| Literature DB >> 24862162 |
Hongbin Yao1, Guangyuan Zheng2, Po-Chun Hsu3, Desheng Kong3, Judy J Cha3, Weiyang Li3, Zhi Wei Seh3, Matthew T McDowell3, Kai Yan3, Zheng Liang3, Vijay Kris Narasimhan3, Yi Cui4.
Abstract
Lithium-sulphur batteries are attractive owing to their high theoretical energy density and reasonable kinetics. Despite the success of trapping soluble polysulphides in a matrix with high surface area, spatial control of solid-state sulphur and lithium sulphide species deposition as a critical aspect has not been demonstrated. Herein, we show a clear visual evidence that these solid species deposit preferentially onto tin-doped indium oxide instead of carbon during electrochemical charge/discharge of soluble polysuphides. To incorporate this concept of spatial control into more practical battery electrodes, we further prepare carbon nanofibers with tin-doped indium oxide nanoparticles decorating the surface as hybrid three-dimensional electrodes to maximize the number of deposition sites. With 12.5 μl of 5 M Li2S8 as the catholyte and a rate of C/5, we can reach the theoretical limit of Li2S8 capacity ~\n1,470 mAh g(-1) (sulphur weight) under the loading of hybrid electrode only at 4.3 mg cm(-2).Entities:
Year: 2014 PMID: 24862162 DOI: 10.1038/ncomms4943
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919