Abstract

Potassium ion batteries are potential energy storage devices owing to their low cost and good K+ diffusion kinetics due to the small Stoke's radius. Here, we report a layered TiS2 cathode material, demonstrating outstanding potassium storage cycling and rate performances in ether-based electrolyte, with a capacity of 80mAhg−1 at 20C and 63mAhg−1 after 600 cycles (1.5–3.0V, corresponding to 4.8Ag−1). The phase transitions during K ion intercalation at the atomic level are explored via High Resolution Transmission Electron Microscopy (HRTEM) and ex-situ X-ray diffraction (XRD) combined with Rietveld refinements. It undergoes a second-stage structure to be K0.11TiS2 and then first-stage K0.56TiS2. The K cations intercalate into trigonal prismatic sites with a sliding of Ti-S plane by 120 degree-rotation, rendering a 3×3 commensurate superstructure along the [001] zone. The K stage intercalation is in favor of a Daumas-Hérold model rather than Rüdorff model. This study demonstrates that the layer structure materials are promising candidates for high performances K-ion batteries and highlights the importance of improving electrochemical performances with electrolyte modification.

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