Rechargeable Li-metal/Li-ion all-solid-state batteries due to their high safety levels and high energy densities are in great demand for different applications ranging from portable electronic devices to energy storage systems, especially for the production of electric vehicles. The LiAlGe(PO) (LAGP) solid electrolyte remains highly attractive because of its high ionic conductivity at room temperature, and thermal stability and chemical compatibility with electrode materials. The possibility of LAGP production by the glass-ceramic method makes it possible to achieve higher total lithium-ion conductivity and a compact microstructure of the electrolyte membrane compared to the ceramic one. Therefore, the crystallization kinetics investigations of the initial glass are of great practical importance. The present study is devoted to the parent glasses for the production of LiAlGeSiPO glass-ceramics. The glass transition temperature is determined by DSC and dilatometry. It is found that decreases from 523.4 ( = 0) to 460 °C ( = 0.5). The thermal stability of glasses increases from 111.1 ( = 0) to 188.9 °C ( = 0.3). The crystallization activation energy of Si-doped glasses calculated by the Kissinger model is lower compared to that of Si-free glasses, so glass-ceramics can be produced at lower temperatures. The conductivity of the glasses increases with the growth of content.
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http://dx.doi.org/10.3390/membranes12121245 | DOI Listing |
Nanoscale
January 2025
Advanced Batteries Research Center, Korea Electronics Technology Institute, 25, Saenari-ro, Seongnam-si, 13509, Republic of Korea.
The SiO electrode interface is passivated with a SiO layer, which hinders the deposition of an inorganic solid electrolyte interphase (SEI) due to its high surface work function and low exchange current density of electrolyte decomposition. Consequently, a thermally vulnerable, organic-based SEI formed on the SiO electrode, leading to poor cycling performance at elevated temperatures. To address this issue, the SEI formation process is thermoelectrochemically activated.
View Article and Find Full Text PDFLangmuir
January 2025
Department of Chemical Engineering, Technion-IIT, Haifa 32000, Israel.
A comprehensive approach enabling a quantitative interpretation of poly-l-arginine (PARG) adsorption kinetics at solid/electrolyte interfaces was developed. The first step involved all-atom molecular dynamics (MD) modeling of physicochemical characteristics yielding PARG molecule conformations, its contour length, and the cross-section area. It was also shown that PARG molecules, even in concentrated electrolyte solutions (100 mM NaCl), assume a largely elongated shape with an aspect ratio of 36.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Frontiers Science Center for High Energy Material, Key Laboratory of Cluster Science, Ministry of Education, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, No. 5, Zhongguancun South Street, Haidian District, Beijing 100081, P. R. China.
The development of solid-state electrolytes has become crucial for promoting the safety and performance of lithium-ion batteries. Herein, the substitution of nodal elements from Si to Ge significantly improved the lithium ionic conductivity in 2D metalloid organic frameworks, resulting in an enhancement of approximately one order of magnitude.
View Article and Find Full Text PDFSci Rep
January 2025
Department of Nutritional Sciences, Auburn University, Auburn, AL, 36849, USA.
Oxidative stress (OS) refers to the disruption in the balance between free radical generation and antioxidant defenses, leading to potential tissue damage. Reactive oxygen species (ROS) can interact with biological components, triggering processes like protein oxidation, lipid peroxidation, or DNA damage, resulting in the generation of several volatile organic compounds (VOCs). Recently, VOCs provided new insight into cellular metabolism and can serve as potential biomarkers.
View Article and Find Full Text PDFNat Mater
January 2025
Department of Materials Science and Engineering, University of Maryland, College Park, MD, USA.
All-solid-state lithium metal batteries promise high levels of safety and energy density, but their practical realization is limited by low Li reversibility, limited cell loading and demand for high-temperature and high-pressure operation, stemming from solid-state electrolyte (SSE) low-voltage reduction and high-voltage decomposition, and from lithium dendrite growth. Here we concurrently address these challenges by reporting that a family of reductive electrophiles gain electrons and cations from metal-nucleophile materials (here a Li sulfide SSE) upon contact to undergo electrochemical reduction and form interphase layers (named solid reductive-electrophile interphase) on material surfaces. The solid reductive-electrophile interphase is electron blocking and lithiophobic, prevents SSE reduction, suppresses Li dendrites and supports high-voltage cathodes.
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