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Se Vacancy Activated Bi 2 Se 3 Nanodots Encapsulated in Porous Carbon Nanofibers for Aqueous Zinc and Ammonium Ion Batteries
Bismuth‐based materials show great potential in aqueous batteries. But it is difficult to design a bifunctional bismuth‐based material for zinc and ammonium ion batteries (ZIBs and AIBs). Herein, a electrospinning method followed by a selenization strategy is used to design Bi 2 Se 3 nanodots embedd...
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Published in: | Advanced functional materials 2024-11, Vol.34 (48) |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Bismuth‐based materials show great potential in aqueous batteries. But it is difficult to design a bifunctional bismuth‐based material for zinc and ammonium ion batteries (ZIBs and AIBs). Herein, a electrospinning method followed by a selenization strategy is used to design Bi
2
Se
3
nanodots embedded in porous carbon nanofibers. Experimental studies coupled with theoretical calculations prove that the designs of nanodot and Se vacancy improve the transfer and storage of Zn
2+
and NH
4
+
. Bi
2
Se
3
nanodots are restricted to porous carbon nanofibers during cyclic test. An insertion‐type mechanism is revealed by ex situ characterizations. As a result, this well‐designed electrode (6 mg cm
−2
) offers high reversible capacities of 270 mA h g
−1
in ZIBs and 192 mA h g
−1
in AIBs at 0.05 A g
−1
and long‐term cycle life (60% capacity retention at 10 A g
−1
after 20 K cycles for ZIBs, 78% capacity retention at 2 A g
−1
after 9 K cycles for AIBs). Remarkably, it still displays satisfactory performances even at an ultrahigh mass loading of 18 mg cm
−2
. Furthermore, Zn
2+
and NH
4
+
full cells offer high reversible capacities of 120 and 90 mA h g
−1
at 0.05 A g
−1
respectively. This work provides a reference for designing a bifunctional electrode. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.202411430 |