材料科学
自行车
锌
期限(时间)
离子
氢
纳米技术
冶金
有机化学
化学
物理
考古
量子力学
历史
作者
Ruheng Jiang,Tuoya Naren,Yuejiao Chen,Chen Zhao,Chunxiao Zhang,Yiman Xie,Libao Chen,Yuyang Qi,Qingfei Meng,Weifeng Wei,Liangjun Zhou
标识
DOI:10.1002/adfm.202411477
摘要
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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