The behavior of the low-frequency electromagnon in multiferroic DyMnO3 has been investigated in external magnetic fields and in a magnetically ordered state. Significant softening of the electromagnon frequency is observed for external magnetic fields parallel to the a-axis (BIIa), revealing a number of similarities to a classical soft mode behavior known for ferroelectric phase transitions. The softening of the electromagnon yields an increase of the static dielectric permittivity which follows a similar dependence as predicted by the Lyddane-Sachs-Teller relation. Within the geometry BIIb the increase of the electromagnon intensity does not correspond to the softening of the eigenfrequency. In this case the increase of the static dielectric permittivity seem to be governed by the motion of the domain walls.
Magnetodielectric materials are characterized by a strong coupling of magnetic and dielectric properties and in rare cases simultaneously exhibit both, magnetic and polar order. Among other multiferroics, TbMnO3 and GdMnO3 reveal a strong magneto-dielectric (ME) coupling and as a consequence fundamentally new spin excitations exist: Electro-active magnons, or electromagnons, i. e. spin waves which can be excited by ac electric fields. Here we show that these excitations appear in the phase with an incommensurate (IC) magnetic structure of the manganese spins. In external magnetic fields this IC structure can be suppressed and the electromagnons are wiped out, thereby inducing considerable changes in the index of refraction from dc up to THz frequencies. Hence, besides adding a new creature to the zoo of fundamental excitations, the refraction index can be tuned by moderate magnetic fields, which allows the design of a new generation of optical switches and optoelectronic devices.
All-electrical control of a dynamic magnetoelectric effect is demonstrated in a classical multiferroic manganite DyMnO3, a material containing coupled antiferromagnetic and ferroelectric orders. Due to intrinsic magnetoelectric coupling with electromagnons a linearly polarized terahertz light rotates upon passing through the sample. The amplitude and the direction of the polarization rotation are defined by the orientation of ferroelectric domains and can be switched by static voltage. These experiments allow the terahertz polarization to be tuned using the dynamic magnetoelectric effect.
We report here a detailed study of AC/DC magnetization and longitudinal/transverse transport properties of La$_{1.2}$Sr$_{1.8}$Mn$_{2}$O$_{7}$ single crystals below $T_{c}$ = 121 K. We find that the resistivity upturn below 40 K is related to the reentrant spin glass phase at the same temperature, accompanied by additional anomalous Hall effects. The carrier concentration from the ordinary Hall effects remains constant during the transition and is close to the nominal doping level (0.4 holes/Mn). The spin glass behavior comes from the competition between ferromagnetic double exchange and antiferromagnetic superexchange interactions, which leads to phase separation, i.e. a mixture of ferromagnetic and antiferromagnetic clusters, representing the canted antiferromagnetic state.
We present sharp magnetization jumps and field induced irreversibility in magnetization in multiferroic Y2CoMnO6. Appearance of magnetic relaxation and field sweep rate dependence of magnetization jumps resemble the martensite like scenario and suggests the coexistence of E*-type antiferromagnetic and ferromagnetic phases at low temperatures. In Y2CoMnO6, the critical field required for the sharp jump can be increased or decreased depening on the magnitude and direction of the cooling field; this is remarkably different from manganites or other metamagnetic materials where the critical field increases irrespective of the direction of the field cooling. The cooling field dependence on the sharp magnetization jumps has been described by considering exchange pinning mechanism at the interface, like in exchange bias model.
Magnetic properties of polycrystalline Sm0.1Ca0.84Sr0.06MnO3 in pristine and metastable states have been investigated in wide range of temperatures and magnetic fields. It was found that below Curie temperature TC = 105 K the pristine state exhibits phase separation comprising ferromagnetic and antiferromagnetic phases. The metastable states with reduced magnetization were obtained by successive number of quick coolings of the sample placed in container with kerosene-oil mixture. By an increasing number of quick coolings (> 6) the long time relaxation appeared at 10 K and the magnetization reversed its sign and became strongly negative in wide temperature range, even under an applied magnetic field of 15 kOe. The observed field and temperature dependences of the magnetization in this state are reversed in comparison with the ordinary ferromagnetic ones. Above TC, the observed diamagnetic susceptibility of the reversed magnetization state at T = 120 K is ~ - 0.9 x 10-4 emu g-1 Oe-1. Only after some storage time at room temperature, the abnormal magnetic state is erasable. It is suggested that the negative magnetization observed results from a specific coupling of the nano/micro-size ferromagnetic regions with a surrounding diamagnetic matrix formed, in a puzzled way, by the repeating training (quick cooling) cycles.