Improving the Energy Efficiency of Direct Formate Fuel Cells with a Pd/C-CeO2 Anode Catalyst and Anion Exchange Ionomer in the Catalyst Layer

Author: Miller Hamish Andrew   Ruggeri Jacopo   Marchionni Andrea   Bellini Marco   Pagliaro Maria Vincenza   Bartoli Carlo   Pucci Andrea   Passaglia Elisa   Vizza Francesco  

Publisher: MDPI

E-ISSN: 1996-1073|11|2|369-369

ISSN: 1996-1073

Source: Energies, Vol.11, Iss.2, 2018-02, pp. : 369-369

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Abstract

This article describes the development of a high power density Direct Formate Fuel Cell (DFFC) fed with potassium formate (KCOOH). The membrane electrode assembly (MEA) contains no platinum metal. The cathode catalyst is FeCo/C combined with a commercial anion exchange membrane (AEM). To enhance the power output and energy efficiency we have employed a nanostructured Pd/C-CeO2 anode catalyst. The activity for the formate oxidation reaction (FOR) is enhanced when compared to a Pd/C catalyst with the same Pd loading. Fuel cell tests at 60 °C show a peak power density of almost 250 mW cm−2. The discharge energy (14 kJ), faradic efficiency (89%) and energy efficiency (46%) were determined for a single fuel charge (30 mL of 4 M KCOOH and 4 M KOH). Energy analysis demonstrates that removal of the expensive KOH electrolyte is essential for the future development of these devices. To compensate we apply for the first time a polymeric ionomer in the catalyst layer of the anode electrode. A homopolymer is synthesized by the radical polymerization of vinyl benzene chloride followed by amination with 1,4-diazabicyclo[2.2.2]octane (DABCO). The energy delivered, energy efficiency and fuel consumption efficiency of DFFCs fed with 4 M KCOOH are doubled with the use of the ionomer.