2D Dynamic Heterogeneous Interface Coupling Endowing Extra Zn 2+ Storage

Aqueous zinc‐ion battery (AZIBs) is expected to be an ideal device for large‐scale energy storage for its high safety and low cost. However, it is still a challenge to achieve both high energy density and high stability. Herein, in situ liquid‐phase growth exfoliation is developed to obtain V 5 O 12...

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Veröffentlicht in:Advanced functional materials 2023-02, Vol.33 (9)
Hauptverfasser: Xiao, Baoquan, Chen, Jie, Hu, Changfa, Mou, Lianshan, Yang, Wenjing, He, Wenhao, Lu, Zhibin, Peng, Shanglong, Huang, Juanjuan
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Sprache:eng
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Zusammenfassung:Aqueous zinc‐ion battery (AZIBs) is expected to be an ideal device for large‐scale energy storage for its high safety and low cost. However, it is still a challenge to achieve both high energy density and high stability. Herein, in situ liquid‐phase growth exfoliation is developed to obtain V 5 O 12 nanosheets, which is then combined with Ti 3 C 2 nanosheets to construct two‐dimensional heterostructure (2D HVO@Ti 3 C 2 ) with interfacial VOTi bonds. 2D HVO@Ti 3 C 2 exhibits a dynamic interface coupling during discharging/charging, accompanied by break/reconstruction of interfacial VOTi bonds. The dynamic interface coupling provides a reversible electron transfer channel and endows the inert Ti 3 C 2 with electrochemical activity in AZIBs, making it an additional electron acceptor and donor, and promoting the insertion of more Zn 2+ . Therefore, a capacity beyond the theoretical capacity of HVO is obtained for the HVO@Ti 3 C 2 . Additionally, the reversible 2D dynamic interface coupling can also effectively alleviate the structural damage during the cycling process. Then, the ultra‐high capacity (457.1 mAh g ‐1 at 0.2 A g ‐1 , over 600 mAh g ‐1 based on the mass of HVO) and high stability (88.9% capacity retention after 1000 cycles at 5 A g ‐1 ) are achieved. This interface coupling mechanism provides an exciting strategy for the high energy density and high stability of AZIBs.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.202211679