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    Solid Ion Conductors under Pressure: In Situ Monitoring of the Tetragonal to Cubic Phase Transition of Na3SbS4Na_3SbS_4 and Na3PS4Na_3PS_4

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    The Na3PnS4(Pn=P,Sb)Na_3PnS_4 (Pn = P, Sb) solid electrolytes are promising candidates for sodium solid-state batteries due to their potential high ionic conductivities. Structural modifications of these materials can induce a tetragonal-to-cubic phase transition, either by increasing temperature or by aliovalent substitutions. In this study, we introduce pressure as an alternative approach to observe the tetragonal-to-cubic phase transition in these materials. In situ synchrotron high-pressure powder X-ray diffraction shows a tetragonal-to-cubic phase transition at pressures of 2.9 GPa for Na3SbS4Na_3SbS_4 and 14.6 GPa for Na3PS4Na_3PS_4. Rietveld refinements and symmetry analysis provide insights into the displacive phase transition mechanism related to the motion of Na+Na^+ and the rotation of the SbS43SbS_4^{3–} tetrahedra. Density functional theory calculations confirm that the cubic phase becomes thermodynamically favorable under high pressure compared to the tetragonal phase. These findings highlight the importance of high-pressure considerations in tailoring the properties of ionic conductors, an area that remains underexplored

    Rapid mineralization of mineral-bound carboxyl-carbon of salicylic acid and phenylalanine

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    Ligand-bound carboxylic acids are considered a stabilized fraction of mineral-adsorbed carbon in soil. Carboxyl-14C labeled phenylalanine or salicylic acid wereadsorbed onto goethite, kaolinite, or illite, and subsequently incubated in both loamy and sandy arable topsoil for three weeks. Contrary to our expectations, moremineral-adsorbed carboxyl-C was mineralized than remaining C in salicylic acid and phenylalanine irrespective of mineral type or soil due to competitive desorptionfollowed by preferential mineralization. Factors that control the desorbability of organic molecules are more important for their stabilization in the soil than sorption strength

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