Abstract
Constructing robust 2D−based energy storage nanomaterials by well−defined pore architectures and rational surface modification are critical yet daunting challenges for rechargeable alkali−ion batteries. Herein, a new−type 2D interwoven multi pores decorated Co3O4@N−doped carbon nanosheet with rich surface defects is proposed as lithium/sodium ion anodes for the first time. The combining experimental researches, microscopic structure characterization and dynamics analysis demonstrate that the multi porous structure provides large numbers of channels to accelerate Li+/Na+ transport, rational surface design creates abundant active sites for fast ions reactions, while robust carbon shell offers excellent ionic/electrical conductivity and structural integrity. The obtained bifunctional composites deliver superior rate performance and long−term cycle stability (~529 mA h g−1 after 2000 cycles in LIBs and ~166 mA h g−1 after 1700 cycles in SIBs) due to the synergistic contribution of the unique structure and surface defects. Furthermore, it still remains a high reversible capacity (>610 mA h g−1 after 1000 cycles) in full cell. Kinetic analysis reveals the designed anode exhibits prominent pseudocapacitive behavior, enabling ultra−fast lithium/sodium storage and ultrahigh−rate capability. This work offers valuable insights for developing high performance energy storage devices.
| Original language | English |
|---|---|
| Article number | 105366 |
| Journal | Nano Energy |
| Volume | 78 |
| DOIs | |
| State | Published - Dec 2020 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 7 Affordable and Clean Energy
Keywords
- 2D nanosheets
- Ion channels
- Lithium ion batteries
- Pseudocapacitive behavior
- Sodium ion batteries
Fingerprint
Dive into the research topics of 'Synergistic engineering of defects and architecture in Co3O4@C nanosheets toward Li/Na ion batteries with enhanced pseudocapacitances'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver