4.7 Article

Stable cathode material enabled by Mg2+ intercalation layered potassium vanadate for high rate and long life potassium ion batteries

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APPLIED SURFACE SCIENCE
卷 633, 期 -, 页码 -

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DOI: 10.1016/j.apsusc.2023.157603

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Cathode material; Potassium ion batteries; Magnesium intercalation; Layered potassium vanadate

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This study achieved significant improvement in the performance of layered potassium vanadate by intercalating magnesium ions, which enhances the electrochemical reaction kinetics and structural stability. The reversible capacity of KVO exceeded 60 mAh/g at 10 mA/g, with 91.5% capacity retention over 1000 cycles at 1000 mA/g. The full cell assembled with Mg-KVO and multi-porous hard carbon demonstrated a reversible capacity of 40.6 mAh/g after 100 cycles at 50 mA/g, with 93% capacity retention. This research provides practical insights for enhancing the electrochemical performance of potassium-ion batteries.
Potassium-ion batteries (PIBs) have become prominent as one kind of next generation electrochemical energy storage technologies recently considering the plentiful potassium resources available. However, the progress of PIBs continues to be impeded by several factors, particularly the large size of K+. As a class of layered oxides with large interlayer spacing, vanadium-based oxides are regarded as promising exploitable cathode materials. Herein, the significant performance improvement of layered potassium vanadate K0.5V2O5 is achieved by the intercalation of Mg2+. The obtained Mg-KVO provides reversible capacity above 60 mAh g  1 at 10 mA g  1, while 91.5% of capacity can be retained at 1000 mA g  1 over 1000 cycles. The full cell assembled with Mg-KVO and multi-porous hard carbon has a reversible capacity of 40.6 mAh g  1 after 100 cycles at 50 mA g  1 with 93% capacity retention, which verifies the superiority of this material in PIBs. Analytical techniques of electro-chemical impedance spectroscopy and galvanostatic intermittent titration technique indicate that the slight amount of Mg2+ endows KVO with better electrochemical reaction kinetics and structural stability by coordi-nating with lattice oxygen during cycling. This study provides practicable insights into enhancing the electro-chemical performance for PIBs.

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