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S-W. Cheong

Publications and source records attributed to S-W. Cheong.

At least 73 records · Page 4Linked to original sources

Direct observation of electronic domains in manganites by spatially resolved spectroscopy

We use a spatially resolved, direct spectroscopic probe for electronic structure with an additional sensitivity to chemical compositions to investigate high-quality single crystal samples of La_{1/4}Pr_{3/8}Ca_{3/8}MnO_{3}, establishing the formation of distinct insulating domains embedded in the metallic host at low temperatures. These domains are found to be at least an order of magnitude larger in size compared to previous estimates and exhibit memory effects on temperature cycling in the absence of any perceptible chemical inhomogeneity, suggesting long-range strains as the probable origin.

cond-mat.mtrl-sci↗

Temperature dependent d-d excitations in manganites probed by resonant inelastic x-ray scattering

We report the observation of temperature dependent electronic excitations in various manganites utilizing resonant inelastic x-ray scattering (RIXS) at the Mn K-edge. Excitations were observed between 1.5 and 16 eV with temperature dependence found as high as 10 eV. The change in spectral weight between 1.5 and 5 eV was found to be related to the magnetic order and independent of the conductivity. On the basis of LDA+U and Wannier function calculations, this dependence is associated with intersite d-d excitations. Finally, the connection between the RIXS cross-section and the loss function is addressed.

cond-mat.str-el↗

First-order nature of the ferromagnetic phase transition in (La-Ca)MnO_3 near optimal doping

Neutron scattering has been used to study the nature of the ferromagnetic transition in single crystals of La_0.7Ca_0.3MnO_3 and La_0.8Ca_0.2MnO_3, and polycrystalline samples of La_0.67Ca_0.33MnO_3 and La_5/8Ca_3/8MnO_3 where the naturally occurring O-16 can be replaced with the O-18 isotope. Small angle neutron scattering on the x=0.3 single crystal reveals a discontinuous change in the scattering at the Curie temperature for wave vectors below ~0.065 A^-1. Strong relaxation effects are observed for this domain scattering, for the magnetic order parameter, and for the quasielastic scattering, demonstrating that the transition is not continuous in nature. There is a large oxygen isotope effect observed for the T_C in the polycrystalline samples. For the optimally doped x=3/8 sample we observed T_C(O-16)=266.5 K and T_C(O-18)=261.5 K at 90% O-18 substitution. The temperature dependence of the spin-wave stiffness is found to be identical for the two samples despite changes in T_C. Hence, T_C is not solely determined by the magnetic subsystem, but instead the ferromagnetic phase is truncated by the formation of polarons which cause an abrupt transition to the paramagnetic, insulating state. Application of uniaxial stress in the x=0.3 single crystal sharply enhances the polaron scattering at room temperature. Measurements of the phonon density-of-states show only modest differences above and below T_C and between the two different isotopic samples.

cond-mat.str-el↗

Average Lattice Symmetry and Nanoscale Structural Correlations in Magnetoresistive Manganites

We report x-ray scattering studies of nanoscale structural correlations in the paramagnetic phases of the perovskite manganites La$_{0.75}$(Ca$_{0.45}$Sr$_{0.55}$)$_{0.25}$MnO$_3$, La$_{0.625}$Sr$_{0.375}$MnO$_3$, and Nd$_{0.45}$Sr$_{0.55}$MnO$_3$. We find that these correlations are present in the orthorhombic $O$ phase in La$_{0.75}$(Ca$_{0.45}$Sr$_{0.55}$)$_{0.25}$MnO$_3$, but they disappear abruptly at the orthorhombic-to-rhombohedral transition in this compound. The orthorhombic phase exhibits increased electrical resistivity and reduced ferromagnetic coupling, in agreement with the association of the nanoscale correlations with insulating regions. In contrast, the correlations were not detected in the two other compounds, which exhibit rhombohedral and tetragonal phases. Based on these results, as well as on previously published work, we propose that the local structure of the paramagnetic phase correlates strongly with the average lattice symmetry, and that the nanoscale correlations are an important factor distinguishing the insulating and the metallic phases in these compounds.

