Issue 44, 2013

Robust and stable intercalated graphene encapsulation of tin nanorods for enhanced cycle and capacity performance for lithium storage

Abstract

Anode materials (Si, Ge, Sn, etc.) in lithium-ion batteries suffer from a remarkable loss of capacity during the charge–discharge cycle, and various carbon-based additions have been widely added to address this issue. In this work, we report on a simple, one-step approach for an intercalated graphene encapsulation of tin nanorods fabricated via the arc-discharge method. Our method is fast, robust, straight-forward and completely catalyst-free. The result is a Sn@G nanocomposite comprising of a single-crystalline Sn nanorod core tightly bonded to a highly-crystalline graphene shell. The as-synthesized Sn@G exhibits superior cycling and rate performance compared to Sn@C nanocomposite: a reversible specific capacity of 846 mA h g−1 after 100 cycles at the current density of 200 mA g−1 and a reversible rate capacity of 488 mA h g−1 at 2 C for Sn@G, in contrast to the 130 mA h g−1 and 48 mA h g−1, respectively for Sn@C. Further, the Sn@G possesses excellent thermal and chemical stabilities against a 950 °C N2 annealing and a 12 h etching in hydrochloric acid, respectively, and has a high mechanical strength as evident by the intercalated core–shell structure maintaining its shape intact in resisting the volume expansion during the 950 °C annealing. These encouraging results indicate that an in situ graphene encapsulated tin rods nanocomposite constitutes a highly feasible candidate for use as an anode material.

Graphical abstract: Robust and stable intercalated graphene encapsulation of tin nanorods for enhanced cycle and capacity performance for lithium storage

Supplementary files

Article information

Article type
Paper
Submitted
02 Aug 2013
Accepted
04 Sep 2013
First published
09 Sep 2013

RSC Adv., 2013,3, 21588-21595

Robust and stable intercalated graphene encapsulation of tin nanorods for enhanced cycle and capacity performance for lithium storage

C. Wang, J. Ju, Y. Yang, Y. Tang, H. Bi, F. Liao, J. Lin, Z. Shi, F. Huang and R. P. S. Han, RSC Adv., 2013, 3, 21588 DOI: 10.1039/C3RA44109A

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