| 1. |
- Aprilis, Georgios, et al.
(författare)
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The Effect of Pulsed Laser Heating on the Stability of Ferropericlase at High Pressures
- 2020
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Ingår i: Minerals. - : MDPI. - 2075-163X. ; 10:6
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Tidskriftsartikel (refereegranskat)abstract
- It is widely accepted that the lower mantle consists of mainly three major minerals-ferropericlase, bridgmanite and calcium silicate perovskite. Ferropericlase ((Mg,Fe)O) is the second most abundant of the three, comprising approximately 16-20 wt% of the lower mantle. The stability of ferropericlase at conditions of the lowermost mantle has been highly investigated, with controversial results. Amongst other reasons, the experimental conditions during laser heating (such as duration and achieved temperature) have been suggested as a possible explanation for the discrepancy. In this study, we investigate the effect of pulsed laser heating on the stability of ferropericlase, with a geochemically relevant composition of Mg0.76Fe0.24O (Fp24) at pressure conditions corresponding to the upper part of the lower mantle and at a wide temperature range. We report on the decomposition of Fp24 with the formation of a high-pressure (Mg,Fe)(3)O(4)phase with CaTi2O4-type structure, as well as the dissociation of Fp24 into Fe-rich and Mg-rich phases induced by pulsed laser heating. Our results provide further arguments that the chemical composition of the lower mantle is more complex than initially thought, and that the compositional inhomogeneity is not only a characteristic of the lowermost part, but includes depths as shallow as below the transition zone.
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| 2. |
- Aslandukov, Andrey, et al.
(författare)
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Anionic N18 Macrocycles and a Polynitrogen Double Helix in Novel Yttrium Polynitrides YN6 and Y2N11 at 100 GPa
- 2022
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Ingår i: Angewandte Chemie International Edition. - Weinheim, Germany : Wiley-VCH Verlagsgesellschaft. - 1433-7851 .- 1521-3773. ; 61:34
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Tidskriftsartikel (refereegranskat)abstract
- Two novel yttrium nitrides, YN6 and Y2N11, were synthesized by direct reaction between yttrium and nitrogen at 100 GPa and 3000 K in a laser-heated diamond anvil cell. High-pressure synchrotron single-crystal X-ray diffraction revealed that the crystal structures of YN6 and Y2N11 feature a unique organization of nitrogen atoms-a previously unknown anionic N-18 macrocycle and a polynitrogen double helix, respectively. Density functional theory calculations, confirming the dynamical stability of the YN6 and Y2N11 compounds, show an anion-driven metallicity, explaining the unusual bond orders in the polynitrogen units. As the charge state of the polynitrogen double helix in Y2N11 is different from that previously found in Hf2N11 and because N-18 macrocycles have never been predicted or observed, their discovery significantly extends the chemistry of polynitrides.
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| 3. |
- Bykov, Maxim, et al.
(författare)
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High-Pressure Synthesis of a Nitrogen-Rich Inclusion Compound ReN8·xN2 with Conjugated Polymeric Nitrogen Chains
- 2018
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773. ; 57:29, s. 9048-9053
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Tidskriftsartikel (refereegranskat)abstract
- A nitrogen-rich compound, ReN(8)xN(2), was synthesized by a direct reaction between rhenium and nitrogen at high pressure and high temperature in a laser-heated diamond anvil cell. Single-crystal X-ray diffraction revealed that the crystal structure, which is based on the ReN8 framework, has rectangular-shaped channels that accommodate nitrogen molecules. Thus, despite a very high synthesis pressure, exceeding 100GPa, ReN(8)xN(2) is an inclusion compound. The amount of trapped nitrogen (x) depends on the synthesis conditions. The polydiazenediyl chains [-N=N-] that constitute the framework have not been previously observed in any compound. Abinitio calculations on ReN(8)xN(2) provide strong support for the experimental results and conclusions.
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| 4. |
- Bykov, Maxim, et al.
