Structural Phase Transformation Research Articles

A highly stable co-doping induced phase structural transformation Sr-free oxygen electrode for reversible solid oxide cells

A highly stable co-doping induced phase structural transformation Sr-free oxygen electrode for reversible solid oxide cells

Uranium Recovery from Uranium Tailings Using the Low-Temperature Chlorination Roasting and Nitric Acid Leaching Process

To address the problems of low leaching efficiency and the fact that the uranium content in leaching residue is higher than the emission standard in the traditional nitric acid leaching uranium tailing and uranium extraction process, the experimental study of low-temperature chlorination roasting and nitric acid leaching was carried out. The effects of roasting temperature, NaCl addition, and roasting time on uranium leaching rate were investigated, and the morphological structure change and phase transformation of roasted minerals were analyzed. After the low-temperature roasting of sodium chloride, the mineral structure was obviously destroyed, the structure became loose, the voids and microcracks increased, and the size of tailing particles decreased. This is mainly due to the reaction of NaCl with metal compounds in minerals. However, when the sodium chloride is excessive, the formation of hydrogen chloride will promote the formation of new compounds, such as Na2Pb2O7 and Zr7O9F10, and form a secondary coating of uranium, resulting in a decrease in the leaching rate. The optimum process conditions of chlorination roasting are as follows: a roasting temperature 250 °C, a 20% addition of NaCl to the tailing mass, a roasting time of 120 min, and a uranium leaching rate of 93.38%. Compared with traditional nitric acid leaching, the leaching rate of uranium increased by 16.64%.

Structural-phase transformations and crystallographic texture in commercial Ti–6Al–4V alloy with globular morphology of α-phase grains: the rolling plane

The commercial Ti–6Al–4V alloy was obtained in an almost single-phase state, formed by finely dispersed globular α-grains with an average size of 12 μm, using thermomechanical processing, including hot rolling. The microtexture and structure of the alloy were studied using X-ray diffractometry and transmission and scanning electron microscopy, including orientation microscopy. It is found that for α-grains the Burgers orientation relationships are satisfied, and twin orientations are ensured in the rolling plane. A significant scattering of the crystallographic orientations of α-grains relative to each other (up to 10°–15°) is established for each group of close Burgers orientations as a result of plastic deformation by rolling at high temperatures. Clusters of microtexture regions in the layered microstructure of grains and the formation mechanisms and mutual crystallographic misorientations of microtexture regions and grains in the alloy have been identified.

Nanocrystalline cerium dioxide reduces recrystallization in cryopreservation solutions

Nanocrystalline cerium dioxide is able to protect living cells from oxidative stress under the influence of various stress factors, in particular under the one of low temperatures. This study investigates the phase-structural transformations in aqueous solutions containing CeO2 nanoparticles (NPs) and their impact on the cryopreservation process. Differential scanning calorimetry and thermomechanical analysis were used to analyse the phase transitions in aqueous suspensions of CeO2 NPs and aqueous solutions of the cryoprotectant dimethyl sulfoxide (Me2SO) with CeO2 NPs. Various concentrations of CeO2 NPs were tested to observe their effects on the crystallization and melting behaviours. The addition of CeO2 NPs significantly altered the temperatures and enthalpies of melting and crystallization in water. Low concentrations of CeO2 NPs promoted crystallization, while higher concentrations inhibited it, reducing supercooling and recrystallization during thawing. In Me2SO solutions, CeO2 NPs raised the glass transition temperature and affected the recrystallization process, with higher concentrations leading to more pronounced vitrification and reduced recrystallization. We also investigated the regularities of the effect of CeO2 NPs on phase transitions in combined cryoprotective media with Ham's F12, fetal bovine serum and Me2SO, which can be used in future to design the cryopreservation protocols. In the complex media, CeO2 NPs decreased the metastability and altered eutectic crystallization patterns, indicating potential cryoprotective effects. In conclusion, CeO2 NPs modulate the thermophysical properties of cryoprotective solutions, enhancing vitrification and reducing recrystallization, which could improve cryopreservation efficiency. Optimizing NP concentrations is crucial for practical applications in cryopreservation.

Giant Topological Hall Effect and Colossal Magnetoresistance in Heusler Ferromagnet near Room Temperature.

