Please use this identifier to cite or link to this item: https://doi.org/10.1063/9.0000054
Title: Ac magnetoresistance and microwave absorption in Sr2FeMoO6
Authors: Das, Rajasree 
Chaudhuri, Ushnish 
Mahendiran, Ramanathan 
Issue Date: 1-Jan-2021
Publisher: American Institute of Physics Inc.
Citation: Das, Rajasree, Chaudhuri, Ushnish, Mahendiran, Ramanathan (2021-01-01). Ac magnetoresistance and microwave absorption in Sr2FeMoO6. AIP Advances 11 (1) : 15026. ScholarBank@NUS Repository. https://doi.org/10.1063/9.0000054
Rights: Attribution 4.0 International
Abstract: This work investigates the microwave absorption property of the ferrimagnetic double perovskite, Sr2FeMoO6 (SFMO) using two different methods: magnetoimpedance (MI) and lock-in based broadband magnetic resonance detection. In the MI method, radio frequency (rf) current (f = 0.001 to 2.8 GHz) is injected into the sample. When dc magnetic field is swept, rf resistance exhibits a single sharp peak centred at H = 0 for f < 0.1 MHz. As f increases, the peak at H = 0 transforms into a dip accompanied by symmetrical double peaks at H = ±HP, which we attribute to the ferromagnetic resonance within the grains. HP increases with increasing frequency of the current. In the lock-in based broadband method the sample, placed on top of a coplanar waveguide, experiences an intense microwave magnetic field from the waveguide, and the field derivative of microwave power absorption is measured as the dc magnetic field is swept. Correlation between MI and microwave power absorption is shown. Landé g factors obtained from both the measurements are close, equal to 2.085, which implies the presence of Fe3+ cations. Large ac magnetoresistance in SFMO compared to its dc value, dominated by the dynamics of transverse permeability and ferromagnetic resonance within grains could be exploited for high-frequency device applications. © 2021 Author(s).
Source Title: AIP Advances
URI: https://scholarbank.nus.edu.sg/handle/10635/233800
ISSN: 2158-3226
DOI: 10.1063/9.0000054
Rights: Attribution 4.0 International
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