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Abstract The key challenges for pursuing high‐energy‐density lithium‐sulfur (Li‐S) batteries lie in struggling sulfur conversions under high‐sulfur‐loading and low electrolyte‐to‐sulfur (E/S) ratio conditions. To mimic high‐efficient natural enzymes, in this work, sulfonated cobalt phthalocyanine (CoPC) is implanted in β‐cyclodextrin (β–CD) cavity for preparing β–CD@CoPC biomimetic catalysts, which enables a good electrochemical contact with solvated lithium polysulfides in a locally enriched electrolyte. Moreover, the dynamic stereo‐conformation evolution of CoPC in hydrophobic β–CD cavity promotes subsequent sulfur redox kinetics and induces the separation of Li 2 S from the catalyst, further improving catalysis efficiency. The catalytic activity is quantified through specific Michaelis–Menten equations for enzymatic reactions and it showed that β–CD@CoPC improved catalytic ability by 3 and 30 times compared to that of the β–CD and CoPC catalysts, respectively. As a result, the Li–S pouch cell with mere 1.0 wt% β–CD@CoPC exhibits a high initial areal capacity of 11.6 mAh cm −2 under high‐sulfur‐loading (12.8 mg cm −2 ) and low E/S ratio (3.5 µL mg −1 ). This strategy provides a feasible way to tackle sulfur conversion issues under lean electrolytes for next‐generation high‐energy batteries.
Dong et al. (Fri,) studied this question.