Colossal magnetoresistance (CMR) is an exotic phenomenon that allows for the efficient magnetic control of electrical resistivity and has attracted significant attention in condensed matter due to its potential for memory and spintronic applications. Heusler alloys are the subject of considerable interest in this context due to the electronic properties that result from the nontrivial band topology. Here, the observation of CMR near room temperature is reported in the shape memory Heusler alloy Ni2Mn1.4In0.6, which is attributed to the combined effects of magnetic field-induced martensite twin variant reorientation (MFIR) and magnetic field-induced structural phase transformation (MFIPT). This compound undergoes a structural phase transition from a cubic (austenite-L21) ferromagnetic (FM) to a monoclinic (martensite) antiferromagnetic (AFM), which leads to an effective increase in the size of the Fermi surface and consequently in CMR. Additionally, it exhibits significant anomalous Hall conductivity in both antiferromagnetic and ferromagnetic phases. Furthermore, it demonstrates a giant topological Hall resistivity (THR) ≈6µΩ.cm in the vicinity of martensite transition due to the enhanced spin chirality resulting from the formation of magnetic domains with Bloch-type domain walls. The findings contribute to the understanding of the magnetotransport of Ni-Mn-In Heusler alloys, which are prospective candidates for room-temperature spintronic applications.

Advanced neutron and [formula omitted]-ray shielding characteristics of nanostructured (90-x)Al-xGd2O3 composites reinforced by tungsten

This study introduces a composite material designed to offer exceptional mechanical strength and superior radiation shielding characteristics. By integrating tungsten into an aluminum Al-matrix with varying Gd2O3 content, we developed composites that meet the needful demands of mechanical durability and radiation protection in nuclear applications. The composites, synthesized via mechanical milling and sintering methods in planetary ball mills, have nominal compositions of (90-x)Al-xGd2O3 (x = 5, 10, 15 wt%) supplemented with 10 %W. The XRD analysis revealed phase structure transformations correlated with increased milling durations, while SEM-EDAX provided detailed morphological and elemental insights. TEM study confirmed a homogeneous distribution of nanocrystalline powders after 30 hours of milling while DSC thermographs indicated variations in thermal properties dependent on the Gd2O3 and tungsten content. The enhanced mechanical strength with higher concentrations of gadolinium and tungsten was characterized by Vickers microhardness tests. Neutron and γ-ray shielding properties were calculated using MCNP6.2 simulation code and Phy-X/PSD software. The thermal neutron macroscopic cross-section increased exponentially with higher Gd2O3 content, achieving values of 23.3 cm⁻¹ for 5 wt%, 48.4 cm⁻¹ for 10 wt%, and 73.7 cm⁻¹ for 15 wt%. Fast neutron removal cross-section also showed an increasing trend. The γ-ray linear attenuation coefficient decreased with increasing energy, but the Al-15Gd2O3-10 %W composite exhibited the highest LAC values, indicating superior γ-ray absorption capabilities. Correspondingly, the HVL values were lowest for the Al-15Gd2O3-10 %W composite. These findings demonstrate that Al-Gd2O3-W composites are promising materials for advanced industrial applications requiring robust mechanical properties and effective radiation shielding.

Identifying patterns in the structural-phase transformations when processing oxide doped waste with the use of carbon reducer

The object of this study is the structural and phase transformations during the carbon reduction of tungsten high-speed steel slag in order to obtain a resource-saving alloying additive. The problem is the loss of precious elements when obtaining and using alloying material from man-made raw materials. Solving the problem is related to the definition of technological parameters to enable the reduction of losses of the corresponding elements. As a result of increasing the degree of scale reduction from 33 % to 72 % and 85 %, the strengthening of the manifestation of the solid solution of carbon and alloying elements in α-Fe relative to FeWO4, FeO and Fe3O4 was revealed. Fe3C, WC, W2C, FeW3C, Fe3W3C, Fe6W6C, VC, V2C, Cr3C2, Cr7C3 and Cr23C6 also appeared. Along with this, rounded and multifaceted particles with different chemical composition and the formation of a spongy microstructure were found. It was established that the most acceptable degree of recovery is 85 %. But achieving a recovery rate of 72 % is also sufficient. This is explained by the fact that the residual carbon in the carbides provides an increased reducing capacity, which is realized during the further reduction of oxides in the liquid metal during alloying. The spongy microstructure results in faster dissolution in contrast to standard ferroalloys, which provides a reduction in melting time while reducing spent resources. No phases with an increased tendency to sublimation were found in the obtained alloying material. That is, no additional conditions are needed that restrain the loss of alloying elements during evaporation with a gaseous phase, which provides an increase in the degree of extraction of the corresponding elements. The properties of the resulting alloying material make it possible to use it in metallurgical production when smelting alloyed steel grades in an electric arc furnace, the composition of which does not have strict restrictions on the carbon content

