Constructing electronic interconnected bimetallic selenide-filled porous carbon nanosheets for stable and highly efficient sodium-ion half/full batteries
Owing to their large theoretical capacity and relatively high electronic conductivity, transition metal selenides have been investigated as potential anodes for energy storage applications. On the other hand, the quick capacity decline induced by volume expansion during cycling and unconnected condu...
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Veröffentlicht in: | Nanoscale 2021-11, Vol.13 (44), p.18578-18585 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Owing to their large theoretical capacity and relatively high electronic conductivity, transition metal selenides have been investigated as potential anodes for energy storage applications. On the other hand, the quick capacity decline induced by volume expansion during cycling and unconnected conducting network of the transition metal selenide-based electrode severely limit their employment in sodium-ion batteries (SIBs). Herein, a simple solvent ultrasonic technique and pyrolysis selenation process were used to make a porous N-doped carbon nanosheet-supported FeSe
2
/CoSe
2
electrode. The electrochemical kinetics could be improved, and the stress generated by volume expansion could be efficiently adjusted by exquisitely constructed boundary of the FeSe
2
/CoSe
2
-CN electrode. As expected, the FeSe
2
/CoSe
2
-CN porous nanosheets exhibited a high Na
+
storage capacity of 350 mA h g
−1
(10 A g
−1
, 1000 cycles). Kinetic studies were conducted to explore the Na
+
storage mechanism of FeSe
2
/CoSe
2
-CN. The as-constructed full sodium-ion batteries, when combined with Na
3
V
2
(PO
4
)
2
O
2
F, have a phenomenal energy density (109 W h kg
−1
), encouraging the exploration of energy-related components with the high-energy density properties.
Owing to their large theoretical capacity and relatively high electronic conductivity, transition metal selenides have been investigated as potential anodes for energy storage applications. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d1nr05521f |