Abstract
The lithium–palladium and lithium–palladium–hydrogen systems are investigated at high pressures at and above room temperature. Two novel lithium–palladium compounds are found below \({18.7}\,{\mathrm{GPa}}\). An ambient temperature phase is tentatively assigned as \(F{\bar{4}}3m\,\hbox {Li}_{17}\hbox {Pd}_{4}\), with \(a = 17.661(1)\) Å at 8.64 GPa, isostructural with \(\hbox {Li}_{17}\hbox {Sn}_{4}\). The other phase occurs at high-temperature and is \(I{\bar{4}}3m\, \hbox {Li}_{11}\hbox {Pd}_{2}\), \(a = 9.218(1)\) Å at 3.88 GPa and 200 \(^\circ {\mathrm{C}}\), similar to \(\hbox {Li}_{11}\hbox {Pt}_{2}\), which is also known at high pressure. The presence of hydrogen in the system results in an \(I{\bar{4}}3m\) structure with \(a = 8.856(1)\) Å at 9.74 GPa. This persists up to \({13.3}\,\mathrm{GPa}\), the highest pressure studied. Below \({2}\,{\mathrm{GPa}}\) an fcc phase with a large unit cell, \(a = 19.324(1)\) Å at 0.39 GPa, is also observed in the presence of hydrogen. On heating the hydrogen containing system at 4 GPa the \(I{\bar{4}}3m\) phases persists to the melting point of lithium. In both systems melting the lithium results in the loss of crystalline diffraction from palladium containing phases. This is attributed to dissolution of the palladium in the molten lithium, and on cooling the palladium remains dispersed.
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Introduction
Lithium and hydrogen are low Z elements which exhibit complex behaviors at high density, in part due to quantum mechanical effects arising from their low masses1,2. Both have maxima in their melting curves3,4,5 and exhibit complex low symmetry crystal structures, despite their apparent simplicity at low pressure6,7. High pressure metal hydrides have attracted considerable attention recently as various novel compounds have been found to form only at high-pressure8,9, some of which have record breaking high Tc superconductivity10,11.
The alkali metals have also been found to form novel intermetallics at high pressure12,13,14,15,16, with a number of high pressure lithides recently reported14,15,16. Alkali metals are more electropositive than many other metals, particularly the noble metals, and charge transfer from the alkali metal to the other component of the intermetallic plays a role in their stability14,17.
Various transition metal – lithium intermetallics are reported in the literature at ambient pressure. Typically, these are synthesized by heating the reactants considerably above the melting point of lithium (180 \(^\circ {\mathrm{C}}\) at ambient pressure), under an inert atmosphere with characterization performed on quenched products. These have attracted attention due to their potential application in energy storage materials as anode materials for lithium ion batteries18. Compared to current intercalation type compounds they offer potentially much higher lithium content and hence energy storage potential15,18, motivating the exploration of lithium-rich intermetallic compounds.
Palladium is a transition metal widely used in catalysis and hydrogen purification. The hydrogen affinity of palladium is very sensitive to pressure with palladium hydride, \(\hbox {PdH}_x\), forming below 1 bar. The hydrogen content increases from \(x=0.6\) at formation to \(x=1\) at a few GPa19. Further compression has not been observed to result in any higher hydride to \({100}\,{\mathrm{GPa}}\)20. A number of lithium palladium intermetallics have been reported at ambient pressure with stoichiometries of \(\hbox {LiPd}_{7}\), \(\hbox {LiPd}_{2}\), \(\hbox {LiPd}\), \(\hbox {Li}_{2}\hbox {Pd}\), \(\hbox {Li}_{3}\hbox {Pd}\), and \(\hbox {Li}_{15}\hbox {Pd}_{4}\)21. All of these were formed at high temperature and quenched to ambient.
