High-pressure Phase Transition Research Articles

High-pressure phase transitions of series of catenated nitrogen energetic crystals Nx (x = 4, 8, 10): A comparative DFT-D study.

High-pressure chemistry has advantages in exploring novel energetic materials and is the key to the development of new high-energy materials. The complexity and danger of experimental processes require a deeper understanding by advanced simulation techniques. Therefore, a high-precision comparative DFT-D study was performed to investigate the effect of pressure on series of catenated nitrogen energetic crystals. The results show that there exist phase transitions for N4, N8, and N10 at 4 GPa, 3 GPa, and 2 GPa respectively, which are embodied in various properties of these crystals. Studies on band gap and DOS indicate pressure-induced improvement on the ability for electrons transition from occupied orbitals to empty ones. Hirshfeld surface analysis qualitatively suggests that hydrogen bonding interactions are becoming dominant inter-molecular interactions. The topological analysis quantitatively reveals that pressure is beneficial to enhancing the inter-molecular hydrogen bonding energy, thereby playing an important role in the stability of high-pressure phases. The discussions on mechanical properties imply that pressure can improve the rigidity of these energetic systems and enhance their mechanical properties. Our findings evidence the high-pressure phase transitions for catenated nitrogen energetic crystals, which lay the theoretical foundation for the development of novel energetic materials. Series of catenated nitrogen energetic crystals N4, N8 and N10 were obtained from experiments. Optimizations were performed by GGA/PBE functional and G06 dispersion correction within the framework of CASTEP code, and the cutoff energies of the plane waves were set to 700 eV. The particular moiety in the crystals was extracted by Multiwfn 3.6 and subsequent analysis was conducted by Gaussian 09W package.

High-pressure phase transition in clinochlore: IIa polytype stabilization

Abstract Structural variations of natural clinochlore with pressure have been studied by in situ single-crystal X-ray diffraction (XRD) in a diamond-anvil cell in the pressure range 0–20 GPa at room temperature. High-resolution XRD data allowed for the identification of a polytypic phase transition at about 9 GPa. Around 4.32(5) GPa, the unit-cell parameters exhibited a significant deviation from linear behavior, particularly the c and β values, abruptly interrupted when the phase transition occurs. XRD patterns showed a drastic reduction of diffuse scattering due to the stabilization of the high-pressure structure, suggesting that the atomic reorganization of the layers led to a disorder reduction. The phase transition showed complete reversibility during the experiment. Ab initio structural refinements identified the transition as polytypic, from the initial IIb-4 triclinic polytype (space group C1) to the IIa-1 monoclinic structure (space group C2/m), with unit-cell parameters a = 5.2058(6) Å, b = 9.0208(4) Å, c = 13.560(7) Å, β = 97.34(3)°. The latter was theoretically derived in the 1960s as the least stable chlorite polytype but has never been observed in natural chlorites. The phase transition also has a significative effect on the bulk modulus, with a reduction from K0 = 81.2(13)t to K0 = 56.0(6) GPa for the high-pressure structure. An isothermal run at 600 K from ambient pressure to 14 GPa showed the same phase transition at 7.8(5) GPa. Its occurrence at lower pressures suggests a negative P/T slope for the transition. Therefore, at high-temperature and high-pressure conditions compatible with impact phenomena, the polytypic phase transition could prevent chlorite from early destabilization and dehydration.

Improved mechanical and corrosion properties through high-pressure phase transition in a biodegradable Zn-1.5Mn alloy

Zn-Mn alloys are considered promising biodegradable metals for orthopedic applications due to their large elongation and favorable osteogenicity. However, the corrosion rate of Zn-Mn alloys could be improved to meet the degradation requirement for orthopedic implants. In this study, a Zn-1.5Mn alloy was prepared via high-pressure solid-solution (HPSS) treatment at 5 GPa and 380 °C for 1 h to cast ingots. Microstructural evaluation revealed the HPSS treatment caused a phase transition from a ζ-MnZn13 phase to an ε-MnZn3 phase. The electrode potential difference between the ε-MnZn3 and the α-Zn was significantly larger than between the ζ-MnZn13 and the α-Zn, leading to an accelerated corrosion rate of the HPSS-treated alloy. It showed an electrochemical corrosion rate of 0.343 mm/y and an immersion degradation rate of 0.028 mm/y, while the as-cast (AC) Zn-1.5Mn displayed an electrochemical corrosion rate of 0.216 mm/y and an immersion degradation rate of 0.026 mm/y. Further, the HPSS-treated Zn-1.5Mn exhibited a compressive yield strength of 202 MPa and a microhardness of 83.48 HV. In addition, the HPSS-treated Zn-1.5Mn exhibited a cell viability toward human umbilical vein endothelial cells (HUVEC) comparable to its AC and atmospheric pressure solid-solution-treated (APSS-treated) counterparts toward HUVEC, along with improved antibacterial activity.

