普鲁士蓝
聚吡咯
吸附
电化学
金属
金属锂
化学工程
化学
材料科学
锂(药物)
无机化学
电解质
硫黄
电极
纳米技术
有机化学
物理化学
医学
工程类
内分泌学
作者
Meng Du,Xuyu Wang,Pengbiao Geng,Qing Li,Yijing Gu,Yang An,Huan Pang
标识
DOI:10.1016/j.cej.2021.130518
摘要
The development of lithium-sulfur (Li-S) batteries is largely hindered by the shuttling and poor electronic conductivity of polysulfide. To solve these two problems simultaneously, we report a new strategy that combines the advantages of Prussian blue analogues (PBAs) with the conductive characteristic of polypyrrole (ppy) to construct FeCoNi PBA-S-ppy composite. The open metal centers in PBAs act as Lewis acid sites with good affinity to the negatively charged polysulfide anions, while the open framework structure allows effective storage of sulfur and confinement of lithium polysulfides (LiPS). Herein, the polysulfide redox reaction mechanism and kinetics are revealed by using in situ X-ray diffraction. The adsorption ability test and electrochemical performance assessment together with density functional theory calculations reveal that the FeCoNi PBA can achieve enhanced LiPS absorption ability and better cycling performance than the FeNi and FeCo PBAs. This can be attributed to the multi-metal synergistic adsorption toward LiPS within FeCoNi PBA, which can act as an effective chemical-anchor to capture LiPS. After combining the FeCoNi PBA with ppy, a physical barrier formed, and the improvement of the conductivity resulted in remarkable electrochemical performance. We believe that PBAs can play a beneficial role in guaranteeing more stable and efficient Li-S batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI