| 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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High-Pressure Yttrium Nitride, Y5N14, Featuring Three Distinct Types of Nitrogen Dimers
- 2021
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Ingår i: The Journal of Physical Chemistry C. - : AMER CHEMICAL SOC. - 1932-7447 .- 1932-7455. ; 125:32, s. 18077-18084
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Tidskriftsartikel (refereegranskat)abstract
- Yttrium nitride, Y5N14, was synthesized by direct reaction between yttrium and nitrogen at similar to 50 GPa and similar to 2000 K in a laser-heated diamond anvil cell. High-pressure single-crystal X-ray diffraction revealed that the crystal structure of Y5N14 (space group P4/mbm) contains three distinct types of nitrogen dimers. Crystal chemical analysis and ab initio calculations demonstrated that the dimers [N-2](x-) are crystallographically and chemically nonequivalent and possess distinct noninteger formal charges (x) that make Y5N14 unique among known compounds. Theoretical computations showed that Y5N14 has an anion-driven metallicity, with the filled part of its conduction band formed by nitrogen p-states. The compressibility of Y5N14, determined on decompression down to similar to 10 GPa, was found to be uncommonly high for dinitrides containing +3 cations (the bulk modulus K-0 = 137(6) GPa).
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| 3. |
- Aslandukov, Andrey, et al.
(författare)
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Stabilization of N6 and N8 anionic units and 2D polynitrogen layers in high-pressure scandium polynitrides
- 2024
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Ingår i: Nature Communications. - : NATURE PORTFOLIO. - 2041-1723. ; 15:1
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Tidskriftsartikel (refereegranskat)abstract
- Nitrogen catenation under high pressure leads to the formation of polynitrogen compounds with potentially unique properties. The exploration of the entire spectrum of poly- and oligo-nitrogen moieties is still in its earliest stages. Here, we report on four novel scandium nitrides, Sc2N6, Sc2N8, ScN5, and Sc4N3, synthesized by direct reaction between yttrium and nitrogen at 78-125 GPa and 2500 K in laser-heated diamond anvil cells. High-pressure synchrotron single-crystal X-ray diffraction reveals that in the crystal structures of the nitrogen-rich Sc2N6, Sc2N8, and ScN5 phases nitrogen is catenated forming previously unknown N-6(6)- and N-8(6)- units and infinity 2(N-5(3-)) anionic corrugated 2D-polynitrogen layers consisting of fused N-12 rings. Density functional theory calculations, confirming the dynamical stability of the synthesized compounds, show that Sc2N6 and Sc2N8 possess an anion-driven metallicity, while ScN5 is an indirect semiconductor. Sc2N6, Sc2N8, and ScN5 solids are promising high-energy-density materials with calculated volumetric energy density, detonation velocity, and detonation pressure higher than those of TNT.
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| 4. |
- Aslandukov, Andrey, et al.
(författare)
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Stabilization Of The CN35− Anion In Recoverable High-pressure Ln3O2(CN3) (Ln=La, Eu, Gd, Tb, Ho, Yb) Oxoguanidinates
- 2023
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773. ; 62:47
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Tidskriftsartikel (refereegranskat)abstract
- A series of isostructural Ln(3)O(2)(CN3) (Ln=La, Eu, Gd, Tb, Ho, Yb) oxoguanidinates was synthesized under high-pressure (25-54 GPa) high-temperature (2000-3000 K) conditions in laser-heated diamond anvil cells. The crystal structure of this novel class of compounds was determined via synchrotron single-crystal X-ray diffraction (SCXRD) as well as corroborated by X-ray absorption near edge structure (XANES) measurements and density functional theory (DFT) calculations. The Ln(3)O(2)(CN3) solids are composed of the hitherto unknown CN35- guanidinate anion-deprotonated guanidine. Changes in unit cell volumes and compressibility of Ln(3)O(2)(CN3) (Ln=La, Eu, Gd, Tb, Ho, Yb) compounds are found to be dictated by the lanthanide contraction phenomenon. Decompression experiments show that Ln(3)O(2)(CN3) compounds are recoverable to ambient conditions. The stabilization of the CN35- guanidinate anion at ambient conditions provides new opportunities in inorganic and organic synthetic chemistry.
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| 5. |
- Aslandukova, Alena, et al.
