The effect of electric field on potentiometric Scanning Electrochemical Microscopic imaging

被引:21
|
作者
Kiss, Andras [1 ,2 ]
Filotas, Daniel [1 ,2 ]
Souto, Ricardo M. [3 ]
Nagy, Geza [1 ,2 ]
机构
[1] Univ Pecs, Dept Gen & Phys Chem, Fac Sci, Ifjusag Utja 6, H-7624 Pecs, Hungary
[2] Univ Pecs, Janos Szentagothai Res Ctr, Ifjusag Utja 20, H-7624 Pecs, Hungary
[3] Univ La Laguna, Dept Chem, POB 456, E-38200 San Cristobal la Laguna, Tenerife, Spain
关键词
Scanning electrochemical microscopy; Potentiometry; Ion-selective microelectrode; Galvanic corrosion; Electric field; VIBRATING ELECTRODE; CONCENTRATION DISTRIBUTIONS; SELECTIVE MICROELECTRODES; AQUEOUS ENVIRONMENTS; SPATIAL-DISTRIBUTION; GALVANIC CORROSION; ALUMINUM; ZN2+;
D O I
10.1016/j.elecom.2017.03.011
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Potentiometric Scanning Electrochemical Microscopy (SECM) is a powerful tool in corrosion science. It allows the selective imaging of a particular ionic species released at the anodic sites in a corrosion micro cell, by using ion-selective microelectrodes (ISMEs) as scanning probes. Galvanic corrosion is a particularly often studied process. The measured potential of the ISME is thought to depend only on the activity of the primary ion. However, an electric field is also formed as a result of the potential difference between the surfaces of the galvanic pair, which has a direct influence on the potential of the sensing microelectrode; the measured potential is the sum of these two contributions. The potential difference caused by the electric field can be substantially large, exceeding that of the potential difference associated with the activity of the primary ion. In this paper, we present experimental evidence of this feature, and investigate the extent to which it influences the final chemically-resolved image. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 141
页数:4
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