Sankaranarayanan V

Bio: Sankaranarayanan V is an academic researcher. The author has contributed to research in topics: Paramagnetism & Irreducible representation. The author has an hindex of 1, co-authored 1 publications receiving 7 citations.

Spin reorientation and disordered rare earth magnetism in Ho$_2$FeCoO$_6$

Abstract: We report the experimental observation of spin reorientation in the double perovskite Ho$_2$FeCoO$_6$. The magnetic phase transitions in this compound are characterized and studied through magnetization and specific heat, and the magnetic structures are elucidated by neutron powder diffraction. Two magnetic phase transitions are observed in this compound - one at $T_\mathrm{N1} \approx$ 250~K, from paramagnetic to antiferromagnetic, and the other at $T_\mathrm{N2} \approx$ 45~K, from a phase with mixed magnetic structures to a single phase through a spin reorientation process. The magnetic structure in the temperature range 200~K - 45~K is a mixed phase of the irreducible representations $\Gamma_1$ and $\Gamma_3$, both of which are antiferromagnetic. The phase with mixed magnetic structures that exists in Ho$_2$FeCoO$_6$ gives rise to a large thermal hysteresis in magnetization that extends from 200~K down to the spin reorientation temperature. At $T_\mathrm{N2}$, the magnetic structure transforms to $\Gamma_1$. Though long-range magnetic order is established in the transition metal lattice, it is seen that only short-range magnetic order prevails in Ho$^{3+}$ - lattice. Our results should motivate further detailed studies on single crystals in order to explore spin reorientation process, spin switching and the possibility of anisotropic magnetic interactions giving rise to electric polarization in Ho$_2$FeCoO$_6$.

B-site disorder driven multiple-magnetic phases: Griffiths phase, re-entrant cluster glass, and exchange bias in Pr2CoFeO6

Abstract: The magnetic spin ordering and the magnetization dynamics of a double perovskite Pr2CoFeO6 have been investigated by employing the (dc and ac) magnetization and neutron powder diffraction techniques. The study revealed that Pr2CoFeO6 adopted a B-site disordered orthorhombic structure (Pnma). Furthermore, ab initio band structure calculations suggested an insulating antiferromagnetic ground state. Magnetization measurements revealed that the system possesses a spectrum of competing magnetic phases, viz., long range canted antiferromagnetic (AFM) spin ordering (TN ∼ 269 K), Griffiths-like phase, re-entrant cluster glass (TG ∼ 34 K), and exchange bias effects. The neutron diffraction study divulged the exhibition of a long range G-type of canted AFM spin ordering. The random nonmagnetic dilution of magnetic Fe3+ (high spin) ions by Co3+ (low spin) ions due to B-site disorder essentially played a crucial role in manifesting such magnetic properties of the system.The magnetic spin ordering and the magnetization dynamics of a double perovskite Pr2CoFeO6 have been investigated by employing the (dc and ac) magnetization and neutron powder diffraction techniques. The study revealed that Pr2CoFeO6 adopted a B-site disordered orthorhombic structure (Pnma). Furthermore, ab initio band structure calculations suggested an insulating antiferromagnetic ground state. Magnetization measurements revealed that the system possesses a spectrum of competing magnetic phases, viz., long range canted antiferromagnetic (AFM) spin ordering (TN ∼ 269 K), Griffiths-like phase, re-entrant cluster glass (TG ∼ 34 K), and exchange bias effects. The neutron diffraction study divulged the exhibition of a long range G-type of canted AFM spin ordering. The random nonmagnetic dilution of magnetic Fe3+ (high spin) ions by Co3+ (low spin) ions due to B-site disorder essentially played a crucial role in manifesting such magnetic properties of the system.

B-site spin-state and anti-site disorder driven multiple-magnetic phases: Griffiths phase, re-entrant cluster glass and exchange bias in double perovskite Pr$_2$CoFeO$_6$

