材料科学
腐蚀
阳极
金属
锆
离子键合
水溶液
导电体
电偶阳极
二氧化锆
水溶液中的金属离子
无机化学
导线
化学工程
图层(电子)
离子
纳米技术
冶金
电极
复合材料
阴极保护
物理化学
有机化学
工程类
化学
作者
Binbin Wei,Jiaxian Zheng,Abhishek Abhishek,Xin Liu,Jingang Wu,Zhengbing Qi,Zhuo Hou,Rui Wang,Jidong Ma,Appala Naidu Gandi,Zhoucheng Wang,Hanfeng Liang
标识
DOI:10.1002/aenm.202401018
摘要
Abstract Aqueous Zn batteries, which use metallic Zn as anodes, have gained significant attention due to their affordability and high safety standards. However, these Zn anodes are plagued by issues such as Zn dendritic growth and side reactions, including corrosion and hydrogen evolution. One straightforward yet effective approach to mitigate these issues is to apply protective coatings to the Zn anodes to enhance their reversibility. It is generally believed that these protective layers should have a high affinity for Zn. Contrarily, this study proposes that non‐conductive coatings should form a strong binding with H + ions while maintaining a weaker interaction with Zn 2+ ions, thereby ensuring a higher selectivity for H + over Zn 2+ . This concept is illustrated using zirconium dioxide (ZrO 2 ), an ionic conductor that meets these criteria and effectively curbs side reactions and dendritic growth of Zn. Remarkably, Zn anodes coated with ZrO 2 layer demonstrate a lifespan exceeding 6000 h at 1 mA cm −2 and 1 mAh cm −2 , significantly outperforming uncoated ones, which last <200 h. This discovery introduces a novel design principle for insulating surface coatings, potentially applicable not only for Zn but also for other metal anodes.
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