Visualizing Nanoscale Distribution of Corrosion Cells by Open-Loop Electric Potential Microscopy
Author(s) -
Kyoko Honbo,
Shoichiro Ogata,
Takuya Kitagawa,
Takahiro Okamoto,
Naritaka Kobayashi,
Itto Sugimoto,
Shohei Shima,
Akira Fukunaga,
Chikako Takatoh,
Takeshi Fukuma
Publication year - 2016
Publication title -
acs nano
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.554
H-Index - 382
eISSN - 1936-086X
pISSN - 1936-0851
DOI - 10.1021/acsnano.5b07552
Subject(s) - corrosion , materials science , cathodic protection , nanoscopic scale , oxide , electrolyte , anode , electrochemistry , kelvin probe force microscope , metallurgy , nanotechnology , electrode , atomic force microscopy , chemistry
Corrosion is a traditional problem but still one of the most serious problems in industry. To reduce the huge economic loss caused by corrosion, tremendous effort has been made to understand, predict and prevent it. Corrosion phenomena are generally explained by the formation of corrosion cells at a metal-electrolyte interface. However, experimental verification of their nanoscale distribution has been a major challenge owing to the lack of a method able to visualize the local potential distribution in an electrolytic solution. In this study, we have investigated the nanoscale corrosion behavior of Cu fine wires and a duplex stainless steel by in situ imaging of local corrosion cells by open-loop electric potential microscopy (OL-EPM). For both materials, potential images obtained by OL-EPM show nanoscale contrasts, where areas of higher and lower potential correspond to anodic areas (i.e., corrosion sites) and cathodic areas, respectively. This imaging capability allows us to investigate the real-time transition of local corrosion sites even when surface structures show little change. This is particularly useful for investigating reactions under surface oxide layers or highly corrosion-resistant materials as demonstrated here. The proposed technique should be applicable to the study of other redox reactions on a battery electrode or a catalytic material. The results presented here open up such future applications of OL-EPM in nanoscale electrochemistry.
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