Papers by Keyword: ORR

Abstract: Metalloporphyrin-based nanostructures were fabricated on 3-aminopropylmethoxysilane-modified indium tin oxide (ITO) surface. UV-visible spectroscopy and cyclic voltammetry are used for investigating electronic absorption spectra and catalytic activity in oxygen reduction reactions as alternative cathode electrochemical catalysts for polymer electrolyte membrane fuel cells (PEMFCs). Using of 5,10,15,20-tetrakis-(4-amiophenyl)-porphyrin-Co (II) as a building block and 1,4-phenylene diisocyanate as a linker, the mixed toluene/chloroform solution-based layer-by-layer process can produce linear growth of 5,10,15,20-tetrakis-(4-amiophenyl)-porphyrin-Co (II) up to 30 layers through urea bonds. The vacuum thermal annealing process demonstrated the improvement of catalytic activity in oxygen reduction reaction.

Abstract: Synthesis and electrochemical characterization of carbon supported platinum nanoparticles dispersed over Nafion-Polyethylene glycol bipolymeric nanocomposite film (Pt/VC/NP) was attempted for catalyzing the oxygen reduction reaction (ORR) in sulfuric acid medium. The nanocomposite films were surface characterized using Scanning electron microscope, X-ray diffraction pattern, X-ray fluorescence spectroscopy and Atomic force microscopy analyses. The electrochemical behavior was studied using cyclic voltammetry and linear scan voltammetry under static and hydrodynamic conditions to check the catalytic ability of the electrocatalyst films towards ORR. A good correlation was seen between the conductivity of the nanocomposite films from electrochemical impedance spectroscopy and the ORR activity. The higher ORR activity was obtained with the onset potential of 1.08 V vs. RHE and the limiting current density of 1.65 mA/cm² for 40 wt. % Pt/VC/NP catalyst film. The ORR kinetic and thermodynamic parameters were calculated and compared with standard Pt/C literature values.

Abstract: Fuel cells, as devices for direct conversion of the chemical energy of a fuel into electricity by electrochemical reactions, are among the key enabling technologies for the transition to a hydrogen-based economy. Among the various types of fuel cells, polymer electrolyte membrane fuel cells (PEMFCs) are considered to be at the forefront for commercialization for portable and transportation applications because of their high energy conversion efficiency and low pollutant emission. Cost and durability of PEMFCs are the two major challenges that need to be addressed to facilitate their commercialization. The properties of the membrane electrode assembly (MEA) have a direct impact on both cost and durability of a PEMFC. An overview is presented on the key components of the PEMFC MEA. The success of the MEA and thereby PEMFC technology is believed to depend largely on two key materials: the membrane and the electro-catalyst. These two key materials are directly linked to the major challenges faced in PEMFC, namely, the performance, and cost. Concerted efforts are conducted globally for the past couple of decades to address these challenges. This chapter aims to provide the reader an overview of the major research findings to date on the key components of a PEMFC MEA.

Abstract: The Mn-doped pyrochlores Pb2Ru1.5Mn0.5O7- (PRMns) samples were synthesized by a precipitation method, followed by heat-treatments at temperatures of 300-800oC. Effects of the heat-treatments on their electrocatalytic activities for oxygen reduction reaction (ORR) were examined by semi-steady state voltammetry with a rotating ring-disk electrode in 0.1 M KOH solution at 70oC. The PRMns showed the best ORR activity for the 500oC-heat-treated PRMn. The onset potential of the ORR current was over 1.0 V vs RHE, and the efficiency of 4-electron reduction was almost 100%. The maximum in the ORR activity for the 500°C-heat-treated PRMn resulted from a trade-off effect between their crystallinity and specific surface areas.

Abstract: The trirutile oxides MTa2O6 (M=Co,Ni,Mg) [MTs] and the substitution products M1-xNxTa2-yLyO6 (N=Mn, L=Sn,Ti,Zr) [M1-xNxTa2-yLy] were prepared by a conventional solid-state reaction. The oxygen reduction reaction (ORR) activities were evaluated with the onset potentials (Eon) of the ORR currents, the disk current densities (iD) and the efficiencies (Eff4) of 4-electron reduction, measured by a rotating ring-disk electrode (RRDE) technique. All the samples showed ORR activities and the Eon values were around +0.8 V vs. RHE in 0.1 M KOH. The CoTa2O6 electrocatalyst showed the best ORR property of the MTs samples: its Eff4 value was as high as ~80%. With substitution of Ti or Sn, the ORR activities of MgTa1.9T0.1O6, CoTa1.8Sn0.2O6 and NiTa1.9Ti0.1O6 were improved in alkaline solution, compared with those of MTa2O6. In acid solution, the same substitution of Ti and Sn resulted in improvement of Eff4, but no significant improvements of Eon and iD.