Abstract
Pressure-induced superconductivity often occurs following structural transition under hydrostatic pressure (PHP) but disappears after the pressure is released. In the alkali-earth metal barium, superconductivity appears after structural transformation from body-centered cubic structure to hexagonal-close-packed (hcp) structure at PHP = 5 GPa, and the superconducting transition temperature (Tc) reaches a maximum of 5 K at PHP = 18 GPa. Furthermore, by stabilizing the low-temperature phase at PHP ~ 30 GPa, Tc reached a higher level of 8 K. Herein, we demonstrate a significantly higher Tc superconductivity in Ba even at ambient pressure. This was made possible through severe plastic deformation of high-pressure torsion (HPT). In this HPT-processed Ba, we observed superconductivity at Tc = 3 K and Tc = 24 K in the quasi-stabilized hcp and orthorhombic structures, respectively. In particular, the latter Tc represents the highest value achieved at ambient pressure among single-element superconducting metals, including intermetallics. The phenomenon is attributed to a strained high-pressure phase, stabilized by residual strains generated from lattice defects such as dislocations and grain boundaries. Significantly, the observed Tc far exceeds predictions from DFT calculations under normal hydrostatic compressions. The study demonstrates the importance of utilizing high-pressure strained phases as quasi-stable superconducting states at ambient pressure.
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Introduction
Superconducting states, which are macroscopic quantum phenomena, are characterized by uniform electron wave function phases. Research into single elements is pivotal for new fundamental insights. Among the 118 elements in the periodic table, about one-fourth are ambient-pressure superconductors, with one-fifth becoming superconductors under hydrostatic pressure1,2,3,4. These are classified as s, s-d, s-p, and s-f electron systems, respectively. In alkali and alkali-earth metals, s-electrons significantly influence electric properties. First, Li and Be exhibit superconductivity at ambient pressure but at extremely low temperatures (Tc = 0.4 mK in Li5, Tc = 26 mK in Be6,7). In particular, for Li, the reduction in the structural symmetry in the unit cell at low temperatures is essential for superconductivity2. Heavier alkali and alkali-earth metals, such as Cs, Ca, Sr, and Ba, exhibit transition into s-d electron superconductors accompanying pressure-induced transformation from body-centered cubic (bcc) to other crystal structures8,9,10,11,12,13,14,15,16,17, where electron transfer from s- to d-orbitals plays a crucial role2. Extensive research, especially on Ba, focuses on hydrostatic contraction effects9,17,18,19,20. Thus, reduction in structural symmetry and structural phase transformation are crucial for stabilizing superconducting state in these metals. Therefore, manipulating lattice strain and crystal structures could feasibly enhance Tc.
In this study, we utilized a high-pressure torsion (HPT) process to introduce shear and compressive strains. The graphical depiction of HPT, as displayed in Extended Data Fig. 1, illustrates that the magnitude of shear strain increases in proportion to the distance from the disk center, as well as the number of revolutions N. Herein, the compressive stress allows only the diagonal components in the strain tensor, whereas the shear strain leads to the nondiagonal components and plays an imperative role in generating possible crystal structures that realize a strain-induced superconducting state. In earlier studies, HPT processing of Re21 and Nb22,23,24 stabilized the superconductivity, and the increase in Tc for Re was due to the increase of the density of states (DOS) at the Fermi level with the expansion of the unit cell volume21, and that for Nb also to the DOS increase with the deformation of the unit cell22,23,24. In general, shear strain is known to introduce not only such simple structural deformations but also an accumulation of dislocations and leads to the formation of a fine-grained structure, resulting in a long-lived quasi-stable state even after releasing stress25,26.
In Ba, the presence of a variety of high-pressure phases under hydrostatic pressure (PHP)16,17,18,19,20 has been reported; in particular, a high-pressure phase Ba-VI (orthorhombic) stabilized at PHP = 12–30 GPa and temperatures below 150 K appears to be the most suitable candidate for high Tc16,17 (Extended Data Fig. 2). In this study, we utilize the HPT process to stabilize such high-pressure hcp and orthorhombic phases even under ambient pressure. Our findings demonstrate that these resulting high-pressure phases maintain their stability even after the stress is released. Notably, the structures achieved through HPT are significantly distinct from those derived sorely from normal hydrostatic compression. The strain at the unit-cell is a crucial factor for attaining superconductivity. Therefor, we anticipate that the HPT-processed Ba will generate appropriately stained structures, potentially leading to an unexpectedly high Tc.
