4.8 Article

Alkalized Ti3C2 MXene nanoribbons with expanded interlayer spacing for high-capacity sodium and potassium ion batteries

期刊

NANO ENERGY
卷 40, 期 -, 页码 1-8

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.nanoen.2017.08.002

关键词

MXene; Alkalization; Nanoribbons; Sodium ion batteries; Potassium ion batteries

资金

  1. National Key R & D Program of China [2016YBF0100100, 2016YFA0200200]
  2. Thousand Youth Talents Plan of China [Y5061921T3]
  3. National Natural Science Foundation of China [51572259]
  4. Natural Science Foundation of Liaoning Province [201602737]
  5. DICP [Y5610121T3]
  6. China Postdoctoral Science Foundation [2016M601349, 2017T100188]

向作者/读者索取更多资源

As post-lithium ion batteries, both sodium ion batteries (SIBs) and potassium ion batteries (PIBs) possess great potential for large scale energy storage. However, the improvements of both SIBs and PIBs for practical applications are facing great challenges in the development of high-performance electrode materials. Here, we demonstrate the fabrication of alkalized Ti3C2 (a-Ti3C2) MXene nanoribbons attained by continuous shaking treatment of pristine Ti3C2 MXene in aqueous KOH solution. Benefited from the expanded interlayer spacing of a-Ti3C2, narrow widths of nanoribbons as well as three-dimensional interconnected porous frameworks for enhanced ion reaction kinetics and improved structure stability, the resulting a-Ti3C2 anodes showed excellent sodium/potassium storage performance, for example, high reversible capacities of 168 and 136 mA h g(-1) at 20 mA g(-1) and 84 and 78 mA h g(-1) at 200 mA g(-1) were obtained for SIBs and PIBs, respectively. Notably, a-Ti3C2 possessed outstanding long-term cyclability at high current density of 200 mA g(-1), delivering a capacity of similar to 50 mA h g(-1) for SIBs and similar to 42 mA h g(-1) for PIBs after 500 cycles, which outperformed most of reported MXene based anodes for SIBs and PIBs. Moreover, this alkalization strategy could be extended as a universal approach for fabricating various alkalized MXene-based frameworks derived from a large family of MAX phases for numerous applications, such as catalysis, energy storage and conversion.

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