We report the observation of spontaneous and ultra-sharp jumps in the low temperature magnetization isotherms of polycrystalline Nd5Ge3. Field-induced and ultra-sharp jumps are also seen in resistivity and heat capacity data. These jumps are accompanied by field-induced irreversibilities. The consistency seen in these three data clearly shows that the spin, electronic and lattice states are strongly coupled. Time-induced growth of the ferromagnetic phase is observed at a constant field and temperature, implying the metastability of the magnetic phase in the low field region. Various experimental findings point towards a strong field-induced magneto-structural irreversibility in this compound.
Low temperature ultrasound velocity measurements are presented on the frustrated spin system SrDy2O4 that allow us to define high resolution phase diagrams with the magnetic field applied along all three principal axes. For H||b, a region of field-induced long range order is delimited by a dome of first-order phase transitions. An unusual magnetization process is observed with significant irreversibility at very low temperatures when passing between the low-field spin liquid phase and the long range ordered phase which we attribute to large energy barriers. For H||c, the system appears to remain effectively one-dimensional, exhibiting two transitions as a function of magnetic field, but no finite-temperature long range order.
We argue that collinearly ordered states which exist in strongly frustrated spin systems for special rational values of the magnetization are stabilized by thermal as well as quantum fluctuations. These general predictions are tested by Monte Carlo simulations for the classical and Lanczos diagonalization for the S=1/2 frustrated square-lattice antiferromagnet.
Five characteristic temperatures of TM = 148 K, TN = 142 K, Tt = 138 K, Tf ~ 125 K and Tg ~ 50 K were found by the measurements of the magnetization curves at various temperature. The spontaneous magnetization appears below TM. It increases up to M_{S} simeq 2 times 10^{-4} mu_{B} at Tt and then decreases steeply below Tt, which qualitatively agrees with the temperature dependence of magnetization obtained under field-cooling (FC) condition. On the other hand, the slope of the magnetization curve, namely the magnetic susceptibility, drops below TN, which coincides with the temperature dependence of magnetization obtained under zero-FC condition, although the magnetization curves were obtained under FC condition. The temperature dependence of the spontaneous magnetization shows a minimum at Tf and a drop at Tg although there is no anomaly in the temperature dependence of FC or ZFC magnetization.
We have used time-resolved x-ray photoemission electron microscopy to investigate the magnetization dynamics induced by nanosecond current pulses in NiFe/Cu/Co nanostripes. A large tilt of the NiFe magnetization in the direction transverse to the stripe is observed during the pulses. We show that this effect cannot be quantitatively understood from the amplitude of the Oersted field and the shape anisotropy. High frequency oscillations observed at the onset of the pulses are attributed to precessional motion of the NiFe magnetization about the effective field. We discuss the possible origins of the large magnetization tilt and the potential implications of the static and dynamic effects of the Oersted field on current-induced domain wall motion in such stripes.
The 1H-NMR spectrum and nuclear relaxation rate 1/T_1 in the antiferromagnetic wheel CsFe8 were measured to characterize the previously observed magnetic field-induced low-temperature phase around the level crossing at 8 T. The data show that the phase is characterized by a huge staggered transverse polarization of the electronic Fe spins, and the opening of a gap, providing microscopic evidence for the interpretation of the phase as a field-induced magneto-elastic instability.
Bibekananda Maji
,K. G. Suresh
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(2010)
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"Observation of spontaneous magnetization jump and field-induced irreversibility in Nd5Ge3"
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Bibekananda Maji
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