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  1. The D" discontinuity, observed at 100-400 km above the core-mantle boundary (CMB), has been commonly attributed to the phase transition from bridgmanite to post-perovskite (ppv). However, the reported transition pressures and thicknesses of the ppv transition in pyrolitic compositions (e.g., Murakami et al., 2005; Ohta et al., 2008; Grocholski et al., 2012) have been inconsistent. Given that subducting slabs may deliver water to the deep lower mantle, it is important to understand the effect of water on the properties of the ppv transition. We conducted experiments on the ppv transition in hydrous pyrolitic compositions using a laser-heated diamond anvil cell (LHDAC) at pressures up to 140 GPa and temperatures up to 2500 K. Between 90 and 140 GPa, we conducted 16 separate LHDAC runs on unheated starting materials. At 2000-2200 K, bridgmanite is stable up to 110 GPa; bridgmanite and post-perovskite exist together between 114-116 GPa; and only post-perovskite was observed above 117 GPa. We found that adding 1-2 wt% H2O to a pyrolitic composition lowers the transition pressure by 20-25 GPa and narrows the boundary thickness to 3-6 GPa (50-100 km in depth). These results show that water not only reduces the transition pressure but also sharpens the transition, potentially resolving discrepancies among previous experimental studies. The potential presence of water in the starting materials of some previous studies may explain the discrepancies. Our results on the ppv boundary are consistent with the sharp D" discontinuity (<30 km thick) reported in regions with subducted slabs and with global variations in D" discontinuity sharpness observed in seismic studies. We propose that water plays a key role in controlling the depth and thickness of the ppv transition and should be considered when interpreting the D" discontinuity in the lowermost mantle. 
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    Free, publicly-accessible full text available December 16, 2026
  2. Free, publicly-accessible full text available May 1, 2027
  3. Abstract Phase transitions in the mantle control its internal dynamics and structure. The post-spinel transition marks the upper–lower mantle boundary, where ringwoodite dissociates into bridgmanite plus ferropericlase, and its Clapeyron slope regulates mantle flow across it. This interaction has previously been assumed to have no lateral spatial variations, based on the assumption of a linear post-spinel boundary in pressure and temperature. Here we present laser-heated diamond anvil cell experiments with synchrotron X-ray diffraction to better constrain this boundary, especially at higher temperatures. Combining our data with results from the literature, and using a global analysis based on machine learning, we find a pronounced nonlinearity in the post-spinel boundary, with its slope ranging from –4 MPa/K at 2100 K, to –2 MPa/K at 1950 K, and to 0 MPa/K at 1600 K. Changes in temperature over time and space can therefore cause the post-spinel transition to have variable effects on mantle convection and the movement of subducting slabs and upwelling plumes. 
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    Free, publicly-accessible full text available December 1, 2026
  4. Abstract The influence of Al substitution on the elastic properties of stishovite and its transition to post-stishovite is of great importance for interpreting the seismic wave velocities of subducted mid-ocean ridge basalt (MORB) within the mantle transition zone and the lower mantle. However, atomistic mechanisms of Al substitution effects on the transition and its associated elasticity remain debated. Here synchrotron single-crystal X-ray diffraction measurements have been performed at room temperature on Al1.3-SiO2 (1.3 mol% Al in the chemical formula of Si0.965(3)Al0.041(1)O2H0.017(4)) and Al2.1-SiO2 (2.1 mol% Al in Si0.948(2)Al0.064(1)O2H 0.018(3)) crystals in diamond anvil cells with Boehler-Almax designed anvils up to 38.0 GPa and 28.5 GPa, respectively. Refinements of the diffraction patterns show that a transformation from stishovite (space group P42/mnm; No. 136) to CaCl2-typed post-stishovite (space group Pnnm; No. 58) is accompanied by splitting of O coordinates. The Al substitution in stishovite results in a faster decrease in the O coordinate, softer apical (Si,Al)-O bonds, and a softer and less distorted (Si,Al)O6 octahedron under compression. This leads to reduced adiabatic bulk modulus (KS), shear modulus (G), shear wave velocity (VS), and compressional wave velocity (VP) in the stishovite phase, explaining seismic wave perturbations in the mantle transition zone. Together with Raman data, Landau theory modeling shows that Al substitution increases the order parameter and excess free energy, stabilizing the post-stishovite phase at lower pressures. Correlation between elasticity and octahedral distortion index (D) reveals that at certain D, the Al substitution reduces KS, G, VS, and VP of the stishovite phase while increasing G, VS, and VP of the post-stishovite phase. Importantly, the maximum shear reduction is slightly enhanced at D = 0.00620(9) at the transition point. Our results help explain the seismically observed small-scale VS anomalies beneath subduction regions in the shallow lower mantle where Al,H-bearing stishovite undergoes the post-stishovite transition. 
