A N–CoSe/CoSe2–C@Cu hierarchical architecture as a current collector-integrated anode for potassium-ion batteries
The highly reversible insertion/extraction of large-radius K + into electrode materials remains a tough goal, especially for conversion-type materials. Herein, we design a current collector-integrated electrode (N–CoSe/CoSe 2 –C@Cu) as an advanced anode for potassium-ion battery (PIBs). The conducti...
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Veröffentlicht in: | Rare metals 2024-08, Vol.43 (8), p.3702-3712 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The highly reversible insertion/extraction of large-radius K
+
into electrode materials remains a tough goal, especially for conversion-type materials. Herein, we design a current collector-integrated electrode (N–CoSe/CoSe
2
–C@Cu) as an advanced anode for potassium-ion battery (PIBs). The conductive CoSe/CoSe
2
heterojunction with rich Se vacancy defects, conductive sp
2
N-doped carbon layer, and the elastic copper foil matrix can greatly accelerate the electron transfer and enhance the structural stability. Consequently, the well-designed N–CoSe/CoSe
2
–C@Cu current collector-integrated electrode displays enhanced potassium storage performance with regard to a high capacity (325.1 mAh·g
−1
at 0.1 A·g
−1
after 200 cycles), an exceptional rate capability (223.5 mAh·g
−1
at 2000 mA·g
−1
), and an extraordinary long-term cycle stability (a capacity fading of only 0.019% per cycle over 1200 cycles at 2000 mA·g
−1
). Impressively, ex situ scanning electron microscopy (SEM) characterizations prove that the elastic structure of copper foil is merged into the cleverly designed N–CoSe/CoSe
2
–C@Cu heterostructure, which buffers the deformation of structure and volume and greatly promotes the cycle life during the potassium/depotassium process.
Graphical abstract |
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ISSN: | 1001-0521 1867-7185 |
DOI: | 10.1007/s12598-024-02788-5 |