.apsusc.2015.06.053 ↗
23. 10.1007/s00269-004-0422-y10.1007/s00269-004-0422-y ↗
24. 10.1088/1742-6596/217/1/01200610.1088/1742-6596/217/1/012006 ↗
25. 10.1016/j.jmmm.2013.04.06410.1016/j.jmmm.2013.04.064 ↗
26. 10.1016/S0022-3697(03)00163-X10.1016/S0022-3697(03)00163-X ↗
27. 10.1021/jp108703b10.1021/jp108703b ↗
28. 10.1016/j.jallcom.2013.02.07710.1016/j.jallcom.2013.02.077 ↗
29. 10.1021/jp067620s10.1021/jp067620s ↗