Guillaume Ozouf

Improving the activity and stability of Ir catalysts for PEM electrolyzer anodes by SnO2:Sb aerogel supports: does V addition play an active role in electrocatalysis?

Low Ir loading oxygen evolution reaction (OER) catalysts with superior activity and durability for proton exchange membrane (PEM) electrolyzers are an important topic in industry and academia. One possible strategy for addressing this challenge is the use of support materials that are stable under highly corrosive acidic environments at a high working potential (>1.4 V). Moreover, highly porous structure is another key criteria for OER catalyst support to achieve a high electrochemical surface area. Here, we report a novel Ir supported on a SnO2:Sb aerogel OER catalyst (Ir/SnO2:Sb-mod-V), which was prepared under ambient pressure by using vanadium additives. It shows an unrivaled activity and enhanced stability, on which vanadium does not play any active role but demonstrates the influences that changes the porosity of the aerogel support and affects the impurity content of the chlorine. By taking advantage of the high porosity of the aerogel substrate, Ir/SnO2:Sb-mod-V allows a decrease of more than 70 wt% for precious metal usage in the catalyst layer while keeping a similar OER activity compared to its unsupported counterpart.

Pt Nanoparticles Supported on Niobium-Doped Tin Dioxide: Impact of the Support Morphology on Pt Utilization and Electrocatalytic Activity

AbstractTwo synthesis routes were used to design high surface area niobium-doped tin dioxide (Nb-doped SnO2, NTO) nanostructures with either loose-tube (fibre-in-tube) morphology using electrospinning or aerogel morphology using a sol-gel process. A higher specific surface area but a lower apparent electrical conductivity was obtained on the NTO aerogel compared to the loose tubes. The NTO aerogels and loose tubes and two reference materials (undoped SnO2 aerogel and Vulcan XC72) were platinized with a single colloidal suspension and tested as oxygen reduction reaction (ORR) electrocatalysts for proton-exchange membrane fuel cell (PEMFC) applications. The specific surface area of the supports strongly influenced the mass fraction of deposited Pt nanoparticles (NPs) and their degree of agglomeration. The apparent electrical conductivity of the supports determined the electrochemically active surface area (ECSA) and the catalytic activity of the Pt NPs for the ORR. Based on these findings, electrospinning appears to be the preferred route to synthesize NTO supports for PEMFC cathode application. Graphical AbstractOn top : SEM images of the synthesized supports : 5.0 at.% Nb-doped SnO2 aerogel (NTO-AG) and loose tubes (NTO-LT) - At the bottom : specific activity (SA0.90) and mass activity (MA0.90) of the synthesized electrocatalysts for the oxygen reduction reaction (ORR) determined at E = 0.90 V vs. RHE as a function of the conductivity of the supports