材料科学
多硫化物
量子点
阳极
电化学
电解质
锂(药物)
纳米技术
化学工程
电池(电)
碳纤维
电极
复合数
复合材料
化学
物理化学
物理
工程类
内分泌学
功率(物理)
医学
量子力学
作者
Yi Liu,Zhiyuan Ma,Guang Yang,Zhen Wu,Yuting Li,Jie Gu,Jagadis Gautam,Xiangxiang Gong,Aadil Nabi Chishti,Suqin Duan,Chong Chen,Ming Chen,Lubin Ni,Guowang Diao
标识
DOI:10.1002/adfm.202109462
摘要
Abstract Lithium‐sulfur batteries have recently attracted academic/industrial attention due to the high theoretical energy density. However, the capacity decay mainly caused by the polysulfides shuttle effect and poor conductivity of sulfur. Herein, in situ growth of ZnCo 2 O 4 quantum dots (ZCO‐QDs) embedded into the hollow carbon‐carrier sphere (HCS) to form the ZnCo 2 O 4 quantum dots nanocapsule (ZCO‐QDs@HCS) as the multifunctional sulfur host is rationally demonstrated. Based on density‐functional theory calculations, in situ spectroscopic techniques, and electrochemical studies, the synergistic effects on anchoring/catalyzing polysulfide of the ZCO‐QDs@HCS composite in Li‐S batteries is investigated. Interestingly, the ZCO‐QDs@HCS also allows for the controlled release of ZCO‐QDs into the Li‐S electrolyte. Subsequently, it is first discovered that these diffused ZCO‐QDs can act as self‐repairing initiators to stabilize Li metal anodes via rebuilding the damaged solid electrolyte interphase and suppressing Li dendrites growth. With this concept, quantum dots‐based catalyst delivery systems is first constructed in a Li‐S battery, which is similar to the use of nanocarrier‐based drug delivery systems in cancer therapy. The Li‐S cells with the S@ZCO‐QDs@HCS cathode display significantly superior electrochemical performances with a high specific capacity (1350.5 mAh·g −1 at 0.1 C) and excellent cycling stability (capacity decay rate of 0.057% per cycle after 1000 cycles at 3.0 C).
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