Crystal structure identification with 3D convolutional neural networks with application to high-pressure phase transitions in SiO2

Efficient, reliable and easy-to-use structure recognition of atomic environments is essential for the analysis of atomic scale computer simulations. In this work, we train two neuronal network (NN) architectures, namely PointNet and dynamic graph convolutional NN (DG-CNN) using different hyperparameters and training regimes to assess their performance in structure identification tasks of atomistic structure data. We show benchmarks on simple crystal structures, where we can compare against established methods. The approach is subsequently extended to structurally more complex SiO2 phases. By making use of this structure recognition tool, we are able to achieve a deeper understanding of the crystallization process in amorphous SiO2 under shock compression. Lastly, we show how the NN based structure identification workflows can be integrated into OVITO using its python interface.

High-pressure phase transition in 3-D printed nanolamellar high-entropy alloy by imaging and simulation insights

We report on the high-resolution imaging and molecular dynamics simulations of a 3D-printed eutectic high-entropy alloy (EHEA) Ni40Co20Fe10Cr10Al18W2 consisting of nanolamellar BCC and FCC phases. The direct lattice imaging of 3D-printed samples shows the Kurdjumov–Sachs (K–S) orientation relation {111} FCC parallel to {110} BCC planes in the dual-phase lamellae. Unlike traditional iron and steels, this alloy shows an irreversible BCC-to-FCC phase transformation under high pressures. The nanolamellar morphology is maintained after pressure cycling to 30 GPa, and nano-diffraction studies show both layers to be in the FCC phase. The chemical compositions of the dual-phase lamellae after pressure recovery remain unchanged, suggesting a diffusion-less BCC–FCC transformation in this EHEA. The lattice imaging of the pressure-recovered sample does not show any specific orientation relation between the two resulting FCC phases, indicating that many grain orientations are produced during the BCC–FCC phase transformation. Molecular dynamics simulations on phase transformation in a nanolamellar BCC/FCC in K–S orientation show that phase transformation from BCC to FCC is completed under high pressures, and the FCC phase is retained on decompression aided by the stable interfaces. Our work elucidates the irreversible phase transformation under static compression, providing an understanding of the orientation relationships in 3-D printed EHEA under high pressures.

High pressure phase transition and its influence on structural, mechanical properties and elastic anisotropy of [formula omitted]: An ab-initio study

Lithium carbide (Li2C2), a promising tritium breeding material with potential applications in magnetic confinement-based fusion reactor blankets, has drawn significant attention due to its recent utilization in lithium-ion batteries. In the current study, we employed first-principles calculations with van der Waals (vdW) force correction to explore the structural and mechanical properties of Immm and Pnma phases of Li2C2 subjected to external hydrostatic pressure. It is demonstrated that inclusion of vdW effects accurately predicts Immm→Pnma phase transition at 16 GPa, aligning closely with experimental transition pressure. In contrast, PBE-GGA calculations underestimate the same by about 21%. Current paper is the first comprehensive study of pressure evolution of mechanical properties and strength determining parameters of Li2C2. Interestingly, this inherently brittle material exhibits ductile characteristics beyond 7.5 GPa. The paper also offers a quantitative comparison of its strength parameters with other prominent tritium breeding materials. Finally, the strong directional dependence due to the presence of C2 dimer is investigated by analyzing the pressure variation of elastic anisotropy. The study has its relevance in assessing structural integrity of Li2C2 during inadvertent buildup of tritium and helium that would generate stress in the solid breeder.

