Journal
SUSTAINABLE ENERGY & FUELS
Volume 4, Issue 5, Pages 2453-2461Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0se00160k
Keywords
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Funding
- National Key Research and Development Program of China [2017YFA0402902]
- National Natural Science Foundation Committee of China Academy of Engineering Physics (NSAF) [U1630108]
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Currently, the search for excellent anode materials for potassium-ion storage is an important research direction. Transition metal selenide has potential application value in alkali metal-ion batteries because of its high theoretical capacity. However, due to its poor conductivity, slow insertion/extraction kinetics, and volume expansion, obtaining stable cycling performance remains challenging. In this paper, we report the design of self-supporting N-rich Cu2Se/C nanowires for use as a binder-free potassium-ion battery (PIB) electrode, which exhibits prolonged cycling life and good rate capacity. Because of the stable three-dimensional (3D) flexible structure, faster reaction kinetics, and high conductance of the as-synthesized nanowires, an excellent ultralong potassium-ion storage stability of similar to 190 mA h g(-1) is achieved over 200 cycles at a current density of 0.1 A g(-1). In addition, a great rate capability is achieved (181 mA h g(-1) at 0.1 A g(-1)vs. 104 mA h g(-1) at 2.0 A g(-1)) due to partial pseudocapacitive behavior. The N-rich Cu2Se/C electrode also exhibits a stable capacity of 78 mA h g(-1) over 1200 cycles when the current density is as high as 2 A g(-1). We are the first to achieve such great performance in Cu-Se-C-based materials, and our work also provides a way to construct advanced transition metal selenide anodes for energy-storage devices.
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