Palladium lithium hydride, \(\hbox {PdLiH}_x\), \(0.7< x < 1\), is also known and has been calculated to exhibit superconductivity with the low mass lithium making a large contribution to the electron-phonon coupling22. Subsequent studies have synthesized it but not observed superconductivity. Various synthesis conditions have been used including sintering equimolar mixtures of LiH and Pd in a hydrogen atmosphere at 10 bar23, heating LiPd in \({270}\,{\mathrm{MPa}}\) of hydrogen gas24, and compressing a sealed mixture of LiH and Pd to \({3}\,{\mathrm{GPa}}\) and heating to \({773}\,{\mathrm{K}}\)25. These all yield P4/mmm \(\hbox {LiPdH}_x\) with x close to 1. Cooling to \({4}\,{\mathrm{K}}\) at ambient pressure23, or at \({270}\,{\mathrm{MPa}}\)24 did not result in superconductivity. Liu et al.25 measured resistivity as a function of temperature and pressure from 2 to \({300}\,{\mathrm{K}}\) up to \({25.2}\,{\mathrm{GPa}}\) and observe a minimum in the resistivity with pressure at \({18.3}\,{\mathrm{GPa}}\) but no superconductivity. They speculate that the discrepancy between theory and experiment may arise from scattering by impurities or hydrogen vacancies.
The application of pressure allows the exploration of exotic chemistry and materials synthesis which does not occur under ambient conditions. To date no study has considered the effect of pressure on the lithium–palladium system, or the lithium–rich lithium–palladium–hydrogen system, nor reported ambient temperature reaction of Pd and Li. Platinum, which lies directly below palladium in the periodic table and shares many properties with it, has been studied under pressure with lithium. It was found to form a \(\hbox {Li}_{11}\hbox {Pt}_{2}\) compound with space group \(I{\bar{4}}3m\) below \({11}\,{\mathrm{GPa}}\), above which it expels lithium to form P6/mmm \(\hbox {Li}_{2}\hbox {Pt}\)14.
Here we study the lithium–rich palladium–lithium and palladium–lithium–hydrogen systems at high pressure, at and above room temperature. All samples exhibited reactions in the cells as loaded, prior to further compression. The initial pressures varied from 0.4 to \({6}\,{\mathrm{GPa}}\). We observe two novel compounds which are isostructural with lithium compounds known in other systems. The presence of hydrogen changes the structure adopted by the compound showing it to play a role in the properties of the system. This also demonstrates that the hydrogen affinity of the compound formed is higher than that of pure lithium, which was present in excess in all samples.
Results
Lithium–palladium
In the absence of hydrogen the lithium and palladium had already reacted at after a few days at \({5.0}\,{\mathrm{GPa}}\), the lowest pressure measured. Figure 1 shows the pressure evolution of the integrated diffraction patterns collected with 0.4246 Å radiation. These indicate no phase transitions below \({18.7}\,{\mathrm{GPa}}\) at ambient temperature. The observed peaks cannot be fitted to any known palladium–lithium or platinum–lithium intermetallic. A weak peak at \(2\theta =2.26^\circ\), corresponding to \(d = 10.77\) Å, at \({6.30}\,{\mathrm{GPa}}\) indicates a large unit cell.
Figure 2 shows a LeBail fit26 to an \(F{\bar{4}}3m\) structure with \(a = 17.661(1)\) Åat \({8.64}\,{\mathrm{GPa}}\). This is similar to known \(\hbox {Li}_{17}\hbox {M}_{4}\) structures with M = Ge, Sn, Pb, which have \(F{\bar{4}}3m\) symmetry and ambient pressure lattice parameters of 18.756, 19.690, and 19.842 Å respectively27. Close inspection of the LeBail fit reveals a few peaks which are not well fitted, particularly in the region of 8.5 to 10.5 degrees. The lithium–palladium system is known to form numerous intermetallics at ambient pressure and some of these peaks may be due to other low-concentration phases. We do note that a slight tetragonal distortion of the unit cell with \(a = 17.656\) Å and \(c = 17.869\) Å results in a much improved fit, see Fig. 3, but the symmetry lowering also results in many allowed reflections so this could be pathological. A similarly improved fit, but with even more possible peaks, may be obtained by a monoclinic distortion. The \(F{\bar{4}}3m\) \(\hbox {Li}_{17}\hbox {M}_{4}\) type structure is the best fit we can obtain to the high-pressure lithium palladium compound, and we tentatively suggest that the structure is this, or closely related to it.
The \(\hbox {Li}_{17}\hbox {M}_{4}\) structure has \(Z = 20\) for a total of 420 atoms per unit cell. This extremely complex structure was previously determined via single crystal X-ray diffraction27. Powder X-ray diffraction in DACs suffers from limited angular range imposed by the geometry of the cell, and limited resolution causing higher angle peaks to overlap. Along with the potential for contaminant peaks this makes a full Rietveld refinement impractical, however a powder X-ray diffraction pattern of the proposed structure can be simulated. Figure 4 compares the observed data with a simulated pattern produced using the literature atomic parameters for \(\hbox {Li}_{17}\hbox {Sn}_{4}\)27, but with Sn exchanged for Pd and the lattice parameter set to match that LeBail fitted to the observed data. The patterns are quite similar which supports the \(F{\bar{4}}3m\) \(\hbox {Li}_{17}\hbox {Pd}_{4}\) structural candidate for the novel palladium lithide.
On heating at \({4}\,{\mathrm{GPa}}\) the appearance of the pattern changes with new peaks appearing at 200 \(^\circ\)C, see Fig. 5. This pattern can be fitted as a mixture of the ambient temperature \(F{\bar{4}}3m\) phase and a bcc phase with \(a = 9.218(1)\) Å at \({3.88}\,{\mathrm{GPa}}\). This is compatible with \(I{\bar{4}}3m\) symmetry and consideration of the density suggests it is \(\hbox {Li}_{11}\hbox {Pd}_{2}\), isostructural with \(\hbox {Li}_{11}\hbox {Pt}_{2}\) observed in the high pressure lithium–platinum system14. This phase has a \(\gamma\)-brass structure and has been observed in other palladium-group intermetallics28,29.
Further heating to 225 \(^\circ\)C melts the lithium and leads to the loss of all crystalline diffraction from palladium. We attribute this to dissolution of the palladium into the large excess of lithium. On cooling, peaks from bcc-lithium reappear, however, those from the palladium intermetallic do not, nor do any new peaks appear. The most likely explanation for the loss of diffraction from the palladium is that it is incorporated into the large excess of bcc lithium. Further compression causes the bcc to fcc transition in lithium near \({7.5}\,{\mathrm{GPa}}\), as expected30, but no peaks other than those of fcc-lithium emerge implying that the palladium remains dispersed.
Lithium–palladium–hydrogen
The presence of hydrogen in cells loaded with palladium, lithium and lithium hydride stabilized different phases under pressure, with a transition occuring between 1 and \({2}\,{\mathrm{GPa}}\), see Fig. 6. Above the transition a single phase is observed. This is well fitted by a bcc structure with and \(a = 8.856(1)\) Å at \({9.74}\,{\mathrm{GPa}}\), compatible with \(I{\bar{4}}3m\) symmetry, similar to the \(\hbox {Li}_{11}\hbox {Pd}_{2}\) phase observed at high-temperature in the lithium–palladium system. An integrated pattern and LeBail fit are shown in Fig. 7. Below \({2}\,{\mathrm{GPa}}\) a second set of peaks are observed, see Fig. 6, which are fitted by an fcc phase with a large unit cell of \(a = 19.324(1)\) Å at \({0.39}\,{\mathrm{GPa}}\). A LeBail fit is shown in Fig. 8. The stoichiometry of the compounds cannot be determined, though hydrogen must be present to cause the structural differences from the lithium–palladium system. Figure 9 shows the similarity between observed diffraction pattern of the bcc phase and simulated powder data based on the structure of \(I{\bar{4}}3m\) \(\hbox {Li}_{11}\hbox {Pt}_{2}\)14.
Between \({0.4}\,{\mathrm{GPa}}\), the lowest pressure the palladium, lithium and lithium hydride system was studied at, and \({1}\,{\mathrm{GPa}}\) an additional fcc phase with a large unit cell is present, see fit in Fig. 8. This is similar to the \(F{\bar{4}}3m\) \(\hbox {Li}_{17}\hbox {Pd}_{4}\) phase proposed for the lithium–palladium system, and may be a related structure. The peaks from this phase are weak by \({1}\,{\mathrm{GPa}}\) and absent at \({2}\,{\mathrm{GPa}}\).
On heating at \({4}\,{\mathrm{GPa}}\), the hydride containing sample showed no phase changes below the melting point of lithium. On melting the lithium, the palladium dissolves, as for the lithium–palladium system, and remains dispersed on cooling.
Discussion
Without hydrogen the lithium–palladium system forms an ambient temperature structure we tentatively assign to be of \(F{\bar{4}}3m\) symmetry and isostructural with \(\hbox {Li}_{17}\hbox {Sn}_{4}\). Interpretation of the powder pattern, Fig. 2, is hindered by the possibility of additional phases or small distortions of the unit cell. Comparison to a simulated pattern for \(\hbox {Li}_{17}\hbox {Pd}_{4}\), Fig. 4, suggests the observed structure is the same, or closely related. This structure has not been observed in any other transition metal - alkali metal intermetallic, however it is observed in the lithides of silicon, germanium, tin and lead27,31 with slightly varying stoichiometry.
Volumetric considerations give further support for the structures of both \(\hbox {Li}_{17}\hbox {Pd}_{4}\) and \(\hbox {Li}_{11}\hbox {Pd}_{2}\) assigned from comparison of the diffraction data to other known lithides. Figure 10 shows pressure-volume data collected on compression for both phases, complete with fitted equations of state of the Vinet form:
Where \(B_0\) and \(V_0\) are the zero-pressure bulk modulus and volume, V is the volume at pressure P, and \(B_0'\) is the pressure derivative of the bulk modulus. The fitted equation of state parameters are given in Table 1. Both compounds exhibit intermediate compressibility between those of lithium, which is highly compressible30,32, and palladium, which has low compressibility20.
Figure 10 also shows the pressure-volume curves for the pure elements at the proposed stoichiometries. In both cases the compounds are denser, with the difference decreasing at higher pressure. Table 2 gives the ratio of the volume of palladium–lithium intermetallics to their elemental constituents and shows the increased density of the intermetallics in this study to be within the range of expected values. In the solid phase the pressure-volume curve of a compound is expected to lie close to that of its constituents of enthalpic grounds. Excess volume will have an increasingly punitive PV term in its free energy, while overly reduced volume would lead to unphysical densities.
In the presence of hydrogen two phases are observed. At low pressure an fcc phase with a large unit cell (\(a = 19.324\) Å at \({0.39}\,{\mathrm{GPa}}\)) coexists with a phase which appears similar to the \(I{\bar{4}}3m\) \(\hbox {Li}_{11}\hbox {M}_{2}\) phase observed in the lithium–platinum system14 and lithium–palladium at high-pressure and high-temperature. Above 1 GPa the fcc phase is lost and only the \(I{\bar{4}}3m\) phase remains. The volume of the low pressure fcc phase observed in the hydride containing system lies off the curve of the \(\hbox {Li}_{17}\hbox {Pd}_{4}\) produced without hydrogen present and both cannot be fitted to a single equation of state. This could arise from hydrogen absorbed into the lattice, or may indicate they have different structures.