High-pressure phase transitions of Fe-bearing orthopyroxene revealed by Raman spectroscopy

Abstract Orthopyroxene is one of the dominant minerals in the Earth’s upper mantle. In this study, we used Raman spectroscopy to investigate the lattice vibration and phase transition of orthopyroxene with four different compositions using diamond-anvil cells up to 34 GPa at 300 K. Our orthopyroxene samples contain 0 (En100), 9% (En91Fs9), 11% (En86Fs11), and 21% (En74Fs21) Fe. At ambient conditions, the Raman modes exhibit a negative dependence on the Fe content, with the exception of the modes at ~850 and 930 cm–1. In contrast, these two Raman modes increase with increasing the Fe content. The phase transition from metastable α- to β-phase was observed at 12.9–15 GPa for samples with <21 mol% Fe and varying Fe content has a minor effect on the phase transition pressure. Besides Fe, incorporation of 2–24 mol% Al can cause an increase in the phase transition pressure from 10–13 to 14–16 GPa. At 29–30.1 GPa, we observed the second apparent change in the Raman spectra for all four investigated samples. For Fe-bearing orthopyroxene, this change in the Raman spectra and frequency shift is associated with the phase transition from β- to γ-phase, whereas for En100, it should be caused by the change of coordination number of Si from 4 to 6 or the presence of α-popx phase. Using the obtained Raman frequency shifts, we calculated the Grüneisen parameters at high pressures. These parameters are useful for understanding the thermoelastic properties of orthopyroxene at high pressures.

High-pressure Phase Transition of Olivine-type Mg2GeO4 to a Metastable Forsterite-III type Structure and their Equation of States

Abstract Germanates are often used as structural analogs of planetary silicates. We have explored the high-pressure phase relations in Mg2GeO4 using diamond anvil cell experiments combined with synchrotron X-ray diffraction and computations based on density functional theory. Upon room temperature compression, forsterite-type Mg2GeO4 remains stable up to 30 GPa. At higher pressures, a phase transition to a forsterite-III type (Cmc21) structure was observed, which remained stable to the peak pressure of 105 GPa. Using a 3rd order Birch Murnaghan fit to the experimental data, we obtained V0 = 305.1 (3) Å3, K0 = 124.6 (14) GPa and K0′ = 3.86 (fixed) for forsterite- and V0 = 263.5 (15) Å3, K0 = 175 (7) GPa and K0′ = 4.2 (fixed) for the forsterite-III type phase. The forsterite-III type structure was found to be metastable when compared to the stable assemblage of perovskite/post-perovskite + MgO, as observed during laser-heating experiments. Understanding the phase relations and physical properties of metastable phases is crucial for studying the mineralogy of impact sites, understanding metastable wedges in subducting slabs and interpreting the results of shock compression experiments.

Electrical Resistivity and Phase Evolution of Fe–N Binary System at High Pressure and High Temperature

Partitioning experiments and the chemistry of iron meteorites indicate that the light element nitrogen could be sequestered into the metallic core of rocky planets during core–mantle differentiation. The thermal conductivity and the mineralogy of the Fe–N system under core conditions could therefore influence the planetary cooling, core crystallization, and evolution of the intrinsic magnetic field of rocky planets. Limited experiments have been conducted to study the thermal properties and phase relations of Fe–N components under planetary core conditions, such as those found in the Moon, Mercury, and Ganymede. In this study, we report results from high-pressure experiments involving electrical resistivity measurements of Fe–N phases at a pressure of 5 GPa and temperatures up to 1400 K. Four Fe–N compositions, including Fe–10%N, Fe–6.4%N, Fe–2%N, and Fe–1%N (by weight percent), were prepared and subjected to recovery experiments at 5 GPa and 1273 K. These experiments show that Fe–10%N and Fe–6.4%N form a single hexagonal close-packed phase (ɛ-nitrides), while Fe–2%N and Fe–1%N exhibit a face-centered cubic structure (γ-Fe). In separate experiments, the resistivity data were collected during the cooling after compressing the starting materials to 5 GPa and heating to ~1400 K. The resistivity of all compositions, similar to the pure γ-Fe, exhibits weak temperature dependence. We found that N has a strong effect on the resistivity of metallic Fe under rocky planetary core conditions compared to other potential light elements such as Si. The temperature-dependence of the resistivity also revealed high-pressure phase transition points in the Fe–N system. A congruent reaction, ε ⇌ γ’, occurs at ~673 K in Fe–6.4%N, which is ~280 K lower than that at ambient pressure. Furthermore, the resistivity data provided constraints on the high-pressure phase boundary of the polymorphic transition, γ ⇌ α, and an eutectoid equilibrium of γ’ ⇌ α + ε. The data, along with the recently reported phase equilibrium experiments at high pressures, enable construction of a phase diagram of the Fe–N binary system at 5 GPa.

