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Lithium indium chloride, LiInCl, is a promising solid-state electrolyte for all-solid-state batteries (ASSBs) due to its high room-temperature ionic conductivity and electrochemical stability. However, its sensitivity to atmospheric moisture leads to the formation of stable crystalline hydrates, which significantly affect both its electrochemical performance and crystal chemistry. In this study, temperature- and time-dependent X-ray diffraction was employed to investigate the underlying mechanisms governing the hydration and dehydration processes of LiInCl and its hydrated counterpart, LiInClHO ( > 2), by monitoring the associated structural transformations. The study reveals a two-step phase transition between the hydrated and dehydrated phases, with the identification of an intermediate phase, LiInCl·HO (1.5 < < 2). Coupled Rietveld refinements of X-ray and neutron powder diffraction data elucidate the crystal structure of this intermediate hydrate, providing crucial insights into the reversible reaction mechanism of LiInCl. Understanding these hydration and dehydration processes is vital for optimizing the electrochemical performance and stability of LiInCl in ASSBs applications.
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http://dx.doi.org/10.1021/acs.inorgchem.5c02094 | DOI Listing |
J Am Chem Soc
September 2025
Laboratory of Inorganic Synthesis and Catalysis (LSCI), Institute of Chemical Sciences and Engineering, École Polytechnique Fédéralede Lausanne (EPFL), Lausanne 1015, Switzerland.
The challenge to produce multicarbon (C) products in high current densities in the electrochemical reduction of carbon dioxide (CORR) has motivated intense research. However, the ability of solvated cations to tune and activate water for C production in the CORR has been overlooked. In this study, we report the incorporation of a covalently grown layer of functionalized phenyl groups on the Cu surface that leads to a 7-fold increase in ethylene production (to -530 mA cm) and a 6-fold increase in C products (to -760 mA cm).
View Article and Find Full Text PDFCureus
August 2025
Vascular Surgery, University Hospitals of Leicester NHS Trust, Leicester, GBR.
Background Fasting during the month of Ramadan is practiced by over a billion Muslims worldwide. This religious observance, which involves complete abstention from food and fluids during daylight hours, may contribute to dehydration and increase the risk of venous thromboembolism (VTE), particularly in hot climates. Despite this theoretical concern, limited clinical evidence exists on the actual incidence and risk of VTE associated with prolonged fasting.
View Article and Find Full Text PDFEvol Med Public Health
July 2025
Department of Evolutionary Anthropology, Duke University, Durham, NC, USA.
Background And Objectives: Water is essential for proper physiological function. As temperatures increase, populations may struggle to meet water needs despite adaptations or acclimation; chronic dehydration can cause kidney damage. We evaluate how daily water requirements are associated with ambient temperature (ambT), wet bulb globe temperature (WBGT), urine specific gravity (USG; marker of hydration status), and albumin:creatinine ratio (ACR; kidney function biomarker) among Daasanach pastoralists living in a hot, dry northern Kenyan climate.
View Article and Find Full Text PDFInorg Chem
September 2025
Malta-Consolider Team and Department of Analytical and Physical Chemistry, University of Oviedo, Oviedo E-33006, Spain.
Hydrated magnesium sulfates (MgSO·HO) are known to form multiple hydration states ( = 0-11) and are essential in planetary science and thermochemical energy storage. Despite their significance in detecting extraterrestrial water reservoirs or in mineral (de)hydration cycles, it is still necessary to understand how the structure-property relationships of these materials evolve at different hydration levels when pressure is applied. Through a systematic first-principles computational investigation, we elucidate the key structural factors governing the densification mechanism under hydrostatic pressure of MgSO·HO crystals.
View Article and Find Full Text PDFInorg Chem
September 2025
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
We report the discovery and comprehensive characterization of the octahydrate phase of magnesium pyrophosphate, MgPO·8HO, synthesized via aqueous reactive crystallization of magnesium chloride and sodium pyrophosphate in Tris buffer at pH 8. While MgPO·3.5HO and MgPO·6HO readily form under these conditions, the octahydrate appears only rarely.
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