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A facile synthesis of CuSe nanosheets for high-performance sodium-ion hybrid capacitors

Due to the low price and abundant reserves of sodium resources, sodium-ion batteries have become the main candidate for the next generation of energy storage equipment, particularly for large-scale grid storage and low-speed electric vehicles. Transition metal selenides have attracted considerable a...

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Detalles Bibliográficos
Autores principales: Chen, Chen, Hu, Qilin, Yang, Fan, Xue, Hongyu, Zhang, Yuning, Yan, Hailong, Lu, Yang, Luo, Yongsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9346626/
https://www.ncbi.nlm.nih.gov/pubmed/35975047
http://dx.doi.org/10.1039/d2ra03206f
Descripción
Sumario:Due to the low price and abundant reserves of sodium resources, sodium-ion batteries have become the main candidate for the next generation of energy storage equipment, particularly for large-scale grid storage and low-speed electric vehicles. Transition metal selenides have attracted considerable attention because of their high reversible capacity, superior electrical conductivity and versatile structures. In this study, two-dimensional CuSe nanosheets are synthesized via a simple hydrothermal reaction. When acting as an electrode material for sodium-ion batteries, the CuSe electrode exhibits an initial coulombic efficiency of 96.7% at a current density of 0.1 A g(−1) and a specific capacity of 330 mA h g(−1) after 100 operation cycles, as well as retains a specific capacity of 211 mA h g(−1) even at a high current density of 10 A g(−1). Moreover, the anode delivers a specific capacity of 236 mA h g(−1) after 3300 cycles at 5 A g(−1) with a capacity retention of 91.2%. In sodium-ion hybrid capacitors (SHICs) with the two-dimensional CuSe nanosheets and Ti(3)C(2)T(x) MXene as the negative and positive materials, respectively, the nanosheets without any pre-sodiation present a lifespan of up to 2000 cycles at 2 A g(−1) and a capacity retention of about 77.7%.