cond-mat↗

X-ray-induced disordering of the dimerization pattern and apparent low-temperature enhancement of lattice symmetry in spinel CuIr$_2$S$_4$

At low temperatures, spinel CuIr$_2$S$_4$ is a charge-ordered spin-dimerized insulator with triclinic lattice symmetry. We find that x-rays induce a structural transition in which the local triclinic structure is preserved, but the average lattice symmetry becomes tetragonal. These structural changes are accompanied by a thousandfold reduction in the electrical resistivity. The transition is persistent, but the original state can be restored by thermal annealing. We argue that x-ray irradiation disorders the lattice dimerization pattern, producing a state in which the orientation of the dimers is preserved, but the translational long-range order is destroyed.

cond-mat↗

Charge Ordering Fluctuation and Optical Pseudogap in La$_{1-x}$Ca$_{x}$MnO$_{3}$

Optical spectroscopy was used to investigate the optical gap (2$Δ$) due to charge ordering (CO) and related pseudogap developments with x and temperature (T) in La$_{1-x}$Ca$_{x}$MnO$_{3}$ (0.48 <= x <= 0.67). Surprisingly, we found 2$Δ$/k_{B}T_{CO} is as large as 30 for x ~0.5, and decreases rapidly with increasing x. Simultaneously, the optical pseudogap, possibly starting from T^* far above T_{CO} becomes drastically enhanced near x=0.5, producing non-BCS T-dependence of 2$Δ$ with the large magnitude far above T_{CO}, and systematic increase of T^* for x~0.5. These results unequivocally indicate systematically-enhanced CO correlation when x approaches 0.5 even though T_{CO} decreases.

cond-mat.str-el↗

Common features of nanoscale structural correlations in magnetoresistive manganites with ferromagnetic low-temperature state

We report x-ray scattering studies of nanoscale structural correlations in Nd$_{1-x}$Sr$_x$MnO$_3$ and La$_{1-x}$(Ca,Sr)$_x$MnO$_3$, $x$=0.2--0.5. We find that the correlated regions possess a temperature-independent correlation length of 2-3 lattice constants which is the same in all samples. The period of the lattice modulation of the correlated regions is proportional to the Ca/Sr doping concentration $x$. Remarkably, the lattice modulation periods of these and several other manganites with a ferromagnetic ground state fall on the same curve when plotted as a function of $x$. Thus, the structure of the correlated regions in these materials appears to be determined by a single parameter, $x$. We argue that these observations provide important clues for understanding the Colossal Magnetoresistance phenomenon in manganites.

cond-mat↗

Magnetic-field-induced collapse of charge-ordered nanoclusters and the Colossal Magnetoresistance effect in Nd(0.3)Sr(0.3)MnO(3)

We report synchrotron x-ray scattering studies of charge/orbitally ordered (COO) nanoclusters in Nd$_{0.7}$Sr$_{0.3}$MnO$_3$. We find that the COO nanoclusters are strongly suppressed in an applied magnetic field, and that their decreasing concentration follows the field-induced decrease of the sample electrical resistivity. The COO nanoclusters, however, do not completely disappear in the conducting state, suggesting that this state is inhomogeneous and contains an admixture of an insulating phase. Similar results were also obtained for the zero-field insulator-metal transition that occurs as temperature is reduced. These observations suggest that these correlated lattice distortions play a key role in the Colossal Magnetoresistance effect in this prototypical manganite.

cond-mat↗

Martensitic accommodation strain and the metal-insulator transition in manganites

In this paper, we report polarized optical microscopy and electrical transport studies of manganese oxides that reveal that the charge ordering transition in these compounds exhibits typical signatures of a martensitic transformation. We demonstrate that specific electronic properties of charge-ordered manganites stem from a combination of martensitic accommodation strain and effects of strong electron correlations. This intrinsic strain is strongly affected by the grain boundaries in ceramic samples. Consistently, our studies show a remarkable enhancement of low field magnetoresistance and the grain size effect on the resistivity in polycrystalline samples and suggest that the transport properties of this class of manganites are governed by the charge-disordered insulating phase stabilized at low temperature by virtue of martensitic accommodation strain. High sensitivity of this phase to strains and magnetic field leads to a variety of striking phenomena, such as unusually high magnetoresistance (10^10 %) in low magnetic fields.