Synergistic contributions of the poling field-induced changes in local structure on the piezoelectric properties of modified BaTiO3 system

Abstract Local structural heterogeneity is a key factor in improving the piezoelectric properties of non-centrosymmetric piezoelectric systems. This work investigates electric field-induced structural and microstructural changes at localized and average scales to elucidate the structure-property correlations that enhance piezoelectric performance in Sn-doped BaTiO3 systems exhibiting coexisting phase boundaries. Despite showing field-induced structural phase transformation, the sample displays variations in piezocoefficient values with the nature of phase boundary compositions. Raman spectroscopy measurements reveal that the TiO6/SnO6 octahedra near the tetragonal-orthorhombic phase boundary exhibit significantly greater poling field-induced structural heterogeneities in local structure compared to those near the orthorhombic-cubic phase boundary. X-ray absorption spectroscopic results on Ti and Sn K-edge in unpoled and poled samples reveal that the dipolar contribution responsible for the piezoelectricity originates from field-induced distortion associated with both TiO6 and SnO6 octahedra. Near the vicinity of the tetragonal-orthorhombic phase boundary, both the TiO6 and SnO6 contributions are cumulative and exhibit better piezoelectricity. On the other hand, at the orthorhombic-cubic phase boundary, the dipolar contributions from these octahedra are counterintuitive, resulting in a reduction of piezoelectricity. These results could provide a pathway to design materials with an enhanced piezoelectric response by considering various phase boundary aspects before applying a poling field prior to making them piezoactive.

Crystal structure stability and phase transition of celsian, BaAl2Si2O8, up to 1100 °C / 22 GPa

Celsian (BaAl2Si2O8) is an important component of aluminosilicate-based ceramics, which is widely used in high temperature/high pressure process. However, limited data available on its high pressure (HP)/high temperature (HT) behavior and HT studies were based on multi-component samples only. Here we present data on crystal structure stability and phase transformation processes of celsian studied under extreme conditions (up to ∼22 GPa/∼1110 °C) using in situ X-ray diffraction. Under HP conditions celsian undergoes three phase transitions: at the pressures below 10 GPa the main changes in the crystal structure of celsian associated with the changes in the coordination Ba-centered polyhedron (celsian-II and celsian-III), whereas at higher pressures AlO4 tetrahedra transforms into AlO6 octahedra (celsian-IV). Though the HP behavior of some isostructural compound has been studied before, the HP transformation of celsian is not similar to any previously studied mineral or synthetic compound. Celsian demonstrate stability and low thermal expansion coefficients (αV = 12 × 10−6 °C−1) in the studied temperature range.

Probing Phase Formation and Structural Transformations in Sodium Extraction and Insertion of NaFe1-yMnyPO4 through First-Principles Calculations.

Manganese (Mn) substitution is a widely explored strategy aimed at sustainably enhancing the energy density of iron (Fe)-based electrode materials by taking advantage of the higher redox potential of the former. However, excessive Mn content can lead to detrimental effects, offsetting the expected improvements. In experimental studies, triphylite NaFe0.8Mn0.2PO4 has been identified as an optimal composition with enhanced electrochemical performance compared to that of its parent phase NaFePO4. Higher Mn contents result in a loss of capacity and increased voltage hysteresis. In this study, density functional theory (DFT) calculations were employed to investigate the phase stability upon desodiation of Mn-poor and -rich NaxFe1-yMnyPO4 compositions. Our findings reveal distinct stability behaviors in antagonistic systems NaxFe0.75Mn0.25PO4 and NaxFe0.25Mn0.75PO4, where the presence of Na-vacancies and charge orderings appear to influence phase stability. In addition, the number of intermediate phases throughout the desodiation process is identified as a crucial factor in buffering the volume changes. This work sheds light on the superior electrochemical performance of lightly Mn-substituted phases and unveils a key parameter for designing future electrode materials with improved performance.

