锰
戒指(化学)
离子
水溶液
电极
化学
无机化学
电荷(物理)
材料科学
光化学
有机化学
物理化学
物理
量子力学
作者
Hyungjin Lee,Amey Nimkar,Netanel Shpigel,Daniel Sharon,Seung‐Tae Hong,Doron Aurbach,Munseok S. Chae
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-10-29
卷期号:9 (11): 5627-5634
被引量:23
标识
DOI:10.1021/acsenergylett.4c02418
摘要
Rechargeable manganese batteries hold promise for large-scale energy storage due to the abundance and eco-friendly nature of manganese. A key challenge is developing cathode materials capable of reversibly inserting Mn ions with a high specific capacity. Here, we demonstrate that perylene-3,4,9,10-tetracarboxylic dianhydride electrodes efficiently and reversibly insert Mn2+ ions in 3 M MnCl2 aqueous electrolyte solutions. Leveraging the carbonyl groups and the π-electron configuration, such compounds can serve as robust redox centers, facilitating reversible interactions with divalent ions such as Mn2+. Through comprehensive studies involving electrochemistry, elemental analyses, spectroscopy, and structural analysis, we explored these systems and found them as promising anode materials for Mn batteries. Demonstrating excellent Mn storage capabilities, such molecules could attain a reversible capacity of approximately >185 mAh g–1 at a current density of 100 mA g–1, maintaining an average voltage of approximately 0.8 V vs Mn/Mn2+, while exhibiting notable capacity retention.
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