The present invention relates to new anion exchange polymers and (blend) membranes made from polymers containing highly fluorinated aromatic groups by means of nucleophilic substitution and processes for their production by means of nucleophilic aromatic substitution and their areas of application in membrane processes, in particular in electrochemical membrane processes such as fuel cells, electrolysis and redox flow batteries.

A polymer electrolyte membrane according to the present invention has a cluster diameter of 2.96 to 4.00 nm and a converted puncture strength of 300 gf/50 μm or more. The polymer electrolyte membrane according to the present invention has a low electric resistance and an excellent mechanical strength.

A polymer electrolyte membrane according to the present invention has a cluster diameter of 2.96 to 4.00 nm and a converted puncture strength of 300 gf/50 μm or more. The polymer electrolyte membrane according to the present invention has a low electric resistance and an excellent mechanical strength.

The present invention relates to a membrane electrode unit comprising a polymer membrane doped with a mineral acid as well as two electrodes, characterized in that the polymer membrane comprises at least one polymer with at least one nitrogen atom and at least one electrode comprises a catalyst which is formed from at least one precious metal and at least one metal less precious according to the electrochemical series.

The present invention relates to a membrane electrode unit comprising a polymer membrane doped with a mineral acid as well as two electrodes, characterized in that the polymer membrane comprises at least one polymer with at least one nitrogen atom and at least one electrode comprises a catalyst which is formed from at least one precious metal and at least one metal less precious according to the electrochemical series.

Method of preparing a proton exchange membrane (PEM) include mixing a precursor of a perfluorosulfonic acid polymer with a second material to form a precursor material in a reduced humidity zone; extruding the precursor material under reduced humidity to form a filament; 3D printing the PEM with the filament; converting the precursor of the perfluorosulfonic acid polymer to the perfluorosulfonic acid polymer within the PEM; and coating the PEM.

Disclosed are a method of manufacturing a membrane-electrode assembly and a membrane-electrode assembly manufactured using the same. The method includes forming a laminated structure, and treating the laminated structure, for example, by drying and heat treating. The laminated structure includes a release film, an anode layer, a porous support layer, and a cathode layer.

Disclosed are redox flow battery membranes, redox flow batteries incorporating the membranes, and methods of forming the membranes. The membranes include a densified polybenzimidazole gel membrane that is capable of incorporating a high liquid content without loss of structure that is formed according to a process that includes in situ hydrolysis of a polyphosphoric acid solvent followed by densification of the gel membrane. The densified membranes are then imbibed with a redox flow battery supporting electrolyte such as sulfuric acid and can operate at very high ionic conductivities of about 50 mS/cm or greater and with low permeability of redox couple ions, e.g. vanadium ions, of about 10.sup.−7 cm.sup.2/s or less. Redox flow batteries incorporating the membranes can operate at current densities of about 50 mA/cm.sup.2 or greater.

Disclosed are redox flow battery membranes, redox flow batteries incorporating the membranes, and methods of forming the membranes. The membranes include a densified polybenzimidazole gel membrane that is capable of incorporating a high liquid content without loss of structure that is formed according to a process that includes in situ hydrolysis of a polyphosphoric acid solvent followed by densification of the gel membrane. The densified membranes are then imbibed with a redox flow battery supporting electrolyte such as sulfuric acid and can operate at very high ionic conductivities of about 50 mS/cm or greater and with low permeability of redox couple ions, e.g. vanadium ions, of about 10.sup.−7 cm.sup.2/s or less. Redox flow batteries incorporating the membranes can operate at current densities of about 50 mA/cm.sup.2 or greater.

A zinc iodine flow battery includes a positive end plate, a positive current collector, a negative current collector, a positive electrode with a flow frame, a membrane, a negative electrode with a flow frame, a negative end plate. The negative electrolyte is circulated between the negative storage tank and the negative cavity by pump. The negative pipe is provided with a branch pipe for the positive electrolyte circulation. The porous membrane between the positive and negative electrodes can realize the conduction of supporting electrolyte and prevent the diffusion of I3− to the negative electrolyte. In a duel-flow battery system, same electrolyte serves as both the positive electrolyte and the negative electrolyte, which is a mixed aqueous solution containing iodized and zinc salt. The membrane is porous membrane does not contain ion exchange group. Both the positive and negative electrolyte are neutral solutions.