Both lithium and hydrogen are low Z and so scatter X-rays very weakly compared to palladium. Therefore, we would not expect to be able to resolve partial replacement of lithium by hydrogen, or additional hydrogen incorporated into the lattice, except on volumetric grounds. This makes the stoichiometries of the phases formed in the palladum–lithium–hydrogen samples impossible to determine, and non-stoichiometric phases cannot be ruled out. Examination of the patterns and comparison to the high temperature lithium–palladium system, and to the literature on the lithium–platinum system, strongly supports the structure being an analog to the \(I{\bar{4}}3m\) \(\hbox {Li}_{11}\hbox {M}_{2}\) (M = Pt, Pd) \(\gamma\)-brass structure. The high-temperature \(I{\bar{4}}3m\) \(\hbox {Li}_{11}\hbox {Pd}_{2}\) phase which forms in the absence of hydrogen has similar volume to the hydrogen bearing \(I{\bar{4}}3m\) phase, see Fig. 10. This limits the quantity of additional hydrogen which can be present and suggests that the structural differences are caused either by substitution of lithium with hydrogen, or very dilute hydrogen present in the lattice. The inclusion of trace impurities has previously been suggested to change the structure of LiPd at ambient pressure21. Inspection of the pressure-volume data of the hydrogen containing \(I{\bar{4}}3m\) structure shows a slight discontinuity at \({8}\,{\mathrm{GPa}}\), this is likely due to small compositional changes such as the incorporation of additional hydrogen, as the diffraction patterns above and below this appear similar.
A \(\hbox {Li}_{15}\hbox {Pd}_{4}\) palladium–lithium intermetallic with \(I{\bar{4}}3d\) symmetry has been reported at ambient pressure21 with \(a = 10.676\) Å. This is not compatible with any diffraction pattens observed in this study. The high-temperature \(\hbox {Li}_{11}\hbox {Pd}_{2}\) and related hydrogen containing \(I{\bar{4}}3m\) phase both have several peaks which are incompatible with the \(I{\bar{4}}3d\) space group. Van Vucht and Buschow21 observed an unknown F-centered cubic lithium–palladium intermetallic with a = 19.009 Å at 10 to 16 at% Pd. While they did not observe satisfactory agreement with the \(\hbox {Li}_{17}\hbox {Pb}_{4}\) structure (wrongly assigned as the \(\hbox {Li}_{22}\hbox {Pb}_{5}\) structure at the time of their publication27) it is possible their fcc phase is the same as, or related to, the one we observe here at higher pressure.
The study of transition metal hydrides and lithides is of interest to various fields including hydrogen storage33, battery technology18,34 and superconductivity22. The phases reported here present a test for theory at high pressure, particularly given the large body of work which exists on the binary hydrides of lithium and palladium19,20,33,35. The reactivity of lithium, lithium hydride and palladium is also relevant to hydrogen storage as both lithium and palladium have proposed applications in the hydrogen economy33,36.
In conclusion, we investigated the palladium–lithium and palladium–lithium–hydrogen systems to 18.7 and \({13.3}\,{\mathrm{GPa}}\) respectively. The palladium–lithium system reveals a single intermetallic at ambient temperature which we tentatively assign to an \(F{\bar{4}}3m\) \(\hbox {Li}_{17}\hbox {M}_{4}\) type structure, possibly with a small distortion. At 200 \(^\circ\)C at \({3.87}\,{\mathrm{GPa}}\) this partially converts to an \(I{\bar{4}}3m\) \(\hbox {Li}_{11}\hbox {Pd}_{2}\) structure analogous to \(\hbox {Li}_{11}\hbox {Pt}_{2}\) in the dense lithium–platinum system. The palladium–lithium–hydrogen system forms an \(I{\bar{4}}3m\) structure similar to \(\hbox {Li}_{11}\hbox {Pd}_{2}\) at all pressures and temperatures studied. Below \({2}\,{\mathrm{GPa}}\) we also observe an fcc phase with a large unit cell in this system. Due to the weak scattering from hydrogen and lithium it is not possible to determine the stoichiometries, though volumetric considerations disallow high concentrations of additional hydrogen in the \(I{\bar{4}}3m\) phase. On heating to the melting point of lithium, diffraction from the palladium compounds disappears in both systems and does not reappear on cooling. This is attributed to the palladium forming a dilute solid solution in the large excess of lithium metal.
Methods
Diamond anvil cells (DACs) were prepared with rhenium gaskets on Boehler-Almax type diamond anvils with culet sizes ranging from 250 to \({400}\,{\upmu {\mathrm{m}}}\). Pressure was determined to an uncertainty of \({0.1}\,{\mathrm{GPa}}\) via the temperature adjusted equation of state37 of a small quantity of tungsten powder (Alfa Aesar, 99.9%) added to each loading. Tungsten was chosen as it is known not to react with lithium4,30, and does not form hydrides below 25 GPa9. Powdered palladium (Alfa Aesar, 99.95%) was added to each cell such that the lithium would be in large excess. Lithium metal (Alfa Aesar, 99.9%) and, for hydrogen containing cells lithium hydride (Alfa Aesar, 99.4%), were loaded under a high purity argon atmosphere. Hydrogen was introduced as lithium hydride because lithium metal fully reacts with hydrogen gas at pressures below \({50}\,{\mathrm{MPa}}\)35 making gas loading an unnecessary complication. The maximum pressure was \({18.7}\,{\mathrm{GPa}}\) to avoid damage to the diamond anvils by lithium at higher pressure3,30,32. There was no evidence of reactions involving the tungsten pressure marker, diamond anvils or rhenium gasket in any cell, nor was there any observable reaction between the lithium and lithium hydride.
Angular dispersive powder X-ray diffraction measurements were carried out at APS beamline 16-ID-B (HPCAT) using 0.4246 Å radiation. Full diffraction maps were taken by rastering the samples with \({5}\,{\upmu }{\mathrm{m}}\) steps taking a diffraction pattern at each location to ensure purity of the loadings. The load on the cells was controlled using a gas membrane with patterns collected on a Dectris Pilatus 1M large area detector with a sample to detector distance of \({200}\,{\mathrm{mm}}\) and \({172}\,{\upmu }{\mathrm{m}}\) pixels. Resistive heating was performed under vacuum with Kapton X-ray windows using the HPCAT resistive heating setup38. Temperature was determined with uncertainty of ± 3 \(^\circ\)C using two type K thermocouples in contact with the cell. Ambient temperature runs were performed in air without the Kapton windows.
Diffraction patterns were integrated using the dioptas software package39. The integrated patterns were further analyzed using jana0640 and powdercell41. LeBail fits determine the unit cell parameters based on the angles of the powder diffraction peaks and can give information on the space group based on systematic absences26, but do not offer details on the location of atoms within the cell. LeBail fits were performed as the complex structures of the intermetallics formed, and limited q-range and resolution possible in diamond anvil cells, made Rietveld fits unstable. Strain and preferred orientation also cannot be ruled out, particularly as the compounds were formed in situ under pressure.
Data availability
The datasets used and/or analysed during the current study available from the corresponding author on reasonable request.
References
Neaton, J. & Ashcroft, N. Pairing in dense lithium. Nature 400, 141–144 (1999).
Bonev, S. A., Schwegler, E., Ogitsu, T. & Galli, G. A quantum fluid of metallic hydrogen suggested by first-principles calculations. Nature 431, 669–672 (2004).
Schaeffer, A. M. J., Talmadge, W. B., Temple, S. R. & Deemyad, S. High pressure melting of lithium. Phys. Rev. Lett. 109, 185702 (2012).
Frost, M. et al. High-pressure melt curve and phase diagram of lithium. Phys. Rev. Lett. 123, 065701 (2019).
Howie, R. T., Dalladay-Simpson, P. & Gregoryanz, E. Raman spectroscopy of hot hydrogen above 200 GPa. Nat. Mater. 14, 495–499 (2015).
Guillaume, C. L. et al. Cold melting and solid structures of dense lithium. Nat. Phys. 7, 211–214 (2011).
