普鲁士蓝
阳极
有机自由基电池
水溶液
储能
电池(电)
电解质
阴极
无机化学
电化学
材料科学
锂(药物)
离子
化学工程
化学
电极
有机化学
物理化学
功率(物理)
内分泌学
工程类
物理
医学
量子力学
作者
Raphael L. Streng,Silvano Reiser,Sabrina Wager,Nykola Pommer,Aliaksandr S. Bandarenka
出处
期刊:Chemsuschem
[Wiley]
日期:2024-10-23
卷期号:18 (6): e202401469-e202401469
被引量:5
标识
DOI:10.1002/cssc.202401469
摘要
Abstract Aqueous alkali‐ion batteries are gaining traction as a low‐cost, sustainable alternative to conventional organic lithium‐ion batteries. However, the rapid degradation of commonly used electrode materials, such as Prussian Blue Analogs and carbonyl‐based organic compounds, continues to challenge the economic viability of these devices. While stability issues can be addressed by employing highly concentrated water‐in‐salt electrolytes, this approach often requires expensive and, in many cases, fluorinated salts. Here, we show that replacing monovalent K + ions with divalent Ca 2+ ions in the electrolyte significantly enhances the stability of both a copper hexacyanoferrate cathode and a polyimide anode. These findings have direct implications for developing an optimized aqueous Ca‐ion battery that demonstrates exceptional fast‐charging capabilities and ultra‐long cycle life and points toward applying Ca‐based batteries for large‐scale energy storage.
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