Affiliation:
1. Key Laboratory of Carbon Materials of Zhejiang Province Wenzhou University Wenzhou 325035 China
2. State Key Laboratory of Silicon and Advanced Semiconductor Materials School of Materials Science and Engineering Zhejiang University Hangzhou 310027 China
3. College of Electrical and Electronic Engineering Wenzhou University Wenzhou 325035 China
Abstract
AbstractThe 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 Li2S 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.
Funder
Natural Science Foundation of Zhejiang Province
National Natural Science Foundation of China
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献