Issue 35, 2015

Double-shelled support and confined void strategy to improve the lithium storage properties of SnO2/C anode materials for lithium-ion batteries

Abstract

As promising anode materials for lithium-ion batteries, SnO2 materials have triggered significant research efforts due to their high theoretical capacity. However, their practical applications are impeded by their poor cycle life, which is caused by structural pulverization and large volume changes during cycling. Thus, the development of strategies to improve the cycling performance of SnO2 anodes is indispensable. Herein, a peculiar nanostructured SnO2/C composite (denoted as SnO2@DSC) with a double-shelled carbon support and confined void is fabricated, in which SnO2 is quasi confined in the void-space between two shells. It is suggested that the as-prepared SnO2@DSC has two unique advantages: on the one hand, SnO2 is quasi encapsulated into the confined void between two shells, huge volume change is largely buffered and its electrical connectivity is guaranteed, because even if SnO2 detaches from the outer shell, it can be immobilized again in the interior shell; on the other hand, the structural integrity of the electrode could be guaranteed by virtue of the dual-support of mechanically flexible double-shelled hollow carbon nanospheres. As a result, the as-prepared SnO2@DSC exhibited an excellent cycling performance, delivering a high reversible capacity of 838.2 mA h gāˆ’1 at 200 mA gāˆ’1 even after 500 cycles.

Graphical abstract: Double-shelled support and confined void strategy to improve the lithium storage properties of SnO2/C anode materials for lithium-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
17 Jun 2015
Accepted
21 Jul 2015
First published
21 Jul 2015

J. Mater. Chem. A, 2015,3, 18036-18044

Double-shelled support and confined void strategy to improve the lithium storage properties of SnO2/C anode materials for lithium-ion batteries

Q. Tian, Y. Tian, Z. Zhang, L. Yang and S. Hirano, J. Mater. Chem. A, 2015, 3, 18036 DOI: 10.1039/C5TA04421A

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