Self-supporting N-rich Cu2Se/C nanowires for highly reversible, long-life potassium-ion storage. Issue 5 (20th March 2020)

• Record Type: Journal Article
• Authors: Zhu, Xingqun; Gao, Jingyu; Li, Jing; Hu, Guojing; Li, Jie; Zhang, Genqiang; Xiang, Bin
• Is Part Of: Sustainable energy & fuels. Volume 4:Issue 5(2020)
• Page Start: 2453
• Page End: 2461
• Publication Date: 2020-03-20
• Subjects: Renewable energy sources -- Periodicals; Fuel cells -- Periodicals; Electric batteries -- Periodicals; Electrochemistry -- Periodicals; 660.297
• DOI: 10.1039/d0se00160k
• Languages: English
• ISSNs: 2398-4902

Abstract

Abstract : Currently, the search for excellent anode materials for potassium-ion storage is an important research direction. Abstract : 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 Cu2 Se/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 ∼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 Cu2 Se/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.