Water Catchers within Sub‐Nano Channels Promote Step‐by‐Step Zinc‐Ion Dehydration Enable Highly Efficient Aqueous Zinc‐Metal Batteries

材料科学 水溶液 阳极 金属 法拉第效率 电解质 水溶液中的金属离子 阴极 化学工程 电偶阳极 无机化学 电化学 纳米- 化学 冶金 电极 有机化学 复合材料 阴极保护 工程类 物理化学
作者
Dongming Xu,Zhe Wang,Chengjun Liu,Haoyu Li,Feng Ouyang,Benqiang Chen,Weihang Li,Xueting Ren,Lishun Bai,Zhi Chang,Shuquan Liang,Haoshen Zhou
出处
期刊:Advanced Materials [Wiley]
标识
DOI:10.1002/adma.202403765
摘要

Abstract Zinc metal suffered from violent and long‐lasting water‐induced side reactions and uncontrollable dendritic Zn growth, which seriously reduced the coulombic efficiency (CE) and lifespan of aqueous zinc‐metal batteries (AZMBs). To suppress the corresponding harmful effects of the highly active water, a stable zirconium‐based metal‐organic framework with water catchers decorated inside its sub‐nano channels was used to protect Zn‐metal. Water catchers within narrow channels can constantly trap water molecules from the solvated Zn‐ions and facilitate step‐by‐step desolvation/dehydration, thereby promoting the formation of an aggregative electrolyte configuration, which consequently eliminate water‐induced corrosion and side reactions. More importantly, the functionalized sub‐nano channels also acted as ion rectifiers and promoted fast but even Zn‐ions transport, thereby leading to a dendrite‐free Zn metal. As a result, the protected Zn metal demonstrated an unprecedented cycling stability of more than 10000 hours and an ultra‐high average CE of 99.92% during 4000 cycles. More inspiringly, a practical NH 4 V 4 O 10 //Zn pouch‐cell was fabricated and delivered a capacity of 98 mAh (under high cathode mass loading of 25.7 mg cm −2 ) and preserved 86.2% capacity retention after 150 cycles. This new strategy in promoting highly reversible Zn metal anodes would spur the practical utilizations of AZMBs. This article is protected by copyright. All rights reserved
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