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Oxygen-Deficient Titanium Dioxide Nanosheets as More Effective Polysulfide Reservoirs for Lithium-Sulfur Batteries

Journal 2017 · IF 5.317 · 23(40): 9666-9673 · 发表于 2017 年 5 月 16 日
作者: Han-Chi Wang,Chao-Ying Fan,Yan-Ping Zheng,Xiao-Hua Zhang,Wen-Hao Li,Si-Yu Liu,Hai-Zhu Sun,Jing-Ping Zhang,Ling-Na Sun,Xing-Long Wu
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摘要

Graphical Oxygen-deficient cathode : A sulfur cathode modified with oxygen-deficient anatase TiO 2 nanosheets (A-TiO 2− x NSs-S cathode) performs better in lithium-sulfur batteries than the A-TiO 2 NSs-S cathode (see figure). Oxygen vacancies on the surface of the A-TiO 2− x NSs provide robustly interactional active sites for lithium polysulfides, which efficiently relieve the shuttle effect, so the A-TiO 2− x NSs-S cathode shows superior electrochemical properties to the A-TiO 2 NSs-S cathode. In this work, oxygen-deficient anatase TiO 2 nanosheets (A-TiO 2− x NSs) are proposed as a substrate to improve the electrochemical properties of sulfur electrodes for lithium-sulfur (Li-S) batteries. The A-TiO 2− x NSs are prepared by partly reducing pristine TiO 2 nanosheets (A-TiO 2 NSs) in NaBH 4 solution. With some oxygen vacancies on the surface of the TiO 2 nanosheets, A-TiO 2− x NSs not only promote electronic transfer, but also act as more effective polysulfide reservoirs to minimize the dissolution of lithium polysulfides (LiPSs) than the A-TiO 2 NSs control. Hence, upon utilization as modifiers for cathodes of Li-S batteries, the A-TiO 2− x NSs-modified sulfur (A-TiO 2− x NSs-S) cathode exhibits a higher reversible specific capacity and greater cycling performance and rate capability than the A-TiO 2 NSs-modified one (A-TiO 2 NSs-S). For example, A-TiO 2− x NSs-S delivers an initial specific capacity of 1277.1 mAh g −1 at 0.1 C and maintains a stable Coulombic efficiency of approximately 99.2 % after the first five cycles; these values are higher than those of 997.3 mAh g −1 and around 96.7 %, respectively, for A-TiO 2 NSs-S. The enhanced electrochemical properties of the A-TiO 2− x NSs-S cathode can be ascribed mainly to the more effective adsorption of dissolvable and diffused LiPSs by the oxygen vacancies. Therefore, utilization of the structure of oxygen vacancies in Li-S batteries demonstrates great prospects for practical application.