插层(化学)
阴极
阳极
化学计量学
电池(电)
石墨
电化学
氧化物
材料科学
储能
过渡金属
无机化学
离子
氧化还原
化学
电极
物理化学
冶金
热力学
物理
催化作用
功率(物理)
有机化学
生物化学
作者
Haegyeom Kim,Dong‐Hwa Seo,Alexander Urban,Jinhyuk Lee,Deok‐Hwang Kwon,Shou‐Hang Bo,Tan Shi,Joseph K. Papp,Bryan D. McCloskey,Gerbrand Ceder
标识
DOI:10.1021/acs.chemmater.8b03228
摘要
K-ion batteries are promising alternative energy storage systems for large- scale applications because of the globally abundant K reserves. K-ion batteries benefit from the lower standard redox potential of K/K+ than that of Na/Na+ and even Li/Li+, which can translate into a higher working voltage. Stable KC8 can also be formed via K intercalation into a graphite anode, which contrasts with the thermodynamically unfavorable Na intercalation into graphite, making graphite a readily available anode for K-ion battery technology. However, to construct practical rocking-chair K-ion batteries, an appropriate cathode material that can accommodate reversible K release and storage is still needed. We show that stoichiometric KCrO2 with a layered O3-type structure can function as a cathode for K-ion batteries and demonstrate a practical rocking-chair K-ion battery. In situ X-ray diffraction and electrochemical titration demonstrate that KxCrO2 is stable for a wide K content, allowing for topotactic K extraction and reinsertion. We further explain why stoichiometric KCrO2 is unique in forming the layered structure unlike other stoichiometric K-transition metal oxide compounds, which form nonlayered structures; this fundamental understanding provides insight for the future design of other layered cathodes for K-ion batteries.
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