Phase Formation and Degradation of Na2ZrO3 under CO2 Cycling Studied by Ex Situ and In Situ Diffraction.

We positively identified and quantified the solid-state phases involved in the carbonation/decarbonation cycle of Na2ZrO3 when used for carbon capture. Previous work had only qualitatively inferred the phases present using diffraction pattern matching and thermogravimetric analysis. Here, we used the Rietveld-refinement method to analyze synchrotron X-ray and neutron powder diffraction data from samples treated ex situ. We then confirmed and extended our findings by in situ diffraction using a purpose-built gas-flow apparatus. This allowed us to resolve discrepancies in the earlier literature concerning which phases are present during the carbonation and regeneration processes. A key finding is the simultaneous presence of the monoclinic and tetragonal phases of ZrO2 and that the "metastable" tetragonal phase is favored by smaller particles and can reincorporate into the bulk but the stable monoclinic phase does not. The result will help optimize the cycling of Na2ZrO3.

Elucidating the Effects of the Composition on Hydrogen Sorption in TiVZrNbHf-Based High-Entropy Alloys.

A number of high-entropy alloys (HEAs) in the TiVZrNbHf system have been synthesized by arc melting and systematically evaluated for their hydrogen sorption characteristics. A total of 21 alloys with varying elemental compositions were investigated, and 17 of them form body-centered-cubic (bcc) solid solutions in the as-cast state. A total of 15 alloys form either face-centered-cubic (fcc) or body-centered-tetragonal (bct) hydrides after exposure to gaseous hydrogen with hydrogen per metal ratios (H/M) as high as 2.0. Linear trends are observed between the volumetric expansion per metal atom [(V/Z)fcc/bct - (V/Z)bcc/hcp]/(V/Z)bcc/hcp with the valence electron concentration and average Pauling electronegativity (χp) of the alloys. However, no correlation was observed between the atomic size mismatch, δ, and any investigated hydrogen sorption property such as the maximum storage capacity or onset temperature for hydrogen release.

Conformational Dynamics in an Organic Ionic Plastic Crystal.

Understanding the short-range molecular motions of organic ionic plastic crystals is critical for the application of these materials as solid-state electrolytes in electrochemical devices such as lithium batteries. However, the theory of short-range-motions was originally developed for simple molecular plastic crystals and does not take account of strong interionic interactions that are present in organic ionic plastic crystals. Here we report a fundamental investigation of the dynamic behavior of an archetypal example triethyl(methyl)phosphonium bis(fluorosulfonyl)amide ([P1222][FSI]) through calorimetry, impedance spectroscopy, synchrotron X-ray diffraction, and solid-state NMR and Raman spectroscopies. For the first time, we show the presence of conformational dynamics in the solid state for the FSI anion. We relate the dynamics to a unique second-order displacive phase transition of [P1222][FSI]. This detailed analysis suggests a new disorder mechanism involving cooperative motion between the cation and FSI anion in the plastic crystal due to strong interionic interactions.