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A Pt-Au alloy catalyst of varying compositions is prepared by codeposition of Pt and Au nanoparticles onto a carbon support to evaluate its electrocatalytic activity toward an oxygen reduction reaction (ORR) with methanol tolerance in direct methanol fuel cells. The optimum atomic weight ratio of Pt to Au in the carbonsupported Pt-Au alloy (Pt-Au/C) as established by cell polarization, linear-sweep voltammetry (LSV), and cyclic voltammetry (CV) studies is determined to be 2:1. A direct methanol fuel cell (DMFC) comprising a carbon-supported Pt-Au (2:1) alloy as the cathode catalyst delivers a peak power density of 120 mW/cm 2 at 70 °C in contrast to the peak power density value of 80 mW/cm 2 delivered by the DMFC with carbonsupported Pt catalyst operating under identical conditions. Density functional theory (DFT) calculations on a small model cluster reflect electron transfer from Pt to Au within the alloy to be responsible for the synergistic promotion of the oxygen-reduction reaction on a Pt-Au electrode.

A new class of corrosion inhibitors, namely, polyamino-benzoquinone (PAQ) has been synthesized and its inhibiting action on the corrosion of mild steel in 1N H2SO, and 1N HC1 has been investigated by various corrosion monitoring techniques. A preliminary screening of the inhibition efficiency of the polymer was carried out by self corrosion studies. PAQ is found to behave better in 1N H2SO, than 1N HC1. Potentiodynamic polarization studies clearly reveal the fact that PAQ is a mixed-type inhibitor. PAQ is able to reduce considerably the permeation current through the steel surface in both the acids. Changes in impedance parameters (R~t and C~) are indicative of adsorption of PAQ on the metal surface leading to the formation of a protective film which grows with increasing exposure time. The adsorption of this polymer is also found to obey Temkin's adsorption isotherm in both acids thereby indicating that the main process of inhibition is by adsorption. UV spectral studies were also carried out to establish the actual mechanism of inhibition of corrosion.

Nafion-silica composite membranes are fabricated by embedding silica particles as inorganic fillers in perfluorosulfonic acid ionomer by a novel water hydrolysis process. The process precludes the use of an added acid but exploits the acidic characteristic of Nafion facilitating an in situ polymerization reaction through a sol-gel route. The use of Nafion as acid helps in forming silica/siloxane polymer within the membrane. The inorganic filler materials have high affinity to water and assist proton transport across the electrolyte membrane of the polymer electrolyte fuel cell ͑PEFC͒ even under low relative humidity ͑RH͒ conditions. In the present study, composite membranes have been tested in hydrogen/oxygen PEFCs at varying RH between 100 and 18% at elevated temperatures. Attenuated total reflectance-Fourier transform infrared spectroscopy and scanning electron microscopy studies suggest an evenly distributed siloxane polymer with Si-OH and Si-O-Si network structures in the composite membrane. At the operational cell voltage of 0.4 V, the PEFC with an optimized silica-Nafion composite membrane delivers a peak power density value five times higher than that achievable with a PEFC with conventional Nafion-1135 membrane electrolyte while operating at a RH of 18% at atmospheric pressures. The polymer electrolyte fuel cell ͑PEFC͒ is an attractive power source for a variety of applications 1 due to its high efficiency and environment-friendly characteristics. The current PEFC technology utilizes perfluorosulfonic acid ͑PFSA͒ polymer membranes, e.g., Nafion, as electrolyte and hence is limited to low-temperature applications. In order to realize the optimum PEFC performance, the Nafion membrane needs to be fully wet as the proton conduction in Nafion relies on the dissociation of protons from the constituent SO 3 H groups in the presence of water.2 However, the performance of PEFCs is enhanced at elevated temperatures by improved kinetics of the cathode and anode reactions and the reduction in adsorption of poisoned species such as CO. [3][4][5][6] To this end, Nafion-composite membranes suitably modified with ceramic/inorganic fillers, namely SiO 2 , TiO 2 , ZrO 2 , etc., are widely used 7-13 to facilitate proton conductivity in the membranes at elevated temperatures even under low relative humidity ͑RH͒ conditions. Watanabe et al. 14 have employed modified Nafion membrane fabricated by incorporating nanosized particles of SiO 2 , TiO 2 , Pt, Pt-SiO 2 , and Pt-TiO 2 to alleviate the humidification requirements of PEFCs. When operated under low humidification, PEFCs with an alternative membrane reportedly exhibited lower ohmic drops in relation to Nafion. In situ platinum particulates with sorption of the water produced on the incorporated oxide fillers attribute such an improvement accompanied with suppression of hydrogen crossover. The benefits of these composite membranes appear to be in the steady operation of PEFCs at about 130°C due to the higher rigidity of the membranes in relation to commercial Nafion membra...

