Semimetallic vanadium molybdenum sulfide for high-performance battery electrodes

The ultrathin thickness and lateral morphology of a two dimensional (2D) MoS 2 nanosheet contribute to its high surface-to-volume ratio and short diffusion path, rendering it a brilliant electrode material for lithium-ion batteries (LIBs). However, the low conductivity and easy restacking character...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (2), p.9411-9419
Hauptverfasser: Zhang, Qingfeng, Wang, Longlu, Wang, Jue, Yu, Xinzhi, Ge, Junmin, Zhang, Hang, Lu, Bingan
Format: Artikel
Sprache:eng
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Zusammenfassung:The ultrathin thickness and lateral morphology of a two dimensional (2D) MoS 2 nanosheet contribute to its high surface-to-volume ratio and short diffusion path, rendering it a brilliant electrode material for lithium-ion batteries (LIBs). However, the low conductivity and easy restacking character of the pure MoS 2 nanosheet during extended cycling result in severe capacity fading and poor cycling performance. In this work, we developed an attractive strategy by using a metal-doping method to engineer chemical, physical and electronic properties of MoS 2 , achieving an outstanding performance in LIBs. The computational results show that V-Mo-S has semimetallic properties. Semimetallic vanadium molybdenum sulfide nanoarrays (V-Mo-S NAs) were prepared to overcome the low conductivity of semiconducting MoS 2 and thus further optimize its performance in LIBs. A reversible capacity as high as 1047 mA h g −1 was achieved at 1000 mA g −1 . It also displayed an excellent stability even after 700 cycles. This fascinating study may pave a way for utilizing semimetallic material-based nanomaterials for batteries. The ultrathin thickness and lateral morphology of a two dimensional (2D) MoS 2 nanosheet contribute to its high surface-to-volume ratio and short diffusion path, rendering it a brilliant electrode material for lithium-ion batteries (LIBs).
ISSN:2050-7488
2050-7496
DOI:10.1039/c8ta00995c