Improving catalytic performance of the oxygen reduction reaction (ORR) of Pt/C catalysts is essential for reducing Pt-loading and the according cost of proton exchange membrane fuel cells (PEMFCs). Herein, we report a new conceptual design of catalyst layers to improve the ORR performance of Pt/C catalysts by replacing perfluorosulfonated ionomers with protic poly(ionic liquid) as a proton conductor. The specific activity of the designed catalyst at 0.9 V under acidic conditions is over three times higher than that of catalyst using Nafion as the proton conductor. Furthermore, the durability test reveals that the introduction of protic poly(ionic liquid) ionomers can protect Pt nanoparticles against aggregation during potential cycles, but it is less durable than Nafion because of the nature of hydrocarbons. Nevertheless, we believe that replacing perfluorosulfonated ionomers with protic poly(ionic liquid) as proton conductors could be a promising strategy to design an efficient cathode for low Pt-loading PEMFCs.
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http://dx.doi.org/10.1021/acsami.8b20587 | DOI Listing |
Nat Commun
May 2024
College of Materials Science and Engineering, Hunan University, Changsha, 410004, China.
The advancement of contemporary adhesives is often limited by the balancing act between cohesion and interfacial adhesion strength. This study explores an approach to overcome this trade-off by utilizing the spontaneous polymerization of a protic ionic liquid-based monomer obtained through the neutralization of 2-acrylamide-2-methyl propane sulfonic acid and hydroxylamine. The initiator-free polymerization process is carried out through a gradual increase in monomer concentration in aqueous solutions caused by solvent evaporation upon heating, which results in the in-situ formation of a tough and thin adhesive layer with a highly entangled polymeric network and an intimate interface contact between the adhesive and substrate.
View Article and Find Full Text PDFPolymers (Basel)
October 2021
Conducting Polymers in Composites and Applications Research Group, Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City 700000, Vietnam.
Polymerized ionic liquids (PILs) are interesting new materials in sustainable technologies for energy storage and for gas sensor devices, and they provide high ion conductivity as solid polymer electrolytes in batteries. We introduce here the effect of polar protic (aqueous) and polar aprotic (propylene carbonate, PC) electrolytes, with the same concentration of lithium bis(trifluoromethane) sulfonimide (LiTFSI) on hydrophobic PIL films. Cyclic voltammetry, scanning ionic conductance microscopy and square wave voltammetry were performed, revealing that the PIL films had better electroactivity in the aqueous electrolyte and three times higher ion conductivity was obtained from electrochemical impedance spectroscopy measurements.
View Article and Find Full Text PDFPolymers (Basel)
October 2020
Polymer Chemistry Research Group, Institute of Materials and Environment Chemistry, Research Centre for Natural Sciences, Magyar tudósok körútja 2, H-1117 Budapest, Hungary.
Despite the great interest in nanoconfined materials nowadays, nanocompartmentalized poly(ionic liquid)s (PILs) have been rarely investigated so far. Herein, we report on the successful alkylation of poly(1-vinylimidazole) with methyl iodide in bicontinuous nanophasic poly(1-vinylimidazole)--poly(tetrahydrofuran) (PVIm--PTHF) amphiphilic conetworks (APCNs) to obtain nanoconfined methylated PVImMe--PTHF poly(ionic liquid) conetworks (PIL-CNs). A high extent of alkylation (~95%) was achieved via a simple alkylation process with MeI at room temperature.
View Article and Find Full Text PDFACS Omega
February 2020
Chemistry Department, College of Science, Ain Shams University, Abasia, Cairo 11566, Egypt.
Catalytic degradation of organic water pollutants has emerged as a cost- and energy-effective technique to treat wastewater. In this work, new silver and magnetite nanoparticles (NPs) were prepared with a protic poly(ionic liquid) (PIL) based on a quaternized diethylethanolamine cation combined with 2-acrylamido-2-methylpropane sulfonate--vinylpyrrolidone (QAMPSA/VP) as a capping and a reducing agent. The morphology, particle size, surface charge, thermal stability, and magnetic properties of QAMPS/VP-Ag and FeO NPs were investigated to determine the efficiency of the PIL as a reducing and a capping agent to protect the produced NPs from oxidation or thermal degradation.
View Article and Find Full Text PDFACS Appl Mater Interfaces
February 2019
College of Physics and Science Technology , Wuhan University, Luojiashan Rd. , Wuhan 430072 , China.
Improving catalytic performance of the oxygen reduction reaction (ORR) of Pt/C catalysts is essential for reducing Pt-loading and the according cost of proton exchange membrane fuel cells (PEMFCs). Herein, we report a new conceptual design of catalyst layers to improve the ORR performance of Pt/C catalysts by replacing perfluorosulfonated ionomers with protic poly(ionic liquid) as a proton conductor. The specific activity of the designed catalyst at 0.
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