Switching Redox-Active Sites by Valence Tautomerism in Prussian Blue Analogues AxMny[Fe(CN)6]•nH2O (A: K, Rb): Robust Frameworks for Reversible Li Storage

被引:174
作者
Okubo, M. [2 ]
Asakura, D. [2 ]
Mizuno, Y. [2 ]
Kim, J-D [3 ]
Mizokawa, T. [4 ]
Kudo, T. [2 ]
Honma, I. [1 ]
机构
[1] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Sendai, Miyagi 9808577, Japan
[2] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058578, Japan
[3] Natl Inst Mat Sci, Tsukuba, Ibaraki 3050044, Japan
[4] Univ Tokyo, Dept Complex Sci & Engn, Chiba 2778581, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2010年 / 1卷 / 14期
关键词
LITHIUM INTERCALATION BEHAVIOR; PHASE-TRANSITION; IN-SITU; ELECTRODE; BATTERIES; LIXFEPO4; SHELL;
D O I
10.1021/jz100708b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The discovery of a new electrode material that provides a reversible Li ion insertion/extraction reaction is of primary importance for Li ion batteries. In this report, electrochemical Li ion insertion/extraction in valence tautomeric Prussian blue analogues A(x)Mn(y)[Fe(CN)(6)] (A: K, Rb) was investigated. Ex situ X-ray diffraction experiments revealed that the K salt without the valence tautomerism exhibits the Li ion insertion/extraction with a redox process of an Fe ion, while the Rb salt with the valence tautomerism exhibits that with a redox process of a Mn ion. Regardless of the redox-active metal ions, highly reversible Li ion storage was achieved. The electronic structure changes during the Li ion insertion/extraction are confirmed by XPS experiments.
引用
收藏
页码:2063 / 2071
页数:9
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