Electron density changes accompanying high-pressure phase transition in AlOOH

Abstract An attempt to compare and describe the differences in the electron density distribution between two phase structures of AlOOH has been made. High-resolution, high-pressure experiments with α-AlOOH diaspore were conducted using single-crystal synchrotron X-ray diffraction data. A multipole model of experimental electron density in the α-AlOOH single crystal was refined. Simultaneously, similar multipole refinement was conducted for another phase of diaspore (δ-AlOOH), this time based on a previously published data set. Both results were compared and supported by density functional theory (DFT) calculations. Although the results are affected by the limited quality of the data, it is clear that the phase transition caused significant changes in the shape and arrangement of the atomic basins. Atomic basins are a much better tool to present subtle electron density distribution changes than traditional polyhedra. Straightforward comparison of datasets available in older scientific papers and current datasets is challenging because of differences in data quality and collection parameters. However, augmenting experimental data with computational results can help reveal important information in even incomplete datasets.

Low-temperature and high-pressure phase transitions of ionic liquid 1-decyl-3-methylimidazolium bromide

The phase behavior of an ionic liquid (IL) was investigated at low temperature (LT) and high pressure (HP). The utilized IL was 1-decyl-3-methylimidazolium bromide ([C10mim][Br]), whose cation possesses a long alkyl side-chain. The LT- and HP-crystal polymorphs of [C10mim][Br] were observed conducting small- and wide-angle X-ray scattering (SWAXS) experiments. Upon cooling, a liquid crystal was formed, which subsequently transformed into crystalline species with the modulated layered structure possessing the double Bragg reflection. In addition to the layered structure, the hybrid layered structure coexisted upon heating. At HP, 00ℓ Bragg reflections representing the layered structure were not observed in SWAXS patterns. The HP-crystal phase of [C10mim][Br] was characterized by double Bragg reflection in the low scattering wavevector region. The non-layered HP-crystal caused the large bulk modulus.

Pressure-induced phase transition and metallization in zirconium disulfide under different hydrostatic environments up to 25.3 GPa

The pressurized behaviours of structure, vibration and electrical transport in zirconium disulfide have been systematically investigated in a diamond anvil cell (DAC) under different hydrostatic environments up to 25.3 GPa utilizing in-situ Raman spectroscopy, electrical conductivity measurement, high-resolution transmission electron microscopy (HRTEM) and first-principles theoretical calculations. Upon compression, our experimental results showed that ZrS2 underwent a phase transition accompanied by a semiconductor-to-metal transformation at 15.4 GPa under non-hydrostatic condition. Under hydrostatic condition, the corresponding phase transition occurred at a higher pressure of 17.5 GPa, indicating that the high-pressure phase transition is sensitive to the hydrostaticity in the sample chamber of DAC. Upon decompression, some absolutely new Raman peaks emerged at the pressures below 4.8 GPa and 2.9 GPa under non-hydrostatic and hydrostatic environments, respectively, which revealed an irreversible phase transition in ZrS2. Furthermore, our observations from selected-area electron diffraction patterns confirmed the irreversibility of the high-pressure phase transformation.

First-principles study of high-pressure structural phase transition and superconductivity of YBeH8.

The theory-led prediction of LaBeH8, which has a high superconducting critical temperature (Tc) above liquid nitrogen under a pressure level below 1 Mbar, has been experimentally confirmed. YBeH8, which has a structural configuration similar to that of LaBeH8, has also been predicted to be a high-temperature superconductor at high pressure. In this study, we focus on the structural phase transition and superconductivity of YBeH8 under pressure by using first-principles calculations. Except for the known face-centered cubic phase of Fm3̄m, we found a monoclinic phase with P1̄ symmetry. Moreover, the P1̄ phase transforms to the Fm3̄m phase at ∼200GPa with zero-point energy corrections. Interestingly, the P1̄ phase undergoes a complex electronic phase transition from semiconductor to metal and then to superconducting states with a low Tc of 40K at 200GPa. The Fm3̄m phase exhibits a high Tc of 201K at 200GPa, and its Tc does not change significantly with pressure. When we combine the method using two coupling constants, λopt and λac, with first-principles calculations, λopt is mainly supplied by the Be-H alloy backbone, which accounts for about 85% of total λ and makes the greatest contribution to the high Tc. These insights not only contribute to a deeper understanding of the superconducting behavior of this ternary hydride but may also guide the experimental synthesis of hydrogen-rich compounds.