Results
Magnetic measurements and XRD analysis
Figure 1a shows the temperature (T) dependence of the in-phase AC magnetization m’ for HPT-processed Ba (PHPT = 6 GPa, N = 10 at room temperature). PHPT is the operational pressure used in HPT processing and differs from PHP, which is the usual hydrostatic pressure. A diamagnetic signal was unambiguously observed at 3 K in HPT-processed Ba. In addition, a small but visible diamagnetic signal was observed at 14 K. We confirmed that neither signal originated from the Al–Mg–Sc cells subjected to HPT processing. The diamagnetic signals shift to the low-temperature side when a DC magnetic field (Hdc) of 100 Oe is applied. Figure 1a shows the results obtained after annealing the HPT-processed Ba at 503 K in a vacuum for one hour. No diamagnetic signals are observed in the sample after annealing. The annealing temperature of 503 K is more than half the melting point of Ba (999 K) and is sufficient to release the residual strain. Figure 1b shows the temperature dependence of the DC magnetization M for the same HPT-processed Ba. The onset temperature Tc for the lower-temperature diamagnetic anomaly exhibited a linear Hdc dependence, as shown in the inset of Fig. 1b. This phenomenon was also confirmed in the other samples (Extended Data Fig. 3). We note that the Tc of 3 K is approximately six times higher than that under the hydrostatic compression of PHP = 6 GPa (Extended Data Fig. 2), thus indicating that the shear strain can induce an enhancement of Tc beyond normal compression. The volume fraction of the superconducting phase VSC was evaluated to be at most 0.6%. Small amount of superconducting volume fraction originates from the large distribution of shear strain and the formation of small grains. The X-ray diffraction (XRD) pattern obtained by the reflection method, shown in Extended Data Fig. 4, reveals that multiple hcp phases existed with multiple bcc phases (see Extended Data Table 2). This feature was also confirmed in other HPT-processed Ba samples, although no diamagnetic signals were observed (sample No.3 in Extended Data Table 1), for which we think that, in the No. 3 sample, superconducting grains whose size was beyond the penetration length of the magnetic field would not occur. Commonly there is a variation of the lattice constant as 4.4–5.0 Å in the bcc structure, which is equivalent to the change in the atomic volume, Vatom = 63.4–41.8 Å3, corresponding to the range of PHP = 0–6 GPa. In the residual hcp phases, Vatom comes to 38.1 and 27.6 Å3 which correspond to PHP ~ 7 GPa (hcp #1) and ~ 18 GPa (hcp #2), respectively (see Extended Data Table 2).
Temperature dependence of in-phase AC magnetization m’ (a) and DC magnetic susceptibility on M/H (b) for Ba subjected to HPT (No. 1) at room temperature (RT), where the pressure of HPT (PHPT) and revolution number (N) were 6 GPa and 10, respectively. During HPT, a Ba disk was encapsulated in an Al-based Al-3%Mg–0.2%Sc cell to prevent oxidization. (a) includes, for comparison, the results after annealing the HPT-processed Ba at 503 K in a vacuum for one hour. During the HPT processing at PHPT = 6 GPa and RT, the targeted high-pressure phase was the hcp phase. The inset in (b) shows the dc magnetic field (Hdc) dependence of Tc for Hdc = 10-300 Oe.
The superconducting properties of HPT-Ba were also investigated at cryogenic temperatures, where HPT processing was performed at PHPT = 12–24 GPa for N = 10, and the processing temperature was maintained at approximately 100 K in liquid nitrogen. We found that HPT processing at cryogenic temperatures generated a high-pressure orthorhombic phase as a quasi-stable state (Extended Data No. 2). Figure 2a shows the T dependence of m’ for the HPT-processed sample at PHPT = 21 GPa, where the magnetic shielding signal appears at approximately 24 K under Hdc = 0 Oe and disappears at Hdc = 300 Oe. The results for the other PHPT are presented in Extended Data Fig. 5. Also, Fig. 2b compares the Hdc dependence of the onset Tc for the HPT samples processed under various PHPT pressures, where we observe that the PHPT = 21 GPa sample gives a highest Tc of 24 K. We emphasize that this Tc is the highest achieved at ambient pressure for pure metals, including intermetallics, although higher values of Tc than 24 K have been reported under the application of high pressures such as scandium (36 K at 260 GPa)27, titanium (26 K at 240 GPa)28,29, and calcium (29 K at 220 GPa)30. The T dependence of m’ in Fig. 2a is rather broad compared to that in Fig. 1a. This is because of the difference in the operating temperature during HPT processing. In general, lowering the operating temperature during HPT processing can result in the loss of sample viscoelasticity, and the HPT processing of such samples produces small sizes and diverse phases. Conversely, HPT processing under high-temperature conditions generates samples with large domains.
(a) Temperature dependence of the AC magnetization m’ for Ba subjected to HPT at liquid-nitrogen temperature, where the PHPT value was 21 GPa. The targeted high-pressure phase is the orthorhombic phase. (b) Hdc dependence of Tc at PHPT = 12, 15, 18, 21, and 24 GPa, along with that at PHPT = 6 GPa (inset of Fig. 1b).
XRD analysis, conducted through the reflection method, was performed on HPT-processed samples at cryogenic temperatures under PHPT = 12, 21, and 24 GPa. We found the coexistence of several orthorhombic, hcp, and bcc phases, as shown in Extended Data Figs. 6–8. The coexistence of these phases was also confirmed using thrubeam XRD, as shown in Extended Data Figs. 9–13. The results of the XRD analysis are summarized in Extended Data Tables 2–3. In HPT processing, many structures with the same crystal symmetry were generated, and different lattice parameters reflected the spatial distribution of the shear strain, as mentioned in detail in the Discussion and Methods sections. Anyway, metastabilization of the high-pressure phase via the residual strain is one of the striking character of the HPT processing. Also, the volume fractions of the high-pressure phases observed in the reflective XRD experiments (Extended Data Table 2) were higher than those detected through the thrubeam method (Extended Data Table 3). This discrepancy suggests that high-pressure phases are more likely to form near the material’s surface, highlighting a unique aspect of material manipulation via HPT processing. Additionally, the magnetic shielding signal was relatively small in the nanosized grain materials, primarily because the magnetic flux can be penetrated near the surface, thus making the Meissner signal to be weakened, even if the grain has superconducting properties. Therefore, the actual VSC can be evaluated to be more than the value via the magnetic measurements.
Phase diagram
Figure 3 summarizes the obtained results. As illustrated in Fig. 3a, a thermodynamic PHP-T phase diagram of Ba is presented, which includes the sequence of PHPT after the revolution processing. Figure 3b, c show the obtained Tc and VSC as a function of PHPT, respectively. It is important to note that the horizontal axis in Fig. 3b, c is PHPT not PHP, and the Tc measurements were performed at ambient pressure. From panel (b), we observe Tc values exceeding 10 K for PHPT values greater than 12 GPa, and Tc = 20–25 K at approximately 10 < PHPT < 20 GPa. In addition, from panel (c), the largest VSC occurs at PHPT = 6 GPa, which is consistent with the trend that HPT processing at high temperatures can generate larger grains compared to those at lower temperatures31,32,33,34, as mentioned above. We infer that the actual VSC for the sample processed using liquid-N2 temperature HPT at PHPT = 21 GPa would approach to that of the sample processed using room-temperature HPT at PHPT = 6 GPa.
(a) Schematic P-T phase diagram of Ba, where the blue and red squares specify the temperature and operating pressure PHPT during the HPT processing. After the HPT processing, the samples are returned to the room temperature and ambient pressure, which is represented as the arrows in (a). PHPT dependence of Tc (b), and volume fraction VSC and Hc (c). Notice that the horizontal axis in the panels (b) and (c) is not the hydrostatic pressure PHP, but the operating pressure PHPT during the HPT processing.
Proving superconductivity through electrical resistance measurement is challenging, as VSC is at most 1%. Additionally, the surface of Ba tends to oxidize slightly during HPT processing and preparation. Preparing electrodes on a room-temperature surface may release residual strain. Therefore, contactless magnetic measurements are more suitable for confirming superconductivity.
Ab initio calculation
To understand the basic properties of Ba, ab initio density functional calculations were performed with normal hydrostatic compressions. Figure 4a shows the enthalpies of the bcc and orthorhombic phases relative to the hcp phase as a function of PHP. The orthorhombic unit cell is equivalent to a double-hcp unit cell. For PHP < 4 GPa, the bcc phase (red dots) is stable; however, as the pressure increases to PHP > 4 GPa, the hcp phase becomes stable. At 18 < PHP < 31 GPa, the orthorhombic phase (blue triangles) becomes stable, whereas at PHP > 31 GPa, the hcp phase becomes stable again. This trend is the same as that reported in previous density functional calculations16. Figure 4b shows the pressure dependence of the calculated Tc based on the McMillan–Allen–Dynes formula35,36. Tc gradually increases with pressure and reaches 10–11 K at approximately PHP = 30 GPa, which is nearly consistent with the experimental results for Tc = 8 K at PHP = 30 GPa compressed at 10 K17. It is known from ab initio calculations that Tc decreases monotonically at pressures higher than PHP = 50 GPa37. Thus, the Tc maximum under normal hydrostatic compression is only of the order of 10 K, which is clearly smaller than the present Tc maximum (approximately 20–25 K) attained in HPT-processed Ba. The reason for this Tc difference remains unclear, and leaves a nontrivial and important issue. As long as we suppose Ba to be a phonon-based superconductor, we must consider that HPT processing works to strengthen the effective electron-lattice interactions.
(a) Structural stability of the bcc (red circles), hcp (green line), and orthorhombic (blue triangles) phases as a function of the hydrostatic pressure PHP, where we plot the enthalpy relative to the hcp phase. (b) PHP dependence of our calculated Tc, where Tc was calculated for the most stable phase at a given hydrostatic pressure.
Discussion
The structural optimization of ab initio density functional calculations provides the structural parameters as follows: bcc (Ba-I) with a = 5.0263(1) Å at PHP = 0 GPa, hcp (Ba-II) with a = 3.6394 (5) Å and c = 5.3921(1) Å at PHP = 15 GPa, and orthorhombic (Ba-VI) a = 5.8269(7) Å, b = 5.0866 (7) Å, and c = 3.3639(2) Å at PHP = 30 GPa. These lattice parameters are consistent with the experimental values under the corresponding PHP16,38. First, for the surface region of HPT-Ba under PHPT = 6 GPa at room temperature, it consists mainly of multiple bcc structures with Vatom corresponding to ≤ 6 GPa as seen in Extended Data Table 2: In bcc #1, strain is perfectly released, and in bcc #4, the strain corresponding to Vatom at PHP = 6 GPa remains. PHP’s for Vatom of bcc #2 and #3 are approximately PHP = 2 and 5 GPa, respectively. Furthermore, the hcp phases remain, which correspond to the crystal lattices at PHP = 7 (hcp #1) and 18 GPa (hcp #2). As shown in Fig. 4, the Tc = 3 K superconductivity of HPT-Ba at PHPT = 6 GPa is attributed to hcp #1 and #2. The inner region does not include bcc #4 or hcp #2, as shown in Extended Data Table 3.
Next, for the cryogenic temperature HPT-Ba, the sample surface is composed of ortho #2, corresponding to PHP > 20 GPa, and ortho #1 and ortho’ #1, corresponding to PHP = + 3 to −1 GPa, respectively. The inner region also exhibits a similar composition; however, an additional bcc #6 corresponding to PHP = 13 GPa exists, and approximately half of the specimen volume recovers bcc #1. The details of the residual phases for PHPT = 21 GPa are shown in Extended Data Fig. 14a. Referring to Fig. 4 and Extended Data Fig. 14a, the Tc > 10 K superconductivity is attributed to strained ortho #2; however, to explain Tc ~ 20 K, an additional factor is needed.
Conclusion
In summary, we successfully stabilized high-pressure Ba hcp and orthorhombic phases at ambient temperature and pressure using HPT processing. The high-pressure phases, hcp and orthorhombic, are more conductive to superconductivity compared to the original bcc phase. Hence, phase stabilization via HPT processing effectively endows Ba with new superconducting properties at ambient pressure. Though preset in small fractions, superconducting transitions as high as 24 K were observed in HPT-processed Ba at ambient pressure. Initially, HPT processing at room temperature led to the discovery of the Ba-II hcp phase with a Tc of ~ 3 K. Subsequent HPT processing at cryogenic temperatures using liquid nitrogen resulted in an increased volume fraction of the strained Ba-VI orthorhombic phase with a Tc of ~ 24 K, the highest Tc ever observed for single-element superconductors at the ambient pressure, except for pressured system. The relationship between the stain nature in the strained phase and the high Tc must be investigated more carefully and microscopically. Contrary to the traditional belief that shear strain negatively impacts the stabilization of the superconducting state by reducing grain size and crystallinity, our study proposes a novel method for developing high Tc superconductors, opening up significant opportunities for advancing electronic property-related functionalities. Ab initio calculations had suggested a Tc of approximately 10 K under normal hydrostatic compression, aligning with previous experimental studies. However, structural analysis of the HPT-processed samples revealed a coexistence of multiple strained phases, and the understanding the electronic states of these strained quasi-stable states is crucial for investigating the origin of the high Tc observed in HPT-processed Ba.
