Issue 8, 2011

Sn-induced low-temperature growth of Ge nanowire electrodes with a large lithium storage capacity

Abstract

We herein present the synthesis of germanium (Ge) nanowires on Au-catalyzed low-temperature substrates using a simple thermal Ge/Sn co-evaporation method. Incorporation of a low-melting point metal (Sn) enables the efficient delivery of Ge vapor to the substrate, even at a source temperature below 600 °C. The as-synthesized nanowires were found to be a core/shell heterostructure, exhibiting a uniform single crystalline Ge sheathed within a thin amorphous germanium suboxide (GeOx) layer. Furthermore, these high-density Ge nanowires grown directly on metal current collectors can offer good electrical connection and easy strain relaxation due to huge volume expansion during Li ion insertion/extraction. Therefore, the self-supported Ge nanowire electrodes provided excellent large capacity with little fading upon cycling (a capacity of ∼900 mA h g−1 at 1C rate).

Graphical abstract: Sn-induced low-temperature growth of Ge nanowire electrodes with a large lithium storage capacity

Supplementary files

Article information

Article type
Paper
Submitted
09 May 2011
Accepted
31 May 2011
First published
12 Jul 2011

Nanoscale, 2011,3, 3371-3375

Sn-induced low-temperature growth of Ge nanowire electrodes with a large lithium storage capacity

Y. Ko, J. Kang, G. Lee, J. Park, K. Park, Y. Jin and D. Kim, Nanoscale, 2011, 3, 3371 DOI: 10.1039/C1NR10471C

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