Jing Zhang , Lin Li , Mannan Yang , Chen Cheng , Na Tian , Yongzheng Zhang , Dongmao Jiao , Hongzhen Lin , Jian Wang
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引用次数: 0
摘要
在低温锂-S 电池(LT-LSB)中,由于 Li+ 扩散动力学迟缓,多硫化物的转化动力学极不稳定,这一问题仍有待解决。在此,通过在锚定于多孔碳网络(ODVO@PCN)的三氧化二钒上引入氧缺陷,设计出了电子定位纳米催化剂。由于 V2+ 位点与硫物种中的 S 位点之间的杂化作用更强,V2+ 状态的重构活性位点更容易与硫物种相互作用,从而增强了 Li+ 在电解质/电极界面上的转化动力学,实现了低温环境下的快速氧化还原反应。因此,在 0 oC 温度下,使用 ODVO@PCN 动力促进剂的电池在 1 C 时可达到 501 mA h g-1,在 0.5 C 时可长期使用 400 次。
Electron-delocalization catalyzers for high performance, low-temperature Li–S batteries†
The extremely depressive conversion kinetics of polysulfides due to sluggish Li+ diffusion kinetics remain to be resolved for low-temperature Li–S batteries (LT-LSB). Herein, the strategy for electron-delocalization of nanocatalysts has been designed through introducing oxygen defects on vanadium trioxide that was anchored on a porous carbon network (ODVO@PCN). The reconstructed active sites of the V2+ state tend to interact with sulfur species more easily due to the stronger hybridization between V2+ sites and S sites in sulfur species, allowing enhanced Li+ transformation kinetics across the electrolyte/electrode interface for a fast redox reaction in the low-temperature surrounding. Consequently, at a low temperature of 0 °C, the cell with the ODVO@PCN kinetic promotor exhibits 501 mA h g−1 at 1C and a long life time of up to 400 cycles at 0.5C. Reduced to ultralow −10 °C, the cell still provides a capacity of 706 mA h g−1 and stabilizes a remarkable capacity retention of 85% after 100 cycles.
期刊介绍:
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