Solvate ionic liquids (SILs), comprising long-lived, Li solvate cations and counter anions, serve as highly Li-ion-conductive and non-flammable electrolytes for use in lithium secondary batteries. In this work, we synthesized a series of novel redox-active glyme(oligoether)-Li salt-based SILs, consisting of a symmetric ([Li(G3)]) or asymmetric ([Li(G3Bu)]) triglyme-Li salt complex and redox-active tetrahalogenoferrate ([FeX] (X = Br, ClBr, Cl)), for use as the catholyte in semi-liquid lithium secondary batteries. The successful formation of stable molten complexes of [Li(G3/G3Bu)][FeX] was confirmed by Raman spectroscopy and thermogravimetry. The melting point ( ) depended on both the molecular weights of the complex anions and the structures of the complex cations. [Li(G3)][FeCl] comprised complex cations with a symmetric structure, and the smallest complex anions showed the lowest of 28.2 °C. The redox properties of the [FeX]/[FeX] couple strongly suggested the suitability of [Li(G3/G3Bu)][FeX] as a catholyte. The discharge capacities of semi-liquid lithium secondary batteries utilizing the [Li(G3/G3Bu)][FeX] catholyte depended on the structure of the SILs, and the cell with [Li(G3)][FeCl] showed the highest capacity with relatively good capacity retention. This study confirmed the feasibility of the glyme-based redox-active SILs as catholytes for scalable redox-flow type batteries.
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http://dx.doi.org/10.1039/c9ra10149g | DOI Listing |
Materials (Basel)
December 2024
School of Physics and School of Materials Science and Engineering, Central South University, Changsha 410083, China.
In order to investigate the effects of the softening point, the addition ratio, and the median particle size (D50) of the asphalt on the performance of secondary particles of artificial graphite anode materials prepared by granulation, ten-kilogram orthogonal experiments were designed. D50 and powder orientation index (OI) value of the prepared secondary particles of artificial graphite anode materials were employed as evaluation index, and the results of the orthogonal experiments were subjected to polarity analysis, analysis of variance (ANOVA), and multiple linear regression analysis. It is demonstrated that the addition ratio of the asphalt exerts the most pronounced influence on D50 and powder OI value of secondary granular artificial graphite anode materials, followed by the softening point.
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December 2024
Faculty of Chemical Technology and Engineering, Bydgoszcz University of Science and Technology, Seminaryjna 3, 85-326 Bydgoszcz, Poland.
The growing demand for alkali metals (AMs), such as lithium, cesium, and rubidium, related to their wide application across various industries (e.g., electronics, medicine, aerospace, etc.
View Article and Find Full Text PDFSmall
December 2024
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, Republic of Korea.
Electrolyte additive engineering enables the creation of long-lasting interfacial layers that protect electrodes, thus extending the lifetime of high-energy lithium-ion batteries employing Ni-rich Li[NiCoMn]O (NCM) cathodes. However, batteries face various limitations if existing additives are employed alone without an appropriate combination. Herein, the study reports the development of a molecular-engineered salt-type multifunctional additive, lithium bis(phosphorodifluoridate) triethylammonium ethenesulfonate (LiPENS), that leverages the different functionalities of phosphorous, nitrogen, and sulfur-embedded motifs, as well as the classical additive vinylene carbonate (VC), to construct protective interfacial layers.
View Article and Find Full Text PDFAdv Mater
December 2024
State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, Guangxi Key Laboratory of Processing for Non-Ferrous Metals and Featured Materials, School of Resources, Environment and Materials, Guangxi University, Nanning, 530004, China.
Lithium metal anode is desired by high capacity and low potential toward higher energy density than commercial graphite anode. However, the low-temperature Li metal batteries suffer from dendrite formation and dead Li resulting from uneven Li behaviors of flux with huge desolvation/diffusion barriers, thus leading to short lifespan and safety concern. Herein, differing from electrolyte engineering, a strategy of delocalizing electrons with generating rich active sites to regulate Li desolvation/diffusion behaviors are demonstrated via decorating polar chemical groups on porous metal-organic frameworks (MOFs).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Fujian Key Laboratory of Pcolymer Materials, College of Materials Science and Engineering, Fujian Normal University, Fuzhou, 350007, China.
Modifying the separator is considered as an effective strategy for achieving high performance lithium-sulfur (Li-S) batteries. However, most modification layers are excessively thick, with catalytic active sites primarily located within the material's interior. This configuration severely impacts Li transport and the efficient catalytic conversion of polysulfides.
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