Two structural transitions in covalent aluminum hydride AlH3 were characterized at high pressure. A metallic phase stable above 100 GPa is found to have a remarkably simple cubic structure with shortest first-neighbor H-H distances ever measured except in H2 molecule. Although the high-pressure phase is predicted to be superconductive, this was not observed experimentally down to 4 K over the pressure range 120-164 GPa. The results indicate that the superconducting behavior may be more complex than anticipated.

Liquids are expected to crystallize at low temperature. The only exception is helium, which can remain liquid at 0 K, owing to quantum fluctuations. Similarly, the atomic magnetic moments (spins) in a magnet are expected to order at a temperature scale set by the Curie-Weiss temperature theta(CW) (ref. 3). Geometrically frustrated magnets represent an exception. In these systems, the pairwise spin interactions cannot be simultaneously minimized because of the lattice symmetry. This can stabilize a liquid-like state of short-range-ordered fluctuating moments well below theta(CW) (refs 5-7). Here we use neutron scattering to observe the spin liquid state in a geometrically frustrated system, Tb(2)Ti(2)O(7), under conditions of high pressure (approximately 9 GPa) and low temperature (approximately 1 K). This compound is a three-dimensional magnet with theta(CW) = -19 K, where the negative value indicates antiferromagnetic interactions. At ambient pressure Tb(2)Ti(2)O(7) remains in a spin liquid state down to at least 70 mK (ref. 8). But we find that, under high pressure, the spins start to order or 'crystallize' below 2.1 K, with antiferromagnetic order coexisting with liquid-like fluctuations. These results indicate that a spin liquid/solid mixture can be induced by pressure in geometrically frustrated systems.

We report magnetic neutron-diffraction and electrical resistivity studies on single crystals of the heavy-fermion antiferromagnet CeRhIn5 at pressures up to 2.3 GPa. These experiments show that the staggered moment of Ce and the incommensurate magnetic structure change weakly with applied pressure up to 1.63 GPa, where resistivity, specific heat and NQR measurements confirm the presence of bulk superconductivity. This work places new constraints on an interpretation of the relationship between antiferromagnetism and unconventional superconductivity in CeRhIn5.

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The pressure-induced structural changes of single-wall carbon nanotubes organized into two-dimensional crystalline bundles are studied by neutron diffraction up to ϳ50 kbar. The strong variation of the ͑10͒ Bragg peak position with pressure is interpreted as a progressive deformation of the tube section from circular to hexagonal, in addition to the van der Waals compression. Data at 50 kbar suggest that the tubes are closed to be fully polygonized at this pressure. The anisotropic behavior of the patterns with pressure is assigned to the presence of a uniaxial pressure component and to preferential orientations of the bundles.

The solid hydrogen compounds D2, HD and H2 remain quantum molecular solids up to pressures in the 100 GPa range. A remarkable macroscopic consequence is the existence of a pressure-induced broken symmetry phase transition, in which the molecules go from a spherical rotational state to an anisotropic rotational state. Theoretical understanding of the broken symmetry phase structure remains controversial, despite numerous studies. Some open questions concern the existence of long- or short-range orientational order; whether a strong isotopic shift on the transition pressure should be assigned to the nuclear zero-point motion or to quantum localization; and whether the structures are cubic, hexagonal or orthorhombic. Here we present experimental data on the structure of the broken symmetry phase in solid D2, obtained by a combination of neutron and X-ray diffraction up to 60 GPa. Our data are incompatible with orthorhombic structures predicted by recent theoretical works. We find that the broken symmetry phase structure is incommensurate with local orientational order, being similar to that found in metastable cubic para-D2.

We have studied the spin liquid Tb2Ti2O7 by single crystal neutron diffraction under high pressure up to 2.8 GPa, together with uniaxial stress, down to 0.1 K, in zero and high magnetic fields up to 7 T. In zero magnetic field, a long-range ordered antiferromagnetic structure is induced by pressure. The Néel temperature and ordered magnetic moment can be tuned by the anisotropic pressure component. Under magnetic field, the antiferromagnetic structure transforms into a canted ferromagnetic one at 0.6 T. Spin canting persists even at 7 T. The magnetic phase diagram under pressure shows a strong increase of the Néel temperature with the field.

Solid oxygen is the only elementary molecular magnet. Under the very high pressure of 96 GPa oxygen transforms into a metal and a superconductor. Theory predicts a nonmagnetic state occurring before the transition into the superconducting xi phase. Nevertheless, until now there was no direct evidence of a magnetic collapse in high-pressure oxygen. For the first time direct information is provided on magnetic properties of the epsilon phase, which is sandwiched between the antiferromagnetic delta phase and the superconducting xi phase. We used magnetic neutron diffraction. The data show that the long-range magnetic order disappears at the delta-epsilon transition. The magnetic collapse occurs at P approximately equal to 8 GPa, far below the pressure of the insulator-metal (superconductor) transition. The collapse is preceded by a decrease in temperature of transition towards the long-range magnetically ordered state (T(LRO)) in the delta phase, at P = 7.6 GPa.