Rb2InCl5·H2O doped with Te4+ for fluorescence thermometry and coordinated water-related structural phase transformation.

Here, we synthesized Rb2InCl5·H2O with x Te4+ doping by the coprecipitation method, which converts the original nonluminance for pure Rb2InCl5·H2O into orange luminescence ascribed to Te4+ incorporation with an emission peak at 648 nm and a full width at half maximum of 142 nm (420.3 meV) at room temperature. The photoluminescence (PL) lifetime of Te4+-doped Rb2InCl5·H2O exhibits a strong temperature dependence, with a maximum absolute sensitivity (SA) of 12 × 10-3 K-1 at 260 K and a relative sensitivity (SR) of 3.5%K-1 at 300 K, demonstrating its capability for non-contact remote temperature measurement. Additionally, we capture the dynamic changes of coordinated water with temperature in Rb2InCl5·H2O through temperature-dependent Raman spectroscopy, analyze the resulting structural phase transformation associated with coordinated water, and investigate the reversibility of this phase transformation.

Pressure-Induced Structural Phase Transitions and Photoluminescence Properties of Micro/Nanocrystals HoF3.

HoF3 crystals of varying sizes and morphologies were synthesized by controlling the amount of water. As the water content gradually decreased, the size of the crystals reduced, transforming from microcrystals to approximately 100 nm nanocrystals with unique morphologies. At room temperature, the pressure-induced phase transitions, and photoluminescence (PL) properties of HoF3 micro/nanocrystals are studied using in situ high-pressure PL technique. The PL spectra show that the HoF3 micro/nanocrystals exhibit two structural phase transformations at 5 (6 GPa for NCs) and 12 GPa. Nanoparticles have higher fluorescence intensity, which initially increases and then decreases with changes in pressure. Based on first-principles calculations, HoF3 transforms from an orthorhombic structure to a hexagonal structure during the phase transition, with the coordination number of holmium atoms increasing from 9 to 11. The high-pressure Raman spectra on lattice modes also confirmed the existence of the two phase transitions. This work not only provides precise structural changes but also facilitates the understanding of two typical structures of rare-earth trifluoride (REF3), which may play an important role in the application of the RE family.

Structural and optical properties of Ce-stabilized tetragonal phase and intense blue emission of monoclinic phase in ZrO2 nanoparticles

Structural and optical properties of Ce-stabilized tetragonal zirconium dioxide (ZrO2) and intense blue emission of monoclinic ZrO2 are presented in this paper. Nanoparticles of ZrO2 in the stabilized tetragonal and monoclinic phases have been prepared by the solution combustion method. X-ray diffraction studies and Rietveld refinement of the diffraction pattern show the stabilization of ZrO2 in the tetragonal phase (t-ZrO2) with Ce doping. It is the host-dopant ionic size mismatch that leads to lattice distortion and hence the t-ZrO2 stabilized phase. Raman modes confirm the phase transformation from the monoclinic to a tetragonal phase of ZrO2. The presence of oxygen vacancies and surface states in the samples play a role in altering the optical band gap. The dopant Ce-ions create defects/oxygen vacancies, which act as the trapping sites for electrons and holes/the donor and vacancy-related impurity levels. It is transition between these levels or between delocalized conduction bands that lead to band gap reduction. Photoluminescence studies reveal the presence of structural phase transformation dependent emission bands. The monoclinic phase (m-ZrO2) exhibits an intense blue emission originating from the asymmetric and unusual oxygen coordination of Zr in the m-ZrO2. The chromaticity coordinates indicate that the prepared material and adopted strategies are suitable in the field of optoelectronic application.

Self-diffusion in < 100 > symmetrical tilt grain boundaries in tungsten: Molecular dynamics simulation

The structure and energy of grain boundaries, the energies of point defects formation in them and grain-boundary self-diffusion coefficients in 18 < 100 > symmetrical tilt grain boundaries in tungsten have been determined by atomistic simulation. The dependences of grain boundary energies, defect formation energies in them and activation energy of grain-boundary self-diffusion on the misorientation angle have been calculated. A structural phase transformation has been discovered in Σ5(310) and Σ5(210) boundaries, which affected the diffusion properties of these grain boundaries. The calculations performed are compared with the available experimental data on self-diffusion in grain boundaries of tungsten.

