We report on a series of experiments that use high-power lasers to ramp-compress aluminum (Al) up to 475 GPa. Under this quasi-isentropic compression, Al remains in the solid state and two solid–solid phase transformations are observed. In situ x-ray diffraction is performed to detect the crystal structure. A velocimetry diagnostic measures particle velocities in order to infer the pressure in the Al sample. We show that a solid–solid phase transition, consistent with a transformation to a hexagonal close-packed (hcp) structure, occurs at 216 ± 9 GPa. At higher pressures, a transformation to a structure consistent with the body-centered cubic (bcc) structure occurs at 321 ± 12 GPa. These phase transitions are also observed in 6061-O (annealed) Al alloy at 175 ± 9 GPa and 333 ± 11 GPa, respectively. Correlations in the high-pressure crystallographic texture suggests the close-packed face-centered cubic (fcc) (111), hcp (002), and bcc (110) planes remain parallel through the solid–solid fcc–hcp and hcp–bcc transformations.

Mechanical equation-of-state data of initially liquid and solid CO2 shock-compressed to terapascal conditions are reported. Diamond-sapphire anvil cells were used to vary the initial density and state of CO2 samples that were then further compressed with laser-driven shock waves, resulting in a data set from which precise derivative quantities, including Grüneisen parameter and sound speed, are determined. Reshock states are measured to 800 GPa and map the same pressure-density conditions as the single shock using different thermodynamic paths. The compressibility data reported here do not support current density-functional-theory calculations, but are better represented by tabular equation-of-state models.

The properties of all materials at one atmosphere of pressure are controlled by the configurations of their valence electrons. At extreme pressures, neighboring atoms approach so close that core-electron orbitals overlap, and theory predicts the emergence of unusual quantum behavior. We ramp-compress monovalent elemental sodium, a prototypical metal at ambient conditions, to nearly 500 GPa (5 million atmospheres). The 7-fold increase of density brings the interatomic distance to 1.74 Å well within the initial 2.03 Å of the Na+ ionic diameter, and squeezes the valence electrons into the interstitial voids suggesting the formation of an electride phase. The laser-driven compression results in pressure-driven melting and recrystallization in a billionth of a second. In situ x-ray diffraction reveals a series of unexpected phase transitions upon recrystallization, and optical reflectivity measurements show a precipitous decrease throughout the liquid and solid phases, where the liquid is predicted to have electronic localization. These data reveal the presence of a rich, temperature-driven polymorphism where core electron overlap is thought to stabilize the formation of peculiar electride states.