阳极
材料科学
水溶液
化学工程
电解质
电化学
极化(电化学)
钝化
电镀
电池(电)
制作
枝晶(数学)
过电位
锌
各向同性腐蚀
纳米技术
阴极
无机化学
过渡金属
蚀刻(微加工)
电偶阳极
氢
三元运算
电极
容量损失
原子层沉积
作者
Yena Jiang,Ting Hu,Hao Zhong,Luoshi Liang,Yanhua Peng,Yuhong Luo,Hanxin Wei,Zhi-Guang Xu,Yongbo Wu,Xiaoming Lin
出处
期刊:Small
[Wiley]
日期:2026-08-13
卷期号:: e74956-e74956
摘要
ABSTRACT Aqueous zinc‐ion batteries (AZIBs) suffer from poor Zn anode stability in aqueous electrolytes, arising from disordered Zn deposition and parasitic reactions. While artificial solid electrolyte interfaces mitigate these issues, their fabrication is complex and time‐consuming. In this study, an ultrafast chemical solution reaction and selective etching are designed to in situ exfoliate a highly durable (002) plane‐exposed GA@Zn layer across the non‐uniform topography of the primary zinc substrate, effectively addressing these problems. Theoretical calculations combined with the experimental characterization show that a specific (002)‐dominant GA@Zn layer, as a multifunctional structure, mitigates the electrodeposition “tip effect” and suppresses dendrite formation. Moreover, the surface polarization field regulates interfacial electric field distribution, guiding uniform Zn 2+ diffusion and deposition, while preventing water‐Zn direct contact, increasing hydrogen evolution overpotential, and eliminating side reactions. Consequently, the 4%GA@Zn symmetric cell maintains stable cycling for more than 4200 h at 2 mA cm −2 , and the Znǁσ‐MnO 2 full battery keeps an 80% capacity retention rate after 1000 cycles at 1 A g −1 . The present investigation offers a straightforward method for developing high‐stability Zn anodes for advanced AZIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI