Search

Highlights • Supercapacitive MFC boosted up power/current pulses. • In-series connection of 4 microbial fuel cells quadrupled voltage and power output. • Fe-catalysts showed high hydrogen evolution reaction rate in neutral media. • Co-generation of electricity and hydrogen using SC-MFCs is here demonstrated., In this work, four different supercapacitive microbial fuel cells (SC-MFCs) with carbon brush as the anode and an air-breathing cathode with Fe-Aminoantipyrine (Fe-AAPyr) as the catalyst have been investigated using galvanostatic discharges. The maximum power (Pmax) obtained was in the range from 1.7 mW to 1.9 mW for each SC-MFC. This in-series connection of four SC-MFCs almost quadrupled Pmax to an operating voltage of 3025 mV and a Pmax of 8.1 mW, one of the highest power outputs reported in the literature. An additional electrode (AdHER) connected to the anode of the first SC-MFC and placed in the fourth SC-MFC evolved hydrogen. The hydrogen evolution reaction (HER) taking place at the electrode was studied on Pt and two novel platinum group metal-free (PGM-free) catalysts: Fe-Aminoantipyrine (Fe-AAPyr) and Fe-Mebendazole (Fe-MBZ). The amount of H2 produced was estimated using the Faraday law as 0.86 mMd−1cm−2 (0.132 L day−1) for Pt, 0.83 mMd−1cm−2 (0.127 L day−1) for Fe-AAPyr and 0.8 mMd−1cm−2 (0.123 L day−1) for Fe-MBZ. Hydrogen evolution was also detected using gas chromatography. While HER was taking place, galvanostatic discharges were also performed showing simultaneous H2 production and pulsed power generation with no need of external power sources.

A new equipment for in situ electrochemical dilatometry is designed and validated by studying the volumetric changes of a model electrode. The contactless measurement system permit to not influence the dilation of the sample during the tests. In addition, different forces can be applied in a selected range. Graphite is selected as model electrode and electrochemical tests in different electrolytes are carried out under different applied forces. The results of the electrodilatometric tests on graphite in EC:DMC- and in PC-based electrolyte reveal not only lithium insertion/deinsertion process, but also the presence of simultaneous phenomena like solvent evaporation, SEI formation and gas evolution. The latter has been detected by applying different forces that affect the gas uptake and release from porous separator. Controlled hydrogen evolution experiments were carried out at different applied forces in order to assess the gassing detection ability of the dilatometer. We demonstrate that with this new equipment it is possible, from thickness variation, to collect information on processes of different nature. Specifically, different applied forces emphasized gas evolution, which is a worth studying phenomenon for increasing battery safety.