We investigated six presolar grains from very primitive regions of the matrix in the unequilibrated ordinary chondrite Semarkona with transmission electron microscopy (TEM). These grains include one SiC, one oxide (Mg-Al spinel), and four silicates. This is the first TEM investigation of presolar grains within an ordinary chondrite host (in situ) and the first TEM study to report on any presolar silicates (in or ex situ) from an ordinary chondrite. Structural and elemental compositional studies of presolar grains located within their meteorite hosts have the potential to provide information on conditions and processes throughout the grains' histories. Our analyses show that the SiC and spinel grains are stoichiometric and well crystallized. In contrast, the majority of the silicate grains are non-stoichiometric and poorly crystallized. These findings are consistent with previous TEM studies of presolar grains from interplanetary dust particles and chondritic meteorites. The individual silicates have Mg#'s ranging from 15 to 98. Internal compositional heterogeneities were observed in several grains, including Al in the SiC, Mg and Al in the spinel, and Mg, Si, Al, and/or Cr in two silicates. We interpret the poorly crystalline nature, non-stoichiometry, more Fe rather than Mg-rich compositions, and/or compositional heterogeneities as features of the formation by condensation under non-equilibrium conditions. Evidence for parent body alteration includes rims with mobile elements (S or Fe) on the SiC grain and one silicate grain. Other features characteristic of secondary processing in the interstellar medium, the solar nebula, and/or on parent bodies, were not observed or are better explained by processes operating in circumstellar envelopes. In general, there was very little overprinting of primary features of the presolar grains by secondary processes (e.g., ion irradiation, grain-grain collisions, thermal metamorphism, aqueous alteration). This finding underlines the need for additional TEM studies of presolar grains located in the primitive matrix regions of Semarkona, to address gaps in our knowledge of presolar grain populations accreted to ordinary chondrites.(c) 2022 Elsevier Ltd. All rights reserved.

Part I shows that quantitative measurements of heat capacity are theoretically possible inside diamond anvil cells via high-frequency Joule heating (100 kHz-10MHz), opening up the possibility of new methods to detect and characterize transformations at high-pressure such as the glass transitions, melting, magnetic orderings, and the onset of superconductivity. Here, we test the possibility outlined in Part I, using prototypes and detailed numerical models. First, a coupled electrical-thermal numerical model shows that specific heat of metals inside diamond cells can be measured directly using similar to 1MHz frequency, with < 10% accuracy. Second, we test physical models of high-pressure experiments, i.e., diamond-cell mock-ups. Metal foils of 2-6 mu m-thickness are clamped between glass insulation inside diamond anvil cells. Fitting data from 10 Hz to similar to 30 kHz, we infer the specific heat capacities of Fe, Pt, and Ni with +/- 20%-30% accuracy. The electrical test equipment generates -80 dBc spurious harmonics, which overwhelm the thermally induced harmonics at higher frequencies, disallowing the high precision expected from numerical models. An alternative Joule-heating calorimetry experiment, on the other hand, does allow absolute measurements with < 10% accuracy, despite the -80 dBc spurious harmonics: the measurement of thermal effusivity, root rho ck (rho, c, and k being density, specific heat, and thermal conductivity), of the insulation surrounding a thin-film heater. Using a similar to 50 nm-thick Pt heater surrounded by glass and 10 Hz-300 kHz frequency, we measure thermal effusivity with 66% accuracy inside the sample chamber of a diamond anvil cell. Published by AIP Publishing.

Numerical simulations of heat transport in diamond anvil cells reveal a possibility for absolute measurements of specific heat via high-frequency modulation calorimetry. Such experiments could reveal and help characterize temperature-driven phase transitions at high-pressure, such as melting, the glass transition, magnetic and electric orderings, or superconducting transitions. Specifically, we show that calorimetric information of a sample cannot be directly extracted from measurements at frequencies slower than the timescale of conduction to the diamond anvils (10s-100s of kHz) since the experiment is far from adiabatic. At higher frequencies, laser-heating experiments allow relative calorimetric measurements, where changes in specific heat of the sample are discriminated from changes in other material properties by scanning the heating frequency from similar to 1 MHz to 1 GHz. But laser-heating generates large temperature gradients in metal samples, preventing absolute heat capacities to be inferred. High-frequency Joule heating, on the other hand, allows accurate, absolute specific heat measurements if it can be performed at high-enough frequency: assuming a thin layer of KBr insulation, the specific heat of a 5 lm-thick metal sample heated at 100 kHz, 1MHz, or 10MHz frequency would be measured with 30%, 8%, or 2% accuracy, respectively. Published by AIP Publishing.

If successfully developed, calorimetry at tens of GPa of pressure could help characterize phase transitions in materials such as high-pressure minerals, metals, and molecular solids. Here, we extend alternating-current calorimetry to 9GPa and 300K in a diamond anvil cell and use it to study phase transitions in H2O. In particular, water is loaded into the sample chambers of diamond-cells, along with thin metal heaters (1 mu m-thick platinum or 20 nm-thick gold on a glass substrate) that drive high-frequency temperature oscillations (20 Hz to 600 kHz; 1 to 10 K). The heaters also act as thermometers via the third-harmonic technique, yielding calorimetric data on (1) heat conduction to the diamonds and (2) heat transport into substrate and sample. Using this method during temperature cycles from 300 to 200 K, we document melting, freezing, and proton ordering and disordering transitions of H2O at 0 to 9 GPa, and characterize changes in thermal conductivity and heat capacity across these transitions. The technique and analysis pave the way for calorimetry experiments on any non-metal at pressures up to similar to 100 GPa, provided a thin layer (several mu m-thick) of thermal insulation supports a metallic thin-film (tens of nm thick) Joule-heater attached to low contact resistance leads inside the sample chamber of a diamond-cell. Published by AIP Publishing.

