PubMed Health⌕ Search

Biomedical subjects

M I Eremets

Publications and source records attributed to M I Eremets.

4 recordsLinked to original sources

Structural transformation of molecular nitrogen to a single-bonded atomic state at high pressures.

The transformation of molecular nitrogen to a single-bonded atomic nitrogen is of significant interest from a fundamental stand point and because it is the most energetic non-nuclear material predicted. We performed an x-ray diffraction of nitrogen at pressures up to 170 GPa. At 60 GPa, we found a transition from the rhombohedral (R3c) epsilon-N(2) phase to the zeta-N(2) phase, which we identified as orthorhombic with space group P222(1) and with four molecules per unit cell. This transition is accompanied by increasing intramolecular and decreasing intermolecular distances. The major transformation of this diatomic phase into the single-bonded (polymeric) phase, recently determined to have the cubic gauche structure (cg-N), proceeds as a first-order transition with a volume change of 22%.

Journal Article↗

Polymerization of nitrogen in sodium azide.

The high-pressure behavior of nitrogen in NaN(3) was studied to 160 GPa at 120-3300 K using Raman spectroscopy, electrical conductivity, laser heating, and shear deformation methods. Nitrogen in sodium azide is in a molecularlike form; azide ions N(3-) are straight chains of three atoms linked with covalent bonds and weakly interact with each other. By application of high pressures we strongly increased interaction between ions. We found that at pressures above 19 GPa a new phase appeared, indicating a strong coupling between the azide ions. Another transformation occurs at about 50 GPa, accompanied by the appearance of new Raman peaks and a darkening of the sample. With increasing pressure, the sample becomes completely opaque above 120 GPa, and the azide molecular vibron disappears, evidencing completion of the transformation to a nonmolecular nitrogen state with amorphouslike structure which crystallizes after laser heating up to 3300 K. Laser heating and the application of shear stress accelerates the transformation and causes the transformations to occur at lower pressures. These changes can be interpreted in terms of a transformation of the azide ions to larger nitrogen clusters and then polymeric nitrogen net. The polymeric forms can be preserved on decompression in the diamond anvil cell but transform back to the starting azide and other new phases under ambient conditions.

Journal Article↗

Superconductivity in boron.

Metals formed from light elements are predicted to exhibit intriguing states of electronic order. Of these materials, those containing boron are of considerable current interest because of their relatively high superconducting temperatures. We have investigated elemental boron to very high pressure using diamond anvil cell electrical conductivity techniques. We find that boron transforms from a nonmetal to a superconductor at about 160 gigapascals (GPa). The critical temperature of the transition increases from 6 kelvin (K) at 175 GPa to 11.2 K at 250 GPa, giving a positive pressure derivative of 0.05 K/GPa. Although the observed metallization pressure is compatible with the predictions of first-principles calculations, superconductivity in boron remains to be explored theoretically. The present results constitute a record pressure for both electrical conductivity studies and investigations of superconductivity in dense matter.

Journal Article↗

Semiconducting non-molecular nitrogen up to 240 GPa and its low-pressure stability.

The triple bond of diatomic nitrogen has among the greatest binding energies of any molecule. At low temperatures and pressures, nitrogen forms a molecular crystal in which these strong bonds co-exist with weak van der Waals interactions between molecules, producing an insulator with a large band gap. As the pressure is raised on molecular crystals, intermolecular interactions increase and the molecules eventually dissociate to form monoatomic metallic solids, as was first predicted for hydrogen. Theory predicts that, in a pressure range between 50 and 94 GPa, diatomic nitrogen can be transformed into a non-molecular framework or polymeric structure with potential use as a high-energy-density material. Here we show that the non-molecular phase of nitrogen is semiconducting up to at least 240 GPa, at which pressure the energy gap has decreased to 0.4 eV. At 300 K, this transition from insulating to semiconducting behaviour starts at a pressure of approximately 140 GPa, but shifts to much higher pressure with decreasing temperature. The transition also exhibits remarkably large hysteresis with an equilibrium transition estimated to be near 100 GPa. Moreover, we have succeeded in recovering the non-molecular phase of nitrogen at ambient pressure (at temperatures below 100 K), which could be of importance for practical use.

Journal Article↗