Abstract

Exploration of advanced carbon anode material is the key to circumventing the sluggish kinetics and poor rate capability for potassium ion storage. Herein, a synergistic synthetic strategy of engineering both surface and structure is adopted to design N, S co-doped carbon nanotubes (NS-CNTs). The as-designed NS-CNTs exhibit unique features of defective carbon surface, hollow tubular channel, and enlarged interlayer space. These features significantly contribute to a large potassium storage capacity of 307mA h g-1 at 1 A g-1 and a remarkable rate performance with a capacity of 151mA h g-1 even at 5 A g-1 . Furthermore, an excellent cyclability with 98% capacity retention after 500 cycles at 2 A g-1 is also achieved. Systematic analysis by in situ Raman spectroscopy and ex situ TEM demonstrates the structural stability and reversibility in the charge-discharge process. Although the kinetics studies reveal the capacitive-dominated process for potassium storage, density functional theory calculations provide evidence that N, S co-doping contributes to expanding the interlayer space to promote the K-ion insertion, improving the electronic conductivity, and providing ample defective sites to favor the K-ion adsorption.

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