Preparation and characterization of a PtRu/C nanocatalyst for direct methanol fuel cells

PtRu/C nanocatalysts were prepared by changing the molar ratio of citric acid to platinum and ruthenium metal salts (CA:PtRu) from 1:1, 2:1, 3:1 to 4:1 using sodium borohydride as a reducing agent. Transmission electron microscopy analysis indicated that well-dispersed smaller PtRu particles (2.6 nm) were obtained when the molar ratio was maintained at 1:1. X-ray diffraction analysis confirmed the formation of PtRu alloy; the atomic percentage of the alloy analyzed by the energy dispersive X-ray spectrum indicated an enrichment of Pt in the nanocatalyst. X-ray photoelectron spectroscopy measurements revealed that 83.34% of Pt and 79.54% of Ru were present in their metallic states. Both the linear sweep voltammetry and chronoamperometric results demonstrated that the 1:1 molar ratio catalyst exhibited a higher methanol oxidation current and a lower poisoning rate among all the other molar ratios catalysts. The CO stripping voltammetry studies showed that the E-TEK catalyst had a relatively higher CO oxidation current than did the 1:1 molar ratio catalyst. Testing of the PtRu/C catalysts at the anode of a direct methanol fuel cell (DMFC) indicated that the in-house PtRu/C nanocatalyst gave a slightly higher performance than did the E-TEK catalyst.     

A glue method for fabricating membrane electrode assemblies for direct methanol fuel cells

We present a simple glue method for fabricating membrane electrode assemblies (MEA) for direct methanol fuel cells (DMFC). Rather than the conventional “dry” hot-pressing method that relies solely on hot-pressing at a high pressure and temperature to form a MEA, the “wet” method developed in this work introduces a binding agent, consisting of Nafion^® solution, between a polymer electrolyte membrane (PEM) and an anode/cathode. The introduced binding agent can provide a better adhesion and stronger binding force between a membrane and an electrode, thereby facilitating a better interfacial contact between the electrode and the Nafion^® membrane, which has been proved by scanning electron microscopy (SEM) analyses to the cross-sectional morphology of the MEA after long-term operation. The cell performance characterization showed the MEA fabricated by the glue method was more stable in cell performance than that fabricated by the conventional hot-pressing method. Cyclic voltammetry (CV) results also demonstrated the MEA fabricated by the glue method exhibited a higher electrochemical surface area (ESA) as a result of the improved interfacial contact between the Nafion^® membrane and the electrodes. Finally, the DMFC with the MEA fabricated by the glue method was characterized by the electrochemical impedance spectroscopy (EIS).     

Magnified expansion and compression of subpicosecond pulses from afrequency-doubled Nd:YLF laser

Pulses from a mode-locked frequency-doubled Nd:YLF laser have been spectrally broadened and subsequently expanded to more than 200 ps and recompressed to 750 fs by grating compressors with magnifying telescopes. The design magnifies the time delay dispersion to a factor 10 times larger than achievable with standard compressors of similar size. The design of the system and its sensitivity to the variations in the position of its optical components is analyzed. The scheme allows efficient amplification of subpicosecond pulses in dye amplifiers     

Preparation and the physical/electrochemical properties of a Pt/C nanocatalyst stabilized by citric acid for polymer electrolyte fuel cells

Pt/C nanocatalysts were prepared by the reduction of chloroplatinic acid with sodium borohydride, with citric acid as a stabilizing agent in ammonium hydroxide solution. These nanocatalysts were obtained by altering the molar ratio of citric acid to chloroplatinic acid (CA/Pt) from 1:1, 2:1, 3:1 to 4:1. Transmission electron microscopy and X-ray diffraction analyses indicated that the well-dispersed Pt nanoparticles of around 3.82 nm in size were obtained when the CA/Pt ratio was maintained at 2:1. X-ray photoelectron spectroscopy measurements revealed that the 2:1, 3:1 and 4:1 molar ratio catalysts had a relatively higher amount of Pt in their metallic state than did the 1:1 molar ratio catalyst. Cyclic voltammetry results demonstrated that the Pt/C nanocatalysts annealed at 400 °C in an N₂ atm provided higher electrocatalytic activity. Among all the molar ratio catalysts, the 2:1 molar ratio catalyst exhibited the largest electrochemical active surface (EAS) area, and its methanol oxidation reaction current was superior to the E-TEK catalyst. The oxygen reduction reaction of the catalysts studied by linear sweep voltammetry and tested in a fuel cell indicated that the catalytic activity of the 2:1 molar ratio catalyst was comparable to that of an E-TEK catalyst.     

