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Abstract Aqueous Zn‐storage behaviors of MoS 2 ‐based cathodes mainly rely on the ion‐(de)intercalation at edge sites but are limited by the inactive basal plane. Herein, an in‐situ molecular engineering strategy in terms of structure defects manufacturing and O‐doping is proposed for MoS 2 (designated as D‐MoS 2 ‐O) to unlock the inert basal plane, expand the interlayer spacing (from 6.2 to 9.6 Å), and produce abundant 1T‐phase. The tailored D‐MoS 2 ‐O with excellent hydrophilicity and high conductivity allows the 3D Zn 2+ transport along both the ab plane and c ‐axis, thus achieving the exceptional high rate capability. Zn 2+ diffusion through the basal plane is verified by DFT computations. As a proof of concept, the wearable quasi‐solid‐state rechargeable Zn battery employing the D‐MoS 2 ‐O cathode operates stably even under severe bending conditions, showing great application prospects. This work opens a new window for designing high‐performance layered cathode materials for aqueous Zn‐ion batteries.
Li et al. (Fri,) studied this question.