Lithium-ion batteries (LIBs) are extensively employed in various fields. Nonetheless, LIBs utilizing ethylene carbonate (EC)-based electrolytes incur capacity degradation in a wide-temperature range, which is attributable to the slow Li transfer kinetics at low temperatures and solvent decomposition during high-rate cycling at high temperatures. Here, we designed a novel electrolyte by substituting nitrile solvents for EC, characterized by low de-solvation energy and high ionic conductivity. The correlation between the carbon chain length of nitrile solvents with reduction stability and the Li-solvated coordination was investigated. The results revealed that the valeronitrile (VN) solvent displayed an enhanced lowest unoccupied molecular orbital energy level and low de-solvation energy, which helped construct robust SEI interfacial layers and improved kinetics of interfacial ion transfer in wide-temperature LIBs. The VN-based electrolyte employed in graphite‖NCM523 pouch cells achieved a discharge capacity of 89.84% at a 20C rate at room temperature. Meanwhile, the cell exhibited 3C rate cycling stability even at a high temperature of 55 °C. Notably, the VN-based electrolyte exhibited a high ionic conductivity of 1.585 mS cm at -50 °C. The discharge capacity of pouch cells retained 75.52% and 65.12% of their room temperature capacity at -40 °C and -50 °C, respectively. Wide-temperature-range batteries with VN-based electrolytes have the potential to be applied in various extreme environments.
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http://dx.doi.org/10.1039/d4sc03890h | DOI Listing |
Dalton Trans
January 2025
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
Silicon-based anode materials experience significant volume changes and low conductivity during the lithiation process, which severely hinders their successful application in lithium-ion batteries. Reducing the size of silicon particles and effectively combining them with carbon-based materials are considered the main strategies to enhance the lithium-ion storage performance of silicon-based anodes. In this study, we employed a "bottom-up" strategy to synthesize Si@C anode materials by cross-linking octa-aminopropyl polyhedral oligomeric silsesquioxane (NH-POSS) with terephthalaldehyde and subsequent high-temperature treatment and low-temperature liquid reduction.
View Article and Find Full Text PDFMacromol Rapid Commun
January 2025
Institut für Chemie, Technische Universität Chemnitz, Straße der Nationen 62, 09111, Chemnitz, Germany.
Aromatic diimides such as naphthalene diimide (NDI) and pyromellitic diimide (MDI) are important building blocks for organic electrode materials. They feature a two-electron redox mechanism that allows for energy storage. Due to the smaller size of MDI compared to NDI its theoretical capacity is higher.
View Article and Find Full Text PDFACS Mater Au
January 2025
Solid State and Structural Chemistry Unit, IISc, Bengaluru 560012, Karnataka, India.
LiNiMnO (LNMO), with its high operating voltage, is a favorable cathode material for lithium-ion batteries. However, Ni and Mn dissolution and the associated low cycle life limit their widespread adoption. In this work, we investigate titanium doping as a strategy to mitigate Mn and Ni dissolution from LNMO electrodes.
View Article and Find Full Text PDFDalton Trans
January 2025
State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
Silicon is utilized as a functional material in various fields such as semiconductors, bio-medicine, and solar energy. To prepare Si materials, researchers have proposed methods including carbothermal reduction, hydrothermal reduction, and magnesiothermal reduction, but these strategies often involve high temperatures or unwanted by-products. Herein, we present a low-temperature ionic liquid reduction system to prepare Si nanospheres based on 1-butyl-3-methylimidazolium chloride-aluminum chloride ([Bmim]Cl-AlCl).
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Inner Mongolia Key Laboratory of Chemistry and Physics of Rare Earth Materials, School of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, P. R. China.
Metal-organic frameworks (MOFs) with well-ordered channels are considered ideal solid-state electrolytes (SSEs) for lithium ionic conductors and are expected to be utilized in all-solid-state Li-ion batteries. However, the outstanding Li conductivity of MOFs, especially the properties at low temperatures, has become a crucial problem to overcome. Herein, a breakthrough is first realized to cope with this challenge a strategy of introducing fluoro-substituted bridging ligands in MOFs.
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