Do you want to publish a course? Click here

Field-temperature phase diagram of magnetic bubbles spanning charge$/$orbital ordered and metallic phases in La$_{1-x}$Sr$_x$MnO$_3$ ($x = 0.125$)

85   0   0.0 ( 0 )
 Publication date 2020
  fields Physics
and research's language is English




Ask ChatGPT about the research

We report formation of magnetic textures in the ferromagnetic (FM) phase of La$_{1-x}$Sr$_x$MnO$_3$ for $x =$ 0.125; these textures are magnetic bubbles, magnetic stripe domains, and forced FM states. In situ Lorentz microscopy (LM) observations show that magnetic bubbles exist in the FM insulating phase accompanying the formation of the charge$/$orbital ordering (CO$/$OO). Furthermore, stable magnetic bubbles still exist in an intermediate temperature region between the CO$/$OO ($T_{CO} =$ 155 K) and FM ($T_c =$ 190 K) transition temperatures. These magnetic bubbles are believed to originate from the magnetocrystalline anisotropy and the dipole-dipole interaction in the FM phase. Based on in situ LM observations as a function of both temperature and the strength of the external magnetic field applied, a magnetic field-temperature phase diagram is constructed, exhibiting the stabilizing regions of the magnetic bubbles in the FM phase of La$_{0.875}$Sr$_{0.125}$MnO$_{3}$.



rate research

Read More

A detailed electronic phase diagram of perovskite-type oxides Sr$_{1-x}$La$_x$FeO$_3$ $(0leq x leq 0.5)$ was established by synchrotron X-ray diffraction, magnetization, and transport measurements for polycrystalline samples synthesized by a high-pressure technique. Among three kinds of helimagnetic phases in SrFeO$_3$ at zero field, two of them showing multiple-${it q}$ helimagnetic spin textures tend to rapidly disappear in cubic symmetry upon the La substitution with $x$ less than 0.1, which accompanies the loss of metallic nature. On the other hand, the third helimagnetic phase apparently remains robustly in Sr$_{1-x}$La$_x$FeO$_3$ with $x$ higher than 0.1, followed by merging to the spin/charge ordered phase with $xsim 1/3$. We propose an important role of itinerant ligand holes on the emergence of multiple-${it q}$ states and a possible link between the third (putative single-${it q}$) helimagnetic phase in SrFeO$_3$ and the spin/charge ordered phase in Sr$_{2/3}$La$_{1/3}$FeO$_3$.
We report low temperature specific heat measurements of Pr$_{1-x}$Ca$_{x}$MnO$_{3}$ ($0.3leq x leq 0.5$) and La$_{0.5}$Ca$_{0.5}$MnO$_{3}$ with and without applied magnetic field. An excess specific heat, $C^{prime}(T)$, of non-magnetic origin associated with charge ordering is found for all the samples. A magnetic field sufficient to induce the transition from the charge-ordered state to the ferromagnetic metallic state does not completely remove the $C^{prime}$ contribution. This suggests that the charge ordering is not completely destroyed by a melting magnetic field. In addition, the specific heat of the Pr$_{1-x}$Ca$_{x}$MnO$_{3}$ compounds exhibit a large contribution linear in temperature ($gamma T$) originating from magnetic and charge disorder.
We report on Raman scattering measurements of single crystalline La$_{1-x}$Sr$_x$MnO$_3$ ($x$=0, 0.06, 0.09 and 0.125), focusing on the high frequency regime. We observe multi-phonon scattering processes up to fourth-order which show distinct features: (i) anomalies in peak energy and its relative intensity and (ii) a pronounced temperature-, polarization-, and doping-dependence. These features suggest a mixed orbiton-phonon nature of the observed multi-phonon Raman spectra.
Neutron powder diffraction measurements, combined with magnetization and resistivity data, have been carried out in the doped perovskite La$_{1-x}$Ca$_x$MnO$_3$ ($x=0.47$, 0.50, and 0.53) to elucidate the structural, magnetic, and electronic properties of the system around the composition corresponding to an equal number of Mn3+ and Mn4+. At room temperature all three samples are paramagnetic and single phase, with crystallographic symmetry Pnma. The samples then all become ferromagnetic (FM) at $T_Capprox 265$ K. At $sim 230$ K, however, a second distinct crystallographic phase (denoted A-II) begins to form. Initially the intrinsic widths of the peaks are quite large, but they narrow as the temperature decreases and the phase fraction increases, indicating microscopic coexistence. The fraction of the sample that exhibits the A-II phase increases with decreasing temperature and also increases with increasing Ca doping, but the transition never goes to completion to the lowest temperatures measured (5 K) and the two phases therefore coexist in this temperature-composition regime. Phase A-II orders antiferromagnetically (AFM) below a N{e}el temperature $T_N approx 160$ K, with the CE-type magnetic structure. Resistivity measurements show that this phase is a conductor, while the CE phase is insulating. Application of magnetic fields up to 9 T progressively inhibits the formation of the A-II phase, but this suppression is path dependent, being much stronger for example if the sample is field-cooled compared to zero-field cooling and then applying the field. The H-T phase diagram obtained from the diffraction measurements is in good agreement with the results of magnetization and resistivity.
Magnetic textures in the ferromagnetic phases of La$_{1-x}$Sr$_x$MnO$_3$ for 0.15 $< x <$ 0.30 have been investigated by Lorentz microscopy combined with small-angle electron diffraction experiments. Various types of magnetic textures characterized by stripe, plate-shaped, and cylindrical (magnetic bubble) domains were found. Two distinct types of magnetic stripe domains appeared in the orthorhombic structure with an inversion symmetry of La$_{0.825}$Sr$_{0.175}$MnO$_3$, depending significantly on magnetocrystalline anisotropy. Based on in-situ observations as functions of temperature and the strength of the external magnetic field, a magnetic field-temperature phase diagram was constructed, showing the stabilization of magnetic bubbles in the ferromagnetic phase of La$_{0.825}$Sr$_{0.175}$MnO$_3$.
comments
Fetching comments Fetching comments
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا