Engineering semicoherent interface with O–Fe–Se coordination for boosting the capacity and rate capability of a battery-type supercapacitor anode
The low capacity and rate capability of the battery-type supercapacitor anode prevent its widespread application. In this paper, we construct a semicoherent heterojunction of Fe 2 O 3 /FeSe 2 as an advanced battery-type supercapacitor anode to overcome the bottleneck. A series of characterization an...
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Veröffentlicht in: | Science China materials 2023-05, Vol.66 (5), p.1767-1778 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The low capacity and rate capability of the battery-type supercapacitor anode prevent its widespread application. In this paper, we construct a semicoherent heterojunction of Fe
2
O
3
/FeSe
2
as an advanced battery-type supercapacitor anode to overcome the bottleneck. A series of characterization and first-principles calculations confirm that the special heterointerface manipulation automatically generates a stronger inherent electric field, thereby enhancing the electron transport rate and the OH
−
adsorption capacity. In addition, it facilitates additional redox reactions between the active materials and OH
−
and makes the reaction system easier to execute. Taking advantage of these benefits, the prepared anode has a high specific capacity of 199.2 mA h g
−1
(1 A g
−1
) and retains 90.2% of its initial capacity after 5000 cycles at 105.8 mA h g
−1
(10 A g
−1
). In addition, an asymmetric supercapacitor device is fabricated with the prepared Fe
2
O
3
/FeSe
2
as the anode, which provides a maximum energy density of 52.55 W h kg
−1
at 0.8 kW kg
−1
and a capacity retention of 91.2% even after 15,000 cycles. In our work, a novel strategy for the optimal design of a battery-type supercapacitor anode with a large capacity and superior rate capability is conceived, significantly advancing the widespread application of transition metal compounds in energy storage systems. |
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ISSN: | 2095-8226 2199-4501 |
DOI: | 10.1007/s40843-022-2330-6 |