(författare)
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High-pressure hP3 yttrium allotrope with CaHg2-type structure as a prototype of the hP3 rare-earth hydride series
- 2023
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Ingår i: Physical Review B. - : AMER PHYSICAL SOC. - 2469-9950 .- 2469-9969. ; 107:1
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Tidskriftsartikel (refereegranskat)abstract
- A high-pressure (HP) yttrium allotrope, hP3-Y (space group P6/mmm), was synthesized in a multi-anvil press at 20 GPa and 2000 K which is recoverable to ambient conditions. Its relative stability and electronic properties were investigated using density functional theory calculations. A hP3-Y derivative hydride, hP3-YHx, with a variable hydrogen content (x = 2.8, 3, 2.4), was synthesized in diamond anvil cells by the direct reaction of yttrium with paraffin oil, hydrogen gas, and ammonia borane upon laser heating to similar to 3000 K at 51, 45 and 38 GPa, respectively. Room-temperature decompression leads to gradual reduction and eventually the complete loss of hydrogen at ambient conditions. Isostructural hP3-NdHx and hP3-GdHx hydrides were synthesized from Nd and Gd metals and paraffin oil, suggesting that the hP3-Y structure type may be common for rare-earth elements. Our results expand the list of allotropes of trivalent lanthanides and their hydrides and suggest that they should be considered in the context of studies of HP behavior and properties of this broad class of materials.
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| 6. |
- Bykov, Maxim, et al.
(författare)
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High-Pressure Synthesis of Dirac Materials: Layered van der Waals Bonded BeN4 Polymorph
- 2021
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Ingår i: Physical Review Letters. - : AMER PHYSICAL SOC. - 0031-9007 .- 1079-7114. ; 126:17
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Tidskriftsartikel (refereegranskat)abstract
- High-pressure chemistry is known to inspire the creation of unexpected new classes of compounds with exceptional properties. Here, we employ the laser-heated diamond anvil cell technique for synthesis of a Dirac material BeN4. A triclinic phase of beryllium tetranitride tr-BeN4 was synthesized from elements at similar to 85 GPa. Upon decompression to ambient conditions, it transforms into a compound with atomic-thick BeN4 layers interconnected via weak van der Waals bonds and consisting of polyacetylene-like nitrogen chains with conjugated pi systems and Be atoms in square-planar coordination. Theoretical calculations for a single BeN4 layer show that its electronic lattice is described by a slightly distorted honeycomb structure reminiscent of the graphene lattice and the presence of Dirac points in the electronic band structure at the Fermi level. The BeN4 layer, i.e., beryllonitrene, represents a qualitatively new class of 2D materials that can be built of a metal atom and polymeric nitrogen chains and host anisotropic Dirac fermions.
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| 7. |
- Bykov, Maxim, et al.
(författare)
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High-Pressure Synthesis of Metal-Inorganic Frameworks Hf4N20 center dot N-2, WN8 center dot N-2, and Os5N28 center dot 3 N-2 with Polymeric Nitrogen Linkers
- 2020
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Ingår i: Angewandte Chemie International Edition. - : WILEY-V C H VERLAG GMBH. - 1433-7851 .- 1521-3773. ; 59:26, s. 10321-10326
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Tidskriftsartikel (refereegranskat)abstract
- Polynitrides are intrinsically thermodynamically unstable at ambient conditions and require peculiar synthetic approaches. Now, a one-step synthesis of metal-inorganic frameworks Hf4N20 center dot N2, WN 8 center dot N2, and Os5N28 center dot 3N2 via direct reactions between elements in a diamond anvil cell at pressures exceeding 100 GPa is reported. The porous frameworks (Hf4N20, WN 8, and Os5N28) are built from transition-metal atoms linked either by polymeric polydiazenediyl (polyacetylene-like) nitrogen chains or through dinitrogen units. Triply bound dinitrogen molecules occupy channels of these frameworks. Owing to conjugated polydiazenediyl chains, these compounds exhibit metallic properties. The high-pressure reaction between Hf and N2 also leads to a non-centrosymmetric polynitride Hf2N11 that features double-helix catenapoly[tetraz-1-ene-1,4-diyl] nitrogen chains [-N-N-N=N-](infinity.)
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| 8. |
- 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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| 9. |
- 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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| 10. |
- Laniel, Dominique, et al.
(författare)
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Front Cover: Revealing Phosphorus Nitrides up to the Megabar Regime: Synthesis of α′-P3N5, δ-P3N5 and PN2 (Chem. Eur. J. 62/2022)
- 2022
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Ingår i: Chemistry - A European Journal. - : Wiley-VCH Verlagsgesellschaft. - 0947-6539 .- 1521-3765. ; 28:62
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- For the last 30 years, the lack of a binary phosphorus nitride containing PN6 octahedra formed a scientific chasm between carbon-group and oxygen-group nitrides, both featuring a variety of solids with XN6 units (X being a non-metal element). Now, the discovery of the δ-P3N5 and PN2 phosphorus nitrides—formed under high pressure and both composed of the elusive PN6 octahedron—builds a long-sought-after bridge between these two groups of nitrides. More information can be found in the Research Article by D. Laniel, F. Trybel, and co-workers (DOI: 10.1002/chem.202201998).
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