Heterogeneous catalysts play a central role in production of a variety of useful chemicals, energy generation and greenhouse gas emissions reduction. A heterogeneous catalyst usually consists of fine metal or metal oxide particles in the nanometer range dispersed on a high surface area supports. The catalytic activity and/or selectivity of the catalyst could be tuned in by using chemical promoters that are added to the catalyst during its fabrication or by choosing a suitable catalyst supports via metal-support interaction (MSI) effect. Another way to efficiently promote catalytic activity and in some instances catalyst selectivity is the use of electrochemistry via Electrochemical Promotion of Catalysis (EPOC), also called Non-faradaic Electrochemical Modification of Catalytic Activity (NEMCA) phenomenon [1, 2]. EPOC or NEMCA is ascribed to significant changes in the catalytic properties of metal or metal oxide catalysts deposited on solid-electrolytes caused by the application of small current (in the range of a few μA) or potential (up to 2V). The application of electric stimuli results in the supply of ionic species from the solid-electrolyte to the active surface, where the catalytic reaction takes place. These ionic species act as promotes and their addition results in significant catalytic rate increase due to changes in the catalyst work function [2-4]. This phenomenon has been applied to over 100 catalytic systems and reactions and continues to make an impact to surface science, catalysis and solid-state electrochemistry. The application of EPOC to nanostructured, highly dispersed catalysts has attracted significant interest in the last decade and several studies have demonstrated dramatic EPOC effect with noble metal (Pt, RuO₂, Pd, etc.) nanoparticles (NPs) as low as 1.5 nm in size and metal loading down to 0.1 mg metal/cm² [5-9]. Despite this tremendous progress, further improvement in metal utilization for practical advancement of EPOC is essential.

In the present work, we investigated EPOC of bi-metallic, highly dispersed Ni₉₀Pd₁₀ and Ru₄₅Fe₅₅ (at. %) nanoparticles for two environmentally important reactions: CH₄ combustion and CO₂ hydrogenation. Both CH₄ and CO₂ are greenhouse gases that have negative impact on the environment and contribute to climate change, therefore methane conversion to CO₂ and CO₂ transformed to useful chemicals have several advantages. Ni₉₀Pd₁₀ and Ru₄₅Fe₅₅ NPs were synthesized using polyol reduction method by using ethylene glycol as reducing and stabilizing agent. TEM/SEM and XRD analysis were carried out to determent the particle and crystallite size, as well as alloy formation in bi-metallic NPs. The resulting colloidal solution containing NPs were deposited on yttria-stabilized zirconia (8 mol % Y₂O₃-ZrO₂, (YSZ)) solid-electrolyte disk (D = 19 mm, thickness = 1 mm) with loading of 0.2 - 0.3 mg metal/cm² and served as a catalyst-working electrode. Inert gold counter and pseudo-reference electrode were deposited on the opposite side of YSZ disk. Gold mesh served a current collector for NPs. The solid-electrolyte cell was placed in the CSTR-type quartz reactor (atm. pressure) [9] for CH₄ combustion (T = 400 – 500 ^oC) and CO₂ hydrogenation (T = 275 – 400 ^oC) reactions. Galvanostatic and potentiostatic EPOC transient experiments were carried out under various gas compositions and temperatures. The EPOC results on bi-metallic nanoparticles will be presented and the role of Ni and Fe on the catalytic activity and EPOC efficiency will be discussed.

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