Fabrication of amorphous Co/Mo–MnSe x electrode materials for high-performance hybrid supercapacitors

The fabrication of polymetallic selenide nanomaterials as supercapacitor electrode materials via a convenient and efficient design route has become the center of attention in energy storage research. However, the design and synthesis of such materials still does not address the major challenges of o...

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Bibliographic Details
Published inNew journal of chemistry Vol. 47; no. 47; pp. 21865 - 21874
Main Authors Zhang, Qian, Wang, Guoxiang, Chen, Taipu, Wu, Hao, Yuan, Rui, Ai, Boyan, Liang, Pengchao, Fang, Dahui, Min, Qingwang
Format Journal Article
LanguageEnglish
Published 04.12.2023
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Summary:The fabrication of polymetallic selenide nanomaterials as supercapacitor electrode materials via a convenient and efficient design route has become the center of attention in energy storage research. However, the design and synthesis of such materials still does not address the major challenges of optimal energy storage. Herein, we present the synthesis of high-performance selenated polymetallic amorphous Co/Mo–MnSe x supercapacitor electrodes with metal MOFs as precursors. The morphology and capacitance of the electrodes are improved by changing the structure of Co/Mo–MOF through ion doping and hydrothermal selenization. At a current density of 1 A g −1 , the Co/Mo–MnSe x electrode material exhibits an ultrahigh specific capacitance of 3679 F g −1 . In particular, the combined hybrid supercapacitor (HBS) has an excellent energy density of 141.3 W h kg −1 at a power density of 496 W kg −1 and even 79.7 W h kg −1 at a power density of 15 105.3 W kg −1 . It can light up light strips 0.5 and 1.0 m in length. In addition, the superb cycling stability of the electrode material can be corroborated by its retention rate of 96.0% after 35 000 cycles. This work synthesized excellent supercapacitor electrode materials through a facile and novel method and provides insights into the design of MOF-based polymetallic materials.
ISSN:1144-0546
1369-9261
DOI:10.1039/D3NJ03859A