arXiv subjects

Anna Pakhomova

Publications and source records attributed to Anna Pakhomova.

8 recordsLinked to original sources

arXiv2026

Exotic centrosymmetric phase of acentric urea under high pressure

Urea is a simple prototype supramolecular crystal that exhibits rich polymorphism at low pressure due to broken and restored N-H-O hydrogen bonds. The high pressure polymorph (phase V') of acentric urea crystallizes in a centrosymmetric structure, which presents an appealing target because of its potential exotic structure, analogous to the symmetric ice phase X. The pressure-induced polymorphism of urea was studied using powder X-ray diffraction, infrared and Raman spectroscopy, second harmonic generation (SHG) measurements up to 20 GPa and ab initio crystal structure prediction (CSP) based on the constrained evolutionary approach. A strong decrease of the SHG signal at the transition pressure 10 GPa reveals that the high-pressure polymorph is indeed centrosymmetric, further confirmed by the selection rules observed in the lattice vibration modes, in contrast to chemical intuition for acentric urea. The structural evolution sequence obtained from X-ray diffraction, SHG and CSP calculations is as follows: phase I (P421m; Z=2) from 0 to 0.5 GPa, Phase III (P212121; Z=4) from 0.5 to 5.2 GPa, and phase V' (P21/m; Z=6) beyond 10.0 GPa which is energetically competitive with the theoretically predicted phase V (Pnma; Z=4). A phase X with distinct spectral and diffraction features forms between 5.2 and 10.0 GPa, which could be explained by a quantum disorder intermediate state between phase III and V', that is ascribed to the difficulty to disrupt the H-bonding network under extremely compressed environment. The softening of N-H vibrations and the change in intensity of the vibrations associated with the hydrogen bonding provide evidence for proton tunneling and charge-transfer interaction in phase X.

cond-mat.mtrl-sci↗

arXiv2025

Prediction and Synthesis of Mg$_4$Pt$_3$H$_6$: A Metallic Complex Transition Metal Hydride Stabilized at Ambient Pressure

The low-pressure stabilization of superconducting hydrides with high critical temperatures ($T_c$s) remains a significant challenge, and experimentally verified superconducting hydrides are generally constrained to a limited number of structural prototypes. Ternary transition-metal complex hydrides (hydrido complexes)-typically regarded as hydrogen storage materials-exhibit a large range of compounds stabilized at low pressure with recent predictions for high-$T_c$ superconductivity. Motivated by this class of materials, we investigated complex hydride formation in the Mg-Pt-H system, which has no known ternary hydride compounds. Guided by ab initio structural predictions, we successfully synthesized a novel complex transition-metal hydride, Mg$_4$Pt$_3$H$_6$, using laser-heated diamond anvil cells. The compound forms in a body-centered cubic structural prototype at moderate pressures between 8-25 GPa. Unlike the majority of known hydrido complexes, Mg$_4$Pt$_3$H$_6$ is metallic, with formal charge described as 4[Mg]$^{2+}$.3[PtH$_2$]$^{2-}$. X-ray diffraction (XRD) measurements obtained during decompression reveal that Mg$_4$Pt$_3$H$_6$ remains stable upon quenching to ambient conditions. Magnetic-field and temperature-dependent electrical transport measurements indicate ambient-pressure superconductivity with $T_c$ (50%) = 2.9 K, in reasonable agreement with theoretical calculations. These findings clarify the phase behavior in the Mg-Pt-H system and provide valuable insights for transition-metal complex hydrides as a new class of hydrogen-rich superconductors.

cond-mat.supr-con↗

arXiv2024

Resolving the pressure induced 'self-insertion' in skutterudite CoSb3

CoSb3, a skutterudite compound, is key in studying thermoelectric materials. Under compression, it undergoes a 'self-insertion' isostructural transition, redistributing large Sb atoms among crystallographic sites. We investigated CoSb3's structural stability up to 70 GPa using single crystal X-ray diffraction and high-resolution X-ray scattering, including Bragg Coherent Diffraction Imaging. We examined the material in three pressure transmitting media (PTMs), exploring how PTMs and nonhydrostatic stresses affect CoSb3. Notably, the 'self-insertion' transition may reduce or even make compressibility negative. Additionally, we report a previously unknown phase transformation from cubic Im-3 to trigonal R-3 above 40 GPa and discuss the phases' distinctive behaviors.

cond-mat.mtrl-sci↗

arXiv2024

Synthesis of Mg$_2$IrH$_5$: A potential pathway to high-$T_c$ hydride superconductivity at ambient pressure

