High energy density potassium-based dual graphite battery with high concentration carbonate electrolyte
Dual ion batteries (DIBs) differ from traditional lithium-ion and sodium-ion batteries in that the electrolyte acts as a significant source of active materials in DIBs, directly influencing the specific capacity, charge-discharge efficiency, and cycle life. Traditional potassium (K)-based dual ion b...
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Veröffentlicht in: | Journal of power sources 2024-12, Vol.624, p.235565, Article 235565 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Dual ion batteries (DIBs) differ from traditional lithium-ion and sodium-ion batteries in that the electrolyte acts as a significant source of active materials in DIBs, directly influencing the specific capacity, charge-discharge efficiency, and cycle life. Traditional potassium (K)-based dual ion batteries use electrolytes with concentrations below 1 m (mol kg−1), which exhibit a comparatively low oxidation potential of ∼4.4 V versus K/K+. This limits the operational longevity and energy density of the batteries. To enhance the electrochemical stability of the electrolyte and improve the capacity and reversibility of anions/cations intercalating into graphite electrodes, this study introduces a 10.0 m potassium bis(fluorosulfonyl)imide (KFSI) in carbonate ester electrolytes. The results show that increasing the electrolyte concentration effectively raises the oxidation potential to 6.1 V vs. K/K+. A K-dual graphite dual ion battery (K-DGDIB) is assembled using 10.0 m KFSI/ethylene carbonate (EC):dimethyl carbonate (DMC) electrolyte and incorporates both a graphite cathode and a graphite anode. This battery provides a discharge capacity of 94.2 mAh g−1 at 100 mA g−1, a discharge medium voltage of ∼4.24 V, and an energy density of ∼5.8 Wh kg−1 considering the total mass of all added electrolyte and the total mass of the active materials.
•The high-concentration strategy expands the electrolyte's voltage window to 6.1 V.•Enhances the intercalation/deintercalation of K+ and FSI− within the graphite layers.•Promotes the main salt decomposition while inhibiting solvent decomposition. |
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ISSN: | 0378-7753 |
DOI: | 10.1016/j.jpowsour.2024.235565 |