Huang Xia, Zhang Kai, Luo Bin, Hu Han, Sun Dan, Wang Songcan, Hu Yuxiang, Lin Tongen, Jia Zhongfan, Wang Lianzhou
Nanomaterials Centre, School of Chemical Engineering and Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, QLD, 4072, Australia.
Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, QLD, 4072, Australia.
Small. 2019 Jul;15(29):e1804578. doi: 10.1002/smll.201804578. Epub 2019 Jan 25.
To realize practical lithium-sulfur batteries (LSBs) with long cycling life, designing cathode hosts with a high specific surface area (SSA) is recognized as an efficient way to trap the soluble polysulfides. However, it is also blamed for diminishing the volumetric energy density and being susceptible to side reactions. Herein, polyethylenimine intercalated graphite oxide (PEI-GO) with a low SSA of 4.6 m g and enlarged interlayer spacing of 13 Å is proposed as a superior sulfur host, which enables homogeneous distribution of high sulfur content (73%) and facilitates Li transfer in thick sulfur electrode. LSBs with a moderate sulfur loading (3.4 mg S cm ) achieve an initial capacity of 1157 and 668 mAh g after 500 cycles at 0.5 C. Even when the sulfur loading is increased to 7.3 mg cm , the electrode still delivers a high areal capacity of 4.7 mAh cm (641 mAh g ) after 200 cycles at 0.2 C. The excellent electrochemical properties of PEI-GO are mainly attributed to the homogeneous distribution of sulfur in PEI-GO and the strong chemical interactions between polysulfides and amine groups, which can mitigate the loss of active phases and contribute to the better cycling stability.
为了实现具有长循环寿命的实用锂硫电池(LSB),设计具有高比表面积(SSA)的阴极主体被认为是捕获可溶性多硫化物的有效方法。然而,它也被指责会降低体积能量密度并易发生副反应。在此,提出了一种具有4.6 m²/g的低SSA和13 Å扩大层间距的聚乙烯亚胺插层氧化石墨(PEI-GO)作为一种优异的硫主体,它能够实现高硫含量(73%)的均匀分布,并促进厚硫电极中的锂转移。具有适度硫负载量(3.4 mg S/cm²)的LSB在0.5 C下循环500次后,初始容量分别为1157和668 mAh/g。即使硫负载量增加到7.3 mg/cm²,该电极在0.2 C下循环200次后仍能提供4.7 mAh/cm²(641 mAh/g)的高面积容量。PEI-GO优异的电化学性能主要归因于硫在PEI-GO中的均匀分布以及多硫化物与胺基之间的强化学相互作用,这可以减轻活性相的损失并有助于实现更好的循环稳定性。