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J. B. Goodenough

Publications and source records attributed to J. B. Goodenough.

24 records · Page 2Linked to original sources

Suppression of the Magnetic Phase Transition in Manganites Close to the Metal-Insulator Crossover

We report the suppression of the magnetic phase transition in La1-xCaxMnO3 close to the localized-to-itinerant electronic transition, i.e. at x = 0.2 and x = 0.5. A new crossover temperature Tf can be defined for these compositions instead of TC. Unlike in common continuous magnetic phase transition the susceptibility does not diverge at Tf and a spontaneous magnetization cannot be defined below it. We propose that the proximity to the doping-induced metal-insulator transition introduces a random field which breaks up the electronic/magnetic homogeneity of the system and explains these effects.

cond-mat.mtrl-sci↗

Chemical, Structural, and Transport Properties of Na1-xCoO2

We report measurement of room-temperature compressibility, thermal expansion, thermoelectric power a(T) at various pressures P < 20 kbar, basal-plane resistivity rab (T), magnetic susceptibility and thermal conductivity k(T) taken on single-crystal or cold-pressed Na0.57CoO2. An enhancement of a large thermopower with a change of slope occurs on heating near 100 K, but this enhancement is progressively suppressed by pressure. The c-axis thermal expansion is large in the interval 150 K <T < 250 K where the c-axis resistivity exhibits a smooth transition from a metallic to a non-metallic temperature dependence; but the basal-plane thermal expansion remains negligible for all temperatures T < 300 K. On the other hand, the basal-plane room-temperature compressibility is large in the interval 0 < P < 22 kbar, becoming negligible in the range 22 < P < 45 kbar, whereas the c-axis room-temperature compressibility is anomalously large in the pressure range 22 < P < 35 kbar. The basal plane resistivity is prop. to T^(3/2) below 175 K where there is 3D metallic conduction; it rises less rapidly with temperature where the metallic conduction is confined to 2D. The phonon contribution to the thermal conductivity of a cold-pressed ceramic sample is not suppressed, as previously reported. These findings are rationalized with the aid of the virial theorem, recognition of a pinning of the nominal Co(IV)/Co(III) redox couple at the top of the O2-:2p6 bands, and a schematic location of the a1T and eT antibonding bands of this couple with respect to the Fermi energy.

cond-mat.mtrl-sci↗

Electron scattering near an itinerant to localized electronic transition

We report an unconventional temperature dependence of the resistivity in several strongly correlated systems approaching a localized to itinerant electronic transition from the itinerant electron side. The observed resistivity, proportioanl to T^(3/2)over the entire range of materials discussed, cannot be explained within the framework of existing theories. We propose a model in which the scattering of the conduction electrons by locally cooperative bond-length fluctuations in a matrix of vibronic and Fermi-liquid electrons can account for the experimental data.

cond-mat.str-el↗

V-V Bond-Length Fluctuations in Vox

We report a significantly stronger suppression of the phonon contribution to the thermal conductivity in VOx than can be accounted for by disorder of the 16 % atomic vacancies present in VO. Since the transition from localized to itinerant electronic behavior is first-order and has been shown to be characterized by bond-length fluctuations in several transition-metal oxides with the perovskite structure, we propose that cooperative V-V bond-length fluctuations play a role in VO similar to the M-O bond-length fluctuations in the perovskites. This model is able to account for the strong suppression of the thermal conductivity, the existence of a pseudogap confirmed by thermoelectric power, an anomalously large Debye-Waller factor, the temperature dependence of the magnetic susceptibility, and the inability to order atomic vacancies in VO.

cond-mat↗

Phase Competition in Ln0.5a0.5mno3 Perovskites

Single crystals of the systems Pr0.5(Ca1-xSrx)0.5MnO3, (Pr1-yYy)0.5(Ca1-xSrx)0.5MnO3, and Sm0.5Sr0.5MnO3 were grown to provide a series of samples with fixed ratio Mn(III)/Mn(IV)=1 having geometric tolerance factors that span the transition from localized to itinerant electronic behavior of the MnO3 array. A unique ferromagnetic phase appears at the critical tolerance factor tc= 0.975 that separates charge ordering and localized-electron behavior for t tc. This ferromagnetic phase, which has to be distinguished from the ferromagnetic metallic phase stabilized at tolerance factors t>tc, separates two distinguishable Type-CE antiferromagnetic phases that are metamagnetic. Measurements of the transport properties under hydrostatic pressure were carried out on a compositions t a little below tc in order to compare the effects of chemical vs. hydrostatic pressure on the phases that compete with one another near t=tc.

cond-mat.mtrl-sci↗

Structural transformation induced by magnetic field and colossal magnetoresistance response above 313 K in MnAs

MnAs exhibits a first-order phase transition from a ferromagnetic, high-spin metal NiAs-type hexagonal phase to a paramagnetic, lower-spin insulator MnP-type orthorhombic phase at T_C = 313 K. Here, we report the results of neutron diffraction experiments showing that an external magnetic field, B, stabilizes the hexagonal metallic phase above T_C. The phase transformation is reversible and constitutes the first demonstration of a bond-breaking transition induced by a magnetic field. At 322 K the hexagonal structure is restored for B > 4 tesla. The field-induced phase transition is accompanied by an enhanced magnetoresistance of about 17 % at 310 K. We discuss the origin of this phenomenon, which appears to be similar to that of the colossal magnetoresistance response observed in some members of the manganese perovskite family.

cond-mat.mtrl-sci↗