Characterisation of MEAs for Electrochemical Energy Conversion Using an Easy Test Technique

The paper describes an EasyTest cell developed for simple, safe and inexpensive to run testing and optimisation of the active materials (catalysts, catalytic supports, polymer membrane electrolytes) and electrode structures utilized in PEM Fuel cells and Electrolysers. The main advantages of the new EasyTest technique are demonstrated by a comparative study on the performance of two types of membrane electrode assemblies for electrochemical energy conversion. Nafion and PBI-based polymer electrolyte membranes covered with catalytic layers containing 20 % Pt dispersed on carbon black (E-TEK, De Nora) are tested as hydrogen electrodes working in a fuel cell and an electrolyser mode at two characteristic temperatures, varying the total partial pressure in the cell. The PBI-based membrane electrode assembly (MEA) gives lower current densities compared to that containing Nafion, while its performance remains stable in a much broader potential range. At overpotentials of about = 300–350 mV the Nafion MEA reaches a limiting current density, while in the case of PBI-based MEA such an effect is not registered in the whole potential range tested

Overpotential analysis of alkaline and acidic alcohol electrolysers and optimized membrane-electrode assemblies

Alcohol electrolysis using polymeric membrane electrolytes is a promising route for storing excess renewable energy in hydrogen, alternative to the thermodynamically limited water electrolysis. By properly choosing the ionic agent (i.e. H+ or OH) and the catalyst support, and by tuning the catalyst structure, we developed membrane-electrode-assemblies which are suitable for cost-effective and efficient alcohol electrolysis. Novel porous electrodes were prepared by Atomic Layer Deposition (ALD) of Pt on a TiO2-Ti web of microfibers and were interfaced to polymeric membranes with either H+ or OH conductivity. Our results suggest that alcohol electrolysis is more efficient using OH conducting membranes under appropriate operation conditions (high pH in anolyte solution). ALD enables better catalyst utilization while it appears that the TiO2-Ti substrate is an ideal alternative to the conventional carbon-based diffusion layers, due to its open structure. Overall, by using our developmental anodes instead of commercial porous electrodes, the performance of the alcohol electrolyser (normalized per mass of Pt) can be increased up to ~30 times

Overpotential analysis of alkaline and acidic alcohol electrolysers and optimized membrane-electrode assemblies

Alcohol electrolysis using polymeric membrane electrolytes is a promising route for storing excess renewable energy in hydrogen, alternative to the thermodynamically limited water electrolysis. By properly choosing the ionic agent (i.e. H+ or OH) and the catalyst support, and by tuning the catalyst structure, we developed membrane-electrode-assemblies which are suitable for cost-effective and efficient alcohol electrolysis. Novel porous electrodes were prepared by Atomic Layer Deposition (ALD) of Pt on a TiO2-Ti web of microfibers and were interfaced to polymeric membranes with either H+ or OH conductivity. Our results suggest that alcohol electrolysis is more efficient using OH conducting membranes under appropriate operation conditions (high pH in anolyte solution). ALD enables better catalyst utilization while it appears that the TiO2-Ti substrate is an ideal alternative to the conventional carbon-based diffusion layers, due to its open structure. Overall, by using our developmental anodes instead of commercial porous electrodes, the performance of the alcohol electrolyser (normalized per mass of Pt) can be increased up to ~30 times