Issue 96, 2015

Synthesis of porous silicon through interfacial reactions and measurement of its electrochemical response using cyclic voltammetry

Abstract

Porous silicon, an excellent material with fascinating physical and chemical properties, is usually formed by anodic polarization of single crystalline silicon in HF based solutions. Here, we show fabrication of porous silicon films ∼0.5–250 μm thick consisting of macropores and mesopores using a contactless electrochemical approach, where the silicon substrate is not under any external bias. Pore dimensions and porosity have been characterized by scanning electron microscopy (SEM) while subsequent cyclic voltammetry (CV) investigations delineate the underlying topographical differences between blanket and porous silicon surfaces. Our work not only offers a new scalable means of fabricating porous silicon structures but also questions the reliability of existing theories that depend on localized collection of electronic hole carriers through anodization of silicon for pore formation. We believe our results will open pathways for development of realistic models for porous silicon formation.

Graphical abstract: Synthesis of porous silicon through interfacial reactions and measurement of its electrochemical response using cyclic voltammetry

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2015
Accepted
07 Sep 2015
First published
08 Sep 2015
This article is Open Access
Creative Commons BY license

RSC Adv., 2015,5, 79157-79163

Synthesis of porous silicon through interfacial reactions and measurement of its electrochemical response using cyclic voltammetry

M. Zhao, R. Balachandran, J. Allred and M. Keswani, RSC Adv., 2015, 5, 79157 DOI: 10.1039/C5RA14592A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements