Supercritical CO2 Deposited Pt-Ir-Co into Carbon Aerogel As a Potential Catalyst for Methanol Oxidation and Oxygen Reduction Reactions
There are several considerations to choose trimetalic PtIrCo alloy as the material of interest. Among them: (i) Pt and Ir in the bulk phase form a stable alloy; (ii) Alloy formation prevents acidic dissolution of transition metal and (iii) Electronic interaction among Pt, Ir and Co in PtIrCo improves electrochemical behavior. In addition, synergistic electrochemical performance of PtIrCo and decrease in binding strength of OH species especially for Pt2IrCo (111) have been observed from recent studies ADDIN EN.CITE ADDIN EN.CITE.DATA [1, 2] . In this context, our work is focused on PtIrCo impregnated into carbon aerogel via supercritical CO2method. The study of structure dependent electrochemical oxidation of methanol and oxygen reduction kinetics is emphasized.
Organic precursors of platinum, iridium and cobalt were used in 2:2:1 ratio in order to impregnate into mesoporous carbon aerogel from Aspen aerogels® in supercritical CO2 vessel at 3000 psi at 80oC. The resultant composite was thermally treated at 600oC and 900oC in inert atmosphere (N2-gas flowing at 100 ml/min) for 1 hour at 10oC/min ramp rate.
Energy dispersive spectrum of as synthesized materials (Fig. 1) shows the relative composition in terms of weight and atomic percentage of Pt, Ir and Co along with scanning electron micrograph image. X-ray diffraction spectrum of as-synthesized catalyst (indicated as PtIrCo/C-SCF in Fig. 2) is compared with that of heat treated materials at 600oC and 900oC. As synthesized materials are mostly amorphous and show partial crystalline phase of PtRuCo along (111). PtIrCo/C catalyst heat treated at 600oC (PtIrCo/C-600oC) improved crystal structure along (111), (220) and (331) planes while PtIrCo/C-900oC forms complete fcc-structure having peaks along (111), (200), (220), (331) and (222) directions. Absence of separate iridium and cobalt peaks confirms the presence of PtIrCo alloy in carbon aerogel.
Morphology of the catalysts from BET surface area analysis and pore size distribution, catalyst structure from TEM study, and X-ray photo-electron spectroscopy (XPS) of the materials will be presented. Electrochemical behavior by means of cyclic voltammetry, linear sweep voltammetry, rotating ring disc electrode (RRDE), CO-stripping, and chronoamperometry in acidic and alkaline media will be discussed. The discussion will specially emphasized on structure dependent electrochemical surface area (ESA), onset potentials for methanol and CO-oxidation, CO-tolerance, ORR over-potential, ORR kinetics regarding 4 electron path, mass activity and specific activity of methanol oxidation and oxygen reduction.
This work is financially supported by NSF EPSCoR grant no: 0903804. Authors would also like to acknowledge partial financial support from Dr. Fong’s group at SDSM&T.
 A. L. Smirnova, Y.-L. Hu, L. Zhang, M. Aindow, P. Menard, P. Singh, et al., "Synthesis of Novel Electrode Materials Using Supercritical Fluids," ECS Transactions, vol. 19, pp. 9-21, 2009.
 R. Loukrakpam, B. N. Wanjala, J. Yin, B. Fang, J. Luo, M. Shao, et al., "Structural and Electrocatalytic Properties of PtIrCo/C Catalysts for Oxygen Reduction Reaction," ACS Catalysis, vol. 1, pp. 562-572, 2011.