The increasing demand for raising the reliability of electronic contacts has led to the development of methods that protect metal surfaces against atmospheric corrosion agents. This severe problem implies an important economic cost annually but small amounts of corrosion inhibitors can control, decrease or avoid reactions between a metal and its environment. In this regard, surfactant inhibitors have displayed many advantages such as low price, easy fabrication, low toxicity and high inhibition efficiency. For this reason, in this article, the spectroelectrochemical behavior of polycrystalline gold electrode modified by reverse micelles (water/polyethyleneglycol-dodecylether (BRIJ 30)/-heptane) is investigated by atomic force microscopy (AFM), potentiodynamic methods and electrochemical impedance spectroscopy (EIS). Main results indicate a strong adsorption of a monolayer of micelles on the gold substrate in which electron tunneling conduction is still possible. Therefore, this method of increasing the corrosion resistance of gold contacts is usable only in conditions of long-term storage but not in the operation of devices with such contacts. In this regard, the micelle coating must be removed from the surface of the gold contacts before use. Finally, the aim of the present work is to understand the reactions occurring at the surfactant/metal interface, which may help to improve the fabrication of novel electrodes.
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http://dx.doi.org/10.3390/molecules26020471 | DOI Listing |
Polymers (Basel)
December 2024
Henan Key Laboratory of Rare Earth Functional Materials, The Key Laboratory of Rare Earth Functional Materials and Applications, Zhoukou Normal University, Zhoukou 466001, China.
Phenoxazine, as an organic-small-molecule chromophore, has attracted much attention for its potential electrochromic applications recently. To develop appealing materials, phenoxazine chromophores were introduced at the N-position of carbazole-thiophene pigment, yielding two novel monomers (DTCP and DDCP), whose chemical structures were characterized by NMR, HRMS and FTIR. The results of the optical property study indicate that little influence could be observed in the presence of the phenoxazine chromophore.
View Article and Find Full Text PDFChem Sci
November 2024
Division of Applied Chemistry, Faculty of Engineering, Hokkaido University Kita 13, Nishi 8, Kita-ku Sapporo Hokkaido 060-8628 Japan
A cyclo[4]pyrrole bearing pyrrole C()-C() direct linkages, a contracted porphyrin analogue with no -carbon bridge, was synthesized from an oligoketone-related precursor. X-ray crystallography and StrainViz analysis revealed a non-planar structure with a total strain of 20.8 kcal mol.
View Article and Find Full Text PDFJ Am Chem Soc
October 2024
The Bernal Institute and Department of Chemical Sciences, School of Natural Sciences, University of Limerick (UL), Limerick V94 T9PX, Ireland.
Conducting polymer (CP) thin films find widespread use, for example in bioelectronic, energy harvesting and storage, and drug delivery technology. Electrosynthesis at a polarizable liquid|liquid interface using an aqueous oxidant and organic soluble monomer provides a route to free-standing and scalable CP thin films, such as poly(3,4-ethylenedioxythiophene) (PEDOT), in a single step at ambient conditions. Here, using the potentiodynamic technique of cyclic voltammetry, interfacial electrosynthesis involving ion exchange, electron transfer, and proton adsorption charge transfer processes is shown to be mechanistically distinct from CP electropolymerization at a solid electrode|electrolyte interface.
View Article and Find Full Text PDFDalton Trans
September 2024
Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Química Inorgánica, Analítica y Química Física, Pabellón 2, Ciudad Universitaria, C1428EHA, Buenos Aires, Argentina.
Chromophore-catalyst assemblies are interesting benchmark molecules for photocatalysis. We have prepared two examples of these assemblies and characterized their behaviour as catalysts for the water oxidation reaction. In the bimetallic complexes [Ru(tpy)(4,4'-X-bpy)(μ-CN)Ru(bda)(DMSO)](PF) (X = -H (1), -OCH (2), tpy = 2,2':6',2''-terpyridine, bpy = 2,2'-bipyridine, Hbda = 2,2'-bipyridine-6,6'-dicarboxylic acid and DMSO = (CH)SO), a Ru(II)-polypiridine chromophore {Ru(tpy)(4,4'-X-bpy)} is linked by a cyanide bridge to a {Ru(bda)} water oxidation catalyst.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2024
Institute of Inorganic and Analytical Chemistry, University of Freiburg, Albertstr. 21, 79104 Freiburg, Germany.
For hydrogenases to serve as effective electrocatalysts in hydrogen biotechnological devices, such as enzymatic fuel cells, it is imperative to design electrodes that facilitate stable and functional enzyme immobilization, efficient substrate accessibility, and effective interfacial electron transfer. Recent years have seen considerable advancements in this area, particularly concerning hydrogenases. However, a significant limitation remains: the inactivation of hydrogenases at high oxidative potentials across most developed electrodes.
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