Layer-by-layer deposition of polyelectrolyte multilayer (PEM) membranes has recently been applied successfully to a number of biomedical applications. This simple and versatile technique provides a broad surface modification platform, for example, for the display of biomolecules such as cell-adhesion peptides. In this work, we investigated the effects of PEM coatings on RGD-immobilization and osteoblast cell culture. RGD-containing peptides were conjugated to the amino groups of poly(allylamine hydrochloride) (PAH), and then adsorbed on top of 10-layer PAH/poly(acrylic acid) (PAA) multilayer membranes that were assembled at either pH 2.0 or pH 6.5. MG63 osteoblast-like cells were then seeded and cultured on the RGD-conjugated surfaces. We found that the cells adhered to and grew better on the RGD-conjugated PEM membranes. Furthermore, the cells grew better on the RGD-conjugated PEM coatings assembled at pH 6.5 than those assembled at pH 2.0. On the other hand, MG63 cells exhibited better differentiated phenotype on the pH 2.0 coatings compared to the pH 6.5 coatings with respect to alkaline phosphatase activity and calcium deposition, while cells did not express osteoblast phenotype on the PAH surfaces. These results clearly show that the base PEM membranes play an important role in RGD-immobilization and osteoblast functions.
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http://dx.doi.org/10.1163/156856209X419095 | DOI Listing |
Sensors (Basel)
December 2024
Institute of Autmatic Control, University of Kaiserslautern-Landau, 67653 Kaiserslautern, Germany.
Harsh operating conditions imposed by vehicular applications significantly limit the utilization of proton exchange membrane fuel cells (PEMFCs) in electric propulsion systems. Improper/poor management and supervision of rapidly varying current demands can lead to undesired electrochemical reactions and critical cell failures. Among other failures, flooding and catalytic degradation are failure mechanisms that directly impact the composition of the membrane electrode assembly and can cause irreversible cell performance deterioration.
View Article and Find Full Text PDFNanomaterials (Basel)
January 2025
Département de Génie Électrique, École de Technologie Supérieure, 1100 Notre-Dame Street West, Montreal, QC H3C 1K3, Canada.
This study explored the influence of graphene oxide (GO) on morphological and mechanical properties of Nafion 115 membranes with the objective of enhancing the mechanical properties of the most widely employed membrane in Proton Exchange Membrane Water Electrolyzers (PEMWE) applications. The membrane surface was modified by ultrasonically spraying a GO solution and different annealing temperatures were tested. Scanning Electron Microscopy (SEM) cross-sectional images revealed that annealing the composite membranes was sufficient to favor an interaction between the graphene oxide and the surface of the Nafion membranes.
View Article and Find Full Text PDFMaterials (Basel)
December 2024
Department of Material Science and Engineering, Universidad Carlos III de Madrid, IAAB, 28911 Leganés, Madrid, Spain.
The production of green hydrogen through proton exchange membrane water electrolysis (PEMWE) is a promising technology for industry decarbonization, outperforming alkaline water electrolysis (AWE). However, PEMWE requires significant investment, which can be mitigated through material and design advancements. Components like bipolar porous plates (BPPs) and porous transport films (PTFs) contribute substantially to costs and performance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Nat Commun
January 2025
School of Materials Science and Engineering, Peking University, Beijing, China.
Using metal oxides to disperse iridium (Ir) in the anode layer proves effective for lowering Ir loading in proton exchange membrane water electrolyzers (PEMWE). However, the reported low-Ir-based catalysts still suffer from unsatisfying electrolytic efficiency and durability under practical industrial working conditions, mainly due to insufficient catalytic activity and mass transport in the catalyst layer. Herein we report a class of porous heterogeneous nanosheet catalyst with abundant Ir-O-Mn bonds, achieving a notable mass activity of 4 A mg for oxygen evolution reaction at an overpotential of 300 mV, which is 150.
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