Abstract: We report the comprehensive experimental results identifying the magnetic spin ordering and the magnetization dynamics of a double perovskite Pr2CoFeO6 by employing the (dc and ac) magnetization, powder neutron diffraction (NPD) and X-ray magnetic circular dichroism (XMCD) techniques. X-ray diffraction and neutron diffraction studies revealed that Pr2CoFeO6 adopts a B-site disordered orthorhombic structure with space group Pnma. Additionally, ab initio band structure calculations performed on this system suggested an insulating anti-ferromagnetic (Fe-Fe) ground state. Magnetometry study showed the system to possess a spectrum of interesting magnetic phases including long range antiferromagnetic (canted) spin ordering (TN ~269 K), Griffiths phase, re-entrant cluster glass (RCG) (TG~ 34 K) and exchange bias. However, the NPD study divulged the exhibition of a long range G-type (below TN ~269 K) of spin ordering by Fe spins. Spin dynamics study by ac susceptibility technique confirmed the system possessing long range ordering at higher temperatureundergoes a RCG transition at ~34 K. Existence of Griffiths phase was confirmed by non-analytic field variation of magnetization and Heisenberg type temporal spin relaxation above long range ordering temperature TN ~269 K. The anti-site disorder related to the B-sites (Co/Fe) is found to be the main driving force forthe observed multiple magnetic phases. Furthermore, the electronic structure probed by the X-ray absorption spectroscopy (XAS) study suggested a nominal valance state of +3 for both of the B-site ions (Co/Fe) which in turn triggered the anti-site disorder in the system. Magnetic, XRD, NPD and XAS analysis yielded a low spin state (LS) for the Co3+ ions. The random non-magnetic dilution of magnetic Fe3+ (HS) ions by Co3+ (LS) ions essentially played a crucial role in manifesting the magnetic properties of the system.

Role of 3d–4f exchange interaction and local anti-site defects in the magnetic and magnetocaloric properties of double perovskite Ho2CoMnO6 compound

Abstract: The strong coupling between 3d and 4f based magnetic sublattices in double perovskite (DP) compounds results in various exotic complex magnetic interactions, and the ground state contains multiple fascinating and remarkable magnetic states. In this article, we have performed a detailed investigation of the crystal structure, magnetic, and magnetocaloric properties of the ordered monoclinic polycrystalline double perovskite Ho 2 CoMnO 6 (HCMO) compound. A study of the magnetization dynamics employing temperature and magnetic field shows a powerful correlation between Ho and Co/Mn sublattices. Due to the presence of the ferromagnetic superexchange interaction in between Co 2 + − O − Mn 4 + networks, the system undergoes an ordered state at the transition temperature, T C ≈ 77 K. Below T C, a clear compensation point continued by negative magnetization is noticed in the virgin state of the compound. The reduction of the saturation magnetization ( M S) in the hysteresis curves (M-H) can be explained by the existence of local anti-site defects or disorders and anti-phase boundaries in the system. Temperature dependence of magnetic entropy change ( − Δ S) curves shows a maximum value of 13.4 J/kg K for Δ H = 70 kOe at a low temperature along with a noticeable inverse magnetocaloric effect. Moreover, the material holds reasonable values of magnetocaloric parameters. The absence of thermal hysteresis along with a large value of | Δ S | makes the system a potential candidate for low temperature as well as liquid nitrogen temperature-based magnetic refrigeration. Additionally, our experimental findings should encourage further detailed studies on the complex 3d–4f exchange interaction in the double perovskite system.

Extraordinary magnetic properties of double perovskite Eu 2 CoMnO 6 wide band gap semiconductor.

Abstract: Some novel magnetic behaviours in double perovskite Eu2CoMnO6 (ECMO) have been reported. The x-ray photoemission spectroscopy study shows the presence of mixed valence states of transition metal ions. The UV-visible absorption spectroscopic study suggests that the ECMO has a direct wide band gap. A second-order magnetic phase transition as a sudden jump in the magnetization curve has been observed around 124.5 K. The large bifurcation between the zero field cooling and field cooling, suggests existence of strong spin frustration in the system. The inverse DC susceptibility confirms the presence of the Griffiths like phase. Sharp steps in magnetization have been observed in the M-H curve at 2 K, which vanishes on increasing temperature. The AC susceptibility study demonstrates the Hopkinson like effect as well as the presence of volume spin-glass-like behaviour. The temperature dependent Raman spectrum shows the presence of spin-phonon coupling.

Roles of Re-entrant cluster glass state and spin-lattice coupling in magneto-dielectric behavior of giant dielectric double perovskite La1.8Pr0.2CoFeO6.

Abstract: La based Co-Fe combined double perovskite (La1.8Pr0.2CoFeO6) was synthesized and the dielectric (zero-field and in-field), magnetic, x-ray absorption and Raman spectroscopy measurements have been investigated for La1.8Pr0.2CoFeO6 double perovskite. The existence of re-entrant cluster glass state is observed. The magneto-dielectric (MD) is found in two temperature regions (25-80 K and 125-275 K). It has been demonstrated that the observed MD at low and high temperatures are respectively due to the spin freezing and the spin-lattice coupling. Furthermore, the very large dielectric constant and the low loss suggest that La1.8Pr0.2CoFeO6 is very important from the application point of view.