材料科学
螯合作用
阳极
水溶液
金属
图层(电子)
生物量(生态学)
无机化学
化学工程
冶金
纳米技术
电极
有机化学
物理化学
化学
海洋学
地质学
工程类
作者
Hao Wu,Hongting Yin,Jin‐Lin Yang,Ruiping Liu
标识
DOI:10.1002/aenm.202501359
摘要
Abstract The detrimental dendrite growth and hydrogen evolution corrosion on Zn metal anode greatly hinder the implement of aqueous zinc batteries. Constructing a stable solid electrolyte interphase (SEI) on Zn anode is considered an effective strategy to prolong the cells life. Herein, by using poly(N‐[2‐(3,4‐dihydroxyphenyl)ethyl]‐2‐methylacrylamide) (PDMA) as a case study, the impact of Zn 2+ chelation effect on SEI layer generation is systematically investigated. The DMA monomer tends to form a robust PDMA layer on Zn anode with a higher crosslinking degree with the assistant of Zn 2+ . The Zn─O interaction between Zn metal and PDMA guarantees the long‐term protection efficiency of the SEI layer and uniformizes the Zn nucleation. Moreover, the Zn 2+ desolvation can be propelled by the zincophilic hydroxyl groups in PDMA. As expected, the Zn symmetric cell with in‐PDMA showcases an extended lifespan of over 3800 h. The Zn||NVO full cell maintains a capacity of 150 mAh g −1 after 1000 cycles at 1 A g −1 . This work is believed to guide the future aqueous Zn anode design based on the protective layer engineering.
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