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With abundant electroactive sites and rapid ion diffusion paths, ultrathin dichalcogenides such as MoS 2 demonstrate enormous potential as anodes for sodium/potassium-ion batteries (SIBs/PIBs). However, ultrahigh-aspectratio nanosheets are very easy to aggregate and re-stack, drastically weakening their intrinsic merits. Here a sustainable dichalcogenide anode is designed via crumpling carbon-pillared atomic-thin MoS 2 nanosheets with CNTs into an elastic ball structure (C-p-MoS 2 /CNTs). In this architecture, the glucose-derived carbon pillars atomic-thin MoS 2 nanosheets and broadens interlayer spacing, ensuring fast Na + /K + diffusion; CNTs act as 3D scaffolds to impede re-stacking of MoS 2 while providing high-speed pathways for electrons; the integration of flexible atomic-thin sheets and high-toughness CNTs further endows the balls with great elasticity to release the cycling stress. Consequently, the C-p-MoS 2 /CNTs material delivers high reversible capacities, outstanding cycling stability, and superior rate performance as anodes for both SIBs and PIBs. Pairing with Na 3 V 2 (PO 4 ) 2 F 3 cathode, the sodiumion coin-cell could operate at a rate up to 50 C at high mass loading of 9.4 mg cm −2 and manifest ultrastable cycling stability at 40 C over 600 cycles. Impressively, the assembled pouch cell can be cycled stably with a high energy density of 188 Wh kg −1 . This study is anticipated to provide inspiration for designing innovative metal dichalcogenides as battery anodes.

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