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A novel ternary sulfur/carbon@tin dioxide composite with polysulfides-adsorptive shell and conductive core as high-performance lithium‑sulfur battery cathodes.

Authors :
Wu, Yong
Zhang, Wen
Han, Tianli
Shen, Zihan
Cheng, Dong
Zhang, Haikuo
Li, Jinjin
Zhang, Huigang
Liu, Jinyun
Source :
Applied Surface Science. Sep2019, Vol. 489, p462-469. 8p.
Publication Year :
2019

Abstract

A polysulfides-adsorptive and conductive host for sulfur (S) cathode is highly required for Li S batteries. Herein, we present a unique ternary S/C@SnO 2 composite consisting of a 3D tubular core-shell structure in which a carbon matrix as the core is coated by a porous SnO 2 shell. Sulfur is coated on carbon inside the tubes. The S/C@SnO 2 exhibits a good electrochemical performance including a stable capacity of 730 mAh g−1 after cycling for 500 times at 0.1C, along with a fading rate as low as 0.07% per cycle. The capacities recover well during two rounds of rate-performance measurements, exhibiting a recovery rate exceeding 96.3%. The composite also delivers stable capacities when cycling at different charge vs. discharge rates. The polysulfides-adsorptive capability of the SnO 2 shell as an efficient protection shield is demonstrated through density functional theory calculation, which confirms a high surface-energy of SnO 2 towards Li 2 S 4 , Li 2 S 6 , and Li 2 S 8. The porous carbon matrix inside the SnO 2 tubes provides a good conductivity for sulfur and spaces for the volume-change of sulfur. Those features of the ternary S/C@SnO 2 enable it to be a promising cathode candidate for Li S batteries. Unlabelled Image • A unique ternary sulfur/carbon@tin dioxide composite is reported. • Polysulfides-adsorptive shell and conductive core are achieved. • Ternary composite exhibits a high performance for Li S battery. • First-principle modeling confirms a high surface energy of SnO 2 shell. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01694332
Volume :
489
Database :
Academic Search Index
Journal :
Applied Surface Science
Publication Type :
Academic Journal
Accession number :
139275458
Full Text :
https://doi.org/10.1016/j.apsusc.2019.06.052