cond-mat.str-el↗

Mesoscopic, Non-equilibrium Fluctuations of Inhomogeneous Electronic States in Manganites

By using the dark-field real-space imaging technique of transmission electron microscopy (TEM), we have observed slow 200 A-scale fluctuations of charge-ordered (CO) phase in mixed-valent manganites under a strong electron beam irradiation. In addition to these unusual fluctuations of the CO phase, we observed the switching-type fluctuations of electrical resistivity in the same sample, which were found to be as large as several percents. Systematic analysis indicates that these two different types of fluctuations with a similar time scale of the order of seconds are interconnected through a meta-stable insulating charge-disordered state. Current dependence of the fluctuations suggests a non-equilibrium nature of this slow dynamics.

cond-mat.str-el↗

Nanoscale anisotropic structural correlations in the paramagnetic and ferromagnetic phases of Nd0.5Sr0.5 MnO3

We report x-ray scattering studies of short-range structural correlations and diffuse scattering in Nd0.5Sr0.5MnO3. On cooling, this material undergoes a series of transitions, first from a paramagnetic insulating (PI) to a ferromagnetic metallic (FM) phase, and then to a charge-ordered (CO) insulating state. Highly anisotropic structural correlations were found in both the PI and FM states. The correlations increase with decreasing temperature, reaching a maximum at the CO transition temperature. Below this temperature, they abruptly collapsed. Single-polaron diffuse scattering was also observed in both the PI and FM states suggesting that substantial local lattice distortions are present in these phases. We argue that our measurements indicate that nanoscale regions exhibiting layered orbital order exist in the paramagnetic and ferromagnetic phases of Nd0.5Sr0.5MnO3.

cond-mat↗

Correlated Polarons in Dissimilar Perovskite Manganites

We report x-ray scattering studies of broad peaks located at a (0.5 0 0)/(0 0.5 0)-type wavevector in the paramagnetic insulating phases of La_{0.7}Ca_{0.3}MnO_{3} and Pr_{0.7}Ca_{0.3}MnO_{3}. We interpret the scattering in terms of correlated polarons and measure isotropic correlation lengths of 1-2 lattice constants in both samples. Based on the wavevector and correlation lengths, the correlated polarons are found to be consistent with CE-type bipolarons. Differences in behavior between the samples arise as they are cooled through their respective transition temperatures and become ferromagnetic metallic (La_{0.7}Ca_{0.3}MnO_{3}) or charge and orbitally ordered insulating (Pr_{0.7}Ca_{0.3}MnO_{3}). Since the primary difference between the two samples is the trivalent cation size, these results illustrate the robust nature of the correlated polarons to variations in the relative strength of the electron-phonon coupling, and the sensitivity of the low-temperature ground state to such variations.

cond-mat.str-el↗

Muon Spin Relaxation Study of (La, Ca)MnO3

We report predominantly zero field muon spin relaxation measurements in a series of Ca-doped LaMnO_3 compounds which includes the colossal magnetoresistive manganites. Our principal result is a systematic study of the spin-lattice relaxation rates 1/T_1 and magnetic order parameters in the series La_{1-x}Ca_xMnO_3, x = 0.0, 0.06, 0.18, 0.33, 0.67 and 1.0. In LaMnO_3 and CaMnO_3 we find very narrow critical regions near the Neel temperatures T_N and temperature independent 1/T_1 values above T_N. From the 1/T_1 in LaMnO_3 we derive an exchange integral J = 0.83 meV which is consistent with the mean field expression for T_N. All of the doped manganites except CaMnO_3 display anomalously slow, spatially inhomogeneous spin-lattice relaxation below their ordering temperatures. In the ferromagnetic (FM) insulating La_{0.82}Ca_{0.18}MnO_3 and ferromagnetic conducting La_{0.67}Ca_{0.33}MnO_3 systems we show that there exists a bi-modal distribution of \muSR rates λ_f and λ_s associated with relatively 'fast' and 'slow' Mn fluctuation rates, respectively. A physical picture is hypothesized for these FM phases in which the fast Mn rates are due to overdamped spin waves characteristic of a disordered FM, and the slower Mn relaxation rates derive from distinct, relatively insulating regions in the sample. Finally, likely muon sites are identified, and evidence for muon diffusion in these materials is discussed.

