Abstract
A comparative study on structural, optical, and magnetic properties of TMxCr2−xO3 (TM = Co and Mn) nanoparticles was synthesized using a simple co-precipitation method with subsequent heat treatment. The structural characterizations of as-prepared nanoparticles were performed using X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. XRD pattern revealed the formation of rhombohedral Cr2O3 phase with space group R3¯c. The FTIR spectra illustrated the shifting of absorption bands of Cr2O3 nanoparticles with Co and Mn substitution due to strain induced within the crystal lattice. X-ray photoelectron spectroscopy (XPS) confirmed the presence of a mixed oxidation state of Cr and oxygen defects in the prepared nanoparticles. Furthermore, XPS spectra also demonstrated the presence of Co and Mn having +2 oxidation state. The reduction in optical band gap of host material was observed with Co and Mn substitution. The magnetic properties of as-synthesized nanoparticles were recorded using a SQUID magnetometer and temperature-dependent magnetic measurements illustrated the decrease of Neel temperature with Co and Mn substitution. It was also demonstrated that magnetization increases below about ∼ 120 K due to spin canting and spin frustration for both TM ions substituted Cr2O3 nanoparticles and is fitted using the 3D spin-wave model with Curie-Weiss law. The magnetic studies revealed the mixed paramagnetic (PM) and antiferromagnetic (AFM) order at room temperature and AFM mix with ferromagnetic (FM) order at low temperature explained using the bound magnetic polarons (BMP) model.
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