4.7 Article

Enhancing sodium-ion storage performance of MoO2/N-doped carbon through interfacial Mo-N C bond

期刊

SCIENCE CHINA-MATERIALS
卷 64, 期 1, 页码 85-95

出版社

SCIENCE PRESS
DOI: 10.1007/s40843-020-1370-x

关键词

topochemical transformation; Mo-N chemical bond; Na-ion batteries; Na-ion capacitor; density functional theory simulations

资金

  1. National Natural Science Foundation of China [51804089]
  2. Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials [EMFM20181114]
  3. research starting foundation of CAEP [PY20200038]

向作者/读者索取更多资源

Na-ion batteries with MoO2/N-doped carbon anode exhibit excellent cycling stability and rate capability, attributed to the formation of chemical bond at the interface between MoO2 and N-doped carbon. Na-ion capacitors constructed based on this strategy show promising energy density and capacitance retention over extended cycles.
Na-ion batteries (SIBs) have attracted considerable attention as promising alternatives to commercial Li-ion batteries (LIBs) due to comparable redox potential, and natural abundance of Na. However, it remains challenging to explore suitable anodes for SIBs. Herein, a MoO2/N-doped carbon (MoO2/N-C) composite composed of MoO2 nanocrystals embedded within carbon matrix with a Mo-N-C chemical bond is prepared by a simple yet effective carbonization-induced topochemical transformation route. Na-ion half-cells using MoO2/N-C exhibit excellent cycling stability over 5000 cycles at 5 A g(-1) and superior rate capability. Physicochemical characterizations and first-principles density functional theory (DFT) simulations reveal that the formation of chemical bond at the interface between MoO2 and N-doped carbon plays an important role in the excellent charge storage properties of MoO2/N-C. More importantly, the interfacial coupling can efficiently promote interface charge transfer. Benefiting from this, Na-ion capacitors (SICs) constructed with the MoO2/N-C anode and activated carbon cathode can deliver an impressive energy density of 15 W h kg(-1) at a power density of 1760 W kg(-1), together with a capacitance retention of 92.4% over 1000 cycles at 10 A g(-1). The proposed strategy in this paper based on interfacial chemical bond may hold promises for the design of high-performance electrodes for energy storage devices.

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