Loubeyre, P., Occelli, F. & Dumas, P. Synchrotron infrared spectroscopic evidence of the probable transition to metal hydrogen. Nature 577, 631–635 (2020).
Matsuoka, T. et al. Beryllium polyhydride \(\text{ Be}_{4}\text{ H}_{8}(\text{ H}_{2})_{2}\) synthesized at high pressure and temperature. Phys. Rev. Mater. 4, 125402 (2020).
Scheler, T. et al. Nanocrystalline tungsten hydrides at high pressures. Phys. Rev. B 87, 184117 (2013).
Drozdov, A. et al. Superconductivity at 250 K in lanthanum hydride under high pressures. Nature 569, 528–531 (2019).
Drozdov, A., Eremets, M., Troyan, I., Ksenofontov, V. & Shylin, S. I. Conventional superconductivity at 203 Kelvin at high pressures in the sulfur hydride system. Nature 525, 73–76 (2015).
Du, X., Lou, H., Wang, J. & Yang, G. Pressure-induced Na–Au compounds with novel structural units and unique charge transfer. Phys. Chem. Chem. Phys. 23, 6455–6461 (2021).
Frost, M., McBride, E. E., Schörner, M., Redmer, R. & Glenzer, S. H. Sodium–potassium system at high pressure. Phys. Rev. B 101, 224108 (2020).
Binns, J. et al. Reactivity of lithium and platinum at elevated densities. Phys. Rev. B 99, 220101 (2019).
Dalladay-Simpson, P. et al. Structures of lithium–zinc compounds at high pressures. J. Chem. Phys. 149, 024306 (2018).
Botana, J. & Miao, M.-S. Pressure-stabilized lithium caesides with caesium anions beyond the \(-1\) state. Nat. Commun. 5, 1–8 (2014).
Spicer, W., Sommer, A. & White, J. Studies of the semiconducting properties of the compound CSAU. Phys. Rev. 115, 57 (1959).
Obrovac, M. & Chevrier, V. Alloy negative electrodes for Li-ion batteries. Chem. Rev. 114, 11444–11502 (2014).
Manchester, F., San-Martin, A. & Pitre, J. The H–Pd (hydrogen–palladium) system. J. Phase Equilib. 15, 62–83 (1994).
Guigue, B., Geneste, G., Leridon, B. & Loubeyre, P. An X-ray study of palladium hydrides up to 100 GPa: Synthesis and isotopic effects. J. Appl. Phys. 127, 075901 (2020).
Van Vucht, J. & Buschow, K. Note on the occurrence of intermetallic compounds in the lithium–palladium system. J. Less Common Metals 48, 345–347 (1976).
Singh, D., Cohen, R. & Papaconstantopoulos, D. Possiblity of LiPdH\(_{{\rm x}}\) as a new ionic superconductor. Phys. Rev. B 41, 861 (1990).
Noréus, D. & Rapp, Ö. Absence of superconductivity above 4 K in LiPdH\(_{{\rm x}}\). Phys. Rev. B 42, 10730 (1990).
Schirber, J., Overmyer, D., Baughman, R. & Morosin, B. Search for high temperature superconductivity in LiPdH\(_{{\rm x}}\). Phys. C Supercond. 172, 465–466 (1991).
Liu, W. et al. Absence of superconductivity in LiPdH\(_{{\rm x}}\). Philos. Mag. 98, 623–631 (2018).
Le Bail, A. Whole powder pattern decomposition methods and applications: A retrospection. Powder Diffract. 20, 316–326 (2005).
Goward, G., Taylor, N., Souza, D. & Nazar, L. The true crystal structure of Li\(_17\)M\(_4\) (M = Ge, Sn, Pb)-revised from Li\(_22\)M\(_5\). J. Alloys Compd. 329, 82–91 (2001).
Gourdon, O. & Miller, G. J. Intergrowth compounds in the Zn–rich Zn–Pd system: Toward 1D quasicrystal approximants. Chem. Mater. 18, 1848–1856 (2006).
