The classic models of metal electrode-electrolyte interfaces generally focus on either covalent interactions between adsorbates and solid surfaces or on long-range electrolyte-metal electrostatic interactions. Here we demonstrate that these traditional models are insufficient. To understand electrocatalytic trends in the oxygen reduction reaction (ORR), the hydrogen oxidation reaction (HOR) and the oxidation of methanol on platinum surfaces in alkaline electrolytes, non-covalent interactions must be considered. We find that non-covalent interactions between hydrated alkali metal cations M(+)(H(2)O)(x) and adsorbed OH (OH(ad)) species increase in the same order as the hydration energies of the corresponding cations (Li(+) >> Na(+) > K(+) > Cs(+)) and also correspond to an increase in the concentration of OH(ad)-M(+)(H(2)O)(x) clusters at the interface. These trends are inversely proportional to the activities of the ORR, the HOR and the oxidation of methanol on platinum (Cs(+) > K(+) > Na(+) >> Li(+)), which suggests that the clusters block the platinum active sites for electrocatalytic reactions.

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The slow rate of the oxygen reduction reaction in the phosphoric acid fuel cell is the main factor limiting its wide application. Here, we present an approach that can be used for the rational design of cathode catalysts with potential use in phosphoric acid fuel cells, or in any environments containing strongly adsorbing tetrahedral anions. This approach is based on molecular patterning of platinum surfaces with cyanide adsorbates that can efficiently block the sites for adsorption of spectator anions while the oxygen reduction reaction proceeds unhindered. We also demonstrate that, depending on the supporting electrolyte anions and cations, on the same CN-covered Pt(111) surface, the oxygen reduction reaction activities can range from a 25-fold increase to a 50-fold decrease. This behaviour is discussed in the light of the role of covalent and non-covalent interactions in controlling the ensemble of platinum active sites required for high turn over rates of the oxygen reduction reaction.

LETTERfactor. 19 A hexagonal unit cell of a = b = 2.775 Å and c = 6.797 Å, where c-axis) Pt [111], was used in our measurements and analysis for convenience.' ASSOCIATED CONTENT b S Supporting Information. Details on the specular rod data and fitting as well as the resonance scattering data and fitting. This material is available free of charge via the Internet at http://pubs.acs.org.

The effect of side-chain structures in perfluoro-sulfonic acid ionomers on the adsorption of the terminal sulfonate moiety on the surface of Pt is investigated with voltammetry and surface-enhanced infrared absorption spectroscopy (SEIRAS). Analyses with lowmolecular-weight model anions with and without an ether group in the perfluoro-alkyl chain indicate that the anions are adsorbed on Pt through one or two oxygen atom(s) of the terminal sulfonate group and that the oxygen atom of the ether group also interacts with the Pt surface, leading to stronger adsorption of the anions with an ether group. On the basis of the results obtained with the model anions, the adsorption of the terminal sulfonate moieties in perfluorinated sulfonic acid ionomers and its effect on oxygen reduction reaction (ORR) is discussed. It is shown that the ionomers having longer side chains more strongly block ORR due to the flexibility of the side chains.

A first principles-based mean field model was developed for the oxygen reduction reaction (ORR) taking account of the coverage- and material-dependent reversible potentials of the elementary steps. This model was applied to the simulation of single crystal surfaces of Pt, Pt alloy and Pt core-shell catalysts under Ar and O(2) atmospheres. The results are consistent with those shown by past experimental and theoretical studies on surface coverages under Ar atmosphere, the shape of the current-voltage curve for the ORR on Pt(111) and the material-dependence of the ORR activity. This model suggests that the oxygen associative pathway including HO(2)(ads) formation is the main pathway on Pt(111), and that the rate determining step (RDS) is the removal step of O(ads) on Pt(111). This RDS is accelerated on several highly active Pt alloys and core-shell surfaces, and this acceleration decreases the reaction intermediate O(ads). The increase in the partial pressure of O(2)(g) increases the surface coverage with O(ads) and OH(ads), and this coverage increase reduces the apparent reaction order with respect to the partial pressure to less than unity. This model shows details on how the reaction pathway, RDS, surface coverages, Tafel slope, reaction order and material-dependent activity are interrelated.

The catalyst poisoning property of a novel ionomer, NBC4, which has two sulfonimide acid groups in its side chain ended with a perfluorobutane, instead of sulfonic acid groups as Nafion does, was theoretically and experimentally compared with that of Nafion. A density functional theory combined with a continuum electrolyte theory showed that the adsorption is weaker for sulfonimide anion than for sulfonate anion on Pt (111) surface. Electrochemical measurements using Pt (111) surfaced single crystal electrodes covered with the ionomer films showed the weaker anion adsorption and higher ORR activity by ca. 50% at 0.82 V vs the reversible hydrogen electrode for NBC4 than for Nafion.) unless CC License in place (see abstract). ecsdl.org/site/terms_use address. Redistribution subject to ECS terms of use (see 131.215.225.9 Downloaded on 2015-06-21 to IP ) unless CC License in place (see abstract). ecsdl.org/site/terms_use address. Redistribution subject to ECS terms of use (see 131.215.225.9 Downloaded on 2015-06-21 to IP ) unless CC License in place (see abstract). ecsdl.org/site/terms_use address. Redistribution subject to ECS terms of use (see 131.215.225.9 Downloaded on 2015-06-21 to IP ) unless CC License in place (see abstract). ecsdl.org/site/terms_use address. Redistribution subject to ECS terms of use (see 131.215.225.9 Downloaded on 2015-06-21 to IP

In recent years, considerable research and development efforts are devoted to improving the performance of polymer electrolyte fuel cells. However, the power density and catalytic activities of these energy conversion devices are still far from being satisfactory for large-scale operation. Here we report performance enhancement via incorporation, in the cathode catalyst layers, of a ring-structured backbone matrix into ionomers. Electrochemical characterizations of single cells and microelectrodes reveal that high power density is obtained using an ionomer with high oxygen solubility. The high solubility allows oxygen to permeate the ionomer/catalyst interface and react with protons and electrons on the catalyst surfaces. Furthermore, characterizations of single cells and single-crystal surfaces reveal that the oxygen reduction reaction activity is enhanced owing to the mitigation of catalyst poisoning by sulfonate anion groups. Molecular dynamics simulations indicate that both the high permeation and poisoning mitigation are due to the suppression of densely layered folding of polymer backbones near the catalyst surfaces by the incorporated ring-structured matrix. These experimental and theoretical observations demonstrate that ionomer’s tailored molecular design promotes local oxygen transport and catalytic reactions.