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Choong-Shik Yoo

Publications and source records attributed to Choong-Shik Yoo.

5 recordsLinked to original sources

Six-fold coordinated carbon dioxide VI.

Under standard conditions, carbon dioxide (CO2) is a simple molecular gas and an important atmospheric constituent, whereas silicon dioxide (SiO2) is a covalent solid, and one of the fundamental minerals of the planet. The remarkable dissimilarity between these two group IV oxides is diminished at higher pressures and temperatures as CO2 transforms to a series of solid phases, from simple molecular to a fully covalent extended-solid V, structurally analogous to SiO2 tridymite. Here, we present the discovery of an extended-solid phase of CO2: a six-fold coordinated stishovite-like phase VI, obtained by isothermal compression of associated CO2-II (refs 1,2) above 50 GPa at 530-650 K. Together with the previously reported CO2-V (refs 3-5) and a-carbonia, this extended phase indicates a fundamental similarity between CO2 (a prototypical molecular solid) and SiO2 (one of Earth's fundamental building blocks). We present a phase diagram with a limited stability domain for molecular CO2-I, and suggest that the conversion to extended-network solids above 40-50 GPa occurs via intermediate phases II (refs 1,2), III (refs 7,8) and IV (refs 9,10). The crystal structure of phase VI suggests strong disorder along the c axis in stishovite-like P42/mnm, with carbon atoms manifesting an average six-fold coordination within the framework of sp3 hybridization.

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Martensitic fcc-to-hcp transformations in solid xenon under pressure: a first-principles study.

First-principles calculations reveal that the fcc-to-hcp pressure-induced transformation in solid xenon proceeds through two mechanisms between 5 and 70 GPa. The dynamics of the phase transition involves a sluggish stacking-disorder growth at lower pressures (path I) that changes to a path involving an orthorhombic distortion at higher pressures (path II). The switchover is governed by a delicate interplay of energetics (enthalpy of the system for the structural stability) and kinetics (energy barrier for the transition). The two types of martensitic transformations involved in this pressure-induced structural transformation are a twinned martensitic transition at lower pressures and a slipped martensitic transition at higher pressures.

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High-pressure-induced phase transitions in pentaerythritol: X-ray and Raman studies.

The high-pressure response of pentaerythritol crystals has been examined to 10 GPa in diamond-anvil cells using angle-dispersive synchrotron X-ray diffraction and Raman spectroscopy. The results reveal two first-order phase transitions: one at 4.8 GPa from phase I, tetragonal I(), to phase II, orthorhombic Pnn2C2v10, with a small approximately 0.5% volume change, and the other at 7.2 GPa to phase III with an unknown crystal structure. We found that phase I exhibits a large crystallographic anisotropy which rapidly decreases with increasing pressure: the ratio of linear compressibilities between two primary crystal axes decreases from betao= 8.1 at 1 atm to betaP = 2.6 at 4 GPa. We suggest that this apparent decrease in crystal anisotropy is due to the disruption of hydrogen bonding in the (001) plane of phase I and eventually leads to an orthorhombic distortion from a quadrilateral network structure in phase I to a quasi one-dimensional structure in phase II. The crystal structure of phase III exhibits a disordered character, and it is likely a conformational variant of phase II.

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High-energy-density extended CO solid.

Covalently bonded extended phases of molecular solids made of first- and second-row elements at high pressures are a new class of materials with advanced optical, mechanical and energetic properties. The existence of such extended solids has recently been demonstrated using diamond anvil cells in several systems, including nitrogen, carbon dioxide and carbon monoxide. However, the microscopic quantities produced at the formidable high-pressure/temperature conditions have limited the characterization of their predicted novel properties, including high-energy content. In this paper, we present experimental evidence that these extended low-Z solids are indeed high-energy-density materials, by milligram-scale high-pressure synthesis, recovery and characterization of polymeric CO (p-CO). Our spectroscopic data reveal that p-CO is a random polymer made of lactonic entities and conjugated C=C with an energy content rivalling or exceeding that of HMX (cyclo-tetramethylene tetranitramine, a commonly used conventional high explosive). Solid p-CO explosively decomposes to CO(2) and glassy carbon, and thus might be used as an advanced energetic material.

Carbon↗

Osmium has the lowest experimentally determined compressibility.

On the basis of high pressure diamond-anvil compression studies for the precious metals Ru, Ir, and Os we report the surprising discovery that metallic osmium has a lower compressibility than covalently bonded diamond. We also find that Ir and Ru are as incompressible as Re. In addition, we have performed first principles calculations that confirm the trend in the measured transition metal compressibilities.

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