4.8 Article

Directionally Tailoring Macroporous Honeycomb-Like Structured Carbon Nanofibers toward High-Capacitive Potassium Storage

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 26, 页码 30693-30702

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c07111

关键词

carbon nanofibers; macroporous honeycomb-like structure; anode; capacitive storage; potassium-ion batteries

资金

  1. National Natural Science Foundation of China [21878195, U20A20145]
  2. Scientific and Technological Achievement Transformation Project of Sichuan Science and Technology Department [21ZHSF0111]

向作者/读者索取更多资源

The use of macroporous honeycomb-like carbon nanofibers as an anode material for high-capacitive potassium storage demonstrated significantly improved kinetics and structural stability. The structural characteristics of the material enabled ultrahigh potassium storage ability and competitive rate capability, even after repeated cycles at high current densities. This work offers a promising strategy for effectively improving K+ diffusion kinetic performance and promoted K+ adsorption/intercalation storage through macropore engineering coupled with an amorphous structure.
Constructing high-capacitive potassium storage materials can avoid the sluggish and unstable bulk diffusion process via a surface-induced process, which is conducive to swift and frequent potassium storage. Herein, we demonstrated the use of macroporous honeycomb-like carbon nanofibers (MHCNFs) as an excellent anode material for high-capacitive potassium storage. The as-made MHCNFs feature abundant well-controlled macropores, an amorphous structure, and a large specific surface area of around 595.9 m(2) g(-1). These structural characteristics could significantly reduce the transferring distance of electrons/ions, offer abundant active sites, enable high-capacitive contribution, and thus substantially improve the kinetics and structural stability of MHCNFs. Experimental investigation demonstrated that MHCNFs enable ultrahigh potassium storage ability (329.1 mAh g(-1) at 100 mA g(-1)) and competitive rate capability (168.5 mAh g(-1) at 5000 mA g(-1)). More impressively, even when cycled at 1000 mA g(-1), the robust structure of MHCNFs can still enable the electrodes a capacity of 252.6 mAh g(-1) over repeating 2500 cycles. This work offers a promising strategy that macropore engineering coupled with amorphous structure can make effectively elevated K+ diffusion kinetic performance and promoted K+ adsorption/intercalation storage possible.

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