材料科学
水溶液
锌
离子
纳米技术
化学工程
工程物理
冶金
有机化学
化学
工程类
作者
Changlei Zhuang,Siwen Zhang,Zhi Gen Yu,Jinzhang Yang,Ying Sun,Hanyu Wen,Haokun Wen,Hui Li,Bosi Yin,Tianyi Ma
标识
DOI:10.1002/adfm.202419351
摘要
Abstract The performance of aqueous zinc‐ion batteries (AZIBs) at high temperatures (HT) is severely compromised by active water corrosion, parasitic reactions, and dendrite growth. Herein, zinc trifluoroacetate is introduced at a low concentration (0.2 m ), dissolved in triethyl phosphate (TEP)and H 2 O. The active water is suppressed due to the reconstructed original hydrogen bond network, which helps inhibit parasitic reactions and severe corrosion. Meanwhile, a solid electrolyte interphase (SEI) formed on the zinc anode due to the decomposition of the introduced zinc salt. The high‐tolerance SEI physically separates the electrolyte and anode, reducing the corrosion caused by active water. Moreover, TEP, as a prevalent fire‐retardant cosolvent, can preferentially anchor on the zinc sheet, serving as a shielding buffer layer. TEP is not only reconstructing the structure of the electric double layer (EDL), decreasing the content of active water, but also accelerating the prompt formation of SEI further. As proof of this synergistic effect, the assembled symmetric Zn.
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