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Redox flow batteries (RFBs) are promising for large-scale long-duration energy storage owing to their inherent safety, decoupled power and energy, high efficiency, and longevity. Membranes constitute an important component that affects mass transport processes in RFBs, including ion transport, redox-species crossover, and the net volumetric transfer of supporting electrolytes. Hydrophilic microporous polymers, such as polymers of intrinsic microporosity (PIM), are demonstrated as next-generation ion-selective membranes in RFBs. However, the crossover of redox species and water migration through membranes are remaining challenges for battery longevity. Here, a facile strategy is reported for regulating mass transport and enhancing battery cycling stability by employing thin film composite (TFC) membranes prepared from a PIM polymer with optimized selective-layer thickness. Integration of these PIM-based TFC membranes with a variety of redox chemistries allows for the screening of suitable RFB systems that display high compatibility between membrane and redox couples, affording long-life operation with minimal capacity fade. Thickness optimization of TFC membranes further improves cycling performance and significantly restricts water transfer in selected RFB systems.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369228 | PMC |
http://dx.doi.org/10.1002/advs.202206888 | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, P. R. China.
Nanofiltration membranes (NFMs) with superior permeability and high rejection of both divalent anions and cations are highly desirable to meet the increasing separation demands of complex systems. Herein, we propose a three-in-one strategy to develop a state-of-the-art dually charged thin-film composite (TFC) nanofiltration membrane consisting of a positively charged electrospun nanofiber substrate (NFS) with surface mineralization and a negatively charged polyamide (PA) selective layer prepared by interfacial polymerization (IP). The highly hydrophilic mineralized nanofiber substrate not only effectively reduces the thickness of the PA selective layer but also crumples its structures by the abundant zirconia nanoparticles on the substrate surface, resulting in excellent water flux (15.
View Article and Find Full Text PDFACS Omega
November 2024
Institute of Membrane Research, Helmholtz-Zentrum Hereon, Max-Planck-Straße 1, 21502 Geesthacht, Germany.
Thin-film composite (TFC) membranes containing metal-polyphenol network (MPN) selective layers were fabricated using a supramolecular self-assembly between tannic acid (TA) and ferric ion (Fe). The TA-Fe thin film was coated on a porous polyacrylonitrile support using aqueous solutions of TA and FeCl via a layer-by-layer deposition technique. The pH of the TA solution was used as a tool to alter the membrane characteristics.
View Article and Find Full Text PDFInd Eng Chem Res
November 2024
School of Engineering, University of Edinburgh, Robert Stevenson Rd., Edinburgh EH9 3FB, United Kingdom.
Membrane-based gas separation processes are a technology in continuous evolution. Various types of polymer membranes have been developed, many exhibiting high CO permeability and selective properties over competing gases such as N and CH. In order to be competitive, membranes must be less-expensive, more stable, and more efficient, and their production must be scalable.
View Article and Find Full Text PDFACS Appl Mater Interfaces
December 2024
Department of Mechanical Engineering, 10-241 Donadeo Innovation Center for Engineering, Advanced Water Research Lab (AWRL), University of Alberta, Edmonton, Alberta T6G 1H9, Canada.
The separation of Li from Mg in salt-lake brines using nanofiltration (NF) has become the most popular solution to meet the rising demand for lithium, particularly driven by the extensive use of lithium-ion batteries. This study presents the fabrication of a uniquely designed polyamide (PA) thin-film nanocomposite (TFN) membranes with ultrahigh Li/Mg selectivity and enhanced water flux by covalently incorporating mixed ligands functionalized silica nanoparticles (F-SiONPs) into the selective PA layer and covalently bonding them to the membrane surface. In this strategy, bare silica nanoparticles (SiONPs) were functionalized with mixed superhydrophilic ligands, including primary amine and quaternary ammonium groups, resulting in a highly positive surface charge primarily from the quaternary ammonium groups and enabling covalent conjugation via amine groups.
View Article and Find Full Text PDFACS Appl Mater Interfaces
November 2024
Environmental Engineering Department, Istanbul Technical University, Maslak 34469, Istanbul, Turkey.
This study investigates the synthesis and characterization of Schiff base network-1 (SNW-1) covalent organic framework (COF) nanomaterials and their application in the fabrication of thin-film nanocomposite (TFN) membranes. The embedding of SNW-1 COF in reverse osmosis (RO) membranes with a polysulfone (PSf) substrate was done using the interfacial polymerization method. The result of the study demonstrated that the porous and hydrophilic structure of the COF increased the hydrophilic properties of the produced RO membranes.
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