Structural parameters, energy states and magnetic properties of the novel Se-doped NiFe2O4 ferrites as highly efficient electrocatalysts for HER
This study is devoted to NiFe2O4 with different masses of Se (NFO + x%Se) (x = 0.0–4.0%) spinel ferrite nanoparticles production and investigation. The results of the crystal structure, microstructure and magnetic properties are presented as a function of the chemical content of the NFO + x%Se. Supe...
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Published in | Ceramics international Vol. 48; no. 17; pp. 24866 - 24876 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.09.2022
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Subjects | |
Online Access | Get full text |
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Summary: | This study is devoted to NiFe2O4 with different masses of Se (NFO + x%Se) (x = 0.0–4.0%) spinel ferrite nanoparticles production and investigation. The results of the crystal structure, microstructure and magnetic properties are presented as a function of the chemical content of the NFO + x%Se. Superparamagnetic (at 300 K) and ferrimagnetic (at 10 K) states are observed for all samples in the wide magnetic field range. The field dependencies of the magnetization show that Se-substitution does not change the main magnetic characteristics when x<2.0%. We observe a non-linear dependence of magnetic parameters for sample with x ≥ 2.0% (for NFO+2%Se, we determine the increase of the main magnetic parameters for 20% of the average values and the minimum values belong to the NFO+3%Se). The undoped sample and NiFe2O4+x%Se are soft magnets and characterized by the low coercivity (varying in the range 560–647 Oe). At T = 10 K squareness ratio (Sq. = Mr/Ms) is in a range of (0.216–0.318). This indicates a preferable single-domain state of crystallites, which differs from the magnetic structure at T = 300 K. Furthermore, the NFO + x%Se (x = 2.0) have a low overpotential of about −327 mV, and a small Tafel slope of 91 mV/dec, which makes it a better for HER (hydrogen evolution reaction) catalyst than the undoped NiFe2O4. |
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ISSN: | 0272-8842 1873-3956 |
DOI: | 10.1016/j.ceramint.2022.05.140 |