Surface and electrochemical studies of a carbon dioxide probe based on conducting polypyrrole

被引:23
作者
Tongol, BJV
Binag, CA [1 ]
Sevilla, FB
机构
[1] Univ Santo Tomas, Grad Sch, Manila 1008, Philippines
[2] Univ Santo Tomas, Res Ctr Nat Sci, Manila 1008, Philippines
[3] Univ Santo Tomas, Coll Sci, Manila 1008, Philippines
关键词
polypyrrole; electrochemical polymerization; carbon dioxide sensor; SEM; XPS;
D O I
10.1016/S0925-4005(03)00180-1
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper reports on the development of a Severinghaus carbon dioxide probe using polypyrrole (PPy) as the pH-indicator electrode. The electrochemically synthesized bicarbonate-doped PPy gave satisfactory potentiometric properties as pH-indicator electrode: sub-Nernstian response with a slope, m, of -39.06 mV pH(-1) at buffer solutions of pH 3-10, excellent linearity, r, of -0.999, and relatively fast response time, average t(r) = 3.6 min for three replicates (n = 3). For the CO2 probe design, the PPy/HCO3--coated Pt electrode was coupled with a miniaturized Ag/AgCl reference electrode. A thin layer (similar to0.5 mm) of 300 mul of 0.001 M NaHCO3 internal electrolyte is sandwiched between the two electrodes and the Teflon gas permeable membrane. The optimized CO2 probe exhibited good potentiometric properties (linearity = 8.78 x 10(-5) to 2.70 x 10(-3) M CO2 with r = -0.993; m = -47.42 mV/decade [CO2] with RSD = 17.04% at n = 3; LOD = 3.93 x 10(-5) M CO2 and t(r) = 4.71 min) when used only in one calibration measurement. Scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) techniques were used to study the surfaces of the CO2 probe components: PPy/HCO3- film and Teflon gas permeable membrane. This study highlights the use of these surface-sensitive techniques to understand the electrochemical behavior of the fabricated CO2 probe. A correlation was made between the surface characteristics of the sensor components with the low reproducibility and repeatability of the sensor responses. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:187 / 196
页数:10
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