Cation and anion co-modulated electrolytes enable highly textured and reversible zinc anodes for durable aqueous batteries

A cation and anion collaboratively regulated electrolyte is developed for durable aqueous Zn batteries. MEP + cations with preferential adsorption on tips promote uniform primary Zn nucleation, followed by dynamic “edge shielding” of existing deposits to guide oriented Zn growth, while Br - anions facilitate reaction kinetics. Meanwhile, both ions of MEPBr contribute to reducing the water activity, thereby inhibiting side reactions. Dendrite formation and side reactions, which originate from uncontrolled zinc (Zn) nucleation and growth and high water activity, remain the two critical challenges that hinder the practical implementation of Zn anodes for rechargeable aqueous batteries. In this work, we propose a cation and anion co-modulation strategy to realize highly textured and durable Zn anodes. As a proof of concept, 1-ethyl-1-methylpyrrolidinium bromide (MEPBr) is selected as a versatile additive to regulate Zn deposition. Specifically, MEP + cations with preferential adsorption on tips/edges first promote uniform primary Zn nucleation on the substrate, followed by dynamic “edge shielding” of existing deposits to guide highly oriented Zn growth. Meanwhile, the incorporation of Br − anions promotes the enrichment of Zn 2+ at the electrode–electrolyte interface (EEI), thereby facilitating Zn deposition kinetics. In addition, both the preferentially adsorbed MEP + cations and Br − anions create a water-poor EEI while the two ionic species disrupt the original hydrogen bond network and reduce water within the solvation structure in the bulk electrolyte through ion-water interactions, thus dramatically reducing water-induced side reactions. As a result, the Zn//Zn symmetric battery with the MEPBr-modulated electrolyte exhibits a remarkable lifespan of over 4000 h at 2 mA cm −2 and 1 mA h cm −2 . More excitingly, the newly designed electrolyte enables a Zn//NaV 3 O 8 ·1.5H 2 O full battery with a thin Zn anode (50 μm) and a high mass-loading cathode (∼10 mg cm −2 ) to operate normally for over 300 cycles with remarkable capacity retention, showcasing its great potential for practical applications.

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Publication Details

Journal
Journal of Energy Chemistry
Published
2025-03-22
DOI
https://doi.org/10.1016/j.jechem.2025.03.010
Citations
20
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
14.61

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article

Cation and anion co-modulated electrolytes enable highly textured and reversible zinc anodes for durable aqueous batteries

Maochun Wu, Ang Li, Zeyu Xu, Xinyu Zhang
20 citations
Journal of Energy Chemistry
Advanced battery technologies research
14.61
article

Cation and anion co-modulated electrolytes enable highly textured and reversible zinc anodes for durable aqueous batteries

Maochun Wu, Ang Li, Zeyu Xu, Xinyu Zhang
article en
20 citations

Abstract

A cation and anion collaboratively regulated electrolyte is developed for durable aqueous Zn batteries. MEP + cations with preferential adsorption on tips promote uniform primary Zn nucleation, followed by dynamic “edge shielding” of existing deposits to guide oriented Zn growth, while Br - anions facilitate reaction kinetics. Meanwhile, both ions of MEPBr contribute to reducing the water activity, thereby inhibiting side reactions. Dendrite formation and side reactions, which originate from uncontrolled zinc (Zn) nucleation and growth and high water activity, remain the two critical challenges that hinder the practical implementation of Zn anodes for rechargeable aqueous batteries. In this work, we propose a cation and anion co-modulation strategy to realize highly textured and durable Zn anodes. As a proof of concept, 1-ethyl-1-methylpyrrolidinium bromide (MEPBr) is selected as a versatile additive to regulate Zn deposition. Specifically, MEP + cations with preferential adsorption on tips/edges first promote uniform primary Zn nucleation on the substrate, followed by dynamic “edge shielding” of existing deposits to guide highly oriented Zn growth. Meanwhile, the incorporation of Br − anions promotes the enrichment of Zn 2+ at the electrode–electrolyte interface (EEI), thereby facilitating Zn deposition kinetics. In addition, both the preferentially adsorbed MEP + cations and Br − anions create a water-poor EEI while the two ionic species disrupt the original hydrogen bond network and reduce water within the solvation structure in the bulk electrolyte through ion-water interactions, thus dramatically reducing water-induced side reactions. As a result, the Zn//Zn symmetric battery with the MEPBr-modulated electrolyte exhibits a remarkable lifespan of over 4000 h at 2 mA cm −2 and 1 mA h cm −2 . More excitingly, the newly designed electrolyte enables a Zn//NaV 3 O 8 ·1.5H 2 O full battery with a thin Zn anode (50 μm) and a high mass-loading cathode (∼10 mg cm −2 ) to operate normally for over 300 cycles with remarkable capacity retention, showcasing its great potential for practical applications.

Journal of Energy ChemistryVol. 106
Hong Kong Polytechnic University (HK)
Hong Kong Polytechnic University
Openalex Percentile: Top 1%
Advanced battery technologies research
14.61
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