Avoiding Errors in Electrochemical Measurements: Effect of Frit Material on the Performance of Reference Electrodes with Porous Frit Junctions

熔块 电极 电解质 多孔性 参比电极 纳米孔 电化学 化学 复合材料 原电池 化学工程 材料科学 电位滴定法 分析化学(期刊) 纳米技术 色谱法 冶金 物理化学 工程类
作者
Maral P. S. Mousavi,Stacey A. Saba,Evan L. Anderson,Marc A. Hillmyer,Philippe Bühlmann
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:88 (17): 8706-8713 被引量:59
标识
DOI:10.1021/acs.analchem.6b02025
摘要

In many commercially available and in-house-prepared reference electrodes, nanoporous glass frits (often of the brand named Vycor) contain the electrolyte solution that forms a salt bridge between the sample and the reference solution. Recently, we showed that in samples with low ionic strength, the half-cell potentials of reference electrodes comprising nanoporous Vycor frits are affected by the sample and can shift in response to the sample composition by more than 50 mV (which can cause up to 900% error in potentiometric measurements). It was confirmed that the large potential variations result from electrostatic screening of ion transfer through the frit due to the negatively charged surfaces of the glass nanopores. Since the commercial production of porous Vycor glass was recently discontinued, new materials have been used lately as porous frits in commercially available reference electrodes, namely frits made of Teflon, polyethylene, or one of two porous glasses sold under the brand names CoralPor and Electro-porous KT. In this work, we studied the effect of the frit characteristics on the performance of reference electrodes, and show that the unwanted changes in the reference potential are not unique to electrodes with Vycor frits. Increasing the pore size in the glass frits from the <10 nm into the 1 μm range or switching to polymeric frits with pores in the 1 to 10 μm range nearly eliminates the potential variations caused by electrostatic screening of ion transport through the frit pores. Unfortunately, bigger frit pores result in larger flow rates of the reference solution through the pores, which can result in the contamination of test solutions.
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