青岛科技大学主页平台管理系统周震芳--中文主页-- Selenium vacancies enable efficient immobilization and bidirectional conversion acceleration of lithium polysulfides for advanced Li-S batteries

Spatial confinement of zeolitic imidazolate framework deposits by porous carbon nanospheres for dual-atom catalyst towards highperformance oxygen reduction reaction: 点击次数：; 关键字：TOTAL-ENERGY CALCULATIONS; REDOX; 摘要：Heterostructures composed of oxides and sulfides (nitrides or carbides) show great potential as sulfur host additives because of the strong adoptability of oxides and catalytic capability of sulfides towards the notorious lithium polysulfides (LiPSs). However, the migration and conversion pathway of LiPSs is seriously confined at a localized interface with inadequate active sites. In this work, the introduction of selenium vacancies into VSe2-x has been demonstrated to successfully synergize the adsorbability and catalytic reactions of LiPSs at an integrated functional surface. The N-doped carbon nanosheets-assembled flower architectures embedded with selenium vacancy-rich VSe2-x and partial vanadium oxides have been controllably synthesized and employed as the cathode additives for lithium-sulfur (Li-S) batteries. Both the experiments and first-principle calculations reveal their strong adsorption to LiPSs and their bidirectional catalytic functionality towards the conversion between S-8 and Li2S. As expected, the charge and discharge kinetics of VSe2-x containing sulfur cathodes is fundamentally improved (an outstanding rate capabilitiy with 693.7 mAh center dot g(-1) at 2 C, a remarkable long-term cyclability within 1,000 cycles at 2 C with S loading 2.27 mg center dot cm(-2), and an excellent areal capacity with 3.44 mAh center dot cm(-2) within 100 cycles at 0.5 C). This work presents an effective resolution to couple the adsorbability and catalytic reactions of LiPSs at the material design perspective, and the insights on bidirectional catalytic functionality are of vital to develop functional materials for advanced Li-S batteries.; 卷号：15; 期号：8; 是否译文：否

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