Issue 48, 2016

Germanium encapsulated in sulfur and nitrogen co-doped 3D porous carbon as an ultra-long-cycle life anode for lithium ion batteries

Abstract

Germanium (Ge) has been considered as a promising anode material for Li-ion batteries because of its theoretical capacity (1600 mA h g−1). However, its poor electrochemical performances resulting from the large volume variation during Li–Ge alloy/dealloy processes prevent its practical application. Herein, we designed a 3D core/shell structure by encapsulation of Ge in a sulfur (S) and nitrogen (N) co-doped three-dimensionally (3D) interconnected macroporous carbon matrix (denoted as Ge@S,N-3DPC). The 3D porous structure can not only buffer the volume change during alloy/dealloy processes, but also facilitate the electrolyte to soak in, offering fast ion/electron pathways. What's more, the co-doping of S and N in carbon could introduce more defects and active sites, which can also help to improve the interfacial adsorption and electrochemical behaviors. When used as an anode material for LIBs, the Ge@S,N-3DPC shows excellent electrochemical performances (1000 mA h g−1 at 200 mA g−1), outstanding cycling stability (94% capacity retention after 300 cycles) and high rate capability (358 mA h g−1 at 10 A g−1). This work develops a general strategy to improve the electrochemical performance of these alloy-type electrode materials with huge volume change in the energy storage area.

Graphical abstract: Germanium encapsulated in sulfur and nitrogen co-doped 3D porous carbon as an ultra-long-cycle life anode for lithium ion batteries

Supplementary files

Article information

Article type
Communication
Submitted
07 Oct 2016
Accepted
01 Nov 2016
First published
04 Nov 2016

J. Mater. Chem. A, 2016,4, 18711-18716

Germanium encapsulated in sulfur and nitrogen co-doped 3D porous carbon as an ultra-long-cycle life anode for lithium ion batteries

C. Yang, Y. Jiang, X. Liu, X. Zhong and Y. Yu, J. Mater. Chem. A, 2016, 4, 18711 DOI: 10.1039/C6TA08681K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements