Al 2 O 3 -Induced Phase Conversion Regulation of WS 2 Anode Enhances the Lithium Storage Reversibility

WS is an attractive anode in alkali metal ion batteries (AMIBs) due to its 2D-layered structure and high theoretical capacity. However, the shuttle effect of sulfur and the spontaneous growth of W nanoparticles are key issues that limit the alkali-ion accommodation ability. Now, it is still a great...

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Veröffentlicht in:ACS applied materials & interfaces 2024-12, Vol.16 (51), p.70596-70605
Hauptverfasser: Zu, Guannan, Zhang, Manchen, Liu, Hexiong, Wang, Juan, Li, Yilong, Wang, Jinshu, Ke, Xiaoxing, Cai, Yongfeng, Chen, Xiaowen, Li, Nan, Fu, Yonghong, Tong, Meijuan, Li, Hongyi
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Sprache:eng
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Zusammenfassung:WS is an attractive anode in alkali metal ion batteries (AMIBs) due to its 2D-layered structure and high theoretical capacity. However, the shuttle effect of sulfur and the spontaneous growth of W nanoparticles are key issues that limit the alkali-ion accommodation ability. Now, it is still a great challenge to achieve in situ control of the microstructure evolution paths in enclosed batteries for extending the cycling reversibility/lifespan. Herein, the phase conversion paths of both film- and powder-type WS anodes are investigated in lithium-ion batteries. It is found that the reversible conversion mechanism is beneficial for alleviating the shuttle effect through strong W-Li S bonding. Also, once the size of the phase-converted W/WS redox pair exceeds ∼10 nm inside the anode layer, the Li storage ability will severely decay due to uncontrollable W precipitation. To maintain high reversibility, amorphous Al O is introduced upon pristine WS . After initializing the battery test, the particle size of the W/WS redox pair is in situ modulated within the range of ∼3-5 nm because of the refinement effect of gradually pulverized Al O . Thus, the decay suppression effect lasting over 750-1400 cycles is obtained with enhanced W ↔ WS conversion efficiency and good capacity retention. This is expected to promote the optimization of Mo-group sulfides/selenides/tellurides toward AMIBs.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.4c17801