Zaghoo et al. [Phys. Rev. B 93, 155128 (2016)] report on the observation of a first-order phase transition to metallic hydrogen at pressures of 100-170 GPa and high temperatures of 1100-1800 K. Here, based on the analysis of their optical spectroscopy data and finite element calculations, we show that the presented data do not support the existence of such a transition at their claimed T-c and are likely related to a continuous band-gap reduction.

Recent theoretical calculations predict that megabar pressure stabilizes very hydrogen-rich simple compounds having new clathrate-like structures and remarkable electronic properties including room-temperature superconductivity. X-ray diffraction and optical studies demonstrate that superhydrides of lanthanum can be synthesized with La atoms in an fcc lattice at 170 GPa upon heating to about 1000 K. The results match the predicted cubic metallic phase of LaH10 having cages of thirty-two hydrogen atoms surrounding each La atom. Upon decompression, the fcc-based structure undergoes a rhombohedral distortion of the La sublattice. The superhydride phases consist of an atomic hydrogen sublattice with H-H distances of about 1.1 angstrom, which are close to predictions for solid atomic metallic hydrogen at these pressures. With stability below 200 GPa, the superhydride is thus the closest analogue to solid atomic metallic hydrogen yet to be synthesized and characterized.

Two new polyhydrides of calcium have been synthesized at high pressures and high temperatures and characterized by Raman spectroscopy, infrared spectroscopy, and synchrotron X-ray diffraction. Above 20 GPa and 700 K, we synthesize a phase having a monoclinic (C2/m) structure with Ca2H5 composition, which is characterized by a distinctive vibration at 3789 cm(-1) at 25 GPa. The observed Raman spectrum is in close agreement with first-principles calculations of a Ca2H5 structure characterized by a lattice containing a central layer of H-2 molecules oriented along the (100) direction. At higher pressures (e.g., 116 GPa and 1600 K), we synthesize another phase, which has the composition of CaH4 and a denser body-centered tetragonal structure. This weakly metallic phase also contains molecular-like H-2 units, and its spectroscopic as well as diffraction signatures match closely with those predicted from first-principles calculations. This phase is observed to persist on decompression to 60 GPa at room temperature. The elongation of the H-H bond in these hydrides is a result of the Ca-H-2 interaction, analogous to what occurs in molecular compounds, where H-2 binds side-on to a d-element, such as in Kubas complex.

Recent computational studies have predicted that rare-earth superhydrides are promising high-temperature superconductors. Of these phases having very high hydrogen content (XHn, n > 6, where X is the rare-earth atom) a cubic phase of lanthanum hydride, recently synthesized at 170 GPa and identified as LaH10 +/- x, is in good agreement with theoretical predictions. The experiments found that the stability of the phase extended to lower pressure and a distorted form was found on decompression. Here we examine the nuclear quantum effects and anharmonic dynamics on LaH10, including the behavior of the hydrogen sublattice in comparison with the predicted atomic metallic hydrogen at higher pressure. We also examine the vibrational dynamics and electronic properties of a distorted lower pressure phase of LaH10 and find that superconducting Tc decreases relative to cubic but remains relatively high (i.e., 229-245 K).

Recent predictions and experimental observations of high T-c superconductivity in hydrogen-rich materials at very high pressures are driving the search for superconductivity in the vicinity of room temperature. We have developed a novel preparation technique that is optimally suited for megabar pressure syntheses of superhydrides using modulated laser heating while maintaining the integrity of sample-probe contacts for electrical transport measurements to 200 GPa. We detail the synthesis and characterization of lanthanum superhydride samples, including four-probe electrical transport measurements that display significant drops in resistivity on cooling up to 260 K and 180-200 GPa, and resistivity transitions at both lower and higher temperatures in other experiments. Additional current-voltage measurements, critical current estimates, and low-temperature x-ray diffraction are also obtained. We suggest that the transitions represent signatures of superconductivity to near room temperature in phases of lanthanum superhydride, in good agreement with density functional structure search and BCS theory calculations.

Hydrogen and helium are the most abundant elements in the universe, and they constitute the interiors of gas giant planets. Thus, their equations of states, phase, chemical state, and chemical reactivity at extreme conditions are of great interest. Applying Raman spectroscopy, visual observation, and synchrotron X-ray diffraction in diamond anvil cells, we performed experiments on H-2-He 1:1 and D-2-He 1:10 compressed gas mixtures up to 100 GPa at 300 K. By comparing with the available data on pure bulk materials, we find no sign of miscibility, chemical reactivity, and new compound formation. This result establishes a new baseline for future investigations of miscibility in the He-H-2 system at extreme P-T conditions. Published under license by AIP Publishing.