Search results for "Passivation"
showing 10 items of 91 documents
Macroscopic and local electrochemical studies of austempered ductile iron in perchlorate solutions.
2006
The corrosion behavior of austempered ductile iron (ADI) in alkaline environment has been investigated at the microscale by means of the electrochemical microcell technique, surface analysis methods, and at the macroscale using classical electrochemical techniques. Local electrochemical investigations have revealed that the matrix (ausferrite), far from spheres, undergoes passivation in 1 M NaClO 4 , pH 10 solution within a wide potential range, from the corrosion potential (of about -280 mV/SCE) until 800 mV/SCE. Surface observations combined with local electrochemical analysis have shown that corrosion of ADI first occurs in the close vicinity of some graphite spheres and then around oxid…
Passivation-Induced Physicochemical Alterations of the Native Surface Oxide Film on 316L Austenitic Stainless Steel
2019
Time of Flight Secondary Ion Mass Spectroscopy, X-Ray Photoelectron Spectroscopy, in situ Photo-Current Spectroscopy and electrochemical analysis were combined to characterize the physicochemical alterations induced by electrochemical passivation of the surface oxide film providing corrosion resistance to 316L stainless steel. The as-prepared surface is covered by a ~2 nm thick, mixed (Cr(III)-Fe(III)) and bi-layered hydroxylated oxide. The inner layer is highly enriched in Cr(III) and the outer layer less so. Molybdenum is concentrated, mostly as Mo(VI), in the outer layer. Nickel is only present at trace level. These inner and outer layers have band gap values of 3.0 and 2.6-2.7 eV, respe…
Ultrafast spectroscopic investigation on fluorescent carbon nanodots: the role of passivation.
2019
Disentangling the respective roles of the surface and core structures in the photocycle of carbon nanodots is a critical open problem in carbon nanoscience. While the need of passivating carbon dot surfaces to obtain efficiently emitting nanoparticles is very well-known in the literature, it is unclear if passivation introduces entirely new surface emitting states, or if it stabilizes existing states making them fluorescent. In this multi-technique femtosecond spectroscopy study, the relaxation dynamics of non-luminescent (non-passivated) carbon dots are directly compared with their luminescent (passivated) counterparts. Non-passivated dots are found to host emissive states, albeit very sho…
Mesoporous SiC with Potential Catalytic Application by Electrochemical Dissolution of Polycrystalline 3C-SiC
2018
Electrochemical dissolution of highly doped (ρ ∼ 1 mΩ·cm, n-type) polycrystalline 3C-SiC in HF/H2O and HF/H2O/ethanol solutions allowed production of porous silicon carbide (por-SiC) and soluble carbon fluorooxide nanoparticles as a byproduct. The por-SiC is a crystalline material with large pore volume, surface area close to 100 m2 g–1, and open mesoporous structure. The surface of por-SiC is covered with a thin carbon-enriched layer, bearing carboxylic acid groups. Depending on the SiC resistivity, etchant composition, and current density, three different types of por-SiC morphology, namely, a macroporous tubular, mesoporous hierarchical, and mesoporous filamentary were revealed. A qualit…
Investigation of the kinetics of growth of anodic oxide films on niobium by galvanostatic and tensiodynamic experiments
1990
Abstract The kinetics of growth of anodic oxide films on niobium has been investigated by interferometric methods. Tensiodynamic experiments allow the growth of the films at constant rate. Photoeffects during the growth of the films under absorbed light give additional information on the growth process.
Two birds with one stone: dual grain-boundary and interface passivation enables >22% efficient inverted methylammonium-free perovskite solar cells
2021
Advancing inverted (p���i���n) perovskite solar cells (PSCs) is key to further enhance the power conversion efficiency (PCE) and stability of flexible and perovskite-based tandem photovoltaics. Yet, the presence of defects at grain boundaries and in particular interfacial recombination at the perovskite/electron transporting layer interface induce severe non-radiative recombination losses, limiting the open-circuit voltage (VOC) and fill factor (FF) of PSCs in this architecture. In this work, we introduce a dual passivation strategy using the long chain alkylammonium salt phenethylammonium chloride (PEACl) both as an additive and for surface treatment to simultaneously passivate the grain b…
Repassivation of the damage generated by cavitation on UNS N08031 in a LiBr solution by means of electrochemical techniques and Confocal Laser Scanni…
2010
Abstract The objective of this work is to study the influence of cavitation on the corrosion behaviour of Alloy 31, a highly-alloyed austenitic stainless steel (UNS N08031), in a LiBr heavy brine solution (992 g/L) at 25 °C. The presence of cavitation shifted the OCP value towards the active direction by 708 mVAg/AgCl, increased anodic current densities and passivation current density, ip, and reduced the pitting potential, Ep. Repassivation behaviour of Alloy 31 has been investigated by using potentiostatic tests at different potentials. The current density transient obtained after interrupting cavitation was used to obtain the repassivation index, n, provided by the slope of the log i(t) …
Monolayer black phosphorus by sequential wetchemical surface oxidation
2018
We report a straightforward chemical methodology for controlling the thickness of black phosphorus flakes down to the monolayer limit by layer-by-layer oxidation and thinning, using water as solubilizing agent.
Influence of sulphite on the passivation of iron
1991
Abstract Mossbauer spectroscopy and electrochemical measurements were used to study the passivation of iron and steels in a sulphite containing solution. The potentiodynamic curves show that passivation occurs at −140 mV potential vs saturated calomel electrode ( sce ). The main phase of the passive layer was found to be γ-FeOOH, while FeSO 4 ·H 2 O on the surface and FeSO 3 ·3H 2 O inside the layer were identified as minor phases in the case of polarization in a solution of pH 3.37. Only γ-FeOOH was observed on the surface of samples polarized at pH 6.6.
Study of Passive Films Formed on AISI 316L Stainless Steel in Non-Polluted and Underwater-Volcano-Polluted Seawater
2014
This work studies the semiconducting behavior of passive films formed on AISI 316L (UNS S31603) in two different sea-water solutions, non-polluted and polluted, collected from the volcano of El Hierro Island. Polarization measurements, potentiostatic passivation tests, electrochemical impedance spectroscopy, and capacitance measurements were performed. Results show that the polluted seawater worsens passivation kinetics. Additionally, passive films formed on AISI 316L stainless steel in polluted seawater have been found to be less protective than those formed in non-polluted seawater, showing a more defective structure, owing to the acidity of the polluted medium.