An overview of all the studies on high-pressure intrusion-extrusion of LiCl aqueous solutions in hydrophobic pure silica zeolites (zeosils) for absorption and storage of mechanical energy is presented. Operational principles of heterogeneous lyophobic systems and their possible applications in the domains of mechanical energy storage, absorption, and generation are described. The intrusion of LiCl aqueous solutions instead of water allows to considerably increase energetic performance of zeosil-based systems by a strong rise of intrusion pressure. The intrusion pressure increases with the salt concentration and depends considerably on zeosil framework. In the case of channel-type zeosils, it rises with the decrease of pore opening diameter, whereas for cage-type ones, no clear trend is observed. A relative increase of intrusion pressure in comparison with water is particularly strong for the zeosils with narrow pore openings. The use of highly concentrated LiCl aqueous solutions instead of water can lead to a change of system behavior. This effect seems to be related to a lower formation of silanol defects under intrusion of solvated ions and a weaker interaction of the ions with silanol groups of zeosil framework. The influence of zeosil nanostructure on LiCl aqueous solutions intrusion-extrusion is also discussed.
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http://dx.doi.org/10.3390/molecules25092145 | DOI Listing |
Adv Mater
January 2025
School of Chemistry and Chemical Engineering, Ministry of Education Key Laboratory of Special Functional Aggregated Materials, Shandong Key Laboratory of Advanced Organosilicon Materials and Technologies, Shandong University, Jinan, 250100, China.
SnO₂ is a widely used electron transport layer (ETL) material in perovskite solar cells (PSCs), and its design and optimization are essential for achieving efficient and stable PSCs. In this study, the in situ formation of a chain entanglement gel polymer electrolyte is reported in an aqueous phase, integrated with SnO₂ as the ETL. Based on the self-polymerization of 3-[[2-(methacryloyloxy)ethyl]dimethylammonium]propane-1-sulfonic acid (DAES) in an aqueous environment, combining the catalytic effect of LiCl (as a Lewis acid) with the salting-out effect, and the introduction of polyvinylpyrrolidone (PVP) as the other polymer chain, a chain entanglement gelled SnO (G-SnO) structure is successfully constructed with a wide range of functions.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China.
J Phys Chem Lett
December 2024
Department of Chemistry-Ångström Laboratory, Uppsala University, Lägerhyddsvägen 1, P.O. Box 538, 75121 Uppsala, Sweden.
Water-in-salt electrolytes with a surprisingly large electrochemical stability window of ≤3 V have revived interest in aqueous electrolytes for rechargeable lithium-ion batteries. However, recent reports of acidic pH measured in concentrated electrolyte solutions appear to be in contradiction with the suppressed activity of the hydrogen evolution reaction (HER). Therefore, the fundamental thermodynamics of proton reactivity in concentrated electrolyte solutions remains elusive.
View Article and Find Full Text PDFSmall
November 2024
Department of Materials Science and Engineering, School of Energy Science and Engineering, Vidyasirimedhi Institute of Science and Technology (VISTEC), Rayong, 21210, Thailand.
Aqueous biphasic systems (ABSs) with water-in-salt electrolytes are gaining significant attention for their role in aqueous biphasic interphase studies, particularly in energy storage devices. Aqueous salt-salt biphasic electrolytes are considered a promising alternative to replace traditional liquid electrolytes commonly used in battery technologies, for example, membrane-less redox flow batteries, owing to their low cost and high ionic conductivity. However, the stability of the interphase over time must be considered, as it can impact the long-term electrochemical performance in various applications.
View Article and Find Full Text PDFJ Phys Chem Lett
November 2024
State Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing, Beijing 100083, People's Republic of China.
The accurate understanding of mass transfer in molten salt contributes to revealing the reaction mechanism and advancing the technologies. The existence of notable natural convection effects has been demonstrated in our previous studies, even though the driving forces for such a high natural convection are still not clear. Herein, we showed that the intense natural convection in molten salts resulted from severe heat dissipation through the electrodes (or the system).
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