Weakly Coordinated Solvent Network‐Induced Ternary Water‐Deficient Eutectic Electrolytes for Low‐Polarization Zn Anodes
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Le résumé fourni par la source
Eutectic electrolytes are attractive for zinc-based energy storage owing to their green chemistry attributes and intrinsic stability; however, their practical deployment is limited by severe polarization stemming from sluggish ion transport and strong solvation. Here, we propose a ternary water-deficient eutectic electrolyte without water solvent whose polarization approaches that of aqueous systems by engineering a weakly coordinated solvent network via solvation-structure restructuring. A strongly coordinated solvent network enables salt dissolution, whereas the introduction of a weakly coordinating co-solvent disrupts the constrained coordination environment and drives a transition to a dynamic, weakly coordinated solvation structure. This restructuring enhances anion participation while suppressing ion bridging, yielding abundant yet size-confined aggregates, thereby accelerating ion-transport kinetics and lowering desolvation barriers. Furthermore, the formation of a robust solid-electrolyte interphase effectively stabilizes the Zn anode. As a result, the ternary water-deficient electrolyte enables highly reversible Zn plating/stripping with low polarization under ambient conditions, while also delivering excellent low-temperature performance. Enhanced kinetics in Zn||PANI cells and consistent performance across both coin cells and printed energy devices highlight the strong potential of this water-deficient eutectic electrolyte for scalable zinc-ion energy storage.
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Le contrôle bibliographique ouvert
DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.
- Titre Crossref
- Weakly Coordinated Solvent Network‐Induced Ternary Water‐Deficient Eutectic Electrolytes for Low‐Polarization Zn Anodes
- Date Crossref
- 06/09/2026
- Éditeur
- Wiley
- Type
- journal-article
Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.
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