Enhanced Hydrogen Bonding Through Strong Water‐Locking Additives for Long‐Term Cycling of Zinc Ion Batteries

Abstract The promising energy storage devices, zinc ion batteries (ZIBs), face challenges such as dendritic growth and side reactions, which hinder their application and development. As a polar group, hydroxyl groups can utilize hydrogen bonding to stably anchor water molecules, preventing contact between water and the anode. Moreover, they can attract and guide Zn 2+ to rapidly and uniformly deposit on the anode. Here, the introduction of multi‐hydroxyl water‐locking additive Lactobionic acid (LA) molecules is proposed into conventional electrolytes. Through an in situ reaction between the highly reactive carboxyl groups on LA molecules and the zinc anode, a stable multi‐hydroxyl protective layer is formed on the anode surface, effectively preventing interface corrosion and dendritic growth. As a result, the Zn||Zn symmetric cell with LA exhibits remarkable performance, cycling for 2300 h under 1 mA cm −2 and 1 mAh cm −2 . Even under more rigorous conditions of 10 mA cm −2 and 10 mAh cm −2 , it maintains over 800 h of cycling durability. Moreover, in the Zn||NH 4 V 4 O 10 full cell configuration, an impressive capacity retention rate of 80.35% after 2000 cycles at a current density of 5 A g −1 . This innovative method can open a new avenue for designing high‐performance ZIBs.

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Institutions

Publication Details

Journal
Advanced Functional Materials
Published
2024-09-23
DOI
https://doi.org/10.1002/adfm.202411477
Citations
69
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
14.40

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article

Enhanced Hydrogen Bonding Through Strong Water‐Locking Additives for Long‐Term Cycling of Zinc Ion Batteries

Qingfei Meng, Tuoya Naren, Liangjun Zhou, Yiman Xie et al.
69 citations
Advanced Functional Materials
Advanced battery technologies research
14.40
article

Enhanced Hydrogen Bonding Through Strong Water‐Locking Additives for Long‐Term Cycling of Zinc Ion Batteries

Qingfei Meng, Tuoya Naren, Liangjun Zhou, Yiman Xie, Weifeng F. Wei, Yuejiao Chen, Ruheng Jiang, Libao Chen, Chunxiao Zhang, Chen Zhao, Yuyang Qi
article en
69 citations

Abstract

Abstract The promising energy storage devices, zinc ion batteries (ZIBs), face challenges such as dendritic growth and side reactions, which hinder their application and development. As a polar group, hydroxyl groups can utilize hydrogen bonding to stably anchor water molecules, preventing contact between water and the anode. Moreover, they can attract and guide Zn 2+ to rapidly and uniformly deposit on the anode. Here, the introduction of multi‐hydroxyl water‐locking additive Lactobionic acid (LA) molecules is proposed into conventional electrolytes. Through an in situ reaction between the highly reactive carboxyl groups on LA molecules and the zinc anode, a stable multi‐hydroxyl protective layer is formed on the anode surface, effectively preventing interface corrosion and dendritic growth. As a result, the Zn||Zn symmetric cell with LA exhibits remarkable performance, cycling for 2300 h under 1 mA cm −2 and 1 mAh cm −2 . Even under more rigorous conditions of 10 mA cm −2 and 10 mAh cm −2 , it maintains over 800 h of cycling durability. Moreover, in the Zn||NH 4 V 4 O 10 full cell configuration, an impressive capacity retention rate of 80.35% after 2000 cycles at a current density of 5 A g −1 . This innovative method can open a new avenue for designing high‐performance ZIBs.

Advanced Functional MaterialsVol. 34(49)
Central South University (CN), City University of Hong Kong (HK), Jiangsu Changjiang Electronics Technology (China) (CN)
National Natural Science Foundation of China, Natural Science Foundation for Distinguished Young Scholars of Hunan Province
Openalex Percentile: Top 1%
Advanced battery technologies research
14.40
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