4.6 Article

Heteroatom doping and activation of carbon nanofibers enabling ultrafast and stable sodium storage

期刊

ELECTROCHIMICA ACTA
卷 276, 期 -, 页码 304-310

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2018.04.207

关键词

Sodium-ion batteries; Activated carbon; Heteroatom doping; Sodium storage mechanism

资金

  1. National Natural Science Foundation of China [21576100, 21536005, 21776098]
  2. National Key Research Program of China [2016YFA0202600]
  3. Guangdong Natural Science Funds for Distinguished Young Scholar [2017A030306022]
  4. Pearl River S&T Nova Program of Guangzhou [201610010062]

向作者/读者索取更多资源

Activation is a common strategy to tailor microstructure of carbon materials. A new activation combined with heteroatom doping of carbon nanofibers is proposed to synthesize the N, S-doped carbon nano fibers (NSCNIFs). After electrospinning and followed thermal treatment with thiourea, the diameter of the as-obtained NSCNEs decreases with much more abundant pore structure and functionalized with S-containing oxygen groups compared with that obtained without activation. The increased specific surface area and pore volume are beneficial to facilitate the Na+ diffusion and provide more active sites to increase adsorption capacitance and facilitate pseudo-capacitive reactions. Also, the S-containing oxygen groups contribute to pseudo-capacitance by faradaic reactions. As a result, capacitive behavior is boosted hence leading to a excellent rate capability and cycling stability. The flexible and freestanding NSCNEs film is directly used as anode for sodium-ion batteries (NIBS) and shows excellent rate capability with reversible capacity of 147 and 133 mA h g(-1) at 10 and 30 A g(-1), respectively. Remarkably, ultra-long cyclic life is also achieved with 90.8% capacity retention after 6000 cycles at 10 A g(-1). Such electrochemical performance makes NSCNEs promising to be used in high power and durable NIBs. This activation strategy can also be expanded to functionalize other carbon materials. (C) 2018 Elsevier Ltd. All rights reserved.

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