Synthesis and superconductivity in yttrium-cerium hydrides at high pressures.

Further increasing the critical temperature and/or decreasing the stabilized pressure are the general hopes for the hydride superconductors. Inspired by the low stabilized pressure associated with Ce 4f electrons in superconducting cerium superhydride and the high critical temperature in yttrium superhydride, we carry out seven independent runs to synthesize yttrium-cerium alloy hydrides. The synthetic process is examined by the Raman scattering and X-ray diffraction measurements. The superconductivity is obtained from the observed zero-resistance state with the detected onset critical temperatures in the range of 97-141 K. The upper critical field towards 0 K at pressure of 124 GPa is determined to be between 56 and 78 T by extrapolation of the results of the electrical transport measurements at applied magnetic fields. The analysis of the structural data and theoretical calculations suggest that the phase of Y0.5Ce0.5H9 in hexagonal structure with the space group of P63/mmc is stable in the studied pressure range. These results indicate that alloying superhydrides indeed can maintain relatively high critical temperature at relatively modest pressures accessible by laboratory conditions.

Compression rate of dynamic diamond anvil cells from room temperature to 10 K.

There is an ever increasing interest in studying dynamic-pressure dependent phenomena utilizing dynamic Diamond Anvil Cells (dDACs), devices capable of a highly controlled rate of compression. Here, we characterize and compare the compression rate of dDACs in which the compression is actuated via three different methods: (1) stepper motor (S-dDAC), (2) gas membrane (M-dDAC), and (3) piezoactuator (P-dDAC). The compression rates of these different types of dDAC were determined solely on millisecond time-resolved R1-line fluorescence of a ruby sphere located within the sample chamber. Furthermore, these different dynamic compression-techniques have been described and characterized over a broad temperature and pressure range from 10 to 300 K and 0-50 GPa. At room temperature, piezoactuation (P-dDAC) has a clear advantage in controlled extremely fast compression, having recorded a compression rate of ∼7 TPa/s, which is also found to be primarily influenced by the charging time of the piezostack. At 40-250 K, gas membranes (M-dDAC) have also been found to generate rapid compression of ∼0.5-3 TPa/s and are readily interfaced with moderate cryogenic and ultrahigh vacuum conditions. Approaching more extreme cryogenic conditions (<10 K), a stepper motor driven lever arm (S-dDAC) offers a solution for high-precision moderate compression rates in a regime where P-dDACs and M-dDACs can become difficult to incorporate. The results of this paper demonstrate the applicability of different dynamic compression techniques, and when applied, they can offer us new insights into matter's response to strain, which is highly relevant to physics, geoscience, and chemistry.

Pressure-induced amorphization and existence of molecular and polymeric amorphous forms in dense SO2.

We report here the pressure-induced amorphization and reversible structural transformation between two amorphous forms of SO2: molecular amorphous and polymeric amorphous, with the transition found at 26 GPa over a broad temperature regime, 77 K to 300 K. The transformation was observed by both Raman spectroscopy and X-ray diffraction in a diamond anvil cell. The results were corroborated by ab initio molecular dynamics simulations, where both forward and reverse transitions were detected, opening a window to detailed analysis of the respective local structures. The high-pressure polymeric amorphous form was found to consist mainly of disordered polymeric chains made of three-coordinated sulfur atoms connected via oxygen atoms, with few residual intact molecules. This study provides an example of polyamorphism in a system consisting of simple molecules with multiple bonds.