多硫化物
硫黄
阳极
锂硫电池
钝化
催化作用
电池(电)
钼
材料科学
氧化还原
化学工程
锂(药物)
化学
无机化学
纳米技术
电极
电化学
有机化学
电解质
图层(电子)
冶金
医学
功率(物理)
物理
物理化学
量子力学
内分泌学
工程类
作者
Min Wu,Zhenyu Xing,Ran Zhu,Xu Liu,Yifan Feng,Wenjie Shao,Rui Yan,Bo Yin,Shuang Li
出处
期刊:Small
[Wiley]
日期:2023-11-08
卷期号:20 (12)
被引量:8
标识
DOI:10.1002/smll.202306991
摘要
Abstract The shuttle effect, which causes the loss of active sulfur, passivation of lithium anode, and leads to severe capacity attenuation, is currently the main bottleneck for lithium‐sulfur batteries. Recent studies have disclosed that molybdenum compounds possess exceptional advantages as a polar substrate to immobilize and catalyze lithium polysulfide such as high conductivity and strong sulfiphilicity. However, these materials show incomplete contact with sulfur/polysulfides, which causes uneven redox conversion of sulfur and results in poor rate performance. Herein, a new type of 2D nano‐channeled molybdenum compounds (2D‐MoN x ) via the 2D organic‐polyoxometalate superstructure for accelerating interfacial polysulfide catalysis toward high‐performance lithium‐sulfur batteries is reported. The 2D‐MoN x shows well‐interlinked nano‐channels, which increase the reactive interface and contact surface with polysulfides. Therefore, the battery equipped with 2D‐MoN x displays a high discharge capacity of 912.7 mAh g −1 at 1 C and the highest capacity retention of 523.7 mAh g −1 after 300 cycles. Even at the rate of 2 C, the capacity retention can be maintained at 526.6 mAh g −1 after 300 cycles. This innovative nano‐channel and interfacial design of 2D‐MoN x provides new nanostructures to optimize the sulfur redox chemistry and eliminate the shuttle effect of polysulfides.
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