Spectral methods of identification of structural transformations in particles of polymineral complexes

Abstract In recent years, new deposits of polymineral complexes have been actively discovered and are beginning to be developed in the Orenburg region of Russia. Knowledge of the structural features of such heterogeneous systems will help provide a controlled structural evolution. Such studies will help shorten the time needed for the introduction of raw materials into production processes of functional ceramics. A selection of physical and chemical methods has been chosen to analyze natural polymineral complexes in order to understand the temperature evolution of their phase composition and structural transformations. The polymineral complexes from deposits in the Orenburg region of Russia are known to be fusible. Infrared spectroscopy and diffractometry methods have been used to identify six to ten crystalline phases in the studied objects. The main phases have been identified as follows: quartz, calcite, kaolinite, montmorillonite, clinochlore, and magnetite. Structural changes were induced by heating the sample to 1200 K at a rate of 10 K/min while recording derivatograms. EPR spectroscopy established that impurity centers have an ambiguous role in the evolution of natural mineral structures. They can both stabilize crystal lattices and cause distortions due to the Jahn-Teller effect. This is particularly true for layered lattices that contain octahedral motifs with a central impurity ion. It has been demonstrated that impurity centers Fe3+ and Mn2+ act as spin labels for structural transformations. As a result of the destruction of crystal components, these impurity centers form clusters with each other and become undetectable by other methods of analysis.

Unveiling Temperature-Induced Structural Phase Transformations and CO2 Binding Sites in CALF-20.

The increase in atmospheric carbon dioxide concentration linked to climate change has created a need for new sorbents capable of separating CO2 from exhaust gases. Recently, an easily produced metal-organic framework, CALF-20, was shown to withstand over 450,000 adsorption/desorption cycles in steam and wet acid gases. Further development and industrial application of such materials require an understanding of the observed processes. Herein, we demonstrate that conditioning as-synthesized CALF-20 single crystal transforms it into a different phase, γ-CALF-20. The transformation resulted in significant structural changes, including the binding of water molecules to Zn(II), accompanied by a reduction of 9% in the unit cell volume. Our experimental findings were supported by the energy-volume dependence of CALF-20 in the presence and absence of water molecules calculated from density functional theory. We have also monitored the sorption process of the dominant greenhouse gas, CO2, on the initial phase of CALF-20 at atomic resolution using in situ single-crystal X-ray diffraction under specific pressure. The new understanding of CALF-20 chemistry from these studies should facilitate development of novel sorbents for gas adsorption technologies.

Order-disorder phase transitions in Fe81Ga19-RE ALLOYS (RE = Dy, Er, Tb, Yb) according to neutron diffraction data

New data on the phase compositions and structural transformations in a number of Fe81Ga19 alloys doped with trace amount (≤ 0.2 at.%) of rare earth elements are presented. The data are obtained in neutron diffraction experiments performed with high resolution and in continuous temperature scanning mode when heated to 900 °C and subsequent cooling. It has been established that structural rearrangements proceed in a generally identical manner both in the original Fe81Ga19 alloy and in its doped analogues. Slow heating and subsequent cooling of the alloys (rate ±2 °C/min) leads to the formation of clusters of the D03 phase with sizes in the range (200–300) Å in the matrix of the disordered A2 phase. The sizes and volume fraction of clusters (~0.3 of the sample volume) weakly depend on the specific composition. The degree of ordering of the clusters atomic structure changes with temperature according to a second-order phase transition and is close to unity at room temperature. The search for structural ordering corresponding to the modified D03 phase, discovered in a number of electron diffraction studies, did not lead to a positive result.

Design and Technological Aspects of Integrating Multi-Blade Machining and Surface Hardening on a Single Machine Base

