Compressibility of M3C60 Fullerene Superconductors: Relation Between Tc and Lattice Parameter

X-ray diffraction and diamond anvil techniques were used to measure the isothermal compressibility of K(3)C(60) and Rb(3)C(60), the superconducting, binary alkali-metal intercalation compounds of solid buckminsterfullerene. These results, combined with the pressure dependence of the superconducting onset temperature T(c) measured by other groups, establish a universal first-order relation between T(c) and the lattice parameter a over a broad range, between 13.9 and 14.5 angstroms. A small secondorder intercalate-specific effect was observed that appears to rule out the participation of intercalate-fullerene optic modes in the pairing interaction.     

Raman Studies of Alkali-Metal Doped AxC60 Films (A = Na, K, Rb, and Cs; x = 0, 3, and 6)

The room temperature Raman spectra of the intramolecular modes between 100 cm(-1) and 2000 cm(-1) are reported for alkali-metal doped AxC(60) films. For A = K, Rb, and Cs, phase separation is observed with the spectra of C(60), K(3)C(60), K(6)C(60), Rb(3)C(60), Rb(6)C(60), and Cs(6)C(60) phases reported. The x = 3 phases show only three Raman active modes: two of Ag symmetry and only the lowest frequency Hg mode. The other Hg modes regain intensity in the x = 6 films, with several mode splittings observed. For A = Na, such phase separation is not clearly observed, and reduced mode shifts are interpreted as due to incomplete charge transfer in these films.     

(RbxK1-x)3C60 Superconductors: Formation of a Continuous Series of Solid Solutions

By means of an approach that employs alkali-metal alloys, bulk single-phase (RbxK1-x)(3)C(6O) superconductors have been prepared for all x between 0 and 1. For x = 1 it is shown that the maximum superconducting fraction, which approaches 100% in sintered pellets, occurs at a Rb to C(60) ratio of 3:1. More importantly, single-phase superconductors are formed at all intermediate values of x, and it is shown that the transition temperature (T(c)) increases linearly with x in this series of materials. The formation of a continuous range of solid solutions demonstrates that the rubidium- and potassium-doped C(60) superconducting phases must be isostructural, and furthermore, suggests that the linear increase in T(c) with x results from a chemical pressure effect.     

Pressure Dependence of Superconductivity in Single-Phase K3C60

The superconducting compound K(3)C(60) (with transition temperature T(c) = 19.3 kelvin at ambient pressure), formed as a single phase by reaction of alkali vapor with solids of the icosahedral C(60) molecule (buckminsterfullerene), shows a very large decrease of T(c) with increasing pressure. Susceptibility measurements on sintered pellets showing bulk superconductivity are reported up to 21 kilobars of pressure, where T(c) is already less than 8 kelvin. The results are consistent with a piling up of the density of states at the Fermi level.     

Superconductivity at 45 k in rb/tl codoped c60 and c60/c70 mixtures

The appearance of superconductivity at relatively high temperatures in alkali metal-doped C(60) fullerene provides the challenge to both understand the nature and origin of the superconductivity and to determine the upper limit of the superconducting transition temperature (T(c)). Towards the latter goal, it is shown that doping with potassium-thallium and rubidium-thallium alloys in the 400 to 430 degrees C temperature range increases the T(c) of C(60)/C(70) mixtures to 25.6 K and above 45 K, respectively. Similar increases in T(c) were also observed upon analogous doping of pure C(60). Partial substitution of potassium with thallium in interstitial sites between C(60) molecules is suggested by larger observed unit cell parameters than for the K(3)C(60) and K(4)C(60) phases. Contrary to previous results for C(60) doped with different alkali metals, such expansion does not alone account for the changes in critical temperature.     

13C NMR Spectroscopy of KxC60: Phase Separation, Molecular Dynamics, and Metallic Properties

The results of (13)C nuclear magnetic resonance (NMR) measurements on alkali fullerides KxC(60) are reported. The NMR spectra demonstrate that material with 0 < x < 3 is in fact a two-phase system at equilibrium, with x = 0 and x = 3. NMR lineshapes indicate that C(3-)(60) ions rotate rapidly in the K(3)C(60) phase at 300 K, while C(6)-(60) ions in the insulating K(6)C(60) phase are static on the time scale of the lineshape measurement. The temperature dependence of the (13)C spin-lattice relaxation rate in the normal state of K(3)C(60) is found to be characteristic of a metal, indicating the important role of the C(3-)(60) ions in the conductivity. From the relaxation measurements, an estimate of the density of electronic states at the Fermi level is derived.     

Oxygen isotope effect in high-temperature oxide superconductors

The effect of oxygen isotope substitution on the superconducting transition temperature, T(c), has been measured for BaBi(0.25)Pb(0.75)O(3) (T(c), approximately 11 K) and Lal(1.85) Ca(0.15)CuO(4) (T(c) approximately 20 K), and is compared to the shifts observed for La(1.85)Sr(0.15)CuO(4) (T(c) approximately 37 K) and YBa(2)Cu(3)O(7) (T(c) approximately 92 K). For all four materials, the transition temperature is shifted to lower temperature upon substitution of oxygen-18 for oxygen-16. The observed shifts demonstrate that phonons are involved in the electron-pairing mechanism in these oxide superconductors.     

Synthesis and Electronic Transport of Single Crystal K3C60

Sizable single crystals of C(6O) have been synthesized and doped with potassium. Above the superconducting transition temperature T(c), the electrical resistivity p(T) displays a classic metal-like temperature dependence. The transition to the superconducting state at T(c) = 19.8 K is extremely sharp, with a transition width DeltaT < 200 mK. In contrast to transport behavior of doped polycrystalline and granular thin films, no anomalous fluctuations are observed near T(c) in single crystal specimens.     

X-ray diffaction evidence for nonstoichiometric rubidium-c60 intercalation compounds

Powder x-ray diffraction at 300 K on equilibrated samples of several nominal compositions chi in Rb(chi)C(60) is reported. In addition to the face-centered cubic (fcc) (chi = 3, superconducting), body-centered tetragonal (chi = 4), and body-centered cubic (bcc) (chi = 6) stoichiometric phases, direct evidence for a dilute fcc doped phase, 0 x c 相似文献   

Organic molecular soft ferromagnetism in a fullerene c60

The properties of an organic molecular ferromagnet [C(60)TDAE(0.86); TDAE is tetrakis(dimethylamino)ethylene] with a Curie temperature ;T(c) = 16.1 kelvin are described. The ferromagnetic state shows no remanence, and the temperature dependence of the magnetization below ;T(c) does not follow the behavior expected of a conventional ferromagnet. These results are interpreted as a reflection of a three-dimensional system leading to a soft ferromagnet.     

Electrical resistivity and stoichiometry of kkhgr c60 films

Electrical resistances of polycrystalline fullerene (C(60)) films were monitored while the films were being doped in ultrahigh vacuum with potassium from a molecular-beam effusion source. Temperature- and concentration-dependent resistivities of K(chi) C(60) films in equilibrium near room temperature were measured. The resistance changes smoothly from metallic at chi approximately 3 to activated as chi --> = 0 or chi --> 6. The minimum resistivity for K(3)C(60) films is 2.2 microohm-centimeters, near the Mott limit. The resistivities are interpreted in terms of a granular microstructure where K(3)C(60) regions form nonpercolating grains, except perhaps at chi approximately 3. Stoichiometries at the resistivity extrema were determined by ex situ Rutherford backscattering spectrometry to be chi = 3 +/- 0.05 at the resistance minimum and chi = 6 +/- 0.05 at the fully doped resistance maximum.     

The oaxaca, Mexico, earthquake of 29 november 1978: a preliminary report on aftershocks

Aftershocks of the 29 November 1978 Oaxaca, Mexico, earthquake (surface-wave magnitude Ms = 7.8) define a rupture area of about 6000 square kilometers along the boundary of the Cocos sea-plate subduction. This area had not ruptured in a large (Ms >/= 7), shallow earthquake since the years 1928 and 1931 and had been designated a seismic "gap." The region has also been seismically quiet for small to moderate (M >/= 4), shallow (depth 相似文献   

Pioneer saturn infrared radiometer: preliminary results

The effective temperature of Saturn, 94.4 + 3 K, implies a total emission greater than two times the absorbed sunlight. The infrared data alone give an atmospheric abundance of H(2) relative to H(2) + He of 0.85 +/- 0.15. Comparison of infrared and radio occultation data will give a more precise estimate. Temperature at the 1-bar level is 137 to 140 K, and 2.5 K differences exist between belts and zones up to the 0.06-bar level. Ring temperatures range from 60 to 70 K on the south (illuminated) side and from < 60 to 67 K in the planet's shadow. The average temperature of the north (unilluminated) side is approximately 55 K. Titan's 45-micrometer brightness temperature is 80 +/- 10 K.     

