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Ionic conductivity

About: Ionic conductivity is a research topic. Over the lifetime, 19412 publications have been published within this topic receiving 519167 citations.


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Journal ArticleDOI
TL;DR: A gel polymer electrolyte (GPE) based on an electrospun polymer membrane of poly(acrylonitrile)/poly(methyl methacrylate) (PAN/PMMA) incorporating with a room-temperature ionic liquid N-methy-N-butylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR14TFSI) was prepared and its performance for lithium ion batteries was investigated as discussed by the authors.

178 citations

Journal ArticleDOI
TL;DR: In this article, the ionic and water transport characteristics of Nafion ionomer membranes were investigated systematically in the mixed cation form of H+ and various kinds of alkali metal cation systems, which were prepared by equilibrating the membranes in the mixtures of HCl and alkali chloride in aqueous solutions of various mixing ratios.
Abstract: Ion and water transport characteristics of Nafion ionomer membranes were investigated systematically in the mixed cation form of H+ and various kinds of alkali metal cation systems, which were prepared by equilibrating the membranes in the mixtures of HCl and alkali chloride in aqueous solutions of various mixing ratios. The membrane cationic composition showed that cations of larger atomic number had a higher affinity to sulfonic acid groups but less water content in the membrane than those of smaller atomic numbers. The net ionic conductivity was decreased, in any case, by the presence of alkali metal cations in the membrane. Different kinds of the interaction mode among cations were observed between H/Li or H/Na systems and H/K, H/Rb, or H/Cs systems. The interaction between alkali metal cations appeared to increase as the atomic number of the alkali metal cation increased. The water transference coefficient (electro-osmosis drag coefficient) increased from 2.5 to more than 10 by the presence of alkali...

177 citations

Journal ArticleDOI
01 Nov 1991-Nature
TL;DR: In this paper, a melt-quenching technique was used to stabilize α-AgI at room temperature and showed diffraction peaks characteristic of the high-temperature phase of AgI and displayed ionic conductivities of about 10−1S cm−1.
Abstract: SINCE the discovery1 that the high-temperature phase of silver iodide (α-AgI) has an ionic conductivity comparable to that of the best liquid electrolytes, solid electrolytes have attracted wide interest. Possible applications of these materials range from solid-state batteries to electrochromic displays and sensors2. Although α-AgI displays conductivities of more than 10 S cm−1 (ref. 3), owing to the almost liquid-like mobility of Ag+ ions, the crystal transforms below 147 °C to the β-phase with a conductivity of only ∼10−5 S cm−1 at room temperature. Efforts to achieve good conductivities at lower temperatures have focused on the addition of a second component to AgI to form solid solutions or new compounds such as RbAg4I5 and Ag2HgI4 (refs 4–7). Here we report our success in depressing the α→β transformation temperature so as to stabilize α-AgI itself at room temperature. We use a melt-quenching technique to prepare crystallites of α-AgI frozen into a silver borate glass matrix. The quenched material showed diffraction peaks characteristic of α-AgI and displayed ionic conductivities of about 10−1S cm−1. Further development of these glass/crystal composites may make the high ionic conductivity of α-AgI available for room-temperature solid-state applications.

177 citations

Journal ArticleDOI
TL;DR: This is the first systematic study on the charge carrier chemistry of peroxides with high relevance for the performance kinetics of Li-oxygen batteries.
Abstract: Bulk Li2O2 is shown to exhibit ionic conductivity via lithium vacancies and electronic conductivity via electron holes (localized as superoxide ions). This is the first systematic study on the charge carrier chemistry of peroxides with high relevance for the performance kinetics of Li-oxygen batteries.

177 citations

Journal ArticleDOI
TL;DR: In this article, 1-methyl-3-propylpyrrolidinium bis(trifluoromethanesulfonyl)imide (P(13)TFSI) is screened out as a particularly promising ionic liquid for applications to rechargeable lithium batteries.
Abstract: Ionic liquids thermodynamically compatible with Li metal are very promising for applications to rechargeable lithium batteries. 1-methyl-3-propylpyrrolidinium bis(trifluoromethanesulfonyl)imide (P(13)TFSI) is screened out as a particularly promising ionic liquid in this study. Dimensionally stable, elastic, flexible, nonvolatile polymer gel electrolytes (PGEs) with high electrochemical stabilities, high ionic conductivities and other desirable properties have been synthesized by dissolving Li imide salt (LiTFSI) in P(13)TFSI ionic liquid and then mixing the electrolyte solution with poly(vinylidene-co-hexafluoropropylene) (PVDF-HFP) copolymer. Adding small amounts of ethylene carbonate to the polymer gel electrolytes dramatically improves the ionic conductivity, net Li ion transport concentration, and Li ion transport kinetics of these electrolytes. They are thus favorable and offer good prospects in the application to rechargeable Li batteries including open systems like Li/air batteries, as well as more "conventional" rechargeable lithium and lithium ion batteries.

177 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20231,167
20222,073
20211,175
20201,117
20191,030
2018966