1. |
- Högström, Jonas, et al.
(författare)
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Cation profiling of passive films on stainless steel formed in sulphuric and acetic acid by deconvolution of angle-resolved X-ray photoelectron spectra
- 2013
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Ingår i: Applied Surface Science. - : Elsevier BV. - 0169-4332 .- 1873-5584. ; 284, s. 700-714
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Tidskriftsartikel (refereegranskat)abstract
- An approach for determining depth gradients of metal-ion concentrations in passive films on stainlesssteel using angle-resolved X-ray photoelectron spectroscopy (ARXPS) is described. The iterative method,which is based on analyses of the oxidised metal peaks, provides increased precision and hence allowsfaster ARXPS measurements to be carried out. The method was used to determine the concentrationdepth profiles for molybdenum, iron and chromium in passive films on 316L/EN 1.4432 stainless steelsamples oxidised in 0.5 M H2SO4 and acetic acid diluted with 0.02 M Na2B4O7 · 10H2O and 1 M H2O,respectively. The molybdenum concentration in the film is pin-pointed to the oxide/metal interface andthe films also contained an iron-ion-enriched surface layer and a chromium-ion-dominated middle layer.Although films of similar composition and thickness (i.e., about 2 nm) were formed in the two electrolytes,the corrosion currents were found to be three orders of magnitude larger in the acetic acid solution.The differences in the layer composition, found for the two electrolytes as well as different oxidationconditions, can be explained based on the oxidation potentials of the metals and the dissolution rates ofthe different metal ions.
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2. |
- Nilsson, Sara, et al.
(författare)
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Electrochemical quartz crystal microbalance study of polyelectrolyte film growth under anodic conditions
- 2013
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Ingår i: Applied Surface Science. - : Elsevier. - 0169-4332 .- 1873-5584. ; 280, s. 783-790
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Tidskriftsartikel (refereegranskat)abstract
- Coating hard materials such as Pt with soft polymers like poly-l-lysine is a well-established technique for increasing electrode biocompatibility. We have combined quartz crystal microgravimetry with dissipation with electrochemistry (EQCM-D) to study the deposition of PLL onto Pt electrodes under anodic potentials. Our results confirm the change in film growth over time previously reported by others. However, the dissipation data suggest that, after the short initial phase of the process, the rigidity of the film increases with time, rather than decreasing, as previously proposed. In addition to these results, we discuss how gas evolution from water electrolysis and Pt etching in electrolytes containing Cl− affect EQCM-D measurements, how to recognize these effects, and how to reduce them. Despite the challenges of using Pt as an anode in this system, we demonstrate that the various electrochemical processes can be understood and that PLL coatings can be successfully electrodeposited.
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