摘要
The multistep redox reactions of lithium–sulfur batteries involve undesirably complex transformation between sulfur and Li2S, and it is tough to spontaneously fragmentate polysulfides into shorter chains Li2S originating from the sluggish redox kinetics of soluble polysulfide intermediates, causing serious polarization and consumption of sulfur. In this work, 3,4,9,10-perylenetetracarboxylic diimide (PTCDI)/G is employed as sulfur host to accelerate the conversion process between polysulfides and sulfur, which could facilitate the process of both charging and discharging. Moreover, PTCDI has strong adsorption capacity with polysulfides to restrain shuttle effect, resulting in promotional kinetics and cycle stability. A high initial capacity of 1496 mAh g−1 at 0.05 C and slight capacity decay of 0.009% per cycle at 5 C over 1500 cycles can be achieved. Moreover, the cathode could also achieve a high energy efficiency over 85% at 0.5 C. This research extends the knowledge into an original domain for designing high-performance host materials.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 1900958 |
| 期刊 | Advanced Science |
| 卷 | 6 |
| 期 | 21 |
| DOI | |
| 出版状态 | 已出版 - 1 11月 2019 |
| 已对外发布 | 是 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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可持续发展目标 7 经济适用的清洁能源
指纹
探究 'Redox Mediator: A New Strategy in Designing Cathode for Prompting Redox Process of Li–S Batteries' 的科研主题。它们共同构成独一无二的指纹。引用此
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