Multi-yolk-shell copper oxide@carbon octahedra as high-stability anodes for lithium-ion batteries

Published

Journal Article

© 2016 Elsevier Ltd. Although transition metal oxides have attracted considerable attention for their high energy density as anode materials of lithium-ion batteries, they suffer from large volume expansion during lithiation process, which usually causes fast capacity degradation. Herein, we report a rational design and facile preparation strategy of copper oxide encapsulated mesoporous carbon multi-yolk-shell octahedra, in which multiple CuO nanoparticles are well-confined in the compartments of micro-scale octahedral carbon scaffolds. The advantages of the novel multi-yolk-shell design are that the three-dimensional carbon scaffolds can buffer the volume change and prevent aggregation of CuO nanoparticles during the charge/discharge cycles, provide pathways for electron transport and Li + diffusion, and restrict the thin solid-electrolyte interphase layer to the outer surface of carbon shells. The results demonstrate how the electrochemical properties of anodes can be significantly improved by the multi-yolk-shell nanostructures with greatly enhanced structural stability and electrochemical actuation. Moreover, the micrometer-size CuO@C octahedra reduce the relative quality of SEI, resulting in high Coulombic efficiency and long cycling stability. In Li-ion cells, the CuO@C multi-yolk-shell octahedra anodes deliver a highly-reversible capacity of 598mAhg -1 at 250mAg -1 , excellent rate capacity of 365mAhg -1 at 3000mAg -1 and exhibit long-term cyclability with a capacity of 512mAhg -1 after 300 cycles at 500mAg -1 .

Full Text

Duke Authors

Cited Authors

  • Chen, T; Hu, Y; Cheng, B; Chen, R; Lv, H; Ma, L; Zhu, G; Wang, Y; Yan, C; Tie, Z; Jin, Z; Liu, J

Published Date

  • February 1, 2016

Published In

Volume / Issue

  • 20 /

Start / End Page

  • 305 - 314

International Standard Serial Number (ISSN)

  • 2211-2855

Digital Object Identifier (DOI)

  • 10.1016/j.nanoen.2015.12.024

Citation Source

  • Scopus