Harbrecht, B., Thimmaiah, S., Armbrüster, M., Pietzonka, C. & Lee, S. Structure and properties of \(\gamma\)-brass-type Pt\(_2\)Zn\(_11\)-\(\delta (0.2 < \delta < 0.3)\). Zeitschrift für anorganische und allgemeine Chemie 628, 2744–2749 (2002).
Frost, M., Levitan, A. L., Sun, P. & Glenzer, S. Equation of state and electron localisation in fcc lithium. J. Appl. Phys. 123, 065901 (2018).
Zeilinger, M., Benson, D., Haussermann, U. & Fässler, T. F. Single crystal growth and thermodynamic stability of Li\(_17\)Si\(_4\). Chem. Mater. 25, 1960–1967 (2013).
Hanfland, M., Loa, I., Syassen, K., Schwarz, U. & Takemura, K. Equation of state of lithium to 21 GPa. Solid State Commun. 112, 123–127 (1999).
Banger, S., Nayak, V. & Verma, U. Hydrogen storage in lithium hydride: A theoretical approach. J. Phys. Chem. Solids 115, 6–17 (2018).
Sun, K. & Peng, Z. Intermetallic interphases in lithium metal and lithium ion batteries. InfoMat 3, 1083–1109 (2021).
Howie, R. T., Narygina, O., Guillaume, C. L., Evans, S. & Gregoryanz, E. High-pressure synthesis of lithium hydride. Phys. Rev. B 86, 064108 (2012).
Schneemann, A. et al. Nanostructured metal hydrides for hydrogen storage. Chem. Rev. 118, 10775–10839 (2018).
Litasov, K. D. et al. Thermal equation of state to 33.5 GPa and 1673 K and thermodynamic properties of tungsten. J. Appl. Phys. 113, 133505 (2013).
Sinogeikin, S. V. et al. Online remote control systems for static and dynamic compression and decompression using diamond anvil cells. Rev. Sci. Instrum. 86, 072209 (2015).
Prescher, C. & Prakapenka, V. B. Dioptas: A program for reduction of two-dimensional X-ray diffraction data and data exploration. High Pressure Res. 35, 223–230 (2015).
Petříček, V., Dušek, M. & Palatinus, L. Crystallographic computing system JANA2006: General features. Zeitschrift für Kristallographie-Crystalline Materials 229, 345–352 (2014).
Kraus, W. & Nolze, G. Powder cell-a program for the representation and manipulation of crystal structures and calculation of the resulting X-ray powder patterns. J. Appl. Crystallogr. 29, 301–303 (1996).
Acknowledgements
The authors would like to thank Eric Rod and Curtis Kenney-Benson. This work was supported by U.S. Department of Energy (DOE) Office of Fusion Energy Sciences funding No. FWP100182. This work was supported by the Department of Energy, Laboratory Directed Research and Development program at SLAC National Accelerator Laboratory, under contract DE-AC02-76SF00515 and as part of the Panofsky Fellowship awarded to E.E.M. Equipment support from Stanford Synchrotron Radiation Light source (SSRL) is acknowledged under DOE Office of Basic Energy Sciences under Contract No. DE-AC02-76SF00515. X-ray diffraction was performed at HPCAT (Sector 16), Advanced Photon Source (APS), Argonne National Laboratory. HPCAT operations are supported by DOE-NNSA’s Office of Experimental Sciences. The Advanced Photon Source is a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357.
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M.F. and S.H.G. conceived the experiment, M.F. and E.E.M. conducted the experiments, J.S. tested and modified equipment and M.F. analysed the results and wrote the manuscript. All authors reviewed the manuscript.
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Frost, M., McBride, E.E., Smith, J.S. et al. The high-pressure lithium–palladium and lithium–palladium–hydrogen systems. Sci Rep 12, 12341 (2022). https://doi.org/10.1038/s41598-022-16694-2
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DOI: https://doi.org/10.1038/s41598-022-16694-2
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