Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces

Microporous silicon membranes, fabricated by lithographic patterning and wet and dry silicon etching processes, were used to create arrays of micro-scale interfaces between two immiscible electrolyte solutions (mITIES) for ion-transfer voltammetry. These membranes served the dual functions of int...

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Main Authors: Zazpe, R., Hibert, C., O'Brien, J., Lanyon, Y., Arrigan, Damien
Format: Journal Article
Published: Royal Society of Chemistry 2007
Online Access:http://hdl.handle.net/20.500.11937/37320
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author Zazpe, R.
Hibert, C.
O'Brien, J.
Lanyon, Y.
Arrigan, Damien
author_facet Zazpe, R.
Hibert, C.
O'Brien, J.
Lanyon, Y.
Arrigan, Damien
author_sort Zazpe, R.
building Curtin Institutional Repository
collection Online Access
description Microporous silicon membranes, fabricated by lithographic patterning and wet and dry silicon etching processes, were used to create arrays of micro-scale interfaces between two immiscible electrolyte solutions (mITIES) for ion-transfer voltammetry. These membranes served the dual functions of interface stabilization and enhancement of the rate of mass-transport to the interface. The pore radii were 6.5 mm, 12.8 mm and 26.6 mm; the pore–pore separations were ca. 20- to 40-times the pore radii and the membrane thickness was 100 mm. Deep reactive ion etching (DRIE) was used for pore drilling through the silicon, which had been previously selectively thinned by potassium hydroxide etching. DRIE produces hydrophobic fluorocarbon-coated internal pore walls. The small pore sizes and large pore–pore separations used resulted in steadystate voltammograms for the transfer of tetramethylammonium cation (TMA+) from the aqueous to the organic phase, whereas the reverse voltammetric sweeps were peak-shaped.
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institution Curtin University Malaysia
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last_indexed 2025-11-14T08:49:34Z
publishDate 2007
publisher Royal Society of Chemistry
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spelling curtin-20.500.11937-373202017-09-13T13:38:14Z Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces Zazpe, R. Hibert, C. O'Brien, J. Lanyon, Y. Arrigan, Damien Microporous silicon membranes, fabricated by lithographic patterning and wet and dry silicon etching processes, were used to create arrays of micro-scale interfaces between two immiscible electrolyte solutions (mITIES) for ion-transfer voltammetry. These membranes served the dual functions of interface stabilization and enhancement of the rate of mass-transport to the interface. The pore radii were 6.5 mm, 12.8 mm and 26.6 mm; the pore–pore separations were ca. 20- to 40-times the pore radii and the membrane thickness was 100 mm. Deep reactive ion etching (DRIE) was used for pore drilling through the silicon, which had been previously selectively thinned by potassium hydroxide etching. DRIE produces hydrophobic fluorocarbon-coated internal pore walls. The small pore sizes and large pore–pore separations used resulted in steadystate voltammograms for the transfer of tetramethylammonium cation (TMA+) from the aqueous to the organic phase, whereas the reverse voltammetric sweeps were peak-shaped. 2007 Journal Article http://hdl.handle.net/20.500.11937/37320 10.1039/b712601h Royal Society of Chemistry restricted
spellingShingle Zazpe, R.
Hibert, C.
O'Brien, J.
Lanyon, Y.
Arrigan, Damien
Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces
title Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces
title_full Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces
title_fullStr Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces
title_full_unstemmed Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces
title_short Ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces
title_sort ion-transfer voltammetry at silicon membrane-based arrays of micro-liquid–liquid interfaces
url http://hdl.handle.net/20.500.11937/37320