Nitrogen and Sulfur Co-Doped Hierarchically Porous Carbon Nanotubes for Fast Potassium Ion Storage

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 307 mA h g(-1) at 1 A g(-1) and a remarkable rate performance with a capacity of 151 mA 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.

Automated summary

A synergistic synthetic strategy of engineering both surface and structure is adopted to design N, S co-doped carbon nanotubes (NS-CNTs), which exhibit unique features of defective carbon surface, hollow tubular channel, and enlarged interlayer space. These features significantly contribute to a large potassium storage capacity and excellent rate performance.