Electrochemical and physical characterisation of Pt-nanocluster activated molybdenum carbide derived carbon electrodes

Oxygen electroreduction (ORR) on Pt-nanoclusters activated electrodes, based on different microporous-mesoporous carbon supports, were studied in 0.5 M H2SO4 solution using cyclic voltammetry, rotating disc electrode (RDE), and impedance methods. The C(Mo2C) carbon supports with variable specific surface area, microporosity-mesoporosity, good electrical conductivity and corrosion stability at positive potentials were prepared from Mo2C at 600 degrees C and 800 degrees C using chlorination synthesis method. Pt-nanoclusters were deposited onto/into carbons using sodium borohydride reduction method. XRD, XRF, XPS, SEM-EDX, and HRTEM data confirm that catalysts under study are free from chlorine, chloride ions, and other residuals of raw materials, and have highly porous hierarchical structure with homogenously dispersed Pt-nanoclusters. RDE data show that the kinetic current densities are higher and half-wave potentials are more positive for Pt-C(Mo2C)800 degrees C than for Pt-C(Mo2C)600 degrees C in 0.5 M H2SO4 solution. The limiting diffusion currents are independent of the catalyst composition used due to the proceeding of ORR process in the outer-diffusion mode. Analysis of impedance data demonstrated nearly capacitive behaviour in low ac frequency region, explained by quick cathodic electroreduction of oxygen followed by slow electrical double-layer formation step limited by adsorption of ions and intermediates at/inside microporous-mesoporous C(Mo2C) and Pt-nanocluster modified electrodes. High series and parallel capacitance values (100-250 Fg(-1)) have been established, attractive also for hybrid supercapacitor applications. High frequency series resistance values are higher for more amorphous C(Mo2C)600 degrees C than for C(Mo2C)800 degrees C supported electrode. (C) 2013 Elsevier Ltd. All rights reserved.