石英晶体微天平
碱金属
电化学
材料科学
电解质
水溶液
离子半径
离子键合
无机化学
X射线光电子能谱
氧化物
晶体结构
同步加速器
超级电容器
化学工程
化学
离子
结晶学
物理化学
电极
吸附
有机化学
工程类
物理
核物理学
冶金
作者
Shin‐Liang Kuo,Nae‐Lih Wu
摘要
Pseudocapacitive charge-storage reaction of in several aqueous alkali and alkaline salts solutions, including , , , , and , has been studied on fine-grained thin films and particles which possess the -type crystal structure. In situ synchrotron X-ray diffraction analysis shows that charge transfer at Mn sites upon reduction/oxidation of is balanced by bulk insertion/extraction of the solution cations into/from the oxide structure, which causes reversible expansion and shrinkage in lattice spacing of the oxide during charge/discharge cycles. Electrochemical quartz-crystal microbalance and X-ray photoelectron spectroscopy data further indicate that plays the predominant role in all cases, while the extent of participation of alkali cations first decreases and then increases with ionic size. The charge-storage reaction can be summarized as: , where is alkali cation.
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