Wichmann Lennart, Aboobacker Adil, Heuvel Steffen, Pfeiffer Felix, Hinz Robert-Tobias, Glorius Frank, Cekic-Laskovic Isidora, Diddens Diddo, Winter Martin, Brunklaus Gunther
Forschungszentrum Jülich GmbH, Helmholtz-Institute Münster, IMD-4, Corrensstr. 48, 48149, Münster, Germany.
International Graduate School for Battery Chemistry, Characterization, Analysis, Recycling and Application (BACCARA), University of Münster, Corrensstr. 40, 48149, Münster, Germany.
Angew Chem Int Ed Engl. 2025 Aug 25;64(35):e202506826. doi: 10.1002/anie.202506826. Epub 2025 Jul 20.
High concentrations of conducting salt in electrolyte formulations enhance the agglomeration of ionic species, which has been demonstrated to yield anion-derived electrode-electrolyte interphases and improved reversibility in several battery configurations. However, industrial application of these electrolytes may be limited due to high costs of electrolyte conducting salts. Here, weakly solvating electrolyte solvents with tailored coordination strength have been established as an approach to achieve ionic agglomeration at moderate conducting salt concentrations and without per-fluorinated diluents. However, the inevitable presence of uncoordinated solvent molecules in this electrolyte concept renders them susceptible to oxidative decomposition. Although previous efforts demonstrated fluorination as an effective design strategy to tailor the oxidative stability of weakly solvating electrolytes, the per-fluorinated solvents are toxic and harmful to the environment. Herein, the incorporation of silicon is evaluated as an eco-friendly approach to dispel electron density of the oxygen lone pair. Though steric demand of substituents is already sufficient to tailor the coordination strength, negative hyperconjugation effectively expands the oxidative stability limit of weakly solvating electrolytes. Combining ion agglomeration and intrinsic oxidative stability, the herein introduced weakly solvating electrolyte enables a notable improvement of reversibility under eco-friendly conditions, presenting a valid alternative to fluorinated electrolyte solvents.
电解质配方中高浓度的导电盐会增强离子物种的团聚,这已被证明会产生源自阴离子的电极 - 电解质界面,并在几种电池配置中提高可逆性。然而,由于电解质导电盐成本高昂,这些电解质的工业应用可能会受到限制。在此,具有定制配位强度的弱溶剂化电解质溶剂已被确立为一种在中等导电盐浓度下且无需全氟稀释剂即可实现离子团聚的方法。然而,在这种电解质概念中不可避免地存在未配位的溶剂分子,这使得它们易于氧化分解。尽管先前的研究表明氟化是一种调整弱溶剂化电解质氧化稳定性的有效设计策略,但全氟溶剂有毒且对环境有害。在此,评估了引入硅作为一种生态友好的方法来消除氧孤对电子的电子密度。尽管取代基的空间需求已经足以调整配位强度,但负超共轭有效地扩展了弱溶剂化电解质的氧化稳定性极限。结合离子团聚和固有的氧化稳定性,本文引入的弱溶剂化电解质在生态友好条件下能够显著提高可逆性,为氟化电解质溶剂提供了一种有效的替代方案。