Construction of a core–double-shell structured Si@graphene@Al 2 O 3 composite for a high-performance lithium-ion battery anode
The vast volume expansion of the Si anode during the charging process leads to rapid cycling performance fading and limits its applications in lithium-ion batteries. In this study, a unique core–double-shell structured porous Si@graphene@glycerin-Al 2 O 3 (p-Si@G@g-Al 2 O 3 ) composite is successful...
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Veröffentlicht in: | New journal of chemistry 2023-03, Vol.47 (13), p.6313-6322 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The vast volume expansion of the Si anode during the charging process leads to rapid cycling performance fading and limits its applications in lithium-ion batteries. In this study, a unique core–double-shell structured porous Si@graphene@glycerin-Al
2
O
3
(p-Si@G@g-Al
2
O
3
) composite is successfully prepared by using a porous Si (p-Si) microsphere as the core and graphene(G)/Al
2
O
3
as the double shell layer
via
an electrostatic self-assembly strategy and a glycerin-involved sol–gel process. The addition of glycerin can reduce the nucleation growth rate of Al(OH)
3
during the sol–gel process and enable more uniform deposition of an ultrathin Al
2
O
3
layer on p-Si@G microspheres. Owing to the crucial role of the lithiated Al
2
O
3
(LiAlO
2
)/G double shell layer in shielding the inner p-Si microsphere from the electrolyte and consolidating the mechanical structure of the p-Si microsphere, the synthesized p-Si@G@g-Al
2
O
3
shows good cycling stability with a high reversible capacity of 1804.5 mA h g
−1
at 0.2 A g
−1
and excellent rate capacity with a capacity of 439 mA h g
−1
at 8 A g
−1
, superior to those of p-Si@G and p-Si electrodes. Moreover, the electrochemical performance of p-Si@G@g-Al
2
O
3
can also be further improved by ∼10% by only adding 5 wt% of carbon nanotubes (CNTs) in a slurry, due to the good capability of CNTs in building the interconnecting network between p-Si@G@g-Al
2
O
3
microspheres. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/D2NJ04909K |