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Acidic polyvinyl alcohol/polyacrylic acid blend hydrogel electrolytes ͑BHEs͒ were prepared by cross-linking with glutaraldehyde and perchloric acid. These acidic BHEs were treated suitably to realize alkaline and neutral BHEs. Amorphicity of BHEs was followed by differential scanning calorimetry. Ionic conduction in acidic BHEs was found to take place by a Grötthus-type mechanism whereas in alkaline and neutral BHEs it was due to a segmental motion mechanism. Ionic conductivity of BHEs was found to range between 10 −3 and 10 −2 S cm −1 . Electrochemical capacitors assembled with acidic polyvinyl alcohol hydrogel electrolyte yielded a maximum capacitance of ϳ60 and 1000 F g −1 with BP carbon and RuO x ·xH 2 O/C electrodes, respectively.

A membrane with interpenetrating networks between poly͑vinyl alcohol͒ ͑PVA͒ and poly͑styrene sulfonic acid͒ ͑PSSA͒ coupled with a high proton conductivity is realized and evaluated as a proton exchange membrane electrolyte for a direct methanol fuel cell ͑DMFC͒. Its reduced methanol permeability and improved performance in DMFCs suggest the new blend as an alternative membrane to Nafion membranes. The membrane has been characterized by powder X-ray diffraction, scanning electron microscopy, time-modulated differential scanning calorimetry, and thermogravimetric analysis in conjunction with its mechanical strength. The maximum proton conductivity of 3.3 ϫ 10 −2 S/cm for the PVA-PSSA blend membrane is observed at 373 K. From nuclear magnetic resonance imaging and volume localized spectroscopy experiments, the PVA-PSSA membrane has been found to exhibit a promising methanol impermeability, in DMFCs. On evaluating its utility in a DMFC, it has been found that a peak power density of 90 mW/cm 2 at a load current density of 320 mA/cm 2 is achieved with the PVA-PSSA membrane compared to a peak power density of 75 mW/cm 2 at a load current density of 250 mA/cm 2 achievable for a DMFC employing Nafion membrane electrolyte while operating under identical conditions; this is attributed primarily to the methanol crossover mitigating property of the PVA-PSSA membrane. Direct methanol fuel cells ͑DMFCs͒ using a proton exchange membrane have been identified as one of the most promising candidates for portable power applications.1,2 Unlike hydrogen-air polymer electrolyte fuel cells, DMFCs do not require a fuel reformer or a high-volume hydrogen storage system. The membrane electrolyte employed with the DMFC, besides exhibiting a good proton conductivity, should act as a physical separator to prevent fuel crossover from the anode to the cathode. At present, Nafion a perfluorosulfonated membrane with a hydrophobic fluorocarbon backbone and hydrophilic sulfonic acid pendant side chains, happens to be the only commercially available and widely used membrane electrolyte in the DMFC. It has been documented that proton conduction in Nafion occurs through the ionic channels formed by micro-or nanophase separation between the hydrophilic proton exchange sites and the hydrophobic domains.3 However, the methanol crossover from anode to cathode across the Nafion membrane brings about a mixed potential at the cathode causing both the loss of fuel and cell polarization impeding their commercial realization. [4][5][6] It has been reported that even over 40% of methanol could be lost in a DMFC due to crossover across the membrane.7 Methanol crossover across the Nafion membrane can be kept to a minimum by controlling the methanol-feed concentration. Alternatively, membranes that are relatively impermeable to methanol have been employed for this purpose. [8][9][10][11][12] Membranes with a lower methanol permeability allow a higher methanol-feed concentration, enhancing the performance of the DMFC. To optimize fuel cell performance, it is neces...

Polymer electrolyte fuel cells (PEFCs) employ membrane electrolytes for proton transport during the cell reaction. The membrane forms a key component of the PEFC and its performance is controlled by several physical parameters, viz. water up-take, ion-exchange capacity, proton conductivity and humidity. The article presents an overview on Nafion membranes highlighting their merits and demerits with efforts on modified-Nafion membranes.