Li Lin, Liu Luojia, Hu Zhe, Lu Yong, Liu Qiannan, Jin Song, Zhang Qiu, Zhao Shuo, Chou Shu-Lei
Key Laboratory of Advanced Energy Materials Chemistry, Renewable Energy Conversion and Storage Center (RECAST), College of Chemistry, Nankai University, Tianjin, 300071, China.
Institute for Superconducting and Electronic Material, Australian Institute for Innovative Materials, University of Wollongong, Innovation Campus, Squires Way, North Wollongong, New South Wales, 2522, Australia.
Angew Chem Int Ed Engl. 2020 Jul 27;59(31):12917-12924. doi: 10.1002/anie.202001966. Epub 2020 May 29.
Graphite shows great potential as an anode material for rechargeable metal-ion batteries because of its high abundance and low cost. However, the electrochemical performance of graphite anode materials for rechargeable potassium-ion batteries needs to be further improved. Reported herein is a natural graphite with superior rate performance and cycling stability obtained through a unique K -solvent co-intercalation mechanism in a 1 m KCF SO diethylene glycol dimethyl ether electrolyte. The co-intercalation mechanism was demonstrated by ex situ Fourier transform infrared spectroscopy and in situ X-ray diffraction. Moreover, the structure of the [K-solvent] complexes intercalated with the graphite and the conditions for reversible K -solvent co-intercalation into graphite are proposed based on the experimental results and first-principles calculations. This work provides important insights into the design of natural graphite for high-performance rechargeable potassium-ion batteries.
由于石墨储量丰富且成本低廉,它作为可充电金属离子电池的负极材料具有巨大潜力。然而,用于可充电钾离子电池的石墨负极材料的电化学性能仍需进一步提高。本文报道了一种天然石墨,通过在1 m KCF SO二甘醇二甲醚电解液中独特的K -溶剂共嵌入机制,获得了优异的倍率性能和循环稳定性。通过非原位傅里叶变换红外光谱和原位X射线衍射证明了共嵌入机制。此外,基于实验结果和第一性原理计算,提出了与石墨嵌入的[K-溶剂]配合物的结构以及K -溶剂可逆共嵌入石墨的条件。这项工作为高性能可充电钾离子电池天然石墨的设计提供了重要见解。