Facile in-situ deposition of Pt nanoparticles on nano-pore stainless steel composite electrodes for high active hydrogen evolution reaction

Hydrogen is regarded as a clean and highly efficient renewable energy. The platinum catalytic electrode is widely used in hydrogen evolution reaction (HER), but it has affected its commercial application because of its high cost. Therefore, the study on cost-effective and high-active catalysts toward HER is required to realise large-scale hydrogen production. In this work, we present a novel Pt/NPSSF catalyst prepared by a one-step in-situ deposition of Pt precursor on a nano-porous stainless-steel film (NPSSF) substrate. The prepared catalyst was evaluated in acidic and alkaline conditions for its HER activities. The preliminary results demonstrate that the Pt/NPSSF electrodes have superior catalytic activity for HER. The hydrogen overpotential of Pt/NPSSF is ?70mV (RHE) in the alkaline solution, which is lower than the Pt electrode of ?184mV. At the same time, we also obtained ?71.2 mV of overpotential for the Pt/NPSSF electrode, which is similar to the ?73mV of Pt electrode in the acid solution. The Tafel graphs plotted from the LSV curves indicate the different HER mechanism in the alkaline and acid solution. The HER kinetics of the Pt/NPSSF were studied using EIS. Comparing Pt/NPSSF to Pt electrode, the multi-pore structures of NPSSF and the Pt nanoparticles active sites decrease the charge transfer-resistance for the HER process. The facile preparation, high efficiency and low value of the Pt/NPSSF composite electrodes demonstrate the promising applications in HER.     

Corrosion of Mg alloys EV31A,WE43B,and ZE41A in chloride- and sulfate-containing solutions saturated with magnesium hydroxide

This study studied corrosion in 0.1 M Na₂SO₄, 0.1 M NaCl, and 0.6 M NaCl, all saturated with Mg(OH)₂, using weight loss, hydrogen evolution, and electrochemical measurements. Corrosion was similar in all cases. Nevertheless, the corrosion rates were alloy-dependent, were somewhat lower in 0.1 M Na₂SO₄ than in 0.1 M NaCl, and increased with NaCl concentration. The corrosion damage morphology was similar for all solutions; the extent correlated with the corrosion rate. The corrosion rates evaluated by the electrochemical methods were lower than those evaluated from hydrogen evolution, consistent with the Mg corrosion mechanism involving the unipositive Mg⁺ ion.     

Improving the corrosion resistance of a-C:H film by a top a-C:H:Si:O layer

During the deposition of a-C:H film, defects (pinholes or discontinuities) caused by excessive stress will inevitably appear, which will reduce the corrosion resistance of the a-C:H film. In this study, top a-C:H:Si:O layers (thickness of approximately 0.3 μm) on the surface of a-C:H films were deposited on a large scale by PACVD technology using acetylene (C₂H₂) and/or hexamethyldisiloxane (HMDSO) as reactants, to improve the corrosion resistance of a-C:H films while ensuring the appropriate overall hardness of the films. The corrosion behaviors of the films were studied by electrochemical impedance spectroscopy (EIS) and Tafel polarization. We found that the a-C:H/a-C:H:Si:O films possess a lower electrolyte penetration rate due to their stronger capacitance characteristics. In addition, the corrosion current density of the a-C:H/a-C:H:Si:O films (10^?10 A cm^?2) were reduced by 2 orders of magnitude compared to the a-C:H film (10^?8 A cm^?2), and by 3 orders of magnitude compared to 316 stainless steel (10^?7 A cm^?2). The impedance results obtained by EIS were simulated using appropriate equivalent circuits, and the corresponding electrical parameters were used to further verify the electrochemical protection behavior of the top a-C:H:Si:O layer.     

Self-healing properties of protective coatings containing isophorone diisocyanate microcapsules on carbon steel surfaces

Microcapsules containing isophorone diisocyanate (IPDI) were used as self-healing additives in the alkyd varnish coatings (AVCs), and their self-healing performance was evaluated in the case of artificial defects on Q235 steel surfaces, using scanning micro-reference electrode technique and Fourier-transform infrared spectroscopy. Comparison of the micromechanical properties between the water-insoluble self-healing products (polyurethanes) and AVCs indicates that the former significantly enhanced the capability of the scratched crevice to successfully endure outer stress. The electrochemical impedance spectroscopy experiments analysed the different stages in the self-healing process. This study successfully demonstrated the self-healing activity of IPDI-AVCs in protecting steel surfaces.     

Super-hydrophobic metal-complex film fabricated electrochemically on copper as a barrier to corrosive medium

Metal-complex film with super-hydrophobic property is fabricated on copper (Cu) surface with one-step electrochemical method in laurylamine/ethanol solution. “Dissolution–coordination–precipitation” model is proposed to illuminate formation mechanism of Cu(II)-laurylamine complex film. The super-hydrophobic film can act as a barrier to corrosion of underlying copper with inhibition efficiency close to 100%, and it maintains stability within a wide potential range. The origin of such corrosion protection property is explained from view point that hierarchical micro-structure of the super-hydrophobic film can maintain a stable air/liquid interface which inhibits erosion of corrosive medium.     

Influence of various surface treated silica nanoparticles on the electrochemical properties of SiO2/polyurethane nanocoatings

Various organosilane-treated SiO₂ nanoparticles were dispersed in a 2-pack polyurethane coating. The influence of surface modification and silica content on the electrochemical behaviour of the resultant nanocoatings was investigated. Electrochemical impedance spectroscopy (EIS) and open circuit potential (OCP) variations were examined. The surface chemistry of nanoparticles and its effect on the resultant nanocoating morphology were also studied utilising FTIR, and TEM analyses. The results reveal that the presence of more hydrophobic groups and longer-lengthed hydrophobic chains on the surface of nanoparticles, greatly improves the interfacial interactions at the polymer/filler interfaces resulting in a better corrosion performance.     

Oxidative post-treatments for enhanced corrosion resistance of aluminium electrodeposited from ionic liquids

In this paper we report the results of a study on the corrosion properties of carbon steel (UNI Fe360B) coated with a thin aluminium layer electrodeposited from ionic liquids and subsequently post-treated in an oxidizing environment. Two different types of treatments were investigated: thermal oxidation in air and electrochemical anodization. We found that heat treatments provided only a modest improvement of the anticorrosion properties while the electrochemical treatment produced a significant improvement.     

A correlation study on the phenolic profiles and corrosion inhibition properties of mangrove tannins (Rhizophora apiculata) as affected by extraction solvents

The objective of this study was to investigate the correlation of phenolic compositions and corrosion inhibition properties of Rhizophora apiculata bark extracts as affected by nine solvent systems. Several phenolic compositions, namely, total phenolic content (TPC), total flavonoid content (TFC), condensed tannin content (CTC) were investigated. In addition, the inhibitive actions of tannin extracts on mild steel in 1 M HCl solution were studied by potentiodynamic polarization and electrochemical impedance spectroscopy. The results showed that extraction solvents had significant effects on TPC, TFC, CTC and inhibition properties of extracts. A correlation between CTC and inhibition properties of R. apiculata bark extracts was revealed.