RESUMO
Oxygen doping is an effective strategy for constructing high-performance carbon anodes in Na ion batteries; however, current oxygen-doped carbons always exhibit low doping levels and high-defect surfaces, resulting in limited capacity improvement and low initial Coulombic efficiency (ICE). Herein, a stainless steel-assisted high-energy ball milling is exploited to achieve high-level oxygen doping (19.33%) in the carbon framework. The doped oxygen atoms exist dominantly in the form of carbon-oxygen double bonds, supplying sufficient Na storage sites through an addition reaction. More importantly, it is unexpected that the random carbon layers on the surface are reconstructed into a quasi-ordered arrangement by robust mechanical force, which is low-defect and favorable for suppressing the formation of thick solid electrolyte interfaces. As such, the obtained carbon presents a large reversible capacity of 363 mAh g-1 with a high ICE up to 83.1%. In addition, owing to the surface-dominated capacity contribution, an ultrafast Na storage is achieved that the capacity remains 139 mAh g-1 under a large current density of 100 A g-1 . Such good Na storage performance, especially outstanding rate capability, has rarely been achieved before.
RESUMO
As one of the most promising candidates for sodium-ion battery anodes, hard carbons suffer from inferior rate performance owing to limited ion transfer rate and sluggish electrochemical kinetics. In this work, novel carbon nanosheets (CNS) with hexagonal ordered conical macropores are prepared. The CNS has a very thin thickness of approximately 370 nm, and the conical pores are penetrated through the whole nanosheet, forming well-connected ion transport freeway. In addition, the carbon microcrystal structure and interlayer spacing can be well tailored by adjusting the carbonization temperature, thereby controlling the sodium storage behavior of carbon electrodes. These structural merits endow CNS with accelerated ion transfer, minimized ion diffusion distance and fast electrochemical kinetics. Consequently, the CNS presents superior electrochemical performance. It delivers a high reversible capacity of 298 mAh g-1 at 0.1 A g-1; and after repeated charge/discharge for 500 times at 1 A g-1, its capacity remains 195 mA h g-1, with no rapid capacity loss. More importantly, CNS exhibits outstanding rate capability. Even under a very high current density of 2 A g-1, it still displays a large capacity of 210 mAh g-1, higher than most of state-of-the-art carbon anodes.
