Issue 14, 2016

Electrocatalytic activity of NiO on silicon nanowires with a carbon shell and its application in dye-sensitized solar cell counter electrodes

Abstract

To improve the catalytic activity of a material, it is critical to maximize the effective surface area by directly contacting the electrolyte. Nanowires are a promising building block for catalysts in electrochemical applications because of their large surface area. Nickel oxide (NiO) decoration was achieved by drop-casting a nickel-dissolved solution onto vertically aligned silicon nanowire arrays with a carbon shell (SiNW/C). Based on the hybridization of the NiO and silicon nanowire arrays with a carbon shell this study aimed to achieve a synergic effect for the catalytic activity performance. This study demonstrated that the resulting nanomaterial exhibits excellent electrocatalytic activity and performs well as a counter electrode for dye-sensitized solar cells (DSSCs). The compositions of the materials were examined using X-ray diffraction, X-ray photoelectron spectroscopy, and energy dispersive spectroscopy. Their micro- and nano-structures were investigated using scanning electron microscopy and transmission electron microscopy. The electrochemical activity toward I/I3 was examined using cyclic voltammetry and electrochemical impedance spectroscopy. The obtained peak power conversion efficiency of the DSSC based on the NiO@SiNW/C counter electrode was 9.49%, which was greater than that of the DSSC based on the Pt counter electrode.

Graphical abstract: Electrocatalytic activity of NiO on silicon nanowires with a carbon shell and its application in dye-sensitized solar cell counter electrodes

Supplementary files

Article information

Article type
Paper
Submitted
23 Nov 2015
Accepted
10 Mar 2016
First published
11 Mar 2016

Nanoscale, 2016,8, 7761-7767

Electrocatalytic activity of NiO on silicon nanowires with a carbon shell and its application in dye-sensitized solar cell counter electrodes

J. Kim, C. Jung, M. Kim, S. Kim, Y. Kang, H. Lee, J. Park, Y. Jun and D. Kim, Nanoscale, 2016, 8, 7761 DOI: 10.1039/C5NR08265J

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