Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties

Here we report on the functionalization of alkyne-terminated alkyl monolayers on highly doped Si(100) using "click" reactions to immobilize ferrocene derivatives. The reaction of hydrogen-terminated silicon surfaces with a diyne species was shown to afford very robust functional surfaces w...

Full description

Bibliographic Details
Main Authors: Ciampi, Simone, Eggers, P., Le Saux, G., James, M., Harper, J., Gooding, J.
Format: Journal Article
Published: American Chemical Society 2009
Online Access:http://hdl.handle.net/20.500.11937/6817
_version_ 1848745186142715904
author Ciampi, Simone
Eggers, P.
Le Saux, G.
James, M.
Harper, J.
Gooding, J.
author_facet Ciampi, Simone
Eggers, P.
Le Saux, G.
James, M.
Harper, J.
Gooding, J.
author_sort Ciampi, Simone
building Curtin Institutional Repository
collection Online Access
description Here we report on the functionalization of alkyne-terminated alkyl monolayers on highly doped Si(100) using "click" reactions to immobilize ferrocene derivatives. The reaction of hydrogen-terminated silicon surfaces with a diyne species was shown to afford very robust functional surfaces where the oxidation of the underlying substrate was negligible. Detailed characterization using X-ray photoelectron spectroscopy, X-ray reflectometry, and cyclic voltammetry demonstrated that the surface acetylenes had reacted in moderate yield to give surfaces exposing ferrocene moieties. Upon extensive exposure of the redox-active architecture to oxidative environments during preparative and characterization steps, no evidence of SiOx contaminants was shown for derivatized SAMs prepared from single-component 1,8-nonadiyne, fully acetylenylated, monolayers. An analysis of the redox behavior of the prepared Si(100) electrodes based on relevant parameters such as peak splitting and position and shape of the reduction/oxidation waves depicted a well-behaved redox architecture whose spectroscopic and electrochemical properties were not significantly altered even after prolonged cycling in aqueous media between -100 and 800 mV versus AglAgCl. The reported strategy represents an experimentally simple approach for the preparation of silicon-based electrodes where, in addition to close-to-ideal redox behavior, remarkable electrode stability can be achieved. Both the presence of a distal alkyne moiety and temperatures of formation above 100 °C were required to achieve this surface stabilization. © Copyright 2009 American Chemical Society.
first_indexed 2025-11-14T06:13:21Z
format Journal Article
id curtin-20.500.11937-6817
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T06:13:21Z
publishDate 2009
publisher American Chemical Society
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-68172017-09-13T14:34:28Z Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties Ciampi, Simone Eggers, P. Le Saux, G. James, M. Harper, J. Gooding, J. Here we report on the functionalization of alkyne-terminated alkyl monolayers on highly doped Si(100) using "click" reactions to immobilize ferrocene derivatives. The reaction of hydrogen-terminated silicon surfaces with a diyne species was shown to afford very robust functional surfaces where the oxidation of the underlying substrate was negligible. Detailed characterization using X-ray photoelectron spectroscopy, X-ray reflectometry, and cyclic voltammetry demonstrated that the surface acetylenes had reacted in moderate yield to give surfaces exposing ferrocene moieties. Upon extensive exposure of the redox-active architecture to oxidative environments during preparative and characterization steps, no evidence of SiOx contaminants was shown for derivatized SAMs prepared from single-component 1,8-nonadiyne, fully acetylenylated, monolayers. An analysis of the redox behavior of the prepared Si(100) electrodes based on relevant parameters such as peak splitting and position and shape of the reduction/oxidation waves depicted a well-behaved redox architecture whose spectroscopic and electrochemical properties were not significantly altered even after prolonged cycling in aqueous media between -100 and 800 mV versus AglAgCl. The reported strategy represents an experimentally simple approach for the preparation of silicon-based electrodes where, in addition to close-to-ideal redox behavior, remarkable electrode stability can be achieved. Both the presence of a distal alkyne moiety and temperatures of formation above 100 °C were required to achieve this surface stabilization. © Copyright 2009 American Chemical Society. 2009 Journal Article http://hdl.handle.net/20.500.11937/6817 10.1021/la803710d American Chemical Society restricted
spellingShingle Ciampi, Simone
Eggers, P.
Le Saux, G.
James, M.
Harper, J.
Gooding, J.
Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties
title Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties
title_full Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties
title_fullStr Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties
title_full_unstemmed Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties
title_short Silicon (100) electrodes resistant to oxidation in aqueous solutions: An unexpected benefit of surface acetylene moieties
title_sort silicon (100) electrodes resistant to oxidation in aqueous solutions: an unexpected benefit of surface acetylene moieties
url http://hdl.handle.net/20.500.11937/6817