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
Hauptverfasser: Song, Jiangnan, Liu, Ting, He, Yinna, Wang, Yiwei, Zhang, Yuxiao, Meng, Alan, Yuan, Xiangcheng, Wang, Lei, Li, Guicun, Zhao, Jian, Li, Zhenjiang
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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.
ISSN:2095-8226
2199-4501
DOI:10.1007/s40843-022-2330-6