Abstract
The real-time composition and structure of the passive film formed on a high nitrogen face-centered-cubic phase (γN) layer at the characterized transient corrosion currents from the electrochemical noise analyses in the borate buffer solution with the pH = 7.7 are investigated by the transmission electron microscope (TEM) with energy dispersion X-ray spectrum (EDS) using the focused ion beam (FIB) sampling. The thicker passive film of the γN phase layer on the nitrided AISI 304L in the borate buffer solutions is observed as two regions structure of O enriched n-type defect spinel γ-Fe2(N,O)3 and hydroxides in the outer region and Cr and N enriched p-type defect spinel (Fe,Cr)3(N,O)4 in the inner region, although few β-(Fe,Cr)OOH compounds are detected due to dehydration. The defect spinel in directions of < 112 >, < 213 > and < 110 > is epitaxially growing on the γN phase matrix during the passivation up to 8 h with a decreasing lattice mismatch from 5.9 to 1%, which is attributed to lattice expansion of the γN phase and the defect spinel. The lattice expansion of the γN phase at the interface with growing passive film is affected by dissolving nitrogen outward to the borate buffer solution. The dissolving nitrogen in the defect spinel induces its lattice expansion by hydrolysis at the interface. The dense and low-defective passive films on the γN phase layer have a significant effect on the corrosion resistance due to inhibition of the absorption of aggressive ion and limitation of the carrier density.
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