Boron isotope effect in superconducting zirconium dodecaboride

The boron isotope effect in ZrB(12) has been determined to be T(c) infinity M(alpha), where alpha is equal to - 0.09 +/- 0.05, M is the boron mass, and T(c) is the supercondiucting transition temperature.     

Structure of haloform intercalated C60 and its influence on superconductive properties

CHCl3 and CHBr3 intercalated C60 have attracted particular interest after a superconductivity transition temperature (Tc) of up to 117 K was discovered. We have determined the structure using synchrotron x-ray powder-diffraction and found that the expansion of the lattice mainly takes place in one dimension (triclinic b axis), leaving planes of C60 molecules on an approximately hexagonal, slightly expanded lattice. We have performed tight-binding band structure calculations for the surface layer. In spite of the slight expansion of the layers, for the range of dopings where a large Tc has been observed, the density of states at the Fermi energy is smaller for C60.2CHCl3 and C60.2CHBr3 than for C60. This suggests that the lattice expansion alone cannot explain the increase of Tc.     

Elasticity of single-crystal MgO to 8 gigapascals and 1600 kelvin

The cross pressure (P) and temperature (T) dependence of the elastic moduli (Cij) of single-crystal samples of periclase (MgO) from acoustic wave travel times was measured with ultrasonic interferometry: partial differential2C11/ partial differentialP partial differentialT = (-1.3 +/- 0.4) x 10(-3) per kelvin; partial differential2C110/ partial differentialP partial differentialT = (1. 7 +/- 0.7) x 10(-3) per kelvin; and partial differential2C44/ partial differentialP partial differentialT = (-0.2 +/- 0.3) x 10(-3) per kelvin. The elastic anisotropy of MgO decreases with increasing pressure at ambient temperature, but then increases as temperature is increased at high pressure. An assumption of zero cross pressure and temperature derivatives for the elastic moduli underestimates the elastic anisotropy and overestimates the acoustic velocities of MgO at the extrapolated high-pressure and high-temperature conditions of Earth's mantle.     

Synthesis and Equation of State of (Mg,Fe) SiO3 Perovskite to Over 100 Gigapascals

Silicate perovskite of composition (Mg(0.88)Fe(0.12)) SiO(3) has been synthesized in a laser-heated diamond-anvil cell to a pressure of 127 gigapascals at temperatures exceeding 2000 K. The perovskite phase was identified and its unit-cell dimensions measured by in situ x-ray diffraction at elevated pressure and room temperature. An analysis of these data yields the first high-precision equation of state for this mineral, with values of the zero-pressure isothermal bulk modulus and its pressure derivative being K(0T) = 266 +/- 6 gigapascals and K'(0T) = 3.9 +/- 0.4. In addition, the orthorhombic distortion of the silicate-perovskite structure away from ideal cubic symmetry remains constant with pressure: the lattice parameter ratios are b/a = 1.032 +/- 0.002 and c/a = 1.444 +/- 0.006. These results, which prove that silicate perovskite is stable to ultrahigh pressures, demonstrate that perovskite can exist throughout the pressure range of the lower mantle and that it is therefore likely to be the most abundant mineral in Earth.     

Vitrification temperature of water

The vitrification temperature (T(g)) of water is an elusive quantity because of the great difficulty in supercooling water sufficiently without initiating its crystallization. Water depresses the vitrification temperature of glycerol (184 degrees K) monotonously, and this property has been used for derivation of an estimate of its T(g). The result, 127 degrees +/- 4 degrees K (-146 degrees +/- 4 degrees C), is the temperature below which water presumably exists as a brittle, glassy substance.     

Excitation Gap in the Normal State of Underdoped Bi2Sr2CaCu2O8+delta

Angle-resolved photoemission experiments reveal evidence of an energy gap in the normal state excitation spectrum of the cuprate superconductor Bi2Sr2CaCu2O8+delta. This gap exists only in underdoped samples and closes around the doping level at which the superconducting transition temperature Tc is a maximum. The momentum dependence and magnitude of the gap closely resemble those of the dx2-y2 gap observed in the superconducting state. This observation is consistent with results from several other experimental techniques, which also indicate the presence of a gap in the normal state. Some possible theoretical explanations for this effect are reviewed.     

Superconductivity of metallic aluminum antimonide

The high-pressure metallic phase of aluminunm antimnonide is super conducting [critical temperature T(c) (P approximately 125 kilobars) = 2.8 degrees +/-0.2 degrees K]. This transition temperature is significantly lower than the transition temperature of metallic germanium under an equivalent high pressure. A similar result had been previously found for superconducting indiumantimonide in comparison to tin.