Single step transformation of sulphur to Li2S2/Li2S in Li-S batteries

被引:161
|
作者
Helen, M. [1 ]
Reddy, M. Anji [1 ]
Diemant, Thomas [2 ]
Golla-Schindler, Ute [3 ]
Behm, R. Juergen [1 ,2 ]
Kaiser, Ute [3 ]
Fichtner, Maximilian [1 ,4 ]
机构
[1] Helmholtz Inst Ulm, D-89081 Ulm, Germany
[2] Univ Ulm, Inst Catalysis & Surface Chem, D-89081 Ulm, Germany
[3] Univ Ulm, Electron Microscopy Grp Mat Sci, Cent Facil Electron Microscopy, D-89081 Ulm, Germany
[4] Karlsruhe Inst Technol, Inst Nanotechnol, D-76021 Karlsruhe, Germany
来源
SCIENTIFIC REPORTS | 2015年 / 5卷
关键词
LONG-LIFE; CATHODE MATERIALS; LITHIUM/SULFUR BATTERIES; PERFORMANCE; CELL; COMPOSITES; DISCHARGE; POLYSULFIDES; ADSORPTION; POROSITY;
D O I
10.1038/srep12146
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lithium-sulphur batteries have generated tremendous research interest due to their high theoretical energy density and potential cost-effectiveness. The commercial realization of Li-S batteries is still hampered by reduced cycle life associated with the formation of electrolyte soluble higher-order polysulphide (Li2Sx, x = 4-8) intermediates, leading to capacity fading, self-discharge, and a multistep voltage profile. Herein, we have realized a practical approach towards a direct transformation of sulphur to Li2S2/Li2S in lithium-sulphur batteries by alteration of the reaction pathway. A coconut shell derived ultramicroporous carbon-sulphur composite cathode has been used as reaction directing template for the sulphur. The lithiation/delithiation and capacity fading mechanism of microporous carbon confined sulphur composite was revealed by analyzing the subsurface using X-ray photoelectron spectroscopy. No higher-order polysulphides were detected in the electrolyte, on the surface, and in the subsurface of the cathode composite. The altered reaction pathway is reflected by a single-step profile in the discharge/charge of a lithium-sulphur cell.
引用
收藏
页数:12
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