Tunable vacancy defect chemistry on free-standing carbon cathode for lithium-sulfur batteries

被引:30
|
作者
Zhang, Xi [1 ]
Liu, Xiaohong [2 ]
Zhang, Wei [3 ]
Song, Yingze [1 ]
机构
[1] Southwest Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Peoples R China
[2] Natl Univ Singapore Chongqing Res Inst, Chongqing 401123, Peoples R China
[3] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Chongqing 400714, Peoples R China
基金
中国国家自然科学基金;
关键词
Li-S chemistry; Tunable vacancy defects; Free-standing cathode; Electrocatalytic activity; Sulfur redox reaction kinetics; POLYSULFIDES; NANOTUBE;
D O I
10.1016/j.gee.2022.03.006
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The defect chemistry is successfully modulated on free-standing and binder-free carbon cathodes for highly efficient Li-S redox reactions. Such rationally regulated defect engineering realizes the synchronization of ion/electron-conductive and defect-rich networks on the three -dimension carbon cathode, leading to its tunable activity for both relieving the shuttle phenomenon and accelerating the sulfur redox reaction kinetics. As expected, the defective carbon cathode harvests a high rate capacity of 1217.8 mAh g-1 at 0.2 C and a superior capacity retention of 61.7% at 2 C after 500 cycles. Even under the sulfur mass loading of 11.1 mg cm -2, the defective cathode still holds a remarkable areal capacity of 8.5 mAh cm -2.(c) 2022 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communi-cations Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:354 / 359
页数:6
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