Methods
High pressure torsion
Processing through high-pressure torsion (HPT) causes severe plastic deformation, as shown in Extended Data Fig. 131,32,33,34. First, a disk sample was uniaxially compressed between opposite-faced anvils, which were made of WC (SR16C, NOTOALLOY Co., Ltd.), using a 50-ton press machine. The lower-side anvil was then rotated with respect to each other for N revolutions. During the revolution process, severe shear strain accumulates, and its magnitude increases in proportion to the distance from the disk center and the number of revolutions. In the early stage, the grain size was reduced, and subsequent recrystallization proceeded, resulting in a balance between these effects.
In this study, HPT was first conducted at room temperature for N = 10 turns under a pressure of PHPT = 6 GPa with a rotation speed of 1 rpm. In this room-temperature HPT process, Ba was easily oxidized and sealed in an Al-based Al-3%Mg-0.2%Sc (Al–Mg–Sc) alloy cell under an Ar atmosphere. A Ba disk (purity 99.9%, 7-mm-diameter, 0.6-mm-thickness) in the Al-alloy cell was then processed using an HPT machine.
The HPT process was also conducted using disks with dimensions of 5 mm in diameter and 1 mm in thickness so that it was possible to control the applied pressure up to a maximum of PHPT = 24 GPa. The HPT process was performed in liquid nitrogen, where liquid and gaseous nitrogen played a role in preventing the oxidation of the Ba disks instead of the Al-alloy cell. A thermocouple was inserted into the upper anvil at a position close to the sample39 such that the processing temperature was maintained at approximately 100 K during the HPT operation in liquid nitrogen40. The thickness after the HPT processing was reduced to 0.54 mm. We previously reported that the grain size after HPT processing under PHPT at 20 GPa was approximately 100 nm for pure Re21. In this experiment, the corresponding HPT processing was conducted at 100 K, resulting in the accumulation of intense strain and the formation of ultrafine grains whose size is much smaller than 100 nm.
Thus, HPT processing was conducted for the state represented by the closed boxes in Fig. 3a. After HPT, the samples were removed from the HPT apparatus via the route represented by the arrows and maintained at 77 K in a liquid nitrogen vessel. The samples were removed from the vessel immediately before the magnetic measurements and XRD experiments. For the magnetic measurements, the samples were placed under ambient pressure conditions, and the temperature was cooled to 1.8 K. XRD experiments were conducted under ambient pressure and room temperature on samples coated with paraffin oil to prevent oxidization.
After the HPT processing, a disk specimen with 4 mm diameter and 0.7 mm thickness and a fragment specimen with a volume < 0.1 × 0.1 × 0.1 mm3 were prepared from the outer-side part excluding the center part for magnetic measurements. The mass of Ba was estimated correctly, where the volume of Ba (maybe 0.3-mm-thickness) could be roughly evaluated. Thirteen specimens were prepared using HPT at both room temperature and approximately 100 K. A summary of these specimens is presented in Extended Table 1.
Magnetic measurements
The T dependence of the in-phase AC magnetization (m') was observed using a commercial superconducting quantum interference device (SQUID) magnetometer (Quantum Design Co. Ltd.) at an AC magnetic field of 3.86 Oe and 10 Hz under certain DC magnetic fields (Hdc). The AC magnetization is intrinsically different from the AC magnetic susceptibility via electromagnetic induction. The former detects the magnetization itself following the AC field, whereas the latter does the time derivative of the magnetization under the AC field.
Temperature dependence of the DC magnetization (M) was also observed at some Hdc's. It should be noted that the HPT-processed samples contained some residual strain even after releasing the stress subjected by HPT processing, whereas their magnetic measurements were performed under ambient pressure conditions. The shear strain increases proportionally to the radial distance from the center of the HPT-processed disks31,32,33,34, such that the broadening of the magnetic shielding signal originates from the wide distribution of the intensity of the residual strain.