A simple method for the synthesis of PtRu nanoparticles on the multi-walled carbon nanotube for the anode of a DMFC

We report the synthesis of PtRu nanoparticles on the multi-walled carbon nanotubes (MWCNTs) by a simple sodium borohydride reduction method. Transmission electron microscopy (TEM) analysis indicated that well-dispersed small (2-3 nm) PtRu particles were formed on the MWCNTs. X-ray diffraction (XRD) analysis confirmed the formation of the PtRu alloy on the MWCNTs. X-ray photoelectron spectroscopy (XPS) measurements revealed that 70.4% Pt and 61.0% Ru are present in their metallic states. Cyclic voltammetry (CV) and chronoamperometry results demonstrated that the PtRu/MWCNT synthesized by this method exhibited a higher methanol oxidation current than did the PtRu/MWCNT synthesized by the more complex method using sodium borohydride as the reducing agent and tetraoctyl ammonium bromide as the stabilizer. Finally, the direct methanol fuel cell (DMFC) performance test showed that the PtRu/MWCNT nanocatalyst used at the anode of the fuel cell yielded higher performance than did the commercial E-TEK PtRu/C catalyst.     

Darzen's glycidic ester condensation reaction on poly(N-vinyl pyrrolidone)

About 38% conversion of carbonyl groups into epoxy functions in the molecular chain of poly(N-vinyl pyrrolidone) using chloracetamide results in the decreased viscosity of the product. De-epoxidation of the epoxy groups introduced shows the most contributing factor towards decreased viscosity is epoxy function.     

Synthesis of branched carbon nanotubes by carbonization of solid polyvinylidene fluoride fibers

Branched carbon nanotubes (b-CNTs) were synthesized by carbonization of polyvinylidene fluoride (PVDF) fibers containing a Pt catalyst. The solid fibrous polymer converted into carbon nanotubes with simultaneous growth of branches on the surface of the tubes during carbonization. The Pt particles were expected to decompose PVDF polymer inside the tubes into volatile carbonaceous species leaving a hollow center, and also to act as catalytic sites for the growth of carbon branches. The resulting b-CNTs had a high degree of graphitization and a large electrochemical surface area, and also showed a possibility as a supporting material for electrocatalysts.     

CW silver ion laser with electron beam excitation

A continuous-wave (CW) laser power of 140 mW was obtained in the 840.39-nm transition of Ag II by electron-beam excitation. The electron-beam excited metal-vapor ion laser is capable of operating using metals with high vaporization temperatures, and is of interest for generation of CW coherent radiation in th 220-260-nm spectral region     

Synthesis and Pyrolysis-Field Ionization Mass Spectrometric Study of an Aromatic Polyamide Having Azo Group in the Main Chain

The reductive coupling of p-nitrobenzoic acid with glucose solution gave 4,4′-azodibenzoic acid and was converted to 4,4′-azodibenzoylchloride using thionyl chloride. This aromatic diacid chloride was condensed with 4,4′-Diaminodiphenyl ether by two different techniques to yield aromatic polyamide. The low temperature polymerization method resulted in comparatively high molecular weight polymer as evidenced by intrinsic viscosity values. The structure of the material was confirmed by IR studies. Detailed pyrolysis-field ionization mass spectral studies carried out indicated two major degradations. In the temperature region (180–200°C), the mass spectrum showed intense peaks at m/z = 166 and 149 which can be explained from the fragmentation of azodicarboxylic acid formed from the polymer. The mass spectrum recorded at 465°C gave clear proof for the structure of the polyamide and also enough evidence was noted for the hydrogenation of the azo group during pyrolysis.     

Fabrication of MEA with hydrocarbon based membranes using low temperature decal method for DMFC

The membrane electrode assembly (MEA) with hydrocarbon (HC) based membranes made by a low temperature decal method has been investigated for the direct methanol fuel cells (DMFCs). The conventional low temperature decal (LTD) transfer method (comprised of three layers; viz., carbon, Nafion bonded electrodes and outer ionomer layers over the decal Teflon substrates) meant for the MEAs made of Nafion type membranes is suitably modified to use with hydrocarbon (HC) based membranes. The modification of conventional LTD method is effected by means of modulating the three-layered structure and optimizing other parameters to facilitate complete transfer of catalyst layers onto the HC membranes. The MEAs prepared by the modified LTD method have yielded 21 % higher DMFC performance compared to that of the MEAs produced by conventional LTD method. The structure and electrochemical properties of the MEAs have been analyzed by the field-emission scanning electron microscopy (FE-SEM) and the electrochemical impedance spectroscopy (EIS).