TY - JOUR
T1 - Jahn-Teller distortions in (Co1-xCux)Cr2O4(x = 0.5, 0.25) nanoparticles
T2 - Structural, magnetic and electronic properties
AU - Mohanty, P.
AU - Sheppard, C. J.
AU - Doyle, B. P.
AU - Carleschi, E.
AU - Prinsloo, A. R.E.
N1 - Publisher Copyright:
© 2021 Author(s).
PY - 2021/2/1
Y1 - 2021/2/1
N2 - The spinel ferrimagnetic compound CoCr2O4 demonstrates a spin spiral (TS) ordering at 25 K, as well as an anomaly at 15 K termed as lock-in transition (TL). From crystallographic perspective CoCr2O4 retains the cubic phase down to 11 K. On the other hand, the normal spinel CuCr2O4 crystallizes into the cubic phase above 850 K, below which Jahn-Teller (J-T) activity of the Cu reduces the crystal symmetry by transforming it to a tetragonal phase. Contraction of CuO4 tetrahedra towards the formation of a square planar structure accounts for the tetragonal to orthorhombic structural transition at ∼130 K associated with the ferrimagnetic Curie temperature (TC). Considering the differences in crystal structure and magnetism of these two compounds, the current work investigates the modification in crystal structure and magnetic behaviour by mixing Co site with Cu in CoCr2O4. To achieve this, (Co1-xCux)Cr2O4 (x = 0.5, 0.25 and 0.75) nanoparticles were prepared by chemical routes. X-ray diffraction (XRD) revealed the retention of cubic structure for the samples calcined at a temperature of 600 °C for x = 0.25 and 0.5. On the other hand, J-T distortion becomes prominent for x = 0.75. Hence, only the compositions with x = 0.25 and 0.5 were studied in detail as unusual cubic phase retention is observed in these compounds. The temperature dependent magnetization studies revealed that the TC values of both the samples, 103 K for (Co0.5Cu0.5)Cr2O4 and 99 K for (Co0.75Cu0.25)Cr2O4, compare well with the value reported for CoCr2O4. However, the feature related to TS is quite prominent for x = 0.25, whereas it is suppressed for x = 0.5. The electronic properties of the cations associated with these compounds, probed using X-ray photoelectron spectroscopy (XPS), indicate that Cu and Co mostly has a 2+ oxidation state whereas that of Cr is 3+.
AB - The spinel ferrimagnetic compound CoCr2O4 demonstrates a spin spiral (TS) ordering at 25 K, as well as an anomaly at 15 K termed as lock-in transition (TL). From crystallographic perspective CoCr2O4 retains the cubic phase down to 11 K. On the other hand, the normal spinel CuCr2O4 crystallizes into the cubic phase above 850 K, below which Jahn-Teller (J-T) activity of the Cu reduces the crystal symmetry by transforming it to a tetragonal phase. Contraction of CuO4 tetrahedra towards the formation of a square planar structure accounts for the tetragonal to orthorhombic structural transition at ∼130 K associated with the ferrimagnetic Curie temperature (TC). Considering the differences in crystal structure and magnetism of these two compounds, the current work investigates the modification in crystal structure and magnetic behaviour by mixing Co site with Cu in CoCr2O4. To achieve this, (Co1-xCux)Cr2O4 (x = 0.5, 0.25 and 0.75) nanoparticles were prepared by chemical routes. X-ray diffraction (XRD) revealed the retention of cubic structure for the samples calcined at a temperature of 600 °C for x = 0.25 and 0.5. On the other hand, J-T distortion becomes prominent for x = 0.75. Hence, only the compositions with x = 0.25 and 0.5 were studied in detail as unusual cubic phase retention is observed in these compounds. The temperature dependent magnetization studies revealed that the TC values of both the samples, 103 K for (Co0.5Cu0.5)Cr2O4 and 99 K for (Co0.75Cu0.25)Cr2O4, compare well with the value reported for CoCr2O4. However, the feature related to TS is quite prominent for x = 0.25, whereas it is suppressed for x = 0.5. The electronic properties of the cations associated with these compounds, probed using X-ray photoelectron spectroscopy (XPS), indicate that Cu and Co mostly has a 2+ oxidation state whereas that of Cr is 3+.
UR - http://www.scopus.com/inward/record.url?scp=85100753064&partnerID=8YFLogxK
U2 - 10.1063/9.0000096
DO - 10.1063/9.0000096
M3 - Article
AN - SCOPUS:85100753064
SN - 2158-3226
VL - 11
JO - AIP Advances
JF - AIP Advances
IS - 2
M1 - 025110
ER -