Modern mechanical engineering faces high competition in global markets, which requires manufacturers of process equipment to significantly reduce production costs while ensuring high product quality and maximum productivity. Metalworking occupies a significant part of industrial production and consumes a significant share of the world’s energy and natural resources. Improving the technology of manufacturing parts with an emphasis on more efficient use of metalworking machines is necessary to maintain the competitiveness of the domestic machine tool industry. Hybrid metalworking systems based on the principles of multi-purpose integration eliminate the disadvantages of monotechnologies and increase efficiency by reducing time losses and intermediate operations. The purpose of this work is to develop and implement a hybrid machine tool system and an appropriate combined technology for manufacturing machine parts. Theory and methods. Studies of the possible structural composition and layout of hybrid equipment at integration of mechanical and surface-thermal processes were carried out, taking into account the basic provisions of structural synthesis and componentization of metalworking systems. Theoretical studies were carried out using the basic provisions of system analysis, geometric theory of surface formation, design of metalworking machines, methods of finite elements, and mathematical and computer modeling. The mathematical modeling of thermal fields and structural-phase transformations during HEH HFC was carried out in ANSYS (version 19.1) and SYSWELD (version 2010) software packages using numerical methods of solving differential equations of unsteady heat conduction (Fourier equation), carbon diffusion (2nd Fick’s law) and elastic–plastic behavior of the material. The verification of the modeling results was carried out using in situ experiments employing the following: optical and scanning microscopy; and mechanical and X-ray methods of residual stress determination. Formtracer SV-C4500 profilograph profilometer was used in the study for simultaneous measurement of shape deviations and surface roughness. Surface topography was assessed using a Walter UHL VMM 150 V instrumental microscope. The microhardness of the hardened surface layer of the parts was evaluated on a Wolpert Group 402MVD. Results and discussion. The original methodology of structural and kinematic analysis for pre-design studies of hybrid metalworking equipment is presented. Methodological recommendations for the modernization of multi-purpose metal-cutting machine tool are developed, the implementation of which will make it possible to implement high-energy heating with high-frequency currents (HEH HFC) on a standard machine tool system and provide the formation of knowledge-intensive technological equipment with extended functionality. The innovative moment of this work is the development of hybrid metalworking equipment with numerical control and writing a unique postprocessor to it, which allows to realize all functional possibilities of this machine system and the technology of combined processing as a whole. Special tooling and tools providing all the necessary requirements for the process of surface hardening of HEH HFC were designed and manufactured. The conducted complex of works and approbation of the technology of integrated processing in real conditions in comparison with traditional methods of construction of technological process of parts manufacturing allowed to obtain the following results: increase in the productivity of processing by 1.9 times; exclusion of possibility of scrap occurrence at finishing grinding; reduction in auxiliary and preparatory-tasking time; and reduction in inter-operational parts backlogs.

Fabricating highly stable and reliable vanadium dioxide thin films: Insights from radio frequency magnetron sputtering

This study establishes an optimization protocol to fabricate a stoichiometric VO2 thin film onto the glass substrate using a single process step in RF magnetron sputtering. An interplay between the substrate temperature and the oxygen-to-argon ratio in process gas is shown to achieve a range of VOx composition (from oxygen-rich to oxygen-deficient phases). The re-sputtering phenomenon is found to be crucial at higher temperature (T ≥ 873 K), leading to a shift in stoichiometry from V2O5 to V2O3. Moreover, a process model for the fabrication of various VOx compounds in thin film form is also established in this study. The crystal structure transformation from M1 to R phase for these VO2 thin films deposited over a range of process conditions is found to be 339 ± 1 K, in close agreement with the reported value for the bulk VO2. In spite of the microstructural variations, these films are found to show consistent phase transition behavior, excellent stability, and reliability in repeated thermal cycles. These films show a semiconductor-to-metal transition, which is correlated to their structural phase transformation temperature. Moreover, this study also establishes a correlation between various external stimuli, widening the usage of this material in a range of applications.

Pressure‐Enhanced Superconductivity and Structural Phase Transition in Layered Sn4P3

High pressure provides a unique tuning method depending on structure modulation to explore the structure–property relationship. Herein, the pressure‐induced structural phase transformation and enhanced superconductivity in a layered binary phosphide Sn4P3 are reported. Comprehensive measurements using in situ synchrotron X‐Ray diffraction and Raman spectroscopy reveal a structural phase transition with mild distortion of SnP3 building blocks and interlayer shrinkage under high pressure. This differs from a conventional trigonal SnAs(P)3 to square SnAs(P)4 topotactic transition in SnAs(P)‐based compound. Through this structure reconstruction under high pressure, electron distribution has been reorganized and phonons have softened, facilitating a high superconducting temperature (Tc) value of 7.8 K at 34.9 GPa, which is almost six times higher than its ambient value. The study introduces a new transition route in layered SnAs/SnP‐based intermetallic materials and provides insight into the structural and electronic changes under high pressure for Sn4P3.