双锰矿
阴极
锰
电解质
材料科学
插层(化学)
储能
Crystal(编程语言)
离子
镁
水溶液
电极
电池(电)
化学工程
无机化学
氧化锰
化学
冶金
有机化学
程序设计语言
功率(物理)
物理化学
工程类
物理
量子力学
计算机科学
作者
Kwan Woo Nam,Sangryun Kim,So‐Yeon Lee,Michael Salama,Ivgeni Shterenberg,Yosef Gofer,Joo Seong Kim,Eunho Yang,Chan Sun Park,Ju Sik Kim,Seok Soo Lee,Won-Seok Chang,Seok Gwang Doo,Yong Nam Jo,Yousung Jung,Doron Aurbach,Jang Wook Choi
出处
期刊:Nano Letters
[American Chemical Society]
日期:2015-05-22
卷期号:15 (6): 4071-4079
被引量:391
标识
DOI:10.1021/acs.nanolett.5b01109
摘要
Rechargeable magnesium batteries have lately received great attention for large-scale energy storage systems due to their high volumetric capacities, low materials cost, and safe characteristic. However, the bivalency of Mg(2+) ions has made it challenging to find cathode materials operating at high voltages with decent (de)intercalation kinetics. In an effort to overcome this challenge, we adopt an unconventional approach of engaging crystal water in the layered structure of Birnessite MnO2 because the crystal water can effectively screen electrostatic interactions between Mg(2+) ions and the host anions. The crucial role of the crystal water was revealed by directly visualizing its presence and dynamic rearrangement using scanning transmission electron microscopy (STEM). Moreover, the importance of lowering desolvation energy penalty at the cathode-electrolyte interface was elucidated by working with water containing nonaqueous electrolytes. In aqueous electrolytes, the decreased interfacial energy penalty by hydration of Mg(2+) allows Birnessite MnO2 to achieve a large reversible capacity (231.1 mAh g(-1)) at high operating voltage (2.8 V vs Mg/Mg(2+)) with excellent cycle life (62.5% retention after 10000 cycles), unveiling the importance of effective charge shielding in the host and facile Mg(2+) ions transfer through the cathode's interface.
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