Encyclopedia of Interfacial Chemistry 2018
DOI: 10.1016/b978-0-12-409547-2.13576-0
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Kinetics of Oxide Growth of Passive Films on Transition Metals

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Cited by 4 publications
(4 citation statements)
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“…There are four aspects related to the oxide film behaviour that influences EAC initiation. First of all, the protective oxide film is a living entity; it grows into the metal at the metal-film interface and dissolves into the aqueous environment at the film-solution interface [22,23]. Second, upon rupture or breakdown of the oxide film, it will reform, i.e.…”
Section: Methodsmentioning
confidence: 99%
“…There are four aspects related to the oxide film behaviour that influences EAC initiation. First of all, the protective oxide film is a living entity; it grows into the metal at the metal-film interface and dissolves into the aqueous environment at the film-solution interface [22,23]. Second, upon rupture or breakdown of the oxide film, it will reform, i.e.…”
Section: Methodsmentioning
confidence: 99%
“…renewable energy sources could induce a breakdown of the passivation layer and an increase in oxide growth. [46][47][48] To study the passivation under alternating conditions, several hundred potential cycles between 0.4 to 1.0 V RHE and 0.4 to 1.4 V RHE were applied. 22 Figure 3a shows the dissolution profiles of the five investigated TMCs during cycling up to 1.0 V RHE .…”
Section: Isotopmentioning
confidence: 99%
“…The explanation is the increased electric field strength between the metal surface and the electrolyte. 46,51 The stronger the electric field, the more are the metal cations dragged towards the oxide/electrolyte interface and the oxide anions towards the metal/oxide interface. NbC exhibits the thickest oxide layer with almost 10 ML while TiC and TaC show oxide overlayers between 5 and 3 ML.…”
Section: Isotopmentioning
confidence: 99%
“…The closeness of the b a ′ values for the Ti and CoCr alloys suggests that these two groups have the same corrosion mechanism, whereby the anodic reaction is controlled by migration through the oxide film with limited growth, because (a) the passive film on these alloys is thin (~2–4 nm, as shown in Table 2), (b) migration of charged species through thin films is considered generally to be rate‐controlling, 23,45 and (c) buffered solutions are thought to impede film growth.…”
Section: Model For Film Growth and Dissolutionmentioning
confidence: 99%