Complexes of alkali metal ions with poly (ethylene oxide)
About: This article is published in Polymer.The article was published on 1973-11-01. It has received 2110 citations till now. The article focuses on the topics: Oxide.
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TL;DR: A brief historical review of the development of lithium-based rechargeable batteries is presented, ongoing research strategies are highlighted, and the challenges that remain regarding the synthesis, characterization, electrochemical performance and safety of these systems are discussed.
Abstract: Technological improvements in rechargeable solid-state batteries are being driven by an ever-increasing demand for portable electronic devices. Lithium-ion batteries are the systems of choice, offering high energy density, flexible and lightweight design, and longer lifespan than comparable battery technologies. We present a brief historical review of the development of lithium-based rechargeable batteries, highlight ongoing research strategies, and discuss the challenges that remain regarding the synthesis, characterization, electrochemical performance and safety of these systems.
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Cites background from "Complexes of alkali metal ions with..."
...Nevertheless, a principal goal has been to search for new, highly conductive salts with a large electrochemical window, which form a eutectic composition with PEO that melts at the lowest possible temperatur...
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TL;DR: The phytochemical properties of Lithium Hexafluoroarsenate and its Derivatives are as follows: 2.2.1.
Abstract: 2.1. Solvents 4307 2.1.1. Propylene Carbonate (PC) 4308 2.1.2. Ethers 4308 2.1.3. Ethylene Carbonate (EC) 4309 2.1.4. Linear Dialkyl Carbonates 4310 2.2. Lithium Salts 4310 2.2.1. Lithium Perchlorate (LiClO4) 4311 2.2.2. Lithium Hexafluoroarsenate (LiAsF6) 4312 2.2.3. Lithium Tetrafluoroborate (LiBF4) 4312 2.2.4. Lithium Trifluoromethanesulfonate (LiTf) 4312 2.2.5. Lithium Bis(trifluoromethanesulfonyl)imide (LiIm) and Its Derivatives 4313
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TL;DR: In this article, various factors that affect the morphology and Coulombic efficiency of Li metal anodes have been analyzed, and the results obtained by modelling of Li dendrite growth have also been reviewed.
Abstract: Lithium (Li) metal is an ideal anode material for rechargeable batteries due to its extremely high theoretical specific capacity (3860 mA h g−1), low density (0.59 g cm−3) and the lowest negative electrochemical potential (−3.040 V vs. the standard hydrogen electrode). Unfortunately, uncontrollable dendritic Li growth and limited Coulombic efficiency during Li deposition/stripping inherent in these batteries have prevented their practical applications over the past 40 years. With the emergence of post-Li-ion batteries, safe and efficient operation of Li metal anodes has become an enabling technology which may determine the fate of several promising candidates for the next generation energy storage systems, including rechargeable Li–air batteries, Li–S batteries, and Li metal batteries which utilize intercalation compounds as cathodes. In this paper, various factors that affect the morphology and Coulombic efficiency of Li metal anodes have been analyzed. Technologies utilized to characterize the morphology of Li deposition and the results obtained by modelling of Li dendrite growth have also been reviewed. Finally, recent development and urgent need in this field are discussed.
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TL;DR: In this article, the authors provide a background overview and discuss the state of the art, ion-transport mechanisms and fundamental properties of solid-state electrolyte materials of interest for energy storage applications.
Abstract: Solid-state electrolytes are attracting increasing interest for electrochemical energy storage technologies. In this Review, we provide a background overview and discuss the state of the art, ion-transport mechanisms and fundamental properties of solid-state electrolyte materials of interest for energy storage applications. We focus on recent advances in various classes of battery chemistries and systems that are enabled by solid electrolytes, including all-solid-state lithium-ion batteries and emerging solid-electrolyte lithium batteries that feature cathodes with liquid or gaseous active materials (for example, lithium–air, lithium–sulfur and lithium–bromine systems). A low-cost, safe, aqueous electrochemical energy storage concept with a ‘mediator-ion’ solid electrolyte is also discussed. Advanced battery systems based on solid electrolytes would revitalize the rechargeable battery field because of their safety, excellent stability, long cycle lives and low cost. However, great effort will be needed to implement solid-electrolyte batteries as viable energy storage systems. In this context, we discuss the main issues that must be addressed, such as achieving acceptable ionic conductivity, electrochemical stability and mechanical properties of the solid electrolytes, as well as a compatible electrolyte/electrode interface. This Review details recent advances in battery chemistries and systems enabled by solid electrolytes, including all-solid-state lithium-ion, lithium–air, lithium–sulfur and lithium–bromine batteries, as well as an aqueous battery concept with a mediator-ion solid electrolyte.
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162 citations
TL;DR: In this paper, an ion-dipole interaction between metal salts and poly(ethylene oxide) has been investigated, and it has been shown that 10% to 30% of the salt in the bulk polymer can significantly reduce crystallinity while retaining compatibility.
Abstract: Evidence is presented for the interaction of metal salts such as potassium iodide with polyethers such as poly(ethylene oxide). This interaction is sufficiently marked that the incorporation of 10–30% of the salt in the bulk polymer markedly reduces crystallinity while retaining compatibility. Examination of electroviscous effects in methanol demonstrates that the salt–polymer adduct behaves as a typical polyelectrolyte at low salt concentrations, while the polymer in absence of salt is essentially insoluble in methanol at room temperature. Measurements of the equilibrium between salt and polymer along with a study of various molecular weight polymers strongly suggest that one salt molecule associates with about nine ethylene oxide units. It is proposed that the association is due to an ion–dipole interaction, and the anion is tentatively postulated as the species directly associating with the polymer. The association of other metal salts and other polymers are interpreted in this light. The significance of these results in interpreting salting-in phenomena is also discussed.
105 citations
90 citations
51 citations
TL;DR: In this article, the reaction between potassium thiocyanate and 2,3,14,15-dibenzo-1,4,7,10,13,16,19,22-octaoxocyclotetracosa-2,14-diene gives a 2:1 complex shown by crystal structure analysis to be centrosymmetrical with two potassium ions each positioned among eight sources of electron density.
Abstract: Reaction between potassium thiocyanate and 2,3,14,15-dibenzo-1,4,7,10,13,16,19,22-octaoxocyclotetracosa-2,14-diene gives a 2:1 complex shown by crystal structure analysis to be centrosymmetrical with two potassium ions each positioned among eight sources of electron density, namely, two nitrogen atoms of bridging thiocyanate groups, five oxygen atoms of the cyclic ether (two of the eight oxygen atoms are shared) and two carbon atoms of a benzene ring.
21 citations