插层(化学)
阴极
石墨
电池(电)
法拉第效率
电解质
钾
材料科学
锂(药物)
钾离子电池
化学工程
电化学
离子
化学
无机化学
电极
磷酸钒锂电池
有机化学
复合材料
物理化学
内分泌学
功率(物理)
冶金
工程类
物理
医学
量子力学
作者
Hong Tan,Dengyun Zhai,Feiyu Kang,Biao Zhang
出处
期刊:Carbon
[Elsevier BV]
日期:2021-03-20
卷期号:178: 363-370
被引量:49
标识
DOI:10.1016/j.carbon.2021.03.027
摘要
Potassium-based dual ion batteries have emerged as promising alternatives to the prevailing lithium-ion batteries due to the advantages in cost and sustainability. Single-anion intercalation into graphite takes place on the cathode side, but it usually delivers a low capacity with poor Coulombic efficiency in potassium-based systems. We demonstrate the performance could be significantly boosted through synergistic dual-anion intercalation of FSI− and PF6−. The presence of PF6− helps the formation of an effective cathode electrolyte interface to allow high anionic stability up to 5.5 V, while FSI− intercalation brings about superior rate capability and long-term cyclic stability. Concurrent intercalation of FSI− and PF6− is tracked by in-situ Raman spectroscopy and ex-situ XRD. It reveals the formation of stage I graphite intercalation compounds (GICs) upon charging, leading to a reversible capacity of over 100 mAh g−1 with an average potential of 4.65 V (vs. K+/K). Furthermore, the graphite-potassium cell delivers an exceptional capacity of 94 mAh g−1 at 0.3 A g−1 and shows capacity retention of 96% after 250 cycles. The strategy provides a novel avenue toward stable dual-ion battery via intercalation chemistry regulation.
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