Abstract
Co3O4 anode materials exhibit poor conductivity and a large volume change, rendering controlling of their nanostructure essential to optimize their lithium storage performance. Carbon-doped Co3O4 hollow nanofibers (C-doped Co3O4 HNFs), for the first time are synthesized using bifunctional polymeric nanofibers as template and carbon source. Compared with undoped Co3O4 HNFs and solid Co3O4 NFs, C-doped Co3O4 HNFs feature a remarkably high specific capacity, excellent cycling stability, and superior rate capacity as anode materials for lithium-ion batteries. The superior performance of C-doped Co3O4 HNFs electrodes can be attributed to their structural features, which confer enhanced electron transportation and Li+ ion diffusion due to C-doping, and tolerance for volume change due to the 1D hollow structure. Density functional theory calculations provide a good explanation of the observed enhanced conductivity in C-doped Co3O4 HNFs. Carbon-doped Co3O4 hollow nanofibers are synthesized, displaying excellent Li+ ion storage properties including high specific capacity, long-term cycling stability, and outstanding rate capacity. Density functional theory calculations reveal a larger delocalization of the band structure as being responsible for the enhanced conductivity observed.
| Original language | English |
|---|---|
| Pages (from-to) | 1428-1436 |
| Number of pages | 9 |
| Journal | Advanced Functional Materials |
| Volume | 26 |
| Issue number | 9 |
| DOIs | |
| State | Published - 2 Mar 2016 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- CoO
- carbon-doping
- hollow nanofibers
- lithium-ion batteries
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