Following long-standing predictions associated with hydrogen, high-temperature superconductivity has recently been observed in several hydride-based materials. Nevertheless, these high-$T_c$ phases only exist at extremely high pressures, and achieving high transition temperatures at ambient pressure remains a major challenge. Recent predictions of the complex hydride Mg$_{2}$IrH$_{6}$ may help overcome this challenge with calculations of high-$T_c$ superconductivity (65 K$~<~T_c~<~$ 170 K) in a material that is stable at atmospheric pressure. In this work, the synthesis of Mg$_{2}$IrH$_{6}$ was targeted over a broad range of $P$-$T$ conditions, and the resulting products were characterized using X-ray diffraction (XRD) and vibrational spectroscopy, in concert with first-principles calculations. The results indicate that the charge-balanced complex hydride Mg$_{2}$IrH$_{5}$ is more stable over all conditions tested up to ca 28 GPa. The resulting hydride is isostructural with the predicted superconducting Mg$_{2}$IrH$_{6}$ phase except for a single hydrogen vacancy, which shows a favorable replacement barrier upon insertion of hydrogen into the lattice. Bulk Mg$_{2}$IrH$_{5}$ is readily accessible at mild $P$-$T$ conditions and may thus represent a convenient platform to access superconducting Mg$_{2}$IrH$_{6}$ via non-equilibrium processing methods.

cond-mat.supr-con↗

arXiv2023

Polytypism of Incommensurately Modulated Structures of Crystalline Bromine upon Molecular Dissociation under High Pressure

Polytypism of incommensurately modulated structures was hitherto unobserved. Here, we found the phenomenon in simple halogen systems of bromine and iodine upon molecular dissociation in the solids under pressure. Single-crystal synchrotron X-ray diffraction in laser heated diamond anvil cells pressurised up to 112 GPa revealed a number of allotropes of bromine and iodine including polytypes of Br-IIIγ (Fmmm(00γ)s00) with γ varying within 0.18 to 0.3.

cond-mat.mtrl-sci↗

arXiv2022

Synthesis of Ultra-Incompressible Carbon Nitrides Featuring Three-Dimensional Frameworks of CN4 Tetrahedra Recoverable at Ambient Conditions

More than thirty years ago, carbon nitrides featuring 3D frameworks of tetrahedral CN4 units were identified as one of the great aspirations of materials science, expected to have a hardness greater than or comparable to diamond. Since then, no unambiguous experimental evidence of their existence has been delivered. Here, we report the high-pressure high-temperature synthesis of the long-sought-after covalent carbon nitrides, tI14-C3N4, hP126-C3N4, and tI24-CN2, in laser-heated diamond anvil cells. Their structures were solved and refined using synchrotron single-crystal X-ray diffraction. In these solids, carbon atoms, all sp3-hybridized, and nitrogen atoms are fully saturated, forming four and three covalent bonds, respectively, leading to three-dimensional arrangements of corner-sharing CN4 tetrahedra. These carbon nitrides are ultra-incompressible, with hP126-C3N4 and tI24-CN2 even rivalling diamond's incompressibility, and superhard. These novel compounds are recoverable to ambient conditions in crystalline form and chemically stable in air. Being wide-band gap semiconductors with intriguing features in their electronic structure, they are expected to exhibit multiple exceptional functionalities besides their mechanical properties, opening new perspectives for materials science.

cond-mat.mtrl-sci↗

arXiv2020

High-pressure polymeric nitrogen allotrope with the black phosphorus structure

Studies of polynitrogen phases are of great interest for fundamental science and for the design of novel high energy density materials. Laser heating of pure nitrogen at 140 GPa in a diamond anvil cell led to the synthesis of a polymeric nitrogen allotrope with the black phosphorus structure, bp-N. The structure was identified in situ using synchrotron single-crystal X-ray diffraction and further studied by Raman spectroscopy and density functional theory calculations. The discovery of bp-N brings nitrogen in line with heavier pnictogen elements, resolves incongruities regarding polymeric nitrogen phases and provides insights into polynitrogen arrangements at extreme densities.

cond-mat.mtrl-sci↗

arXiv2019

High-pressure synthesis of ultraincompressible hard rhenium nitride pernitride Re$_{2}$(N$_{2}$)N$_{2}$ stable at ambient conditions

Here we report the synthesis of metallic, ultraincompressible (bulk modulus $K_{0}$ = 428(10) GPa) and very hard (nanoindentation hardness 36.7(8) GPa) rhenium (V) nitride pernitride Re$_{2}$(N$_{2}$)N$_{2}$. While the empirical chemical formula of the compound, ReN$_{2}$, is the same as for other known transition metals pernitrides, e.g. IrN$_{2}$, PtN$_{2}$, PdN$_{2}$ and OsN$_{2}$, its crystal chemistry is unique. The known pernitrides of transition metals consist of a metal in the oxidation state +IV and pernitride anions N$_{2}^{4-}$. ReN$_{2}$ contains both pernitride N$_{2}^{4-}$ and discrete N$^{3-}$ anions, which explains its exceptional properties. Moreover, in the original experimental synthesis of Re$_{2}$(N$_{2}$)N$_{2}$ performed in a laser-heated diamond anvil cell via a direct reaction between rhenium and nitrogen at pressures from 40 to 90 GPa we observed that the material was recoverable at ambient conditions. Consequently, we developed a route to scale up its synthesis through a reaction between rhenium and ammonium azide, NH$_{4}$N$_{3}$, in a large-volume press at 33 GPa. Our work resulted not only in a discovery of a novel material with unusual crystal chemistry and a set of properties attractive for potential applications, but also demonstrated a feasibility of surmounting conceptions common in material sciences.

cond-mat.mtrl-sci↗