在金属有机框架中通过氧化插入阳离子的双离子电池阴极
Michael L Aubrey1,2, Jeffrey R Long1,2
1Department of Chemistry, University of California , Berkeley, California 94720, United States.
Journal of the American Chemical Society
|October 6, 2015
概括
一种新型的氧化还原活性金属有机框架Fe2 ((dobpdc) 证明了潜在的电池应用的可逆离子插入. 这种框架对开发先进的储能设备具有前景.
科学领域:
- 材料科学
- 电化学
- 能量储存
背景情况:
- 金属有机框架 (MOF) 为各种应用提供可调节的特性.
- 反氧活性MOF对电化学能量储存具有兴趣.
研究的目的:
- 研究Fe2的离子插入反应.
- 探索Fe2 ((dobpdc) 作为电池中的阴极材料的潜力.
主要方法:
- 合成和表征Fe2 ((dobpdc).
- 用各种离子进行拓性氧化插入反应.
- 电化学测量包括循环电压测量和静电循环.
- 制造和测试一个双离子电池原型.
主要成果:
- Fe2 ((dobpdc) 经历了可逆的,低协调性离子的氧化插入.
- 阳离子插入取决于阳离子大小和溶剂,受到纳米限制的影响.
- 该材料具有很高的初始降解潜力和50个循环的稳定性.
- 一个使用Fe2的双离子电池原型实现了316Wh/kg的特定能量.
结论:
- 由于其可逆的离子插入,Fe2 ((dobpdc) 是离子电池的一个有前途的阴极材料.
- 该研究强调了基于MOF的电化学系统中阴离子大小和溶剂效应的重要性.
- 这项工作为设计高性能能量存储的先进MOF材料铺平了道路.
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