Current-density dependence of Li2S/Li2S2 growth in lithium-sulfur batteries

被引:135
作者
Kong, Long [1 ]
Chen, Jin-Xiu [1 ,2 ]
Peng, Hong-Jie [1 ]
Huang, Jia-Qi [3 ]
Zhu, Wancheng [2 ]
Jin, Qi [1 ,4 ]
Li, Bo-Quan [1 ]
Zhang, Xi-Tian [4 ]
Zhang, Qiang [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Beijing Key Lab Green Chem React Engn & Technol, Beijing 100084, Peoples R China
[2] Qufu Normal Univ, Dept Chem Engn, Jining 273165, Shandong, Peoples R China
[3] Beijing Inst Technol, Adv Res Inst Multidisciplinary Sci, Beijing 100081, Peoples R China
[4] Harbin Normal Univ, Sch Phys & Elect Engn, Key Lab Far Photon & Elect Bandgap Mat, Minist Educ, Harbin 150025, Heilongjiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
LI-S BATTERIES; ENERGY DENSITY; PERFORMANCE; REDOX; MECHANISM; KINETICS; POLYSULFIDES; COMPOSITES; CATHODE; DESIGN;
D O I
10.1039/c9ee01257e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur (Li-S) batteries with a high theoretical energy density basedonmulti-electron redox reactionswere strongly considered. The lithium disulfide/sulfide (Li2S2/Li2S, denoted as Li2S1/2) precipitation is critical to achieve high sulfur utilization. However, the kinetic effect on Li2S1/2 precipitation in a working battery has been rarely investigated. Herein, the current-density-dependent Li2S1/2 nucleation/growth was explored and such a dependence served as the guiding principle for the construction of high-sulfur-loading/content Li-S batteries. Generally, the Li2S1/2 nucleation density is proportional to two-third the power of the current density and the shift from a high to low current density alters the Li2S1/2 precipitation pathway from surface deposition to solution-mediated growth. The in-solution growth rate was found to be restricted by the mobilities of polysulfide intermediates and Li2S1/2 in conventional ether electrolytes. The rationalized guideline directed the design of a lightweight, high-surface-area, and open-pore conductive framework for sulfur cathodes, which enabled an extremely high sulfur content of 93.4 wt% in the whole electrode and a high capacity (1269 mA h g(-1)). The present work affords a kinetic understanding of the liquid-solid conversion in working Li-S batteries and optimization schemes for practical operation parameters.
引用
收藏
页码:2976 / 2982
页数:7
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