The loss of sulfur cathode material as a result of polysulfide dissolution causes significant capacity fading in rechargeable lithium/sulfur cells. Here, we use a chemical approach to immobilize sulfur and lithium polysulfides via the reactive functional groups on graphene oxide. This approach enabled us to obtain a uniform and thin (around tens of nanometers) sulfur coating on graphene oxide sheets by a simple chemical reaction-deposition strategy and a subsequent low-temperature thermal treatment process. Strong interaction between graphene oxide and sulfur or polysulfides enabled us to demonstrate lithium/sulfur cells with a high reversible capacity of 950-1400 mA h g(-1), and stable cycling for more than 50 deep cycles at 0.1C (1C = 1675 mA g(-1)).

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The electrocatalytic activity of well-characterized Pt-Ru alloy electrodes toward the electrooxidation of CO in acidic electrolyte at room temperature was measured on alloy surfaces prepared in UHV (ultrahigh vacuum).Clearly defined surface composition was determined via LEIS (low-energy ion scattering). Electrocatalytic activities were measured by CO stripping voltammetry as well as by potentiostatic oxidation of adsorbed CO.It was found that the property of Ru atoms to nucleate oxygen-containing species at low potentials produced a strong enhancement in the catalytic activity of sputter-cleaned Pt-Ru alloy electrodes compared to pure Pt, thereby supporting the concept of the bifunctional character of the oxidation process of these alloys. A further synergistic effect of the alloy with a Ru surface composition of 4 0 atom % Ru was observed, with a catalytic shift in the CO electrooxidation current of -0.25 and -0.15 V compared to those of pure Pt and pure Ru surfaces, respectively. This synergism was attributed to a uniquely active state of OH& on Pt-Ru pair sites. The different electrocatalytic activities of sputter-cleaned uersus annealed Pt-Ru alloy electrodes with essentially identical Ru surface compositions are discussed in terms of Ru clustering during annealing.

The kinetics of methanol electro‐oxidation on well‐characterized Pt‐Ru alloy surfaces were measured in sulfuric acid solution as a function of temperature. The alloy surfaces were prepared in ultrahigh vacuum with the surface composition determined by low energy ion scattering. It was found that the activity of Ru towards the dissociative adsorption of methanol is a strong function of temperature. This change in the adsorptive nature of the Ru sites with temperature produced a variation in the optimum surface composition with temperature. The optimum surface had an Ru content which increased with increasing temperature, from close to ≈10 atomic percent (a/o) Ru at 25°C to a value in the vicinity of ≈30 a/o at 60°C. The shift in optimum composition with temperature was attributed to a shift in the rate‐determining step from methanol adsorption/dehydrogenation at low temperature to the surface reaction between the dehydrogenated intermediate and surface oxygen at high temperature. The apparent activation energies were consistent with this change in the rate‐determining step.