Abstract

We report the structural and magnetic properties of NdCe x CrO3 () single-phase samples to classify the influence of Ce substitution on the Nd-site. The electron density profile indicates the possible covalent nature of Cr–O bonds. The x-ray photoelectron spectroscopy confirms a mixed Ce valency with a constant ratio of Ce3+/Ce4+ ions in all substituted compounds and the charge neutralization through the oxygen vacancies. The magnetization measurements reveal an increase in antiferromagnetic ordering temperature () and spin-reorientation transition temperature () and unfold soft spin-reorientation attributed to diluted superexchange interactions upon Ce incorporation. The presence of mixed Ce ions induces the merging of the hysteresis loop with a significant exchange bias (EB) field. We demonstrate for the first time that the magnitude of the magnetization is different for the same applied field in positive and negative directions, indicating the existence of two different magnetic states. The difference between these two magnetic states possibly arises from the pinning of Cr3+ spins, which requires an additional Zeeman energy for it to rotate. This maximum Zeeman energy from the normalized magnetic susceptibility vs. temperature curves correlates with the maximum EB field, validating unusual EB in these compounds.

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