(författare)
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High-pressure synthesis of ultraincompressible hard rhenium nitride pernitride Re-2(N-2)(N)(2) stable at ambient conditions
- 2019
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Ingår i: Nature Communications. - : NATURE PUBLISHING GROUP. - 2041-1723. ; 10
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Tidskriftsartikel (refereegranskat)abstract
- High-pressure synthesis in diamond anvil cells can yield unique compounds with advanced properties, but often they are either unrecoverable at ambient conditions or produced in quantity insufficient for properties characterization. Here we report the synthesis of metallic, ultraincompressible (K-0 = 428(10) GPa), and very hard (nanoindentation hardness 36.7(8) GPa) rhenium nitride pernitride Re-2(N-2)(N)(2). Unlike known transition metals pernitrides Re-2(N-2)(N)(2) contains both pernitride N-2(4-) and discrete N3- anions, which explains its exceptional properties. Re-2(N-2)(N)(2) can be obtained via a reaction between rhenium and nitrogen in a diamond anvil cell at pressures from 40 to 90 GPa and is recoverable at ambient conditions. We develop a route to scale up its synthesis through a reaction between rhenium and ammonium azide, NH4N3, in a large-volume press at 33 GPa. Although metallic bonding is typically seen incompatible with intrinsic hardness, Re-2(N-2)(N)(2) turned to be at a threshold for superhard materials.
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| 5. |
- Gorelova, Liudmila, et al.
(författare)
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Edge-sharing BO4 tetrahedra and penta-coordinated silicon in the high-pressure modification of NaBSi3O8
- 2022
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Ingår i: Inorganic Chemistry Frontiers. - : ROYAL SOC CHEMISTRY. - 2052-1545 .- 2052-1553. ; 9:8, s. 1735-1742
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Tidskriftsartikel (refereegranskat)abstract
- The high-pressure behavior of the borosilicate reedmergnerite NaBSi3O8 has been studied using in situ single-crystal X-ray diffraction and Raman spectroscopy up to 35 GPa. The crystal structure of NaBSi3O8 contracts homogeneously upon compression up to 12 GPa, while at higher pressures it undergoes two phase transitions. Above 16 GPa the unit-cell volume is doubled, whereas the coordination numbers of all cations and the structural topology are preserved. Above 25 GPa the crystal structure of NaBSi3O8 contains extremely rare dimers of edge-sharing BO4 tetrahedra and earlier unknown Si2O5 groups consisting of edge-sharing SiO5 square pyramids. The structural model was corroborated by DFT calculations. This HP modification results in the first example of a borosilicate compound with edge-sharing BO4 tetrahedra.
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| 6. |
- Laniel, Dominique, et al.
(författare)
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A reentrant phase transition and a novel polymorph revealed in high-pressure investigations of CF4 up to 46.5 GPa
- 2022
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Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 156:4
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Tidskriftsartikel (refereegranskat)abstract
- The high-pressure behavior of simple molecular systems, devoid of strong intermolecular interactions, provides a unique avenue toward a fundamental understanding of matter. Tetrahalides of the carbon group elements (group 14), lacking all intermolecular interactions but van der Waals, are among the most elementary of molecular compounds. Here, we report the investigation of CF4 up to 46.5 GPa-the highest pressure up to which any tetrahalides of group 14 elements have been studied so far-by a combination of single-crystal x-ray diffraction (SC-XRDp), Raman spectroscopy, and ab initio calculations. These measurements reveal a pressure-induced reentrant phase transition (phase II phase III phase IIR) Room temperature and the formation of a previously unknown CF4 cubic polymorph, named phase IV, after the laser heating of CF4 at 46.5 GPa. In this work, the structures of phases II(R), III, and IV were solved and the atomic coordinates were refined on the basis of SC-XRDp. A comparison of tetrahalides of group 14 elements underlines that reducing the intermolecular halogen-halogen distances leads to a structural rearrangement from close packing of the tetrahedral molecules to close packing of the halogen atoms.