cond-mat.str-el↗

Raman scattering study of anomalous charge-, spin-, and lattice-dynamics in the charge-ordered phase of ${\bf Bi}_{1-x}{\bf Ca}_x{\bf MnO}_3$ ($x>0.5$)

We report an inelastic light scattering study of the effects of charge-ordering on the spin-, charge-, and lattice-dynamics in ${\rm Bi}_{1-x}{\rm Ca}_{x}{\rm MnO}_3$ $(x>0.5)$. We find that charge-ordering results in anomalous phonon behavior, such as the appearance of `activated' modes. More significantly, however, the transition to the CO phase results in the appearance of a quasielastic scattering response with the symmetry of the spin chirality operator ($T_{1g}$); this scattering response is thus indicative of magnetic or chiral spin fluctuations in the AFM charge-ordered phase.

cond-mat.str-el↗

Multiphase segregation and metal-insulator transition in single crystal La(5/8-y)Pr(y)Ca(3/8)MnO3

The insulator-metal transition in single crystal La(5/8-y)Pr(y)Ca(3/8)MnO3 with y=0.35 was studied using synchrotron x-ray diffraction, electric resistivity, magnetic susceptibility, and specific heat measurements. Despite the dramatic drop in the resistivity at the insulator-metal transition temperature Tmi, the charge-ordering (CO) peaks exhibit no anomaly at this temperature and continue to grow below Tmi. Our data suggest then, that in addition to the CO phase, another insulating phase is present below Tco. In this picture, the insulator-metal transition is due to the changes within this latter phase. The CO phase does not appear to play a major role in this transition. We propose that a percolation-like insulator-metal transition occurs via the growth of ferromagnetic metallic domains within the parts of the sample that do not exhibit charge ordering. Finally, we find that the low-temperature phase-separated state is unstable against x-ray irradiation, which destroys the CO phase at low temperatures.

cond-mat↗

High Temperature Charge-Ordering Fluctuation in Manganites

High temperature (T) studies of La_{1-x}Ca_{x}MnO_{3} show that charge and phonon transport is significantly suppressed in a narrow doping region of x~1/2 and in a wide T range up to 900 K, which accompanies anomalous broadening of x-ray Bragg peaks. Contrarily, ferromagnetic (FM) correlation above Curie T is sharply enhanced at x~3/8. All these observations indicate the presence of short-range charge ordering (CO) correlation at high T, possibly in the form of a FM "zigzag", a small segment of the CE-type CO state. The decoupling and coupling of the FM zigzags for x~3/8 and 1/2, respectively, is consistent with our results.

cond-mat.str-el↗

Anomalous field-dependent specific heat in charge-ordered Pr$_{1-x}$Ca$_x$MnO$_3$ and La$_{0.5}$Ca$_{0.5}$MnO$_3$

We report low temperature specific heat measurements of Pr$_{1-x}$Ca$_{x}$MnO$_{3}$ ($0.3\leq x \leq 0.5$) 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 ($γT$) originating from magnetic and charge disorder.

cond-mat.str-el↗

Thermal/Electronic Transport Properties and Two-Phase Mixtures in La_{5/8-x}Pr_{x}Ca_{3/8}MnO_{3}

We measured thermal conductivity, k, thermoelectric power, S, and dc electric conductivity, sigma, of La_{5/8-x}Pr_{x}Ca_{3/8}MnO_{3}, showing an intricate interplay between metallic ferromagnetism (FM) and charge ordering (CO) instability. The change of k, S and sigma with temperature (T) and x agrees well with the effective medium theories for binary metal-insulator mixtures. This agreement clearly demonstrates that with the variation of T as well as x, the relative volumes of FM and CO phases drastically change and percolative metal-insulator transition occurs in the mixture of FM and CO domains.

cond-mat.str-el↗