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Magnetic exchange interactions and non-Debye relaxation in spin-3/2 frustrated Kagomé magnet Co 3 V 2 O 8 .

Harshita SinghM SkoulatosDeep C JoshiPrativa PramanikMouli Roy ChowdhurySayandeep GhoshSuchit Kumar JenaJayjit Kumar DeySubhash Thota
Published in: Journal of physics. Condensed matter : an Institute of Physics journal (2024)
We report the experimental determination of the magnetic exchange parameter (J/kB= 2.88 ± 0.02 K) for the Spin-3/2 ferromagnetic (FM) Kagomé lattice system: Co 3 V 2 O 8 using the temperature dependence of dc-magnetic susceptibility χ ( T ) data by employing the fundamental Heisenberg linear chain model. Our results are quite consistent with the theoretically reported nearest neighbor dominant FM exchange coupling strengthJex-NN∼2.45 K. Five different magnetic phase transitions (6.2-11.2 K) and spin-flip transitions (9.6-7.7 kOe) have been probed using the∂(χT)/∂Tvs. T , heat capacity ( C P - T ) and differential isothermal magnetization curves. Among such sequence of transitions, the prominent ones being incommensurate antiferromagnetic (AFM) state at 11.2 K, commensurate AFM state at 8.8 K, and commensurate FM state across 6.2 K. All the successive magnetic phase transitions have been mapped onto a single H-T plane through which one can easily distinguish the above-mentioned different phases. The magnetic contribution of the C P - T near T N (11.2 K) has been analyzed using the power-law expressionCM=A|T-TN|-αresulting in the critical exponent α = 0.18 ± 0.01 (0.15 ± 0.003) for T < T N ( T > T N ), respectively for the Co 3 V 2 O 8 . It is interesting to note that non-Debye type dipole relaxation is quite prominent in Co 3 V 2 O 8 and was evident from the Kohlrausch-Williams-Watts analysis of complex modulus and impedance spectra (0⩽β⩽1). Mott's variable-range hopping of charge carriers process is evident through the resistivity analysis (ρac- T -1/4) in the temperature range 275  ∘ C-350  ∘ C. Moreover, the frequency-dependent analysis ofσac( ω ) follows Jonscher's power law yielding two distinct activation energies (Ea∼0.37 and 2.29 eV) between the temperature range 39  ∘ C-99  ∘ C and 240  ∘ C-321  ∘ C.
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