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| 7. |
- Laniel, Dominique, et al.
(författare)
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Aromatic hexazine [N6]4− anion featured in the complex structure of the high-pressure potassium nitrogen compound K9N56
- 2023
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Ingår i: Nature Chemistry. - : NATURE PORTFOLIO. - 1755-4330 .- 1755-4349. ; 15:5, s. 641-646
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Tidskriftsartikel (refereegranskat)abstract
- The recent high-pressure synthesis of pentazolates and the subsequent stabilization of the aromatic [N-5](-) anion at atmospheric pressure have had an immense impact on nitrogen chemistry. Other aromatic nitrogen species have also been actively sought, including the hexaazabenzene N-6 ring. Although a variety of configurations and geometries have been proposed based on ab initio calculations, one that stands out as a likely candidate is the aromatic hexazine anion [N-6](4-). Here we present the synthesis of this species, realized in the high-pressure potassium nitrogen compound K9N56 formed at high pressures (46 and 61 GPa) and high temperature (estimated to be above 2,000 K) by direct reaction between nitrogen and KN3 in a laser-heated diamond anvil cell. The complex structure of K9N56-composed of 520 atoms per unit cell-was solved based on synchrotron single-crystal X-ray diffraction and corroborated by density functional theory calculations. The observed hexazine anion [N-6](4-) is planar and proposed to be aromatic.
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| 8. |
- Pakhomova, Anna, et al.
(författare)
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Penta- and hexa-coordinated beryllium and phosphorus in high-pressure modifications of CaBe2P2O8
- 2019
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Ingår i: Nature Communications. - : NATURE PUBLISHING GROUP. - 2041-1723. ; 10
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Tidskriftsartikel (refereegranskat)abstract
- Beryllium oxides have been extensively studied due to their unique chemical properties and important technological applications. Typically, in inorganic compounds beryllium is tetrahedrally coordinated by oxygen atoms. Herein based on results of in situ single crystal X-ray diffraction studies and ab initio calculations we report on the high-pressure behavior of CaBe2P2O8, to the best of our knowledge the first compound showing a step-wise transition of Be coordination from tetrahedral (4) to octahedral (6) through trigonal bipyramidal (5). It is remarkable that the same transformation route is observed for phosphorus. Our theoretical analysis suggests that the sequence of structural transitions of CaBe2P2O8 is associated with the electronic transformation from predominantly molecular orbitals at low pressure to the state with overlapping electronic clouds of anions orbitals.
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| 9. |
- Serovaiskii, Aleksandr, et al.
(författare)
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Fate of Hydrocarbons in Iron-Bearing Mineral Environments during Subduction
- 2019
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Ingår i: Minerals. - : MDPI. - 2075-163X. ; 9:11
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Tidskriftsartikel (refereegranskat)abstract
- Subducted sediments play a key role in the evolution of the continental crust and upper mantle. As part of the deep carbon cycle, hydrocarbons are accumulated in sediments of subduction zones and could eventually be transported with the slab below the crust, thus affecting processes in the deep Earth's interior. However, the behavior of hydrocarbons during subduction is poorly understood. We experimentally investigated the chemical interaction of model hydrocarbon mixtures or natural oil with ferrous iron-bearing silicates and oxides (representing possible rock-forming materials) at pressure-temperature conditions of the Earth's lower crust and upper mantle (up to 2000(+/- 100) K and 10(+/- 0.2) GPa), and characterized the run products using Raman and Mossbauer spectroscopies and X-ray diffraction. Our results demonstrate that complex hydrocarbons are stable on their own at thermobaric conditions corresponding to depths exceeding 50 km. We also found that chemical reactions between hydrocarbons and ferrous iron-bearing rocks during slab subduction lead to the formation of iron hydride and iron carbide. Iron hydride with relatively low melting temperature may form a liquid with negative buoyancy that could transport reduced iron and hydrogen to greater depths.
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