In the technologically important field of anticorrosion coatings, it is imperative to form well-defined and characterized films to protect the metal surface from corrosion. Phosphonate-based corrosion mitigation approaches are currently being exploited. Herein, the synergistic action of alkaline-earth metal ions and two carboxy-diphosphonates, PAIBA [-bis(phosphonomethyl)-2-aminoisobutyric acid] and BPMGLY [-(phosphonomethyl)glycine], is explored. Also, a family of four novel hybrid metal phosphonate materials is reported, Mg-PAIBA, Ca-PAIBA, Sr-PAIBA, and Sr-Na-PAIBA, whose topological analysis revealed a variety of underlying networks with the 6,10T9, , SP 1-periodic net (4,4)(0,2), and unique topologies. The synergistic metal/carboxy-diphosphonate blends were tested for their anticorrosion performance on carbon steel at preselected concentrations (0.1-1.0 mM) and pH values (4.0-6.0). The results showed an enhanced inhibitory performance in the presence of metal cations at higher concentrations. The inhibition of corrosion at pH 5.0 in the presence of BPMGLY, PAIBA, and their combination with Sr was investigated in detail using electrochemical measurements. Enhanced inhibition was achieved with a 1:1 Sr/BPMGLY (or PAIBA) binary system. Polarization curves indicated that the system is a "mixed" inhibitor. This study widens the family of carboxyphosphonate coordination polymers, showing their potential as attractive hybrid coatings with anticorrosion performance.
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http://dx.doi.org/10.1021/acs.inorgchem.4c02545 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Department of Battery and Chemical Engineering, Hanyang University, Ansan, Gyeonggi-do 15588, Republic of Korea.
Designing and constructing hierarchically structured materials with heterogeneous compositions is the key to developing an effective catalyst for overall water-splitting applications. Herein, we report the fabrication of hollow-structured selenium-doped nickel-cobalt hybrids on carbon paper as a self-supported electrode (denoted as Se-Ni|Co/CP, where Ni|Co hybrids consist of nickel-cobalt alloy-incorporated nickel-cobalt oxide). The procedure involves direct growth of zeolitic imidazolate framework-67 (ZIF-67) on bimetal-based nickel-cobalt hydroxide (NiCoOH) electrodeposited on CP, followed by selenous etching and pyrolysis to obtain the final Se-Ni|Co/CP electrocatalytic system.
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January 2025
Institute of Physics and Astronomy, University of Potsdam, Karl-Liebknecht-Straße 24/25, 14476, Germany.
Two-dimensional transition metal dichalcogenides (2D TMDCs) can be combined with organic semiconductors to form hybrid van der Waals heterostructures. Specially, non-fullerene acceptors (NFAs) stand out due to their excellent absorption and exciton diffusion properties. Here, we couple monolayer tungsten diselenide (ML-WSe) with two well performing NFAs, ITIC, and IT-4F (fluorinated ITIC) to achieve hybrid architectures.
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January 2025
Marquette University School of Dentistry, Milwaukee, Wisconsin, USA.
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View Article and Find Full Text PDFNat Commun
January 2025
State Key Laboratory of Superhard Materials, Synergetic Extreme Condition High-Pressure Science Center, College of Physics, Jilin University, Changchun, China.
Metal-organic frameworks that feature hybrid fluorescence and phosphorescence offer unique advantages in white-emitting communities based on their multiple emission centers and high exciton utilization. However, it poses a substantial challenge to realize superior white-light emission in single-component metal-organic frameworks without encapsulating varying chromophores or integrating multiple phosphor subunits. Here, we achieve a high-performance white-light emission with photoluminescence quantum yield of 81.
View Article and Find Full Text PDFNanoscale
January 2025
Laboratoire Softmat, Université de Toulouse, CNRS UMR 5623, 118 route de Narbonne, 31062 Toulouse Cedex 9, France.
Hybrid polyionic complexes (HPICs) are colloidal structures with a charged core rich in metal ions and a neutral hydrophilic corona. Their properties, whether as reservoirs or catalysts, depend on the accessibility and environment of the metal ions. This study demonstrates that modifying the coordination sphere of these ions can tune the properties of HPICs by altering the composition of the complexing block or varying formulation conditions.
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