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Nonaqueous redox flow batteries (NARFBs) have been plagued by the lack of appropriate separators to prevent crossover. In this article, the synthesis and characterization of poly(norbornene) (PNB) anion-exchange membranes (AEMs) were studied. PNB is a copolymer of butyl norbornene (BuNB) and bromobutyl norbornene (BrBuNB) with varying amounts of tetramethyl hexadiamine cross-linker. The performance of the AEMs was investigated in nonaqueous redox flow batteries under ideal conditions. Performance evaluation encompassed several key factors, including durability in a nonaqueous solvent, charge-carrying ions permeability, electric cell resistance, crossover of redox-active molecules, and mechanical properties. The BuNB-based AEMs outperformed the commercial Fumasep membrane in battery cycling tests, showcasing their superior performance characteristics. Long-term performance tests showed that the top performing PNB membrane exhibited an impressive 83% total capacity retention over 1000 charge/discharge cycles. The low loss was primarily due to minimal crossover. In contrast, the FAPQ-375 commercial membrane experienced significantly lower capacity retention, measuring only 28%, due to high crossover.
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http://dx.doi.org/10.1021/acsami.4c18366 | DOI Listing |
Sustain Energy Fuels
August 2025
Electrochemical Materials and Systems, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology P.O. Box 513 5600 MB Eindhoven The Netherlands
Understanding reactive mass transport in redox flow reactors is key to improving performance, yet conventional characterization techniques often rely on cell-averaged metrics and fail to resolve local transport phenomena. In this study, we employ neutron radiography to visualize concentration distributions in redox flow cells with non-aqueous electrolytes, leveraging the high attenuation of hydrogen-containing organic molecules and boron-containing supporting ions. Symmetric flow cell experiments were conducted with three electrode types (paper, cloth, and a hierarchical porous electrode fabricated by non-solvent induced phase separation), and two flow field designs (parallel and interdigitated).
View Article and Find Full Text PDFChem Sci
July 2025
Department of Chemical Engineering, University of Utah Salt Lake City UT USA
Nonaqueous magnesium redox flow batteries (Mg RFBs) are attractive for low-cost, high-energy-density and long-cycle-life stationary energy storage applications. However, state-of-the-art cathode redox-active molecules suffer from low solubility and low redox potential. Herein, we screened a range of cathode redox-active molecules and identified amine molecules as optimal to couple with the Mg anode.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Department of Physics, University School of Sciences, Gujarat University, Ahmedabad 380 009, India. Electronic address:
Lithium-oxygen batteries are next-generation battery devices due to lightweight nature and high energy density with compared to conventional Li-ion batteries. These batteries consist a metal anode terminal and an oxygen diffused cathode terminal, in which oxygen is used as a reactant with metal atoms from surrounding air. Nonetheless, these systems facing the problems related to sluggish kinetics and higher overpotential due to formation of insoluble products at negative electrode during redox reaction.
View Article and Find Full Text PDFChemSusChem
August 2025
Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, South Korea.
Redox flow batteries (RFBs) offer a scalable and safe solution for storing energy from intermittent renewable sources. Naphthalene diimide (NDI) with its π-conjugated core enables stable two-electron redox reactions, making it a promising redox-active material. However, its limited solubility, diffusivity, and crossover in nonaqueous solvents restrict practical applications.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemistry, Bankura University, Bankura, West Bengal, 722155, India.
Eight mononuclear complexes have been synthesized, namely: [(L1)Cu]ClO (1), [(L2)Cu]ClO·CHCN (2·CHCN), [(L2)Cu(DMF)](ClO)·2DMF·HO (3·2DMF·HO), [(L1)Cu(MeCN)](ClO) (4), [(L1)Cu(Cl)]PF (5), [(tren)Cu(MeCN)](ClO) (6), [(tren)Cu(Cl)]PF (7) and [(L2')Cu(DMF)](ClO)·DMF·HO (8·DMF·HO). In these complexes, copper atoms are coordinated to tetradentate ligands such as tris-(4-(4-(-butyl))benzyl-3-aza-3-butenyl)amine (L1), tris(2-aminoethyl)amine (tren), tris-(4-pyren-1-yl-3-aza-3-butenyl)amine (L2) and bis-(4-pyren-1-yl-3-aza-3-butenyl)aminoethylamine (L2'). The complexes were structurally characterized by X-ray crystallography, along with various spectroscopic techniques.
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