High-pressure phase transitions in a laser directed energy deposited Fe-33Cu Alloy

Additively manufactured Fe-Cu alloys contain both equilibrium face-centered cubic (FCC) and metastable body-centered cubic (BCC) crystal structure Cu precipitates depending on their size. However, the stability of these nanoscale precipitates under extreme conditions such as high pressures has not been reported. This study investigates the phase transformations and microstructural stability of laser directed energy deposition (DED-LB) made Fe67Cu33 alloy (nominal composition in at.%) under high static pressure deformation using in-situ synchrotron X-ray diffraction under pressure, postmortem high-resolution scanning transmission electron microscopy (HR-STEM), and molecular dynamics (MD) simulations. In-situ XRD results reveal a reversible phase transformation from BCC to the hexagonal close-packed (HCP) structure in the Fe grains at an onset pressure of 16.4 GPa, significantly higher than reported in the literature for pure Fe. Although no high-pressure phase transition was observed in the FCC Cu grains through XRD, HR-STEM analysis uncovers a phase transition to the HCP structure in nanoscale metastable BCC Cu precipitates within the BCC Fe matrix. After decompression, the Fe matrix reverted back to the BCC structure with periodic lath martensite, while regions of the nanoscale BCC Cu precipitates retained the metastable HCP structure. MD simulations support the BCC → HCP transition in the embedded nanoscale coherent Cu precipitates, consistent with the classical Burgers mechanism. Thus, by leveraging in-situ XRD observation, postmortem high-resolution S/TEM microscopy, and MD simulations, this study offers profound insights into the distinctive phase transformations induced by high pressure in DED-LB Fe67Cu33 alloy, which is distinguished by its hierarchical microstructure.

Elastic and piezoelectric properties of β-glycine - a quantum crystallography view on intermolecular interactions and a high-pressure phase transition.

The effect of hydrostatic compression on the elastic and electronic properties of β-glycine was studied using a quantum crystallography approach. The interrelations between the changes in the microscopic quantum pressure in the electronic continuum, macroscopic compressibility and piezoelectricity were considered. The geometries and energies of hydrogen bonds in the crystal structure of β-glycine were considered as functions of pressure before and after a phase transition into the β'-phase in relation to the mechanism of this phase transition.

Damage evolution and removal behaviors of GaN crystals involved in double-grits grinding

Elucidating the complex interactions between the work material and abrasives during grinding of gallium nitride (GaN) single crystals is an active and challenging research area. In this study, molecular dynamics simulations were performed on double-grits interacted grinding of GaN crystals; and the grinding force, coefficient of friction, stress distribution, plastic damage behaviors, and abrasive damage were systematically investigated. The results demonstrated that the interacted distance in both radial and transverse directions achieved better grinding quality than that in only one direction. The grinding force, grinding induced stress, subsurface damage depth, and abrasive wear increase as the transverse interacted distance increases. However, there was no clear correlation between the interaction distance and the number of atoms in the phase transition and dislocation length. Appropriate interacted distances between abrasives can decrease grinding force, coefficient of friction, grinding induced stress, subsurface damage depth, and abrasive wear during the grinding process. The results of grinding tests combined with cross-sectional transmission electron micrographs validated the simulated damage results, i.e. amorphous atoms, high-pressure phase transition, dislocations, stacking faults, and lattice distortions. The results of this study will deepen our understanding of damage accumulation and material removal resulting from coupling between abrasives during grinding and can be used to develop a feasible approach to the wheel design of ordered abrasives.

