首页> 外文期刊>Advanced functional materials >Multifunctional ZnCo_2O_4 Quantum Dots Encapsulated In Carbon Carrier for Anchoring/Catalyzing Polysulfides and Self-Repairing Lithium Metal Anode in Lithium-Sulfur Batteries
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Multifunctional ZnCo_2O_4 Quantum Dots Encapsulated In Carbon Carrier for Anchoring/Catalyzing Polysulfides and Self-Repairing Lithium Metal Anode in Lithium-Sulfur Batteries

机译:封装在碳载体中的多功能ZnCo_2O_4量子点,用于锚定/催化锂硫化物和锂金属负极的自修复

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摘要

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 ZnCo2O4 quantum dots (ZCO-QDs) embedded into the hollow carbon-carrier sphere (HCS) to form the ZnCo2O4 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 center dot 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).
机译:锂硫电池由于理论能量密度高,最近引起了学术界/工业界的关注。但容量衰减主要是由多硫化物穿梭效应和硫导电性差引起的。本文合理地证明了ZnCo2O4量子点(ZCO-QDs)嵌入空心碳载流球(HCS)中形成ZnCo2O4量子点纳米胶囊(ZCO-QDs@HCS)作为多功能硫主体。基于密度泛函理论计算、原位光谱技术和电化学研究,研究了ZCO-QDs@HCS复合材料在Li-S电池中锚定/催化多硫化物的协同效应。有趣的是,ZCO-QDs@HCS 还允许将 ZCO-QD 受控释放到 Li-S 电解液中。随后,首次发现这些扩散的ZCO-QDs可以作为自修复引发剂,通过重建受损的固体电解质界面和抑制Li枝晶生长来稳定Li金属阳极。有了这个概念,基于量子点的催化剂递送系统首先构建在锂硫电池中,这类似于在癌症治疗中使用基于纳米载体的药物递送系统。采用S@ZCO QDs@HCS正极的Li-S电池表现出显著优异的电化学性能,具有高比容量(0.1 C时中心点g(-1)为1350.5 mAh)和优异的循环稳定性(在3°C下循环1000次后,容量衰减率为0.057%。0个分类)。

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