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Nanoscale electrochemical visualization of grain-dependent anodic iron dissolution from low carbon steel

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Yule, Lewis C., Shkirskiy, Viacheslav, Aarons, Jolyon, West, Geoffrey D., Shollock, Barbara A., Bentley, Cameron Luke and Unwin, Patrick R. (2020) Nanoscale electrochemical visualization of grain-dependent anodic iron dissolution from low carbon steel. Electrochimica Acta, 332 . 135267. doi:10.1016/j.electacta.2019.135267 ISSN 0013-4686.

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Official URL: http://dx.doi.org/10.1016/j.electacta.2019.135267

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Abstract

The properties of steels and other alloys are often tailored to suit specific applications through the manipulation of microstructure (e.g., grain structure). Such microscopic heterogeneities are also known to modulate corrosion susceptibility/resistance, but the exact dependency remains unclear, largely due to the challenge of probing and correlating local electrochemistry and structure at complex (alloy) surfaces. Herein, high-resolution scanning electrochemical cell microscopy (SECCM) is employed to perform spatially-resolved potentiodynamic polarisation measurements, which, when correlated to co-located structural information from electron backscatter diffraction (EBSD), analytical scanning electron microscopy (SEM) and scanning transmission electron microscopy (STEM), reveal the relationship between anodic metal (iron) dissolution and the crystallographic orientation of low carbon steel in aqueous sulfuric acid (pH 2.3). Considering hundreds of individual measurements made on each of the low-index planes of body-centred cubic (bcc) low carbon steel, the rate of iron dissolution, and thus overall corrosion susceptibility, increases in the order (101) < (111) < (100). These results are rationalized by complementary density functional theory (DFT) calculations, where the experimental rate of iron dissolution correlates with the energy required to remove (and ionise) one iron atom at the surface of a lattice, calculated for each low index orientation. Overall, this study further demonstrates how nanometre-resolved electrochemical techniques such as SECCM can be effectively utilised to vastly improve the understanding of structure-function in corrosion science, particularly when combined with complementary, co-located structural characterisation (EBSD, STEM etc.) and computational analysis (DFT).

Item Type: Journal Article
Subjects: Q Science > QC Physics
Q Science > QD Chemistry
Q Science > QH Natural history
T Technology > TS Manufactures
Divisions: Faculty of Science, Engineering and Medicine > Science > Chemistry
Faculty of Science, Engineering and Medicine > Science > Physics
Faculty of Science, Engineering and Medicine > Engineering > WMG (Formerly the Warwick Manufacturing Group)
Library of Congress Subject Headings (LCSH): Scanning electrochemical microscopy, Electrons -- Backscattering , Electrons -- Diffraction, Scanning electron microscopy , Scanning transmission electron microscopy , Density functionals, Metals -- Anodic oxidation
Journal or Publication Title: Electrochimica Acta
Publisher: Pergamon
ISSN: 0013-4686
Official Date: 1 February 2020
Dates:
DateEvent
1 February 2020Published
13 November 2019Available
10 November 2019Accepted
Volume: 332
Article Number: 135267
DOI: 10.1016/j.electacta.2019.135267
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Open Access (Creative Commons)
Date of first compliant deposit: 20 November 2019
Date of first compliant Open Access: 20 November 2019
RIOXX Funder/Project Grant:
Project/Grant IDRIOXX Funder NameFunder ID
UNSPECIFIED[EPSRC] Engineering and Physical Sciences Research Councilhttp://dx.doi.org/10.13039/501100000266
UNSPECIFIEDTata Steelhttp://dx.doi.org/10.13039/501100007220
792948 (NELMA)[ERC] Horizon 2020 Framework Programmehttp://dx.doi.org/10.13039/100010661
UNSPECIFIEDRamsay Memorial Fellowships Trust, University College Londonhttp://dx.doi.org/10.13039/501100000685
Wolfson Research Merit Award[RS] Royal Societyhttp://dx.doi.org/10.13039/501100000288
EP/R018820/1[EPSRC] Engineering and Physical Sciences Research Councilhttp://dx.doi.org/10.13039/501100000266

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