Regulation of the Ice Ⅰ to Ice III high pressure phase transition meta-stability in milk and its bactericidal effects

This study was focused on a novel approach of creating perturbations under high pressure (HP) meta-stable Ice Ⅰ to Ice Ⅲ phase transition and its bactericidal effects. Experiments were carried out under subzero high pressure processing conditions using Escherichia coli suspended in milk, and the microbial inactivation before and after the meta-stable state regulation was compared. The phase transition position of unperturbed milk was 302 MPa/–37.5 °C. The volume change resulting from the phase transition was employed as the perturbation mechanism. Glucose (5 %, 20 %) and sodium chloride solutions (5 %, 20 %) were used as regulatory sources. Glucose solutions accelerated the phase change of the milk better than the sodium chloride solution and resulted in an optimum phase transition position of milk at 243 MPa/–30.6 °C. The induced perturbations accelerated meta-stable transformation and enhanced the microbial destruction. At 330 MPa/3s, compared to the unfrozen samples, the lethality of E. coli in the frozen-regulated samples significantly increased by 1.79 log. The relationship between the E. coli inactivation within the phase change pressure range and the pressure was not continuous, but a segmented one, both before and after meta-stable state regulation. A higher level of E. coli destruction was accomplished by a 5 min pressure-holding of frozen samples at 220 MPa and 280 MPa as compared to the one-pulse and two-pulses treatments without holding time. The maximum lethality of 6.73 log was achieved at 280 MPa/5 min in the frozen-regulated application.

Propagation behavior of coal crack induced by liquid CO2 phase change blasting considering blasting pressure effects.

To investigate the crack propagation mechanisms in low-permeability coal seams induced by liquid CO2 phase change blasting under different blasting pressures, this research presents an experimental study conducted on a small liquid CO2 phase change blasting test system. The failure mode, crack morphology, and distribution characteristics of the coal rock model specimens under different liquid CO2 phase change blasting pressure were revealed, analyzing the crack shapes and expansion process. The results show that with increasing blasting pressure, both the number and complexity of cracks significantly increase under liquid CO2 phase change blasting, evolving from simple linear cracks to more complex multi-directional networks. Furthermore, the process of crack generation and expansion during liquid CO2 phase change blasting in coal and rock is controlled by the interaction of shock waves and quasi-static stress resulting from high-pressure CO2 phase transition in the borehole. Cracks form in distinct zones: the broken zone, where shock waves cause severe crushing near the borehole; the crack zone, where quasi-static tensile stress drives crack propagation. Higher confining and CO2 blasting pressures increase crack propagation. The research results offer valuable insights for optimizing blasting design in liquid CO2 phase change fracturing.

High-pressure phase and pressure-induced phase transition of Ag3YCl6

Hexagonal Ag3YCl6 was found to transform into a monoclinic structure above ∼1.5 GPa.

High-pressure structure and reactivity of crystalline bibenzyl: Insights and prospects for the synthesis of functional double-core carbon nanothreads.

The high-pressure synthesis of double-core nanothreads derived from pseudo-stilbene crystals represents a captivating approach to isolate within the thread chromophores or functional groups without altering its mechanical properties. These entities can be effectively utilized to finely tune optical properties or as preferential sites for functionalization. Bibenzyl, being isostructural with other members of this class, represents the ideal system for building co-crystals from which we can synthesize double-core nanothreads wherein bridging chromophores, such as the azo or ethylene moieties, are embedded in the desired concentration within a fully saturated environment. To achieve this, a critical step is the preliminary characterization of the high-pressure behavior of crystalline bibenzyl. We report here an accurate investigation performed through state-of-the-art spectroscopic techniques, Raman and Fourier transform infrared spectroscopy, and x-ray diffraction up to 40GPa. Our findings reveal a strongly anisotropic compression of the crystal, which determines, at pressures between 1 and 2GPa, consistent modifications of the vibrational spectrum, possibly related to a torsional distortion of the molecules. A phase transition is detected between 9 and 10GPa, leading to a high pressure phase where, above 24GPa, the nanothread formation is observed. However, the observed reaction was limited in extent and required significantly higher pressures in comparison to other members of the pseudo-stilbene family. This comprehensive study is imperative in laying the foundation for future endeavors, aiming to synthesize double-core nanothreads from pseudo-stilbene crystals, and provides crucial insights into the high-pressure behavior and phase transitions of crystalline bibenzyl.