4.8 Article

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

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 1, Issue 14, Pages 2063-2071

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jz100708b

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Funding

  1. New Energy and Industrial Development Organization (NEDO) of Japan

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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.

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