材料科学
电极
硫黄
互连性
电化学
结(造纸)
阴极
合理设计
离子
多硫化物
吸附
纳米技术
化学工程
复合材料
计算机科学
工程类
电解质
物理化学
人工智能
有机化学
化学
冶金
作者
Chunlong Dai,Linyu Hu,Xinyu Li,Qiyong Xu,Rui Wang,Heng Liu,Hao Chen,Shu−Juan Bao,Yuming Chen,Graeme Henkelman,Chang Ming Li,Maowen Xu
出处
期刊:Nano Energy
[Elsevier BV]
日期:2018-11-01
卷期号:53: 354-361
被引量:72
标识
DOI:10.1016/j.nanoen.2018.08.065
摘要
Rational design of Li-S batteries requires efficient prevention of sulfur mobility and fast redox kinetics while accommodating the volumetric expansion of the sulfur cathode. Herein, we propose a multifunctional Chinese knot-like electrode design for advanced Li-S batteries. NiCo2S4 nanotubes are closely interwoven to form Chinese knot-like designs as a sulfur host. The unique interconnectivity of the 2D Chinese knot-like networks constructed by 1D nanostructured nanotubes enables fast electron transfer for high capacity. Furthermore, the hollow structure can simultaneously provide enough space for volumetric expansion of sulfur and confine lithium polysulfides (LiPSs) in the internal void space by structural encapsulation. Besides these, experimental and theoretical analysis demonstrates that NiCo2S4 can effectively capture the LiPSs and then catalyze the captured LiPSs into solid Li2S2/Li2S. More importantly, the transition between low-spin and high-spin of Co ions, induced by extra sulfur atoms from LiPSs, provides an electronic way to stabilize the adsorption system and reduce system energy, leading to the inhibition of the shuttle effect in Li-S batteries. As a result, the Chinese knot-like [email protected]2S4 electrodes show a high capacity of 1348 mA h g−1 at 0.1 C and long cycling life up to 1000 cycles with a slow capacity decay of 0.02% per cycle at 1 C. Even with a higher sulfur loading of 5 mg cm−2, the electrodes still deliver good electrochemical performance.
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