阳极
材料科学
水溶液
电化学
电池(电)
铵
阴极
储能
离子
化学工程
溶解
钾离子电池
无机化学
纳米技术
电极
化学
有机化学
磷酸钒锂电池
功率(物理)
物理化学
工程类
物理
量子力学
作者
Zhengnan Tian,Vinayak S. Kale,Simil Thomas,Sharath Kandambeth,Issatay Nadinov,Yizhou Wang,Wandi Wahyudi,Yongjiu Lei,Abdul‐Hamid Emwas,Mickaële Bonneau,Osama Shekhah,Osman M. Bakr,Omar F. Mohammed,Mohamed Eddaoudi,Husam N. Alshareef
标识
DOI:10.1002/adma.202409354
摘要
Abstract Aqueous ammonium ion batteries have garnered significant research interest due to their safety and sustainability advantages. However, the development of reliable ammonium‐based full batteries with consistent electrochemical performance, particularly in terms of cycling stability, remains challenging. A primary issue stems from the lack of suitable anode materials, as the relatively large NH 4 + ions can cause structural damage and material dissolution during battery operation. To address this challenge, an Aza‐based covalent organic framework (COF) material is introduced as an anode for aqueous ammonium ion batteries. This material exhibits superior ammonium storage capabilities compared to existing anode materials. It operates effectively within a negative potential range of 0.3 to‒1.0 V versus SCE, achieves high capacity even at elevated current densities (≈74 mAh g −1 at 10 A g −1 ), and demonstrates exceptional stability, retaining a capacity over 20 000 cycles at 1.0 A g −1 . Furthermore, by pairing this COF anode with a Prussian blue cathode, an ammonium rocking‐chair full battery is developedd that maintains 89% capacity over 20 000 cycles at 1.0 A g −1 , surpassing all previously reported ammonium ion full batteries. This study offers insights for the design of future anodes for ammonium ion batteries and holds promise for high‐energy storage solutions.
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