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With abundant electroactive sites and rapid ion diffusion paths, ultrathin dichalcogenides such as MoS2 demonstrate enormous potential as anodes for sodium/potassium‐ion batteries (SIBs/PIBs). However, ultrahigh‐aspect‐ratio 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 MoS2 nanosheets with CNTs into an elastic ball structure (C‐p‐MoS2/CNTs). In this architecture, the glucose‐derived carbon pillars atomic‐thin MoS2 nanosheets and broadens interlayer spacing, ensuring fast Na+/K+ diffusion; CNTs act as 3D scaffolds to impede re‐stacking of MoS2 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‐MoS2/CNTs material delivers high reversible capacities, outstanding cycling stability, and superior rate performance as anodes for both SIBs and PIBs. Pairing with Na3V2(PO4)2F3 cathode, the sodium‐ion 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. [ABSTRACT FROM AUTHOR]

Electrode microstructure is one of the primary factors determining the electrochemical properties of all‐solid‐state batteries (ASSBs). However, the key principles of electrode design to realize fast ionic/electronic transport pathways are not well elucidated. Herein, the correlation between electrode microstructure and electrochemical behaviors is studied through different electrode design in terms of energy‐density‐related electrode composition and Ni‐rich layered oxides particle size distribution. A positive relation between particle size and mass fraction in electrode design is revealed, that is, as the particle size increases, more cathode materials are required to enable the fast reaction kinetics. The well interconnected active particles and solid electrolytes construct the highly percolated ionic/electronic transfer networks, which determines the overall electrochemical properties. The findings in this work give a new insight into electrode design to promote the development of high‐energy and high‐power ASSBs. [ABSTRACT FROM AUTHOR]