Abstract
We present magnetic properties of NiMn2O4−δ (nickel manganite) which was synthesized by complex polymerization synthesis method followed by successive heat treatment and final calcinations in air at 1200°C. The sample was characterized by using X-ray powder diffractometer (XRPD), scanning electron microscopy (SEM), field-emission scanning electron microscopy (FE-SEM) and superconducting quantum interference device (SQUID) magnetometer. The XRPD and FE-SEM studies revealed NiMn2O4−δ phase and good crystallinity of particles. No other impurities have been observed by XRPD. The magnetic properties of the sample have been studied by measuring the temperature and field dependence of magnetization. Magnetic measurements of M(T) reveal rather complex magnetic properties and multiple magnetic phase transitions. We show three magnetic phase transitions with transition temperatures at TM1=35K (long-range antiferromagnetic transition), TM2=101K (antiferromagnetic-type transition) and TM3=120K (ferromagnetic-like transition). We found that the TM1 transition is strongly dependent on the strength of the applied magnetic field (TM1 decreases with increasing applied field) whereas the TM3 is field independent. Otherwise, the TM2 maximum almost disappears in higher applied magnetic fields (H=1kOe and 10kOe). Magnetic measurements of M(H) show hysteretic behavior below TM3. Moreover, hysteresis properties measured after cooling of the sample in magnetic field of 10kOe show exchange bias effect with an exchange bias field |HEB|=196Oe. In summary, the properties that distinguish the investigated NiMn2O4-δ sample from other bulk, thin film, ceramic and nanoparticle NiMn2O4-δ systems are the triple magnetic transitions with sharp increase of the ZFC and FC magnetizations at 120K and the exchange bias effect. The analysis of the results and comparison with literature data allowed us to conjecture that the mixed oxidation states of Mn ions, ferromagnetic and antiferromagnetic sublattice orders and surface effects in the sample tailor these interesting magnetic properties.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.