Chronoamperometric response at nanoscale liquid-liquid interface arrays

被引:24
作者
Sairi, Masniza [1 ]
Strutwolf, Joerg [2 ]
Mitchell, Rowan A. [1 ]
Silvester, Debbie S. [1 ]
Arrigan, Damien W. M. [1 ]
机构
[1] Curtin Univ, Dept Chem, Nanochem Res Inst, Perth, WA 6845, Australia
[2] Univ Tubingen, Inst Organ Chem, D-72076 Tubingen, Germany
关键词
nanoITIES arrays; Silicon nitride membranes; Potential step chronoamperometry; Charging time; Response time; IMMISCIBLE ELECTROLYTE-SOLUTIONS; FACILITATED ION TRANSFER; DISK ELECTRODE; MICROPIPET ELECTRODES; ELECTROCHEMICAL CHARACTERIZATION; NANOELECTRODE ARRAYS; MICRODISK ELECTRODES; MASS-TRANSPORT; POTASSIUM-ION; VOLTAMMETRY;
D O I
10.1016/j.electacta.2012.11.062
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this work, potential step chronoamperomety (PSCA) was used to study the behaviour of arrays of nanoscale interfaces between two immiscible electrolyte solutions (nanoMES). The nanoITIES arrays were formed at nanoporous silicon nitride membranes containing 400 nanopores in a hexagonal close-packed arrangement. Three membrane designs, with nanopore radii of 75, 50 and 17 nm, were studied by ion-transfer of tetrapropylammonium cations across the nanopore array-supported water vertical bar 1,6-dichlorohexane interface. The cell time constants and charging times were determined prior to experimental PSCA. The three membrane designs studied exhibited charging times in the range of 0.08-0.46 s, with the smallest pore configuration (17 nm radius) exhibiting the longest charging time. The experimental steady-state currents were 30-50% lower than of the calculated inlaid disc model currents, due to diffusion zone overlap at adjacent interfaces. The three nano-interface arrays studied also showed response times of 6 +/- 1 s, being the time required to reach 95% of the steady-state current. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:177 / 185
页数:9
相关论文
共 56 条
[1]   Bioanalytical Detection Based on Electrochemistry at Interfaces between Immiscible Liquids [J].
Arrigan, Damien W. M. .
ANALYTICAL LETTERS, 2008, 41 (18) :3233-3252
[2]   Nanoelectrodes, nanoelectrode arrays and their applications [J].
Arrigan, DWM .
ANALYST, 2004, 129 (12) :1157-1165
[3]  
Bard A.J., 2001, ELECTROCHEMICAL METH, P216
[4]   An accurate microdisc simulation model for recessed microdisc electrodes [J].
Bartlett, PN ;
Taylor, SL .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 453 (1-2) :49-60
[5]   INVESTIGATION OF THE KINETICS OF ASSISTED POTASSIUM-ION TRANSFER BY DIBENZO-18-CROWN-6 AT THE MICRO-ITIES BY MEANS OF STEADY-STATE VOLTAMMETRY [J].
BEATTIE, PD ;
DELAY, A ;
GIRAULT, HH .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1995, 380 (1-2) :167-175
[6]   INVESTIGATION OF THE KINETICS OF ION AND ASSISTED ION TRANSFER BY THE TECHNIQUE OF AC-IMPEDANCE OF THE MICRO-ITIES [J].
BEATTIE, PD ;
DELAY, A ;
GIRAULT, HH .
ELECTROCHIMICA ACTA, 1995, 40 (18) :2961-2969
[7]   A COMPARISON OF THE CHRONOAMPEROMETRIC RESPONSE AT INLAID AND RECESSED DISK MICROELECTRODES [J].
BOND, AM ;
LUSCOMBE, D ;
OLDHAM, KB ;
ZOSKI, CG .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1988, 249 (1-2) :1-14
[8]   OHMIC POTENTIAL DROP AT ELECTRODES EXHIBITING STEADY-STATE DIFFUSION CURRENTS [J].
BRUCKENSTEIN, S .
ANALYTICAL CHEMISTRY, 1987, 59 (17) :2098-2101
[9]  
Cattrall R.W., 1997, CHEM SENSORS, P25
[10]  
Cottrell FG, 1903, Z PHYS CHEM-STOCH VE, V42, P385