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Improving the operating voltage is an effective strategy for enhancing the energy density of lithium-ion batteries. However, this approach raises critical challenges, including oxidative decomposition of the electrolyte and degradation of electrode materials, which urgently require solutions. In this context, nitrile compounds, characterized by their strong electron-withdrawing effect, high dielectric constant, and excellent oxidation stability, have emerged as ideal materials for optimizing high-voltage electrolytes. While some studies have reported the impact of linear nitrile compounds on battery performance, research on cyclic nitrile compounds remains scarce. To address this research gap, we designed a series of nitrile-substituted cyclic carbonates based on ethylene carbonate (EC) and propylene carbonate (PC) and conducted quantum chemical calculations and molecular dynamics simulations. Quantum chemical calculation results demonstrate that introducing a cyano group (-CN) at the methylene or methine position can form a conjugation effect with the C═O group, thereby enhancing the molecular oxidation stability. With the same number of nitrile substituents, the substitution position (methylene vs methine) or cis/trans configuration has a minor influence on the oxidation potential, but the reduction potential of the cis configuration is higher than that of the trans configuration. Geminal disubstitution and methyl-permethyl substitution significantly increase the reduction potential due to synergistic effects. Molecular dynamics simulation results indicate that the introduction of cyano groups restructures the solvation shell, influencing the kinetics of lithium-ion coordination and transport. This work emphasizes the importance of selecting the number and position of nitrile substituents in cyclic carbonates. Based on quantum chemical and molecular dynamics calculation results, we provide candidate molecule screening recommendations for cathode/anode film-forming additives and solvents, aiming to offer practical strategies for improving the electrochemical performance of high-voltage lithium metal/lithium-ion batteries.
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http://dx.doi.org/10.1021/acs.jpcb.5c04193 | DOI Listing |
JMIR Res Protoc
September 2025
Service of Clinical Pharmacology, Department of Medicine, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Background: Janus kinase inhibitors (JAKIs) are small molecules used orally to treat inflammatory and hematological disorders. They have demonstrated impressive efficacy across multiple indications. However, concerns have emerged regarding their safety profile.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2025
Computational Inorganic Chemistry Group, Department of Chemistry, Indian Institute of Technology Hyderabad, Kandi, Sangareddy, Telangana 502284, India.
Over the past few years, alkali and alkaline earth metals have emerged as alternative catalysts to transition metal organometallics to catalyze the hydroboration of unsaturated compounds. A highly selective and cost-effective lithium-catalyzed method for the synthesis of an organoborane has been established based on the addition of a B-H bond to an unsaturated bond (polarized or unpolarized) using pinacolborane (HBPin). In the present work, the neosilyllithium-catalyzed hydroboration of nitriles, aldehydes, and esters has been investigated using high-level DLPNO-CCSD(T) calculations to unravel the mechanistic pathways and substrate-dependent reactivity.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2025
Institut für Anorganische und Analytische Chemie, Technische Universität Braunschweig, Hagenring 30, D-38106 Braunschweig, Germany.
In the structure of the title compound, CHN·CHNOS·CHNOS, the central pyridinic rings are approximately coplanar to the benzo-thia-zole moieties. The phenyl groups are appreciably angled to the central rings [inter-planar angles of 57.30 (3)° for the anion and 79.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2025
Laboratory of Matter Environmental and Solar Energy Sciences Research Team: Crystallography and Molecular Physics Félix Houphouët-Boigny University, Abidjan,Ivory Coast.
The structure of the title compound, CHClN, was determined at low temperature (100 K). In the crystal, the mol-ecules are connected through C-H⋯N and C-H⋯Cl inter-molecular hydrogen bonds generating a network that extend along the [010] direction. In addition, C-H⋯π and π-π stacking inter-actions as well as inter-molecular contacts contribute to the cohesion of the structure.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
September 2025
The structure of 2-[4-(di-cyano-meth-yl)cyclo-hexa-2,5-dien-1-yl]propane-bis-(nitrilium) bis-(hexa-fluorido-arsenate), CHN ·2AsF , has ortho-rhom-bic () symmetry. The compound exhibits a layer structure, which is formed by hydrogen bonds between the semi-protonated nitrile groups. Unexpectedly, no H⋯F contacts are observed.
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