X-ray diffraction
We performed reflection-type X-ray diffraction (XRD) at room temperature using SmartLab (Rigaku) para-focusing optics with Cu (Kα1 and Kα2) radiation. We also used thrubeam-type XRD analysis using synchrotron radiation with an X-ray energy of 60 keV at the beamline (BL04B1) of SPring-8 at the Japan Synchrotron Radiation Research Institute (JASRI), and 16 keV at the beamline (BL-8B) of the Photon Factory at the Institute of Materials Structure Science, High Energy Accelerator Research Organization. The observed diffraction peaks were deconvolved using the Voight function into those associated with each Ba phase by multipeak fitting. The lattice constants were calculated from the relationship between the lattice constants and the plane indices determined from the Bragg peak angles of the deconvoluted peaks. All the crystal structures were evaluated based on the assumption that the atomic positions did not change.
The reflection type mainly detects crystal structures at the surface area, whereas the thrubeam type detects the entire area across the thickness, including the surface. The XRD patterns of the samples subjected to HPT processing at cryogenic temperatures are shown in Extended Data Fig. 6–13, and the analytical results are presented in Extended Data Tables 2–3. The hydrostatic pressure PHP corresponding to the atomic volume Vatom was estimated using Extended Data Fig. 14, which was constructed from the XRD data reported in the literature at a hydrostatic pressure38.
Herein, we describe the crystal structure of HPT-processed Ba obtained using these two methods. First, we picked up important experimental facts in the reflection method (see Extended Data Table 2) for the Ba specimens subjected to room-temperature HPT at PHPT = 6 GPa, whose conditions are suitable for stabilizing the hcp phase called the Ba-II phase: (1) More than half of the sample volume is a bcc phase, and they have an atomic volume Vatom corresponding to PHP < PHPT. The smallest Vatom corresponds to PHP = 5.3 GPa. The maximum PHP = 5.3 GPa did not exceed PHPT 6 GPa. (2) Most of the bcc phases were bcc#1, corresponding to PHP = 0 GPa. (3) The hcp phase also existed with Vatom corresponding to PHP > PHPT = 6 GPa (i.e., 7 and 18 GPa), and their volume fractions were almost equal. Next, in the thrubeam method (see Extended Data Table 3), (1) More than two-thirds are the bcc phases, which have Vatom corresponding to PHP ≤ 2.5 GPa. (2) A single hcp phase with Vatom corresponding to PHP = 7 GPa was observed. Summarizing the difference between the two methods, the surface regions had more varied and compressed phases than those in the interior.
In HPT-processed Ba at cryogenic temperatures, the PHPT values varied from 12 to 24 GPa. These conditions are suitable for stabilizing the orthorhombic phase, which is called the Ba-VI phase. At first, we pick up important experimental facts in the reflection method (see Extended Data Table 2): (1) Approximately half of the sample volume belongs to bcc phases with Vatom corresponding to PHP ≤ 5.0 GPa. This feature was commonly observed in room-temperature HPT-Ba at PHPT = 6 GPa. The value of PHPT = 5 GPa is consistent with the upper threshold value of the PHP region for the Ba-I phase. This suggests that approximately half of the compressed Ba sample recovered the bcc state of the Ba-I phase during the stress release after HPT processing. The residual bcc states were not uniform, and some candidates corresponded to PHP = 0–5 GPa. (2) The hcp phase remained in the stress-release process after HPT processing. The hcp phase has Vatom corresponding to approximately PHP = 12 GPa, which is close to the threshold value of PHP between Ba-II (hcp) and Ba-VI (ortho). This phenomenon was commonly observed in samples with PHPT = 12, 21, and 24 GPa. (3) The two types of orthorhombic structures were stabilized after HPT processing. One is ortho #1 and #2, with the space group Pnma, which is the same as the structure of Ba-VI stabilized under hydrostatic pressure16,17. The other is ortho’ #1, with the space group of Cmcm, created by shear strain under severe compression at cryogenic temperatures. Thus, three states exist: ortho #1, ortho #2, and ortho’ # 1. Both ortho #1 and ortho’ #1 have Vatom corresponding to PHP ~ 0 GPa, and they cannot be created by typical hydrostatic compression. This is simply the effect of the shear stress under severe compression at cryogenic temperatures. In contrast, ortho #2 has Vatom corresponding to PHP = 22–26 GPa. Next, in the thrubeam method (see Extended Data Table 3), new phenomena appear compared to those observed in the reflection method: (1) new bcc states with Vatom corresponding to PHP ~ 13 GPa appear, and the volume fraction occupies approximately 10%. (2) At PHPT = 12, 15, and 18 GPa, the hcp phase only has a state with Vatom corresponding to PHP ~ 12 GPa, which is close to the threshold value of PHP between Ba-II (hcp) and Ba-VI (ortho). However, for larger PHPT conditions with PHPT = 21 and 24 GPa, there also appears the hcp state with Vatom corresponding to PHP = 14–16 GPa. (3) Three orthorhombic states were confirmed in the interior, and ortho #2 has Vatom corresponding to PHP = 19–24 GPa. The volume fraction of the ortho #2 phase in the interior is smaller than that on the surface.
