Issue 41, 2017

Highly mesoporous C nanofibers with graphitized pore walls fabricated via ZnCo2O4-induced activating-catalyzed-graphitization for long-lifespan lithium-ion batteries

Abstract

Transition metals (TMs), e.g. Fe, Co, and Ni, are normally unsuitable for the fabrication of highly porous C materials with graphitized C layers since in situ formed carbides on the surface of the TMs impede their catalytic graphitization effect. In this paper, we report on highly mesoporous sponge-like C nanofibers (SLCNFs) with graphitized pore-walls fabricated through novel activating-catalyzed-graphitization using ZnCo2O4 as a source of ZnO and metallic Co. During the carbonization, the ZnO functions as an in situ activating agent to provide O species to oxidize the inert Co3C to active Co; the original transient “amorphous C/Co–graphite/Co3C” process induced by the metallic Co can be translated into a cyclic “amorphous C/Co–graphite/Co3C–COx/Co” system, to fabricate a sponge-like well-interconnected mesoporous structure. This gives SLCNFs a high reversible capacity (900 mA h g−1 at 0.1 A g−1 after 100 cycles), good rate performance, and excellent super-long-term cycle stability (460 mA h g−1 at 1.67 A g−1 after 2000 cycles) when used as the anode of a lithium-ion battery. The usability of SLCNFs as a conductive substrate for sulfur is also demonstrated, indicating their excellent potential for application to energy storage and conversion.

Graphical abstract: Highly mesoporous C nanofibers with graphitized pore walls fabricated via ZnCo2O4-induced activating-catalyzed-graphitization for long-lifespan lithium-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
22 Jun 2017
Accepted
20 Sep 2017
First published
21 Sep 2017

J. Mater. Chem. A, 2017,5, 21679-21687

Highly mesoporous C nanofibers with graphitized pore walls fabricated via ZnCo2O4-induced activating-catalyzed-graphitization for long-lifespan lithium-ion batteries

R. Chen, Y. Hu, Z. Shen, X. He, Z. Cheng, P. Pan, K. Wu, X. Zhang and Z. Tang, J. Mater. Chem. A, 2017, 5, 21679 DOI: 10.1039/C7TA05445A

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