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  5. Free, publicly-accessible full text available December 1, 2026
  6. Abstract Understanding how microscopic structural domains govern macroscopic electronic properties is central to advancing hydride superconductors, yet such correlations remain poorly resolved under pressure. We report the synthesis and characterization of (La0.9Y0.1)H10superhydrides exhibiting coexisting cubic$${Fm}\bar{3}m$$ Fm 3¯ m and hexagonal$$P{6}_{3}/{mmc}$$ P 63 /mmc clathrate phases observed over the pressure range from 168 GPa down to 136 GPa. Using synchrotron-based X-ray diffraction imaging at the upgraded Advanced Photon Source, we spatially resolved μm-scale distributions of these phases, revealing structural inhomogeneity across the sample. Four-probe resistance measurements confirmed superconductivity with two distinct transitions: an onset at 244 K associated with the cubic phase and a second near 220 K linked to the hexagonal phase. Notably, resistance profiles collected from multiple current and voltage permutations showed variations in transition width and onset temperature that correlated with the spatial phase distribution. These findings demonstrate a direct connection between local structural domains and superconducting behavior. 
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    Free, publicly-accessible full text available December 1, 2026
  7. Abstract Carbon and nitrogen are considered as candidate light elements present in planetary cores. However, there is limited understanding regarding the structure and physical properties of Fe‐C‐N alloys under extreme conditions. Here diamond anvil cell experiments were conducted, revealing the stability of hexagonal‐structured Fe7(N0.75C0.25)3up to 120 GPa and 2100 K, without undergoing any structural transformation or dissociation. Notably, the thermal expansion coefficient and Grüneisen parameter of the alloy exhibit a collapse at 55–70 GPa. First‐principles calculations suggest that such anomaly is associated with the spin transition of iron within Fe7(N0.75C0.25)3. Our modeling indicates that the presence of ∼1.0 wt% carbon and nitrogen in liquid iron contributes to 9–12% of the density deficit of the Earth's outer core. The thermoelastic anomaly of the Fe‐C‐N alloy across the spin transition is likely to affect the density and seismic velocity profiles of (C,N)‐rich planetary cores, thereby influencing the dynamics of such cores. 
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  8. Abstract Davemaoite (CaSiO3 perovskite) is considered the third most abundant phase in the pyrolytic lower mantle and the second most abundant phase in the subducted mid-ocean ridge basalt (MORB). During the partial melting of the pyrolytic upper mantle, incompatible titanium (Ti) becomes enriched in the basaltic magma, forming Ti-rich MORB. Davemaoite is considered an important Ti-bearing mineral in subducted slabs by forming a Ca(Si,Ti)O3 solid solution. However, the crystal structure and compressibility of Ca(Si,Ti)O3 perovskite solid solution at relevant pressure and temperature conditions had not been systematically investigated. In this study, we investigated the structure and equations of state of Ca(Si0.83Ti0.17)O3 and Ca(Si0.75Ti0.25)O3 perovskites at room temperature up to 82 and 64 GPa, respectively, by synchrotron X-ray diffraction (XRD). We found that both Ca(Si0.83Ti0.17)O3 and Ca(Si0.75Ti0.25)O3 perovskites have a tetragonal structure up to the maximum pressures investigated. Based on the observed data and compared to pure CaSiO3 davemaoite, both Ca(Si0.83Ti0.17)O3 and Ca(Si0.75Ti0.25)O3 perovskites are expected to be less dense up to the core-mantle boundary (CMB), and specifically ~1–2% less dense than CaSiO3 davemaoite in the pressure range of the transition zone (15–25 GPa). Our results suggest that the presence of Ti-bearing davemaoite phases may result in a reduction in the average density of the subducting slabs, which in turn promotes their stagnation in the lower mantle. The presence of low-density Ti-bearing davemaoite phases and subduction of MORB in the lower mantle may also explain the seismic heterogeneity in the lower mantle, such as large low shear velocity provinces (LLSVPs). 
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  9. Abstract Germanates are often used as structural analogs of planetary silicates. We have explored the high-pressure phase relations in Mg2GeO4 using diamond-anvil cell experiments combined with synchrotron X-ray diffraction and computations based on density functional theory. Upon room temperature compression, forsterite-type Mg2GeO4 remains stable up to 30 GPa. At higher pressures, a phase transition to a forsterite-III type (Cmc21) structure was observed, which remained stable to the peak pressure of 105 GPa. Using a third-order Birch Murnaghan fit to the experimental data, we obtained V0 = 305.1(3) Å3, K0 = 124.6(14) GPa, and K0′ = 3.86 (fixed) for forsterite-type Mg2GeO4 and V0 = 263.5(15) Å3, K0 = 175(7) GPa, and K0′ = 4.2 (fixed) for the forsterite-III type phase. The forsterite-III type structure was found to be metastable when compared to the stable assemblage of perovskite/post-perovskite + MgO, as observed during laser-heating experiments. Understanding the phase relations and physical properties of metastable phases is crucial for studying the mineralogy of impact sites, understanding metastable wedges in subducting slabs, and interpreting the results of shock compression experiments. 
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