Given the above experimental facts, we can imagine the appearance of quasi-stable states during the stress-release process after HPT.
Ab initio calculations
To analyze the structural stability of the bcc, hcp, and orthorhombic phases of Ba at a given external pressure, we performed ab initio density functional calculations for these systems using the QUANTUM ESPRESSO package41,42. We used the Perdew–Burke–Ernzerhof type43 for the exchange–correlation functional, and norm-conserving pseudopotentials were generated by the code ONCVPSP (Optimized Norm-Conserving Vanderbilt PSeudopotential)44 and obtained from PseudoDojo45. We used a 20 × 20 × 20 Monkhorst–Pack k-mesh for the Brillouin zone integration. The kinetic energy cutoff was set to 144 Ry for the wave functions and 576 Ry for the charge density. The Fermi energy was estimated by Gaussian smearing with a width of 0.136 eV46. The crystal structures were optimized with a total energy convergence better than 1 meV/atom. We verified that these conditions ensured a better convergence and enabled a quantitative comparison of the enthalpies of each phase. The phonon modes were calculated using the density-functional linear-response method47,48. The calculation conditions for the electron–phonon coupling are as follows: For the bcc, 14 × 14 × 14 k-mesh and 7 × 7 × 7 q-mesh are used for the electronic structure and phonon mode calculations, respectively. To ensure the convergence of the electron–phonon-coupling matrix elements, a large 28 × 28 × 28 k-mesh (kfit) was used with Gaussians of width 0.136 eV. For hcp, the sizes of the k-mesh, q-mesh, and kfit-mesh were 12 × 12 × 12, 6 × 6 × 6, and 24 × 24 × 24, respectively. For the orthorhombic phase, the k-mesh, q-mesh, and kfit-mesh values were 12 × 12 × 12, 4 × 4 × 4, and 24 × 24 × 24, respectively. The superconducting transition temperatures were estimated using the McMillan–Allen–Dynes formula35,36 with an effective Coulomb pseudopotential (μ* = 0.1). Electron–phonon coupling λ and characteristic frequency ωln were numerically evaluated using the frequency integral of the Eliashberg function. Density functional calculations prove that an orthorhombic structure based on Pnma can be ideal for realizing a high Tc superconducting state in Ba.
Data availability
Data supporting the findings of this study are available from the corresponding authors upon reasonable request.
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Acknowledgements
This study was supported by a Grant-in-Aid for Scientific Research, Grant No. 23H01126, from MEXT, Japan. The synchrotron radiation experiments were performed at BL04B1 of SPring-8 with the approval of the Japan Synchrotron Radiation Research Institute (JASRI) (Proposal Nos. 2022A1393 and 2022B1391) and BL-8B of the Photon Factory at the Institute of Materials Structure Science, High Energy Accelerator Research Organization (Proposal No. 2021G534).
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M. M., H. T. Y. T., and Z. H. performed the high-pressure torsion tests. M. M., T. T., Y. T., and Z. H. performed structural analyses. K. N. performed DFT calculations. M. M. wrote the manuscript, which was edited by K. N. and Z. H. All authors discussed the results and commented on the manuscript. M. M. and Z. H. supervised the study.
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Mito, M., Tsuji, H., Tajiri, T. et al. Superconductivity of barium with highest transition temperatures in metallic materials at ambient pressure. Sci Rep 14, 965 (2024). https://doi.org/10.1038/s41598-023-50940-5
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DOI: https://doi.org/10.1038/s41598-023-50940-5
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